Skip to main content


Front. Endocrinol., 18 September 2018
Sec. Experimental Endocrinology
Volume 9 - 2018 |

Progestin and Nuclear Progestin Receptor Are Essential for Upregulation of Metalloproteinase in Zebrafish Preovulatory Follicles

Dong Teng Liu1,2, Nichole J. Carter2, Xin Jun Wu2, Wan Shu Hong1, Shi Xi Chen1* and Yong Zhu1,2*
  • 1State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, China
  • 2Department of Biology, East Carolina University, Greenville, NC, United States

Ovulation requires proteinases to promote the rupture of ovarian follicles. However, the identity of these proteinases remains unclear. In our previous studies using RNA-seq analysis of differential expressed genes, we found significant down-regulation of five metalloproteinases: adam8b (a disintegrin and metalloproteinase domain 8b), adamts8a (a disintegrin and metalloproteinase with thrombospondin motif 8a), adamts9, mmp2 (matrix metalloproteinase 2), and mmp9 in the nuclear progestin receptor knockout (pgr−/−) zebrafish that have failed to ovulate. We hypothesize that these metalloproteinases are responsible for ovulation and are regulated by progestin and Pgr. In this study, we first determined the expression of these five metalloproteinases and adamts1 in preovulatory follicles at different times within the spawning cycle in pgr−/− and wildtype (wt) zebrafish and under varying hormonal treatments. We found that transcripts of adam8b, adamts1, adamts9, and mmp9 increased drastically in the preovulatory follicular cells of wt female zebrafish, while changes of adamts8a and mmp2 were not significant. This increase of adam8b, adamts9, and mmp9 was significantly reduced in pgr−/−, whereas expression of adamts1 was not affected in pgr−/− zebrafish. Among upregulated metalloproteinases, adamts9 mRNA was found to be expressed specifically in follicular cells. Strong immunostaining of Adamts9 protein was observed in the follicular cells of wt fish, and this expression was reduced drastically in pgr−/−. Interestingly, about an hour prior to the increase of metalloproteinases in wt fish, both Pgr transcript and protein increased transiently in preovulatory follicular cells. The results from in vitro experiments showed that adamts9 expression markedly increased in a dose, time and Pgr-dependent manner when preovulatory follicles were exposed to a progestin, 17α,20β-dihydroxy-4-pregnen-3-one (DHP). Taken together, our results provide the first evidence that upregulation of adamts9 occurs specifically in preovulatory follicular cells of zebrafish prior to ovulation. Progestin and its receptor (Pgr) are essential for the upregulation of metalloproteinases.


Ovulation is essential for successful reproduction to occur. In vertebrates, ovulation is triggered by a surge of luteinizing hormone (LH) and mediated by progesterone (P4) (15). Ovulation also requires upregulation of proteolytic enzymes (6). These proteinases promote the rupture of follicles releasing mature oocytes. Studies have shown correlations between increased expression of proteolytic enzymes and elevated levels of P4 or its receptor (a.k.a. the progestin receptor, PGR). For instance, induction of transcripts of Adamts1 (a disintegrin and metalloproteinase with thrombospondin motifs 1) by human chorionic gonadotropin (hCG), a popular substitute for LH, was reduced in PGR knockout (Pgr−/−) mice (7). A synthetic PGR agonist, R5020, could reverse the inhibitory effect of mifepristone (RU486) on the LH induced expression of ADAMTS1 and ADAMTS9 mRNA in granulosa cells of cattle (8). In a teleost medaka, mmp15 (matrix metalloproteinase 15) was found to be upregulated by Pgr within LH exposed follicles (9). Further, plasminogen activator and several other MMPs were also reported to be regulated by PGR during ovulation (3, 10, 11). Though the relationships between PGR and these proteases have implicated their involvement in the ovulation process, our knowledge of the regulation and functions of these proteases is extremely limited. So far, knockout studies of these metalloproteinases in mice have provided little information on the functions of these proteases, mainly due to null mice either dying in utero or exhibiting no observable defects (1216). One exception is ADAMTS1 knockout mice that were found to be sub-fertile, but ultimately they were still able to ovulate (17). By comparison, anovulatory PGR knockout mice were completely infertile (18). Furthermore, ADAMTS1 is not expressed in cumulus cells (19), ADAMTS1 gene does not have P4 receptor response element (20) and is believed not to be regulated by Pgr in high mammalian species (personal communication). These studies suggest that there may be critical protease(s) other than ADAMTS1 necessary for ovulation that has not yet been identified.

Zebrafish is an established model for studying gene functions and signaling pathways in conserved ovarian events such as oogenesis, oocyte maturation, and ovulation (2123). Our previous results show that pgr−/− female zebrafish were unable to ovulate demonstrating the conserved function of Pgr in ovulation from fish to mice (18, 24, 25). Furthermore, compared to pgr−/− zebrafish, a genome-wide analysis of transcripts revealed conserved signaling pathways and higher expression levels for adamts8a, adamts9, mmp2, mmp9, and adam8b (a disintegrin and metalloproteinase domain 8b) in the follicular cells of wildtype (wt) fish (26). We hypothesized that some of these genes are likely obligatory for follicular rupture and ovulation in zebrafish. In this study, we aimed to elucidate the expression and hormonal regulation of these proteinases in zebrafish ovarian follicles. We first determined the expression changes of five abovementioned metalloproteinases and adamts1. We found dramatic increases of adam8b, adamts1, adamts9, and mmp9 in the follicular cells prior to ovulation. Interestingly, expression of adamts9, adam8b, and mmp9 were significantly reduced in pgr−/− fish, whereas that of adamts1 was not affected. Then, we found that 17α,20β-dihydroxy-4-pregnen-3-one (DHP) stimulated adamts9 expression in preovulatory follicles in a dose, time and Pgr-dependent manner. Our study suggests progestin and Pgr are critical for the upregulation of metalloproteinases prior to ovulation in zebrafish.

Materials and Methods

Zebrafish Husbandry

The wt zebrafish used in this study are a Tübingen strain initially obtained from the Zebrafish International Resource Center and propagated in our lab. Pgr gene knockout lines used in this study were generated and characterized previously (24, 27). Fish were kept under a photoperiod of 14 h (h) light and 10 h dark (lights on at 09:00, lights off at 23:00), at a water temperature around 28.5°C, pH ~7.2, and salinity conductivity ranging from 500 to 1,200 μS in automatically controlled zebrafish rearing systems (Aquatic Habitats Z-Hab Duo systems, Florida, USA). Fish were fed three times daily to satiation with a commercial food (Otohime B2, Reed Mariculture, CA, USA) containing high protein content and supplemented with newly hatched brine shrimp Artemia (Brine Shrimp Direct, Utah, USA). The Institutional Animal Care and Use Committees (IACUC) at both Xiamen University and East Carolina University have approved all experimental protocols.

Collection of Stage I–IV Follicles

Thirty mature females from wt or pgr−/− were collected at 08:00 (1 h before lights turned on) from group housed tanks in conditions described as in section Zebrafish Husbandry. These fish were deeply anesthetized in a lethal dose of MS-222 (300 mg/L buffered solution) for 10 min. To ensure death, the spinal cord and blood supply behind the gill cover were cut off using sharp scissors. Ovaries were removed immediately and placed in a 90-mm petri dish containing 60% L-15 media (Sigma, in 15 mM HEPES, pH 7.2). Thereafter, ovaries were cut into ~4 mm3 pieces, and then transferred to a 15-ml centrifuge tube. Individual oocytes were separated by pipetting up and down using a disposable glass pipette with a polished 3 mm opening. Hereafter, we will use “follicles” to specifically refer to follicular cells and their enclosed oocytes to distinguish them from follicular cells or defolliculated oocytes (i.e., denuded oocytes). Individual follicles of various sizes (Table 1) were separated into five stages according to an established oocyte classification system in zebrafish with modification (28). We further subdivided stage IV follicles into two stages, immature stage IVa (before germinal vesicle breakdown, i.e., GVBD) and mature stage IVb (after GVBD has occurred but prior to ovulation). Though the outside appearance of stage IVb follicles is transparent, same as stage V, distinguishing stage IVb follicles from stage V mature ova is straightforward since stage IVb mature follicles are scattered around the ovary, surrounded by follicular cells and other immature follicles. Whereas, stage V ovulated oocytes are grouped together and pushed to the posterior part of the ovary in vivo (26). Stage V ovulated oocytes were not collected for two reasons: (1) Our targeted genes are expressed mainly in the follicular cells, and stage V mature oocytes do not have follicular cells; (2) It was not possible to collect stage V oocytes from pgr−/− fish due to their inability to ovulate.


Table 1. Classification of different developmental stages of zebrafish follicles.

Collection of Follicular Cells and Denuded Oocytes From Stage IV Follicles During a Spawning Cycle

In group housing conditions, zebrafish skip spawning frequently in part due to intense competition for space and food. To increase and monitor individual spawning, we set up multiple spawning tanks with a pair of approximate 3-month old mature male and female wt fish for each tank. Everyday around 22:00 (1 h prior to lights off), water in spawning tanks was replaced with clean water along with an inner tank insert that allows fertilized eggs to drop through to the bottom to prevent the eating of the eggs by the adults. Spawning and release of fertilized eggs (~150 embryos/day) were visually confirmed and recorded for each pair of fish every morning. At 12:00, fish were transferred to a new spawning tank with clean water but without an insert, so they could access the commercial fish food and newly hatched brine shrimp. Fish food and brine shrimp were supplemented every 3 h. In this setup and enhanced feeding condition, the majority of the pairs (7–8 out of 10 pairs) spawn almost daily.

At 1 week following the setup of spawning, the mature female zebrafish of the pairs were sacrificed, their ovaries removed, and stage IV follicles were collected as described in section Zebrafish Husbandry. Stage IV follicles from wt fish were collected at four different time points: 13:00 (stage IVa, from fish that skipped spawning that morning); 21:00 (stage IVa, 2 h before lights off); 06:00 (stage IVa, onset of oocyte maturation and 3 h before lights on); and 08:00 (stage IVb, after oocytes have matured but before ovulation, 1 h before lights on). To determine the effect of Pgr knockout, stage IVb follicles at 08:00 were also collected from 3-month old virgin female pgr−/− fish that were paired with fertile wt male at the same time. Follicular cells (collected from ~100 follicles/fish) and their enclosed oocytes (collected from ~10 follicles/fish) were separated from stage IV follicles using a pair of small glass needles. Respective samples were pooled and homogenized immediately in RNAzol solution according to an established procedure (26, 29).

Various Hormone Treatments of Stage IVa Fully-Grown Immature Follicles in vitro

Stage IVa follicles (>650 μm) with visible germinal vesicles (GV) were collected from females at ~05:30. Briefly, intact follicles with no obvious damage were selected and transferred into a 24-well tissue culture plate containing 60% L15 medium (25 follicles per well). These follicles were incubated for 2.5 h at 25°C with DHP (1–1,000 nM), testosterone (T, 500 nM), or RU486 (0.01–10 μM), alone or in combination. An exposure time of 2.5-h was selected to conduct the various hormone treatment based on results from our time course experiments (up to 6 h). Follicles that underwent final oocyte maturation, indicated by transparent yolk and GVBD, were easily determined under a dissecting microscope at the end of incubation. Excluding broken follicles, the number of transparent follicles that completed GVBD were counted and presented as a percentage of the total follicles. Thereafter, all the follicles were collected and homogenized immediately in RNAzol for qPCR analyses of gene expression, or in 1X SDS sample buffer for Western blot analyses of protein expression.

RNA Extraction, Reverse Transcription, and Real-Time Quantitative PCR

Total RNA was extracted using RNAzol (MRC, Cincinnati, Ohio, USA) and a Qiagen RNeasy kit. According to the manufacturer's protocol, BAN solution (4-bromoanisole) was added to purify the RNA and eliminate genomic DNA following the first precipitation step with water. After the second precipitation, an equal volume of cold 100% ethanol was added. The mixture was then loaded onto a RNeasy free spin column, centrifuged (8,000 g, for 30 s), washed twice with 650 μL 75% ethanol, and eluted in RNase-free water. We used 15–30 μL depending on the initial amount of sample. The approximate concentration and purity of samples were determined using a Nanodrop 2000 Spectrophotometer. RNA samples with concentrations >100 ng/μL, OD 260/280 >1.8, and OD 260/230 >1.3 were retained for further analyses. Reverse transcription was performed using SuperScript III Reverse Transcriptase and 0.5 μg of total RNA from each sample in a reaction volume of 10 μL, per manufacturer's instructions (Invitrogen, Carlsbad, CA). Gene expression was determined by quantitative real time PCR (qPCR) analyses according to previously established protocols (26, 29) using gene specific qPCR primers for targeting genes for adam8b, adamts1, adamts8a, adamts9, mmp2, mmp9, and pgr (Table 2). To avoid genomic DNA contamination, forward and revise primers were designed to be in two different exons of each target gene. Authentic single qPCR product for each gene was confirmed by melting curve analyses, gel electrophoresis, and sequencing. The absolute transcript levels, expressed as copies/μg total RNA, were determined using Ct-values of samples and standard curves corresponding to different target genes generated from known serial plasmid concentrations (102-107 copies/μL). We did not use the comparative Ct method for this study because house-keeping-genes including actb1, actb2, and ef1a vary between different developmental stages of follicles (data not shown).


Table 2. Primers used in the study.

Western Blotting

Total protein was extracted from 10 stage IVa or IVb follicles from newly sacrificed fish at various time points during an ovulatory cycle, or from in vitro incubation. Collected follicles were homogenized immediately by sonication in 100 μl of 1X SDS sample buffer (62.5 mM Tris-Cl pH 6.8, 2% SDS, 10% glycerol, 100 mM Dithiothreitol) with 0.1% protease inhibitor cocktail (Sigma, Saint Louis, MO) on ice for about 10 short bursts (1–2 s for each burst, Sonic Dismembrator, Fisher Scientific). Samples were then boiled immediately for 10 min and stored in −20°C until analysis. Samples were loaded onto an 8% SDS PAGE gel (10 μL is equivalent to one follicle), separated by electrophoresis, and transferred to a nitrocellulose membrane. The membrane was pre-incubated for 2 h with a blocking solution containing 5% BSA (albumin from bovine serum, Sigma-Aldrich Catalog# A7906) in TBST (50 mM Tris, 100 mM NaCl, 0.1% Tween 20, pH 7.4). Then incubated overnight with a primary antibody [zebrafish PGR primary antibody, 1:250 dilution (29); or α-tubulin primary antibody, Sigma catalog#T5168, 1:5,000 dilution] in 1% BSA blocking solution. The following day, the membrane was washed with 1X TBST five times for 5 min each, incubated for 1 h with horseradish peroxidase (HRP) conjugated secondary antibody (goat anti-mouse antibody HRP for α-tubulin, Fisher catalog# PI31430, 1:5,000 dilution; goat anti-rabbit antibody HRP for Pgr, Cell Signaling catalog#7074S, 1:3,000 dilution). Then washed again with TBST buffer five times for 5 min each. The membrane was developed using Super Signal West Extended Dura Substrate (Pierce, Rockford, IL) and visualized using a Fluor Chem 8900 imaging station (Alpha Innotech, San Leandro, CA). Protein size was calibrated using a biotinylated protein ladder (Cell Signaling) and a pre-stained protein ladder (Fermentas).

Immunohistochemistry and Hematoxylin and Eosin (HE) Stain

Two commercial antibodies for human ADAMTS9 were used in the immunohistochemical staining (Triple Point Biologics, Forest Grove, Oregon, USA). These antibodies target domains in human ADAMTS9 that share sequence homology to those in zebrafish adamts9. One antibody, catalog# RP5-ADAMTS-9, targets 44 amino acid residues of metalloprotein domain, and shares 85.7% sequence homology with zebrafish Adamts9. The other antibody, catalog# RP1-ADAMTS-9, targets the 44 amino acid residues of propeptide domain and shares 41% sequence homology with zebrafish Adamts9. Mature ovaries for the studies were collected from wt or pgr−/− fish at 08:00 (1 h prior to lights on) and fixed in 10% buffered formalin for overnight. Samples were washed in tap water for 30 min, dehydrated through increasing concentrations of ethanol, and embedded in paraffin. A series of 8-μm sections were made deparaffined in xylene, rehydrated in decreased concentration of ethanol, then subjected to HE stains (hematoxylin staining for 2 min, rinsed in running tap water for 5 min, and eosin staining for 30 s), or immunohistological staining according to previously established protocols with a few modifications (24, 30). Briefly, sections were deparaffinized sequentially by 5-min treatment with 100% xylene (twice), 100% ethanol (twice), 95% ethanol, 70% ethanol, and PBS (137 mM NaCl, 2.7 mM KCl, 10 mM Na2HPO4·12H2O, 2 mM KH2PO4) twice for each section. Then sections were incubated with 0.1% testicular hyaluronidase (Sigma catalog# H3506, 1 mg/mL in 30 mM sodium acetate, 125 mM sodium chloride, pH 5.2) at 37°C for 1 h for antigen retrieval. Thereafter, sections were washed with PBS twice, then incubated in 0.3% H2O2 for 30 min to reduce endogenous activities of horseradish peroxidase. Following three washes with PBS, sections were blocked with normal goat serum for 30 min, and then incubated with ADAMTS9 primary antibodies (1:1,000 dilution for RP5-ADAMTS-9; 1:250 dilution for RP1-ADAMTS-9) or normal rabbit serum (1:1,000 dilution) overnight. After three washes with PBS, immunoreaction was developed using the Vectastain ABC kit (Vector Laboratories, Burlingame, California) according to the manufacturer's protocol.

Statistical Analyses

For the comparison of two data sets (e.g., wt vs. pgr−/−, or DHP vs. vehicle control), unpaired students' t-test was used to determine significant differences. For multiple group comparison, one-way ANOVA followed by Tukey's test or Dunnett's test was used. All experiments were repeated at least three times, and the results of one representative experiment is shown in the following section.


Changes of Metalloproteinase Expression in Stage I–IV Follicles in Mature Female Zebrafish

We hypothesized that metalloproteinases required for ovulation should be expressed highly in late stage follicles such as stage IVa or IVb follicles. Therefore, we separated follicles according to their sizes and stages, and determined expression of six representative metalloproteinases in early (stage I) through late stage (IVb) follicles (Figure 1). Expression of adamts9 remained at extremely low levels (<300 copies/μg total RNA) and was sometimes undetectable from stage I through stage IVa fully-grown immature follicles; however, its expression increased drastically in stage IVb mature follicles in both wt and pgr−/− fish. This increased expression of adamts9 in pgr−/− (3,000–4,000 copies/μg total RNA) was only one-tenth of that in wt fish (~40,000 copies/μg total RNA). Intriguingly, high expression of adam8b, adamts1, mmp2, and mmp9 were observed in all stages of follicles (>10,000 copies/μg total RNA), whereas expression of adamts8a remained at low levels (<2,000 copies/μg total RNA). Surprisingly, none of these five metalloproteinases (adam8b, adamts1, adamts8a, mmp2, mmp9) showed significant difference in their expression between pgr−/− and wt.


Figure 1. Expression of representative metalloproteinases in various stages of follicles (follicular cells-enclosed oocytes) in wildtype (wt, solid line with filled circles) and Pgr knockout zebrafish (pgr−/−, dashed line with open circles) in vivo. All transcripts were determined and expressed as absolute value according to standard curves established with known concentrations of serially diluted plasmids using real-time quantitative PCR (qPCR). Stages of zebrafish follicles were classified per Selman et al. (28). Stage IV follicles were further sub-divided into stage IVa and stage IVb. Stage IVa follicles were fully-grown immature follicles prior to oocyte maturation. Stage IVb follicles were follicular cells enclosed mature oocytes that have gone through oocyte maturation, but not yet ovulated (also see Table 1 for detail). Different letters (uppercase for wt; lowercase for pgr−/−) indicate significant differences among different follicular stages in wt or pgr−/− fish. Significant differences between wt or pgr−/− fish at the same developmental stage of follicles are indicated by asterisks. *p < 0.05, *****p < 0.00001. N = 6. The metalloproteinases examined were adam8b, a distintegrin and metalloproteinase domain 8b; adamts1, a disintegrin and metalloproteinase with thrombospondin type 1 motif 1; adamts8a; adamts9; mmp2, matrix metalloproteinase 2; and mmp9, matrix metalloproteinase 9, respectively.

Pgr Mediates the Upregulation of Metalloproteinases in Preovulatory Follicular Cells

We then hypothesized that changes of metalloproteinases in late stage follicles, especially in the follicular cells, could be important for ovulation but their activity may be masked by differential expression and/or high levels of metalloproteinase transcripts in large oocytes when entire follicles (follicular cells and their enclosed oocytes) are used. Hence, we focused on changes of transcripts in stage IVa and IVb fully grown follicles. We also separated the follicular cell layers from their enclosed oocytes and determined gene expression in both cell types during the ovulatory cycle in wt female zebrafish (Figure 2). In follicular cells, expression of adam8b, adamts1, adamts9, and mmp9 remained relatively low at most times but increased significantly at about 1 h (08:00) prior to ovulation that occurred at around 09:00 when lights were turned on. The changes of adamts8a and mmp2 transcripts were not significant during the daily spawning cycle. In denuded oocytes, the expression of adamts8a and adamts9 was extremely low and nearly undetectable (<300 copies/μg total RNA). By contrast, expression of adam8b, adamts1, mmp2, and mmp9 in denuded oocytes was relatively high (>5,000 copies/μg total RNA) but did not significantly change during the ovulatory cycle.


Figure 2. Expressions of adam8b, adamts1, adamts9, and mmp9 transcripts significantly increased in stage IV preovulatory follicular cells during a daily spawning cycle in wildtype (wt) fish in vivo. Transcripts of representative metalloproteinases were determined in stage IV follicular cells (solid line with filled circles) or denuded oocytes (dash line with open circles) separately during a daily spawning cycle in wt fish. (A) A schematic drawing showing the daily ovulatory cycle of zebrafish. Day and night cycles are indicated by open or black bars, respectively. Lights were switched on at 09:00 and off at 23:00. Approximate time for daily oocyte maturation, ovulation and spawning in zebrafish are indicated on top of the bar. Samples were collected from four representative time points, indicated by triangles: 13:00 (after spawning), 21:00 (2 h before lights off), 06:00 (prior to oocyte maturation), and 08:00 (after oocyte maturation but prior to ovulation). (B) Expression of representative metalloproteinase transcripts were determined by qPCR. Asterisks indicate a significant increase of transcripts compared to the previous sampling time point in follicular cells (solid line with black circles). No significant change was observed in the denuded oocytes (dash line with open circles). **p < 0.01, ****p < 0.0001. N = 5.

Because the expression of metalloproteinases was upregulated in preovulatory stage IVb follicles (mature but not ovulated follicles) sampled at 08:00, we hypothesized that Pgr is an upstream regulator for these metalloproteinases. We found significantly reduced expression of adam8b, adamts9, and mmp9 in follicular cells of pgr−/− fish compared to those in wt fish (Figure 3). Expression of adamts1 was not affected by Pgr knockout as ADAMTS1 is not regulated by PGR in high mammalian species. In denuded oocytes, the expression of all aforementioned metalloproteinases was not significantly different between wt and pgr−/− fish (data not shown).


Figure 3. Expressions of adam8b, adamts9, and mmp9 were significantly reduced in the follicular cells of preovulatory follicles (stage IVb) in pgr−/− than those in wildtype (wt) in vivo. Transcripts of representative metalloproteinases were determined by quantitative real-time PCR (qPCR) in follicular cells of stage IVb preovulatory follicles (at 08:00) in both wt and pgr−/−. Asterisks indicate significant differences between follicular cells of wt and pgr−/−. *p < 0.05, ****p < 0.0001. N = 6.

Changes of Pgr Expression During Ovulatory Cycle

We hypothesized that upstream regulators of these metalloproteinases, especially Pgr would be upregulated prior to the upregulation of these metalloproteinases. As we predicated, expression of Pgr (transcript and protein) in follicular cells began to increase in the early morning (05:00, prior to maturation), reached a peak level in the middle of maturation (06:00–07:00), then decreased gradually thereafter (Figure 4).


Figure 4. Transient increase of nuclear progestin receptor (Pgr) in follicular cells prior to ovulation in vivo. (A) Changes of pgr transcript. Transcripts were determined by quantitative real-time PCR (qPCR) in the follicular cells of stage IV follicles in an ovulatory cycle in wildtype (wt) zebrafish. Asterisks indicate significant change of transcripts compared to the previous time point. **p < 0.01, ****p < 0.0001. N = 5. (B) Western analysis of Pgr protein expression in stage IV follicles in pgr−/− or wt. Arrow indicates the specific band of zebrafish Pgr at the approximate size of 69 kDa in wt fish. No band was observed in pgr−/−. (C) (Top) Representative images of a Western blot of Pgr proteins from stage IV (IVa or IVb) follicles sampled at various time of a spawning cycle. α-tubulin was used as an internal control for normalization of expression of Pgr protein; (Bottom) normalized Pgr expression at various time compared to Pgr expression at 21:00. Asterisks indicate significant difference compared to the value at 21:00. Experiment was repeated three times with results of one representative experiment presented as mean ± SEM. *p < 0.05. N = 3.

Exogenous DHP Exposure Directly Upregulates adamts9 in Follicles in vitro

To determine if low expression of metalloproteinases found in pgr−/− zebrafish is due to direct effect of progestin and its receptor (Pgr) in the follicular cells, we chose an in vitro oocyte maturation assay (29), and focused on hormonal regulation of adamts9 because only adamts9 meets all following criteria: (1) Expressed specifically in follicular cells but not in the oocytes (Figures 2, 5); (2) Expressed differently between wt and pgr−/− (Figures 2, 3, and 5); and (3) Increases significantly prior to ovulation (Figures 1, 2).


Figure 5. Strong immunostaining of Adamts9 was observed in the follicular cells of wildtype (wt) fish (A). (A) Representative images of a stage IVb follicle stained with hematoxylin and eosin or immunostained with an antibody against metalloproteinase domain of human ADAMTS9 (RP5-ADMTS-9, Triple Point Biologics, Forest Grove, Oregon), (B) Representative images of a stage IVb follicle of Pgr-KO zebrafish fish stained at same time, (C) Negative control, representative images of a stage IVb follicle of wildtype zebrafish fish stained at same time but the primary antibody was replaced with normal rabbit serum. Pictures located on the bottom of panels are magnified images of the areas outlined on the top panels. Immunostaining are shown on the left side of panels, while HE stains of adjacent sections are shown on the right side of panels. Arrows indicate follicular cells. Similar results were obtained when RP1-ADAMTS-9 antibody used (data not shown).

Consistent with expression of adamts9 transcripts, expression of Adamts9 protein was also observed specifically in the follicular cells of zebrafish and was relative high in the follicular cells of wt than in pgr−/− fish in vivo (Figure 5). Exposure of stage IVa follicles to DHP in vitro significantly upregulated adamts9 expression in a dose dependent manner (Figure 6A). The increase of adamts9 correlated well with the occurrence of oocyte maturation in vitro (Figure 6B). DHP-induced adamts9 expression was transient (Figure 6C), peaking at 2 h post incubation with DHP (100 nM) when about 90% of stage IV oocytes had matured (Figure 6D), but then decreased gradually to basal levels after an additional 2 h of in vitro incubation.


Figure 6. Dose- and time-dependent and transient increase of adamts9 in stage IV follicles exposed to progestin in wildtype (wt) zebrafish in vitro. (A,B) Effects of various doses of progestin (17α,20β-dihydroxy-4-pregnen-3-one, DHP) on the expression of adamts9 transcript and oocyte maturation, i.e., germinal vesicle breakdown (GVBD) during in vitro incubation. (C,D) Effects of DHP (100 nM) on adamts9 expression and GVBD at various time points of in vitro incubation. Asterisks indicate significant difference in hormone treated samples compared to vehicle treatment at the same time point. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Experiment was repeated three times with results of one representative experiment presented as mean ± SEM. N = 4.

RU486 Did Not Affect Expression of adamts9 but Triggered Oocyte Maturation in Follicles in vitro

Exposure to the mammalian P4 antagonist, RU486, did not block DHP-induced oocyte maturation (Figure 7A). RU486 also did not inhibit adamts9 expression induced by DHP (Figure 7B). Intriguingly, at a high dosage (10 μM) by itself, RU486 induced oocyte maturation, but had no effect on the expression of adamts9 (Figure 7).


Figure 7. RU486 induced oocyte maturation but did not attenuate DHP-induced expression of adamts9. (A) Percentage of germinal vesicle breakdown (GVBD), (B) Expression of adamts9 transcripts. Letters on the bars indicate significant differences (p < 0.0001). Experiment was repeated three times with results of one representative experiment presented as mean ± SEM. N = 4.

Effect of DHP on the Increased Expression of adamts9 Is Blocked in Pgr−/− Fish in vitro

As expected, DHP-induced oocyte maturation was not impaired in pgr−/− fish (Figure 8A) because DHP signaling is mediated via the membrane progestin receptor (mPR) at the oocyte surface (24, 29, 31, 32). However, DHP-induced expression of adamts9 was completely blocked in pgr−/− fish in vitro (Figure 8B).


Figure 8. Complete inhibition of DHP induced adamts9 expression in stage IVa follicles from Pgr knockout zebrafish in an in vitro incubation indicates a direct regulation of progestin in metalloproteinase. (A) Percentage of germinal vesicle breakdown (GVBD), (B) Expression of adamts9 transcript. White bar, pgr−/−; black bar, wt. Different letters on the bars indicate significant differences (p < 0.05). Experiment was repeated three times with results of one representative experiment presented as mean ± SEM. N = 4.

DHP Downregulates Pgr Protein

Because we observed downregulation of Pgr during oocyte maturation (GVBD) in vivo, we hypothesized this downregulation of receptor is progestin (DHP) specific but not GVBD specific. Therefore, we tested our hypothesis by examining direct effect of DHP, RU486 and T on Pgr expression in an in vitro incubation of follicles. All three steroids induced GVBD in preovulatory follicles (stage IVa) following an 2.5 h in vitro incubation (data not shown). As expected, DHP treatment induced significant reduction of Pgr protein expression, whereas treatments of RU486 or T had no such effect on the expression of Pgr protein, comparable to the vehicle control (Figure 9).


Figure 9. Exposure of exogenous DHP significantly reduced Pgr protein, while RU486 or T exposure had no effect on Pgr protein expression in stage IVa follicles in zebrafish in vitro. (Top) Representative images of a Western blot of Pgr proteins following treatments. (Middle) Representative image of a Western blot analysis of α-tubulin that was used as an internal control for normalization of expression of Pgr protein. (Bottom) Normalized Pgr expression in each treatment compared to vehicle control. Asterisks indicate significant difference compared to vehicle treatment. Experiment was repeated three times with results of one representative experiment presented as mean ± SEM. **p < 0.01.


In the present study, we provide the first evidence that expression of adam8b, adamts1, adamts9, and mmp9 increased drastically within the preovulatory follicular cells of zebrafish, a basal vertebrate model. A significant increase of Pgr was required for this increase. Using follicles from pgr−/− fish, we showed that expression of adamts9, adam8b, and mmp9 was severely reduced in the knockout. One main cause for anovulation in pgr−/− fish is likely due to this dramatically reduced expression of these metalloproteinases, which was caused by the loss of progestin signal in the Pgr knockout fish. Our study indicates a direct regulation of metalloproteinase by progestin and Pgr in preovulatory follicles, which likely is essential for ovulation in zebrafish.

In this study, we found Pgr was expressed throughout the daily ovulatory cycle in late stage follicles and was significantly elevated at the onset of oocyte maturation in zebrafish. This increase of Pgr corresponds to the transient appearance and increase of PGR prior to ovulation in mammals (2, 5, 29, 3335), supporting the idea of conserved regulation and roles for Pgr in vertebrate ovulation (24, 26). Ligand-dependent down-regulation of PGR has been shown in multiple reproductive tissues in mammals (36, 37). This down-regulation of PGR was suggested to be concomitant with its transcriptional hyperactivity (38). In fact, production of DHP in zebrafish ovarian tissue increased significantly at 3.5 h prior to lights turned on (39), which could contribute to the down-regulation of Pgr in zebrafish. In the present study, Pgr protein level was downregulated either in vitro by DHP exposure or in vivo likely by endogenous progestin. Our results support previous studies and indicate that the appropriate Pgr expression in preovulatory follicles is required for the increase of metalloproteinase expression in zebrafish.

Suppression of the stimulatory effect of DHP on metalloproteinase expression in Pgr knockout indicates an indispensable role of Pgr in metalloproteinase expression in zebrafish ovary. Interestingly, expression of adamts9 increased significantly during oocyte maturation in vivo in pgr−/− fish, though the magnitude of increase was greatly reduced in pgr−/− fish in comparison to those in wt fish. It has been suggested that LH and PGR have distinct but coordinate effects on transactivation of the Adamts1 gene in mice granulosa cells (40). Whether gonadotropin stimulates adamts9 and other metalloproteinase expression via Pgr-independent signaling pathway deserves further investigation. An interesting finding from the current study is failure of RU486 in inhibition of Pgr-dependent and DHP induced adamts9 expression. One possible scenario is that RU486 has low or no binding affinity to zebrafish Pgr. A single amino acid substitution of glycine by cysteine in the hormone binding domain (HBD) of the human PGR abrogates binding of RU486 (41). Alignment of the zebrafish Pgr HBD with other species, including humans and chickens, has shown a glycine substitution by cysteine in the zebrafish Pgr (30, 42). Alternatively, instead of acting as an antagonist, RU486 can act as partial agonist (43). Indeed, our study shows that high doses of RU486 can induce oocyte maturation, which suggests that RU486 acts as an agonist of progestin activating mPRα and/or Pgr signaling in zebrafish. Further studies are required for elucidation of actions and molecular mechanisms of RU486 in fish.

Most likely, several proteinases are required for the appropriate remodeling of the extracellular matrix (ECM) and basal membranes that lead to follicular rupture and ovulation in vertebrates. Knockout of PGR, or administration of P4 inhibitors, significantly reduced hCG-induced expression of Adam8 in mice granulosa cells (44). In agreement with this, we observed the expression of adam8b was also dramatically reduced in the follicular cells of pgr−/− zebrafish, suggesting a conserved signaling pathway for the regulation of this metalloproteinase in preovulatory follicular cells. Unfortunately, knockout of Adam8 in mice had no noticeable effect on fertility, which might be due to the overlapping roles of other proteinases as multiple metalloproteinases could target the same substrate (15). MMPs have also been postulated to play critical roles in ECM remodeling associated with ovulation (45). Transcript of MMP9 was elevated in rhesus monkey granulosa cells exposed to LH in vitro (46). Another study also suggested that MMP9 played a critical role in LH-induced steroidogenesis during ovulation in mouse granulosa cells (47). In line with these studies, we found significant increase of mmp9 expression in zebrafish follicular cells prior to ovulation, and this increase was significantly reduced in pgr−/− fish. Increase of Adamts1 transcripts were observed in mice granulosa cells of periovulatory follicles after LH stimulus, but not in small follicles or in denuded oocytes (7). Other studies suggest that ADAMTS1 may cleave versican, a proteoglycan located in the basal follicular region and COC matrix (17). This cleavage of versican promotes changes in the ECM of preovulatory follicle required for the successful ovulation of a fertilizable oocyte in mice. In concert with these findings, our results showed that expression of adamts1 increased remarkably in zebrafish follicular cells after oocyte maturation, supporting its role in ovulation. In human preovulatory granulosa cells, gene expression of ADAMTS9 exhibited a significant upregulation (40-fold) following hCG treatment (48). In cattle, mifepristone inhibited the effects of LH on the expression of ADAMTS9 transcripts in granulosa cells in vitro (8). In this study, we showed expression of adamts9 in zebrafish was extremely low in immature follicles (stage I–IVa), negligible in denuded oocytes, and dramatically increased to its peak level specifically in the follicular cells of mature follicles (stage IVb) prior to ovulation. Additionally, knocking out Pgr indeed severely reduced the expression of adamts9. These results suggest that Adamts9 may also be responsible for follicular rupture. In summary, the preovulatory increases of adam8b, mmp9, adamts1, and adamts9 in follicular cells support the requirement of multiple metalloproteinases for ovulation in zebrafish. Future studies including changes of protein contents and enzyme activities, and the effects of knockouts of these metalloproteinases in zebrafish are required to determine relative importance of each metalloproteinase in ovulation in zebrafish.

Author Contributions

DL performed experiments, analyzed results, and wrote the paper. NC, XW performed experiments. SC and WH supervised the project and discussed the results. YZ conceived and supervised the project, analyzed results, and wrote the paper.


This work was supported by NIH GM100461, National Natural Science Foundation of China (No. 31672628 and 41276129), the fund for Doctor Station of the Ministry of Education, China (No. 20120121110029), Fundamental Research Funds for the Central Universities (No. 20720180123), and Program for New Century Excellent Talents in Fujian Province University.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


We want to thank Dr. Myon-Hee Lee and Dr. Dong Suk Yoon at Brody School of Medicine in East Carolina University for their assistance in Western blotting. We thank Mr. Christopher M. Anderson at Department of Biology in East Carolina University for proofreading.


1. Kohda H, Mori T, Ezaki Y, Nishimura T, Kambegawa A. A progesterone-dependent step in ovulation induced by human chorionic gonadotrophin in immature rats primed with pregnant mare serum gonadotrophin. J Endocrinol. (1980) 87:105–7.

PubMed Abstract | Google Scholar

2. Park OK, Mayo KE. Transient expression of progesterone receptor messenger RNA in ovarian granulosa cells after the preovulatory luteinizing hormone surge. Mol Endocrinol. (1991) 5:967–78. doi: 10.1210/mend-5-7-967

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Richards JS, Russell DL, Robker RL, Dajee M, Alliston TN. Molecular mechanisms of ovulation and luteinization. Mol Cell Endocrinol. (1998) 145:47–54. doi: 10.1016/S0303-7207(98)00168-3

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Wlizla M, Falco R, Peshkin L, Parlow AF, Horb ME. Luteinizing Hormone is an effective replacement for hCG to induce ovulation in Xenopus. Dev Biol. (2016) 426:442. doi: 10.1016/j.ydbio.2016.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Richards JS, Ascoli M. Endocrine, paracrine, and autocrine signaling pathways that regulate ovulation. Trends Endocrinol Metab. (2018). 29:315–25. doi: 10.1016/j.tem.2018.02.012

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Robker RL, Akison LK, Russell DL. Control of oocyte release by progesterone receptor-regulated gene expression. Nucl Recept Signal (2009) 7:e012. doi: 10.1621/nrs.07012

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Robker RL, Russell DL, Espey LL, Lydon JP, O'Malley BW, Richards JS. Progesterone-regulated genes in the ovulation process: ADAMTS-1 and cathepsin L proteases. Proc Natl Acad Sci USA. (2000) 97:4689–94. doi: 10.1073/pnas.080073497

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Fortune JE, Willis EL, Bridges PJ, Yang CS. The periovulatory period in cattle: progesterone, prostaglandins, oxytocin and ADAMTS proteases. Anim Reprod. (2009) 6:60–71.

PubMed Abstract | Google Scholar

9. Ogiwara K, Takahashi T. Involvement of the nuclear progestin receptor in LH-induced expression of membrane type 2-matrix metalloproteinase required for follicle rupture during ovulation in the medaka, Oryzias latipes. Mol Cell Endocrinol. (2017) 450:54–63. doi: 10.1016/j.mce.2017.04.016

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Curry TE Jr, Osteen KG. The matrix metalloproteinase system: changes, regulation, and impact throughout the ovarian and uterine reproductive cycle. Endocr Rev. (2003) 24:428–65. doi: 10.1210/er.2002-0005

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Ogiwara K, Hagiwara A, Rajapakse S, Takahashi T. The role of urokinase plasminogen activator and plasminogen activator inhibitor-1 in follicle rupture during ovulation in the teleost medaka. Biol Reprod. (2015) 92:10. doi: 10.1095/biolreprod.114.121442

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Carmeliet P, Kieckens L, Schoonjans L, Ream B, van Nuffelen A, Prendergast G, et al. Plasminogen activator inhibitor-1 gene-deficient mice. I Generation by homologous recombination and characterization. J Clin Invest. (1993) 92:2746–55. doi: 10.1172/JCI116892

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Peschon JJ, Slack JL, Reddy P, Stocking KL, Sunnarborg SW, Lee DC, et al. An essential role for ectodomain shedding in mammalian development. Science (1998) 282:1281–4. doi: 10.1126/science.282.5392.1281

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Vu TH, Werb Z. Matrix metalloproteinases: effectors of development and normal physiology. Genes Dev. (2000) 14:2123–33. doi: 10.1101/gad.815400

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Kelly K, Hutchinson G, Nebenius-Oosthuizen D, Smith AJ, Bartsch JW, Horiuchi K, et al. Metalloprotease-disintegrin ADAM8: expression analysis and targeted deletion in mice. Dev Dyn. (2005) 232:221–31. doi: 10.1002/dvdy.20221

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Enomoto H, Nelson CM, Somerville RP, Mielke K, Dixon LJ, Powell K, et al. Cooperation of two ADAMTS metalloproteases in closure of the mouse palate identifies a requirement for versican proteolysis in regulating palatal mesenchyme proliferation. Development (2010) 137:4029–38. doi: 10.1242/dev.050591

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Brown HM, Dunning KR, Robker RL, Boerboom D, Pritchard M, Lane M, et al. ADAMTS1 cleavage of versican mediates essential structural remodeling of the ovarian follicle and cumulus-oocyte matrix during ovulation in mice. Biol Reprod. (2010) 83:549–57. doi: 10.1095/biolreprod.110.084434

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Lydon JP, DeMayo FJ, Funk CR, Mani SK, Hughes AR, Montgomery CA Jr, et al. Mice lacking progesterone receptor exhibit pleiotropic reproductive abnormalities. Genes Dev. (1995) 9:2266–78.

PubMed Abstract | Google Scholar

19. Shimada M, Nishibori M, Yamashita Y, Ito J, Mori T, Richards JS. Down-regulated expression of A disintegrin and metalloproteinase with thrombospondin-likerepeate-1 by progesterone receptor antagonist is associated with impaired expansion of porcinecumulus-oocyte complexes. Endocrinology. (2004) 145:4603–14. doi: 10.1210/en.2004-0542

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Lima MA, da Silva SV, Freitas VM. Progesterone acts via the progesterone receptor to induce adamts proteases in ovarian cancer cells. J Ovarian Res. (2016) 9:9. doi: 10.1186/s13048-016-0219-x

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Ge W. Intrafollicular paracrine communication in the zebrafish ovary: the state of the art of an emerging model for the study of vertebrate folliculogenesis. Mol Cell Endocrinol. (2005) 237:1–10. doi: 10.1016/j.mce.2005.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Spence R, Gerlach G, Lawrence C, Smith C. The behaviour and ecology of the zebrafish, Danio rerio. Biol Rev Camb Philos Soc. (2008) 83:13–34. doi: 10.1111/j.1469-185X.2007.00030.x

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Clelland E, Peng C. Endocrine/paracrine control of zebrafish ovarian development. Mol Cell Endocrinol. (2009) 312:42–52. doi: 10.1016/j.mce.2009.04.009

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Zhu Y, Liu D, Shaner ZC, Chen S, Hong W, Stellwag EJ. Nuclear progestin receptor (pgr) knockouts in zebrafish demonstrate role for pgr in ovulation but not in rapid non-genomic steroid mediated meiosis resumption. Front Endocrinol. (2015) 6:37. doi: 10.3389/fendo.2015.00037

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Kubota K, Cui W, Dhakal P, Wolfe MW, Rumi MA, Vivian JL, et al. Rethinking progesterone regulation of female reproductive cyclicity. Proc Natl Acad Sci USA. (2016) 113:4212–7. doi: 10.1073/pnas.1601825113

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Liu DT, Brewer MS, Chen S, Hong W, Zhu Y. Transcriptomic signatures for ovulation in vertebrates. Gen Comp Endocrinol. (2017) 247:74–86. doi: 10.1016/j.ygcen.2017.01.019

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Wang C, Liu D, Chen W, Ge W, Hong W, Zhu Y, et al. Progestin increases the expression of gonadotropins in pituitaries of male zebrafish. J Endocrinol. (2016) 230:143–56. doi: 10.1530/joe-16-0073

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Selman K, Wallace RA, Sarka A, Qi X. Stages of oocyte development in the zebrafish, Brachydanio rerio. J Morphol. (1993) 218:203–24. doi: 10.1002/jmor.1052180209

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Hanna RN, Zhu Y. Controls of meiotic signaling by membrane or nuclear progestin receptor in zebrafish follicle-enclosed oocytes. Mol Cell Endocrinol. (2011) 337:80–8. doi: 10.1016/j.mce.2011.02.004

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Hanna RN, Daly SC, Pang Y, Anglade I, Kah O, Thomas P, et al. Characterization and expression of the nuclear progestin receptor in zebrafish gonads and brain. Biol Reprod. (2010) 82:112–22. doi: 10.1095/biolreprod.109.078527

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Zhu Y, Rice CD, Pang Y, Pace M, Thomas P. Cloning, expression, and characterization of a membrane progestin receptor and evidence it is an intermediary in meiotic maturation of fish oocytes. Proc Natl Acad Sci USA. (2003) 100:2231–6. doi: 10.1073/pnas.0336132100

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Thomas P, Pang Y, Dong J, Groenen P, Kelder J, de Vlieg J, et al. Steroid and G protein binding characteristics of the seatrout and human progestin membrane receptor alpha subtypes and their evolutionary origins. Endocrinology (2007) 148:705–18. doi: 10.1210/en.2006-0974

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Hild-Petito S, Stouffer RL, Brenner RM. Immunocytochemical localization of estradiol and progesterone receptors in the monkey ovary throughout the menstrual cycle. Endocrinology (1988) 123:2896–905. doi: 10.1210/endo-123-6-2896

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Press MF, Greene GL. Localization of progesterone receptor with monoclonal antibodies to the human progestin receptor. Endocrinology (1988) 122:1165–75. doi: 10.1210/endo-122-3-1165.

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Bayaa M, Booth RA, Sheng Y, Liu XJ. The classical progesterone receptor mediates Xenopus oocyte maturation through a nongenomic mechanism. Proc Natl Acad Sci USA. (2000) 97:12607–12. doi: 10.1073/pnas.220302597

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Wei LL, Krett NL, Francis MD, Gordon DF, Wood WM, O'Malley BW, et al. Multiple human progesterone receptor messenger ribonucleic acids and their autoregulation by progestin agonists and antagonists in breast cancer cells. Mol Endocrinol. (1988) 2:62–72. doi: 10.1210/mend-2-1-62

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Savouret JF, Bailly A, Misrahi M, Rauch C, Redeuilh G, Chauchereau A, et al. Characterization of the hormone responsive element involved in the regulation of the progesterone receptor gene. Embo J. (1991) 10:1875–83.

PubMed Abstract | Google Scholar

38. Shen T, Horwitz KB, Lange CA. Transcriptional hyperactivity of human progesterone receptors is coupled to their ligand-dependent down-regulation by mitogen-activated protein kinase-dependent phosphorylation of serine 294. Mol Cell Biol. (2001) 21:6122–31. doi: 10.1128/MCB.21.18.6122-6131.2001

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Lister AL, Van Der Kraak GJ. Regulation of prostaglandin synthesis in ovaries of sexually-mature zebrafish (Danio rerio). Mol Reprod Dev. (2009) 76:1064–75. doi: 10.1002/mrd.21072

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Doyle KM, Russell DL, Sriraman V, Richards JS. Coordinate transcription of the ADAMTS-1 gene by luteinizing hormone and progesterone receptor. Mol Endocrinol. (2004) 18:2463–78. doi: 10.1210/me.2003-0380

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Benhamou B, Garcia T, Lerouge T, Vergezac A, Gofflo D, Bigogne C, et al. A single amino acid that determines the sensitivity of progesterone receptors to RU486. Science (1992) 255:206–9.

PubMed Abstract | Google Scholar

42. Moudgil VK, Lombardo G, Hurd C, Eliezer N, Agarwal MK. Evidence for separate binding sites for progesterone and RU486 in the chick oviduct. Biochim Biophys Acta (1986) 889:192–9. doi: 10.1016/0167-4889(86)90104-7

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Bagowski CP, Myers JW, Ferrell JE Jr. The classical progesterone receptor associates with p42 MAPK and is involved in phosphatidylinositol 3-kinase signaling in Xenopus oocytes. J Biol Chem. (2001) 276:37708–14. doi: 10.1074/jbc.M104582200

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Sriraman V, Eichenlaub-Ritter U, Bartsch JW, Rittger A, Mulders SM, Richards JS. Regulated expression of ADAM8 (a disintegrin and metalloprotease domain 8) in the mouse ovary: evidence for a regulatory role of luteinizing hormone, progesterone receptor, and epidermal growth factor-like growth factors. Biol Reprod. (2008) 78:1038–48. doi: 10.1095/biolreprod.107.066340

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Cooke RG III, Nothnick WB, Komar C, Burns P, Curry JTE. Collagenase and gelatinase messenger ribonucleic acid expression and activity during follicular development in the rat ovary. Biol Reprod. (1999) 61:1309–16. doi: 10.1095/biolreprod61.5.1309

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Duffy DM, Stouffer RL. Luteinizing hormone acts directly at granulosa cells to stimulate periovulatory processes: modulation of luteinizing hormone effects by prostaglandins. Endocrine (2003) 22:249–56. doi: 10.1385/ENDO:22:3:249

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Light A, Hammes SR. LH-induced steroidogenesis in the mouse ovary, but not testis, requires matrix metalloproteinase 2- and 9-mediated cleavage of upregulated EGF receptor ligands. Biol Reprod. (2015) 93:65. doi: 10.1095/biolreprod.115.130971

CrossRef Full Text | Google Scholar

48. Rosewell KL, Al-Alem L, Zakerkish F, McCord L, Akin JW, Chaffin CL, et al. Induction of proteinases in the human preovulatory follicle of the menstrual cycle by human chorionic gonadotropin. Fertil Steril. (2015) 103:826–33. doi: 10.1016/j.fertnstert.2014.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: ovulation, adamts9, progestin, Pgr, metalloproteinase

Citation: Liu DT, Carter NJ, Wu XJ, Hong WS, Chen SX and Zhu Y (2018) Progestin and Nuclear Progestin Receptor Are Essential for Upregulation of Metalloproteinase in Zebrafish Preovulatory Follicles. Front. Endocrinol. 9:517. doi: 10.3389/fendo.2018.00517

Received: 08 June 2018; Accepted: 17 August 2018;
Published: 18 September 2018.

Edited by:

Chun Peng, York University, Canada

Reviewed by:

Xin Qi, Ocean University of China, China
Oliana Carnevali, Università Politecnica delle Marche, Italy

Copyright © 2018 Liu, Carter, Wu, Hong, Chen and Zhu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Shi Xi Chen,
Yong Zhu,