Original Research ARTICLE
The 3-Phosphoinositide-Dependent Protein Kinase 1 Inhibits Rod Photoreceptor Development
- 1Department of Anatomy and Cell Biology, East Carolina University, Greenville, NC, United States
- 2Department of Neural and Behavioral Sciences, Penn State College of Medicine, Hershey, PA, United States
The transition of rod precursor cells to post-mitotic rod photoreceptors can be promoted by extrinsic factors such as insulin-like growth factor 1 (IGF-1), which regulates phosphatidylinositide concentration, and consequently the 3-phosphoinositide-dependent protein kinase-1 (PDPK-1). PDPK-1 is a 63 kDa cytoplasmic kinase that controls cell proliferation and differentiation. In the mouse retina, PDPK-1 and its phosphorylated derivative p-PDPK-1 (Ser241), showed peak expression during the first postnatal (PN) day with a substantial decline by PN7 and in the adult retina. Though initially widely distributed among cell types, PDPK-1 expression decreased first in the inner retina and later in the outer retina. When PDPK-1 is inhibited in neonatal retinal explants by BX795, there is a robust increase in rod photoreceptor numbers. The increase in rods depended on the activity of PKC, as BX795 had no effect when PKC is inhibited. Inhibition of PDPK-1-dependent kinases, such as P70-S6K, but not others, such as mTORC-1, stimulated rod development. The P70-S6K-dependent increase in rods appears to be correlated with phosphorylation of Thr252 and not at Thr389, a substrate of mTORC-1. This pathway is also inactive while PKC activity is inhibited. We also found that inhibition of the kinase mTORC-2, also stimulated by insulin activity, similarly increased rod formation, and this effect appears to be independent of PKC activity. This may represent a novel intracellular signaling pathway that also stimulates photoreceptor development. Consistent with previous studies, stimulation of STAT3 activity is sufficient to prevent any PDPK-1, P70-S6K, or mTORC2-dependent increase in rods. Together the data indicate that PDPK-1 and other intrinsic kinases downstream of IGF-1 are key regulators of rod photoreceptor formation.
Cells within the retina develop in stereotyped order that is well conserved across vertebrates (Young, 1985; La Vail et al., 1991; Stiemke and Hollyfield, 1995). In the rodent retina, these terminal cell divisions occur between embryonic days 10–12 (Barnstable, 1985; Rapaport et al., 2004) and postnatal days 11–12 (Barnstable, 1985; Young, 1985). Rod photoreceptors are the most abundant developing cell of the rodent retina and also among the last to be born, with peak rod generation occurring shortly after birth (Young, 1985; Ezzeddine et al., 1997). The development of these cells requires a combination of intrinsic (Cepko, 1999; Mears et al., 2001; Pinzon-Guzman et al., 2011) and extrinsic signaling molecules (Kelley et al., 1994; Davis et al., 2000) that can regulate the transition of multi-potent stem cells to rod precursors (Lu and Barnstable, 2017) and the differentiation of precursors in to post-mitotic retinal cells (Pinzon-Guzman et al., 2011).
Extrinsic insulin-like growth factor 1 (IGF-1) signaling is one such signal that promotes the transition of rod precursor cells to post-mitotic photoreceptors (Yi et al., 2005; Pinzon-Guzman et al., 2011). Canonically, IGF-1 stimulates phosphatidylinositol-3-kinase (PI3K) activity, increasing phosphorylation of the 3′-hydroxyl on intracellular phosphatidylinositol (PIP3) (Alessi et al., 1996, 1997; Alessi and Downes, 1998). PIP3 is a common second messenger, and one of its major effects is to interact with a central regulator of intracellular signaling, the 3-phosphoinositide-dependent protein kinase-1 (PDPK-1).
3-Phosphoinositide-dependent protein kinase-1 controls cell cycle progression (Nakamura et al., 2008), size (Lawlor et al., 2002), survival (Ito et al., 2009), and differentiation (Dainichi et al., 2016). It is expressed ubiquitously during embryonic stages of mouse development, and PDPK1 null pups do not survive past embryonic day 9.5, indicating the biological importance of this protein (Lawlor et al., 2002). The cellular composition of phospholipids regulates the subcellular localization of PDPK-1, which influences some of its activity. For example, PIP3 binding to the PDPK-1 pleckstrin homology domain targets it to the plasma membrane and allows it to phosphorylate protein kinase B (AKT1/PKB) at Thr308 (Alessi et al., 1997; Andjelković et al., 1997; Stephens et al., 1998; Bayascas et al., 2008).
In the adult retina, IGF-1 stimulates classical PI3K pathway activity to phosphorylate downstream effectors such as Akt at Ser473. In the PN1 retina, IGF-1 does not appear to have the same effects and decreases Akt (Ser473) phosphorylation. This alteration in IGF-1 signaling is correlated with decreased phosphorylation of the PI3K regulatory subunit P55 (PIK3R3). This shift in PI3K regulation likely decreases PDPK-1 activity and signaling to it’s downstream effectors (Pinzon-Guzman et al., 2011). Under these conditions, non-canonical IGF-1-dependent signaling increases photoreceptor development in a pathway that requires conventional protein kinase C (PKC) isoforms-β1 and -γ. PKC is critical for the activation of downstream tyrosine phosphatases Ship1/2 and to decrease activation of the signal transducer and activator of transcription 3 (STAT3) (Pinzon-Guzman et al., 2010, 2015). STAT3 is a potent regulator of gene expression, and an endpoint in multiple growth factor signaling cascades (Zhang et al., 2004). Activation of STAT3 with cytokines such as CNTF or LIF decreases rod generation (Ezzeddine et al., 1997; Zhang et al., 2004), and infection of ex vivo retinas with a dominant negative form of STAT3 prevents basal or CNTF-stimulated inhibition of photoreceptor development (Zhang et al., 2004). While we have defined upstream and downstream intracellular signals that enhance rod development, the intermediate signals in this pathway are not yet clear. Specifically, the mechanism through which PI3K inhibition leads to a PKC-dependent decrease in STAT3 activation is not yet known.
As a key intermediate between PI3K and downstream signal pathways, we hypothesized that PDPK-1 and its downstream effectors (mTOR, P70-S6K, and PKC) are important signals in rod photoreceptor development. In this study we show that inhibiting PDPK-1 greatly increases the development of rod photoreceptors in retinal explants, in part through PKC-STAT3 signaling and in part through other pathways.
Materials and Methods
This study was carried out in accordance with the National Research Council’s Guide for the Care and Use of Laboratory Animals (8th edition). The protocol was approved by the Pennsylvania State University College of Medicine Institutional Animal Care and Use Committee.
C57B1/6J mice were purchased from Jackson laboratory (Bar Harbor, ME, United States) and housed in a room with an ambient temperature of 25°C, 30–70% humidity, a 12-h light–dark cycle, and ad libitum access to rodent chow. All ex vivo explant culture experiments used retinal tissue from early postnatal day 1 (PN1) mice.
Retinal Isolation and Culture
Photoreceptor development was studied using a previously described ex vivo retinal explant cultured system (Zhang et al., 2002; Pinzon-Guzman et al., 2011). Briefly, mouse retinas were dissected from PN1 pups and cultured in a defined medium (UltraCulture, Cambrex BioScience) supplemented with 10 μg/mL gentamicin and maintained at 37°C in a 5% CO2. Half of this culture medium was changed every 48 h. Table 1 lists the reagents added to the basal retinal explant culture medium to interrogate the effects of the IGF-1 pathway on photoreceptor development.
Retinal explants for Western blotting were first cultured for 5 h in medium, and then cultured for 30 min in medium supplemented with various reagents at the concentrations listed in Table 1, prior to lysis. Explants destined for immunohistochemical studies were cultured for 96 h with or without these reagents prior to fixation.
Western blots were performed as previously described (Zhang et al., 2004; Pinzon-Guzman et al., 2015). Briefly, retinas were lysed in CytoBuster Protein Extraction Reagent (Novagen) containing EDTA, protease inhibitors (Thermo Scientific), and phosphatase inhibitors (Roche). Samples underwent three freeze-thaw cycles at -20°C, and supernatant was collected after centrifugation. Equal amounts (10–20 μg) of protein were loaded onto polyacrylamide gels (Any kD, Bio-Rad), and separated by standard SDS–PAGE. Proteins were transferred to poly-vinylidene difluoride (PVDF) or nitrocellulose membranes (Bio-Rad) using a standard semi-dry transfer system. Gels were saved for coomassie labeling and normalization to the three histone bands as implemented previously (Popova et al., 2013; Ferreira et al., 2017), and membranes were blocked for 1 h with 5% non-fat dry milk in Tris-buffered saline with 0.1% Tween-20. Membranes were incubated with primary antibody overnight at 4°C, followed by incubation with horseradish peroxidase-conjugated secondary antibodies for 1–2 h at room temperature (See Table 2 for antibody specificities and dilutions). Semi-quantitative analysis of band intensity was performed using ImageJ1.
Histology and Immunocytochemistry
Immunolabeling of retinal tissue was performed as previously described (Pinzon-Guzman et al., 2011). Briefly, explanted retinas and whole eyes were fixed in 4% paraformaldehyde (Electron Microscopy Sciences, Hatfield, PA, United States) in 1× PBS for 24 h at 4°C. Fixed retinas were either dehydrated through a series of graded ethanol concentrations, embedded in paraffin and sectioned at a 7 μm thickness, or embedded in a 2:1 mixture of 20% sucrose and OCT (Electron Microscopy Sciences), frozen at -20°C, and sectioned at a 5–10 μm thickness. Samples for each experiment were located on the same slide to control for section thickness and assay variability.
Prior to immunohistochemical labeling of deparaffinized or frozen tissue section, we unmasked antigens in a sodium citrate buffer (pH 6.0). Sections were permeabilized in 0.2% Triton-X-100 in PBS, blocked in 5% non-fat milk, and incubated in primary antibodies (See Table 2 for dilutions) overnight at 4 °C. The following day, sections were washed and incubated in secondary antibody for 3 h, followed by incubation in 1 μg/mL Hochest-33258 for 20 min. After three washes, slides were mounted with 0.5% n-propyl gallate in 1:1 glycerol: PBS. Sections were imaged using an Olympus FLUOVIEW FV1000 confocal microscope. In each set of experiments, acquisition parameters for each antibody were held constant. Fluorescent intensity measurements were derived using the ImageJ measurement tool.
RNA Isolation and Quantitative Real-Time PCR
RNA was isolated from PN1 retinas using TRIzol (Invitrogen) and purified using RNeasy Mini Kits (Qiagen) as per the manufacturer’s instructions. Final RNA concentration was measured on a Gene Spect III (Hitachi) spectrophotometer. 2 μg RNA samples were reverse transcribed in a total reaction volume of 50 μL using SuperScript III reverse transcriptase (Invitrogen). Quantitative PCR annealing temperatures were set at 60°C for 40 cycles on a Bio-Rad iCycler, followed by a melt curve analysis to confirm primer specificity. Primer sequences are listed in Table 3. We quantified relative gene expression using the ΔΔCt method with GAPDH (QuantiTect; Qiagen) as a reference gene.
All statistical analyses were performed using GraphPad Prism. To compare the means of two groups, we used a two-tailed, unpaired t-test. For the statistical analysis of more than two groups, we used a one-way ANOVA with a Newman–Keuls post hoc test.
Developmental Expression of PDPK-1 in Mouse Retina
In the mouse retina, the protein levels of PDPK-1 and its active form, phosphorylated at Ser241, significantly declined between postnatal days (PN) 1, 7, and 28. Relative to PN1, total PDPK-1 protein decreased to 82 ± 15% at PN7 and 31.4% at PN28 (p < 0.01; Figure 1A). Similarly, p-PDPK-1 (Ser241) levels declined to 72 ± 7% at PN7 (p < 0.05) and 65 ± 5% at PN28 (p < 0.05; Figure 1B). To determine whether PDPK-1 protein was expressed in specific retinal cell populations we labeled retinas fixed at PN1, PN7, or PN28 with antibodies recognizing PDPK-1 or p-PDPK-1 (Ser241). During PN1, both forms of PDPK-1 were widely distributed across the retina, from the outer neuroblast layer to inner neuroblast layer. At PN7, much of the labeling had disappeared and the heaviest labeling of PDPK-1 (but not pPDPK-1) was on cell bodies at the outer edge of the inner nuclear layer and suggests that PDPK-1 is present in horizontal cells (Figure 1C). At PN28, outer plexiform labeling remained strong, and the inner plexiform layer was diffusely labeled. We tested whether the p-PDPK-1-expressing population of cells of the outer neuroblast layer were dividing or post-mitotic by labeling fixed PN1 retinas for both proliferating cell nuclear antigen (PCNA; green), and p-PDPK-1 (Ser241) (red; Figure 1D and Supplementary Figure S4). Though many cells were only labeled with a single marker, there was co-localization (yellow) of PDPK-1 and PCNA in cells proximal to the outer limiting membrane (Figure 1D). This shows that pPDPK-1 is present in a portion of dividing cells of the early postnatal retina.
FIGURE 1. PDPK-1 and p-PDPK-1 expression decline following retinal development. Western blots and corresponding histograms representing (A) PDPK-1 and (B) p-PDPK-1 Ser241 levels in wild-type PN 1, 7 and adult mouse retinas, normalized to the three histone bands on a coomassie stain of the gel. (C) Immunofluorescent labeling of PDPK-1 and p-PDPK-1 Ser241 (red) and Hoechst-33258 (blue) in 10 μm sections of the postnatal days 1, 7, and 28 wild-type mouse retina. (D) The same set of retinas, fluorescently labeled for p-PDPK-1 (red), PCNA (green), and Hoechst-33258 (blue). In this set of images, the objective is focused on the outer neuroblast or nuclear layers. ONBL, outer neuroblast layer; INBL, inner neuroblast layer; OS, outer segments; ONL, outer nuclear layer; OPL, outer plexiform layer; INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer. n = 3 biological replicates/measure ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001.
PDPK-1 Is a Critical Inhibitor of Rod Photoreceptor Differentiation
To determine the role of PDPK-1 in photoreceptor development, we treated retinal explants with the competitive inhibitor, BX795 (IC50: 6 nM) at concentrations ranging from 10 nM to 20 μM for 96 h. BX795 significantly increased rhodopsin labeling, with a peak effect on rhodopsin (340 ± 25% of control) observed at 1 μM (Figures 2A,C). Concentrations of BX795 greater than 1 μM decreased rhodopsin labeling, suggesting off-target or non-specific effects that negatively impact rod development. Notably, we see the same pattern of rhodopsin labeling in explats treated with increasing concentrations of an alternative PDPK-1 inhibitor, GSK2334470 (Supplementary Figure S1; Barnstable, 1980). To prevent possible effects, we used 100 nM BX795 in all subsequent experiments, which gives a significant though sub-maximal increase in opsin expression. p-AKT-1 (Thr308) is a PDPK-1 target (Alessi et al., 1997), and as a verification of inhibitor activity, we found a concentration dependent decrease in p-AKT-1 (Thr308) with increasing concentrations of BX795 (Figure 2B). To determine whether the action of BX795 was on rod photoreceptors, rather than just on opsin, we tested the expression of a variety of other markers. Though some rod genes (Crx and Sag) showed little change, the expression of others (Nrl, Pde6B, and Otx2) significantly increased, suggesting that the action of BX795 was on more than a single rod gene (Figure 2D), and that in our experiments, rhodopsin is a valid proxy for overall photoreceptor development.
FIGURE 2. BX795 is a PDPK-1 inhibitor that enhances rod photoreceptor precursor development. In P1 retinal explant cultures, PDPK-1 was inhibited with 0, 0.1, 1, 5, 10, 20, and 40 μM BX795. (A) Quantification of rhodopsin labeling intensity as a function of log10 (BX795 concentration), relative to untreated controls. (B) Protein levels of p-AKT1Thr308 as a function of BX795 concentration. The inset contains an example western blot with duplicate lanes for each concentration of BX795 (n = 3). (C) Representative images for the curve in A, 96 h retinal explants were sectioned and labeled for rhodopsin (green) and the DNA stain Hoechst-33258 (blue). (D) cDNA levels corresponding to the expression of photoreceptor and photoreceptor precursor-related genes. n = 3 biological replicates/measure. ∗p < 0.05 and ∗∗p < 0.01.
PDPK-1 Inhibits Rod Development in a PKC-Dependent Manner
Our previous studies have documented the stimulatory effects of IGF-1 on rod photoreceptor development via a pathway involving activation of PKC (Pinzon-Guzman et al., 2010, 2011). We tested whether the effect of BX795 on rhodopsin was PKC-dependent. As in previous experiments, 50 μg/mL IGF-1 increased rhodopsin labeling to 403 ± 47% (p < 0.0001) relative to untreated control explants. Treatment of explants with 50 nM of the PKC inhibitor Go7874 or the combination of IGF-1 and Go7874 decreased rhodopsin labeling to 69 ± 7% (n.s.), and 54 ± 16% (n.s.) of control, respectively (Figure 3A).
FIGURE 3. IGF-1 and BX795 enhance rod development in a PKC-dependent manner. Quantification (top) and representative images (bottom) of rhodopsin (green) and Hoechst-33258 (blue) labeled retinal explants following a 96-h exposure to nothing (controls) or (A) 50 nM IGF-1, 100 nM Go7874, or both; (B) 100 nM Go7874, 100 nM BX795, or both. n = 3 biological replicates/measure. ∗p < 0.05 and ∗∗∗p < 0.001.
BX795 also significantly increased rhodopsin levels relative to controls (202 ± 39%, p < 0.05) (Figure 3B). When Go7874 was co-applied with BX795 there was a decrease in rhodopsin labeling (51 ± 40%) relative to controls, similar to the level of labeling seen with Go7874 alone (48 ± 49%). These data show that the BX795-mediated increase in rhodopsin levels requires PKC activity.
Inhibition of mTORC-1 Does Not Alter Rod Photoreceptor Development
3-Phosphoinositide-dependent protein kinase-1 lies upstream of AKT1 and thus mTORC-1 signaling (Saxton and Sabatini, 2017). To test whether inhibition of mTORC-1 can influence rhodopsin levels, we treated explants with 10 nM rapamycin for 96 h (Beretta et al., 1996; Sehgal, 2003). This treatment did not significantly alter rhodopsin fluorescence (Figure 4), suggesting that mTORC-1 does not normally regulate photoreceptor development. To confirm that the inhibitory effects of rapamycin were still active over similar time periods, we tested the effect of 30 min and 48 h rapamycin treatment on phosphorylation of the mTORC1 target p-P70-S6K (Thr389). Our data suggest that rapamycin is even more effective at decreasing Thr389 levels over this time period than at 30 min, confirming our result (Supplementary Figure S2).
FIGURE 4. Inhibition of mTORC-1 does not affect rod photoreceptor development. Quantification and representative images of rhodopsin (green) and Hoechst-33258 (blue) labeled retinal explants following a 96-h exposure to nothing (controls) or 10 nM rapamycin.
Inhibition of P70-S6K Enhances Rod Differentiation in a PKC Dependent Manner
P70-S6K is major substrate of both PDPK-1 and mTORC-1. Using the P70-S6K inhibitor PF4708671 (IC50 = 160 nM) (Pearce et al., 2010), we tested whether inhibition of P70-S6K altered rhodopsin levels. 200 nM PF4708671 significantly increased rhodopsin (242 ± 39%, p < 0.01, Figures 5A,B), though to a lesser extent than with 100 nM BX795. Concurrent inhibition of PDPK-1 and P70-S6K (941 ± 167%, p < 0.01) greatly increased rhodopsin levels, but the increase in rhodopsin was not statistically different from inhibition of PDPK-1 alone (Figures 5A,B), suggesting that PDPK-1 and P70-S6K may work in the same pathway to regulate photoreceptor development.
FIGURE 5. Inhibition of P70-S6K with PF4708671 enhances rod photoreceptor development. (A) Representative rhodopsin (green) and Hoechst-33258 (blue) labeling in retinal explants following a 96 h exposure to nothing (control), 100 nM BX795, 200 nM PF4708671, BX795 and PF4708671, 100 nM Go7874, or Go7874 and PF4708671. (B,C) Quantification of treatment groups represented in (A). (D) Example western blots and densitometric analysis of retinal explants left untreated or treated with 10 nM Rapamycin for 30 min. Lysate from these retinas was labeled with antibodies to detect P70-S6K Thr252, P70-S6K Thr389, and β-actin. (E) The same proteins were detected in lysate from retinal explants treated with 100 nM BX795 for 30 min. n = 3 biological replicates/measure. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001.
To test more directly if P70-S6K is upstream of PKC, we treated explants with 200 nM PF4708671, 50 nM Go7874, or a combination of these inhibitors for 96 h (Figures 5A,C). As shown earlier, rhodopsin levels were reduced in Go7874-treated retinas (59 ± 5% of controls, n.s.). Similarly, rhodopsin was elevated in explants treated with PF4708671 (267 ± 89%, p < 0.01). When explants were treated with Go7874 and PF4708671, opsin levels increased to a lower extent than with PF4708671 alone (156 ± 40%, n.s.). These data suggest that while much of the action of P70-S6K is dependent on PKC, the remaining increase in rhodopsin in Go7874 plus PF4708671-treated retinas suggests that part of P70-S6K’s effect on rhodopsin is independent of PKC.
mTORC-1 and PDPK-1 activate P70-S6K kinase activity on separate amino acid residues (mTORC1 phosphorylates Thr389 in mouse and human, whereas PDPK-1 phosphorylates Thr229 in human and Thr252 in mouse) (Burnett et al., 1998; Pullen et al., 1998). Using rapamycin and BX795, we tested whether either or both of these residues was important for retinal development. Application of the mTORC-1 inhibitor rapamycin significantly decreased phosphorylation of P70-S6K Thr389 (p < 0.05) but not at Thr252 (Figure 5D). On the other hand, BX795 significantly decreased both Thr389 phosphorylation (47% of control, p < 0.05) and Thr252 phosphorylation (77% of control, p < 0.05; Figure 5E). This suggests that the effects of P70-S6K on rod photoreceptor development are particularly dependent on its phosphorylation at Thr252.
Inhibition of mTORC2 Enhances Rod Differentiation
The mTORC2 complex is a regulator of cell growth and metabolism, and the mTORC2 component rictor is a downstream target of P70-S6K (Treins et al., 2010). We hypothesized that like P70-S6K inhibition, mTORC2 inhibition is also able to regulate rod development. There are no known selective inhibitors of mTORC-2, but since mTORC-1 did not influence rod development, we interrogated mTORC-2-dependent effects using the mTORC-1/2 inhibitor KU0063794 (KU; IC50 = 10 nM). Treatment of explants with 100 nM KU0063794 enhanced rod photoreceptor development by 236 ± 15% relative to untreated control explants (p < 0.05, Figures 6A,B). The combined use of KU0063794 and BX795 also stimulated rod development (750 ± 141% of control, p < 0.01) approximately to the same extent as BX795 alone (941 ± 167% of control, p < 0.001, Figure 6A). These data show that mTORC-2 inhibition is likely a component of PDPK-1-inhibition-dependent photoreceptor development.
FIGURE 6. Inhibition of mTORC-1/2 with KU0063794 enhances rod photoreceptor development independently of PKC. (A) Example images and (B,C) quantification of rhodopsin labeling in retinal explants following a 96-h exposure to nothing (controls) or (B) 100 nM KU0063794, 100 nM BX795, or both; (C) 100 nM KU0063794, or both. n = 3 biological replicates/measure. ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001.
To determine whether mTORC-2 requires PKC to inhibit rod development, we tested the ability of Go7874 to block the KU0063794 induced increase in rhodopsin levels. As shown in Figure 6B, co-application of Go7874 with KU0063794 to retinal explants led to a 210 ± 21% increase in rhodopsin above control, not significantly different from the increase seen with KU0063794 alone (272 ± 58%, p < 0.05). These data suggest that the action of mTORC-2 on rod photoreceptor development is independent of PKC.
STAT3 Activation Prevents BX795-, PF4708671-, and KU0063794-Dependent Rod Formation
Activation of STAT3 by phosphorylation of Tyr705 blocks rod photoreceptor development. We hypothesized that inhibitors which increase rhodopsin levels would do so through a pathway that ultimately decrease p-STAT3 Tyr705 levels. 100 nM BX795, but not 100 nM KU0063794 or 200 nM PF4708671, significantly decreased resting p-STAT3 Tyr705 (Figures 7A,B). We also tested whether these inhibitors would be sufficient to overcome levels of STAT3 activation stimulated by cytokines such as leukemia inhibitory factor (LIF). We tested the effect of 20 ng/mL LIF on rod photoreceptor development induced by 100 nM BX795, 100 nM KU0063794, or 200 nM PF4708671, and found that LIF-induced STAT3 activity completely halts photoreceptor development, regardless of the presence of BX795, KU0063794, or PF4708671 (Figures 7C,D). We also confirmed that the actions of LIF are STAT3 dependent, since while no rods develop in explants treated with 20 ng/mL LIF and 100 nM BX795, rhodopsin labeling is rescued in explants treated with a cocktail of 100 nM BX795, 20 ng/mL LIF, and 50 μM of the STAT3 inhibitor Stattic (Supplementary Figure S3). These data suggest STAT3 activity is a prominent regulator of cell fate in the developing retina, perhaps more so than the factors we have studied that stimulate rod development.
FIGURE 7. STAT3 activation suppresses rod photoreceptor development, which is prevented by BX795. (A) Quantification and (B) example western blot demonstrating the effects of 30 min exposures to BX795, PF4708671, and KU0063794 on STAT3 Tyr705 phosphorylation in retinal explants. (C) Quantification and (D) representative images of rhodopsin (green) and Hoechst-33258 (blue)-labeled retinas following a 96 h exposure to nothing (control), 100 nM BX795, 100 nM KU0063794, 200 nM PF4708671 (left column), or any of the above in combination with 20 ng/mL LIF (right column). ∗p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.001.
Our previous work has demonstrated the presence of an IGF-1-PI3K-PKC-Shp-1/2-STAT3 axis in the early postnatal retina that regulates rod photoreceptor development. The present study has demonstrated that PDPK-1, a key downstream effector of the PI3K pathway, is part of this axis. Also, we have found that additional pathways downstream of PDPK-1, particularly P70-S6K and mTORC-2, also have a strong inhibitory influence rod photoreceptor development.
Both the normal and active forms of PDPK-1 are expressed in the developing retina and decline during later stages (Figures 1A,B). In the early postnatal retina when PDPK-1 levels are greatest, both active and total PDPK-1 are evenly distributed across the tissue (Figure 1C), suggesting that PDPK-1 may play a role in the terminal differentiation of multiple retinal cell types. Developing retinal cells extend radial processes across much of the retina. This makes it difficult to measure the co-localization of the cytoplasmic PDPK-1 enzyme and the nuclear proliferation marker PCNA. Nevertheless, we did find some double-labeled cells at the outer margin of the retina, where developing cells undergo mitosis. Interestingly PCNA is cytosolic in these cells, which in granulocytes correlates with differentiation in to neutrophils (Bouayad et al., 2012). We propose that cytosolic PCNA in the retina corresponds to terminally differentiated retinal cells as well. Later in postnatal development, PDPK-1 localized more distinctly to the outer plexiform layer of the retina, with strong staining in horizontal cells (Figure 1C), suggesting that it may have a unique function within this cell type. However, the overall decline in PDPK-1 levels suggests that the developmental role of PDPK-1 has concluded by PN7. We did not find any significant perinuclear localization of the active or inactive form of the enzyme, as has been reported by others (Alajajian et al., 2009; Sephton et al., 2009). It is unclear whether this reflects differences in PDPK-1’s role in different tissues or during different developmental stages.
A previously characterized developmental shift in PI3K subunits results in IGF-1 inhibiting canonical downstream signaling intermediates such as AKT-1 in the newborn retina, but activating them at later ages (Pinzon-Guzman et al., 2011). As a major regulator of AKT-1, PDPK-1 is also likely inhibited in the early postnatal retina. We modeled this effect by using the PDPK-1 inhibitor BX795 (Feldman et al., 2005). PDPK-1 inhibition caused a significant increase rhodopsin levels (Figure 2). Our data showed that this effect is dose dependent up to 1 μM BX795, but the decrease in rhodopsin labeling at greater concentrations suggest that it can affect other proteins at higher concentrations (Figures 2A,C). We used 100 nM BX795 in our studies, as it has high specificity for PDPK-1 and a minimal effect on downstream factors such as AKT-1 (Figure 2B). While this concentration lessened the magnitude of effect on rhodopsin, we feel that the increased specificity make our results easier to interpret. Additionally, this dose of BX795 was sufficient to increase the expression of multiple rod genes (Figure 2D), and we would expect an even greater effect at concentrations of BX795 closer to 1 μM.
Our previous work had shown that the basal or IGF-1 stimulated formation of photoreceptors is dependent on PKC activity (Pinzon-Guzman et al., 2010, 2011). IGF-1 is upstream of PDPK-1 and PKC is downstream of PDPK-1 (Alessi et al., 1997; Le Good et al., 1998) in most biological contexts, and we tested the hypothesis that as with IGF-1, PKC is also downstream of PDPK-1. Our data support this hypothesis, showing that while BX795 and IGF-1 can each significantly increase rhodopsin levels, they are unable to do so when PKC is inhibited (Figure 3).
3-Phosphoinositide-dependent protein kinase-1 activity leads to the phosphorylation of a number of targets including AKT-1/PKB, mTORC-1, P70-S6K, and mTORC-2. Canonically, PDPK-1 phosphorylates and activates AKT-1/PKB at Thr308, which then indirectly activates mTORC-1. mTORC-1 is has been implicated in the regulation of many diverse processes within cells, from increasing survival to regulating energy homeostasis and cell growth (Guertin and Sabatini, 2007). Despite the ubiquitous number of mTORC-1 targets, mTORC-1 does not appear to regulate rod development (Figure 4). This was not completely unexpected, as direct inhibition of AKT/PKB also does not appear to regulate rod development (Pinzon-Guzman et al., 2011). However, PDPK-1 and mTORC-1 share several downstream targets (Figure 8). One such target that is key in mediating PDPK-1 signaling is P70-S6K, which increases translational activity within a cell by phosphorylating the S6 ribosomal subunit (Pullen et al., 1998; Dufner and Thomas, 1999; Mora et al., 2004; Fenton and Gout, 2011). We inhibited P70-S6K with PF4708671, and noted a significant increase in rhodopsin levels that occurred to a much lesser extend when PKCs were inhibited, suggesting that PKC is downstream of P70-S6K in the determination of rod numbers (Figure 5). This finding, while significant, initially seemed to conflict with the lack of effect we observed in rapamycin-treated retinas, as both mTORC-1 and PDPK-1 increase P70-S6K activity. However, these kinases target different activating residues on P70-S6K (Thr389 for mTORC-1 and both Thr389 and Thr252 for PDPK-1). While rapamycin strongly inhibited phosphorylation of Thr389 (without affecting Thr252), BX795 decreased phosphorylation at both sites (Figure 5). Comparing these effects, and the ability of P70-S6K inhibition to increase rod photoreceptor development, we suggest that PDPK-1 suppresses photoreceptor development by activating Thr252 of P70-S6K. To our knowledge, this is the first demonstration of the differential effects of phosphorylating these amino acid residues on P70-S6K.
FIGURE 8. Pathway diagram representing the pathways and interacting factors that control rod photoreceptor development.
The protein mTOR can be a component of two multi-protein complexes, mTORC-1 and mTORC-2. mTORC-2 is a rapamycin-insensitive protein complex that is responsive to growth factor signaling cascades, and regulates cell proliferation, survival, and metabolism (Saxton and Sabatini, 2017). mTORC-2 can influence rod development, but the stimulatory effect of the mTORC-1/2 inhibitor KU0063794 on rhodopsin levels was insensitive to treatment with Go7874, suggesting that it operates through a pathway that does not involve PKC (Figure 6). Like mTORC1, mTORC2 is activated in response to PI3K signaling (Wahane et al., 2014), and is a direct target of P70-S6K (Treins et al., 2010), though the functional impact of mTORC2 activation by P70-S6K has not yet been fully explored. It can also phosphorylate AKT-1/PKB or conventional PKC isoforms (Ikenoue et al., 2008), and thus interacts with many different signaling factors that regulate rod development. Overall, mTORC-2 signaling may be one component in a novel pathway that stimulates rod development (Figure 8).
Additionally, it may be possible that P70-S6K stimulates rod development through interactions with both PKC- and mTORC2-dependent developmental pathways. If this is the case, it would explain why the rod-stimulating effects of PF4708671 do not appear to be fully silenced by PKC inhibition, though rhodopsin levels in explants treated with PF4708671 were not statistically distinct from those in explants treated with PF4708671 and Go7874. Regardless, it is still remains to be seen specific role this alternate pathway plays in the developmental cellular physiology of photoreceptors.
One central characteristic of rod photoreceptor development is that it is fully inhibited by STAT3 activity (Ezzeddine et al., 1997; Zhang et al., 2004). PKC activation promotes rod development in part by decreasing STAT3 Tyr705 phosphorylation through the phosphatases Ship1/2 (Pinzon-Guzman et al., 2015). In the present study, we found that inhibition of PDPK-1, but not of P70-S6K or mTORC-2 effectively decreased STAT3 activation. This suggests that PDPK-1 has multiple targets which inhibit rod development. One major pathway involves PKC and STAT3m as we have previously described. In addition we have found a pathway involving P70-S6K and mTORC2 that can influence rod development without altering STAT3 activity. The PDPK-1 inhibition-dependent decrease in STAT3 activation may explain the more intense increase in rhodopsin levels induced by BX795 treatment relative to KU0063794 and PF4708671. LIF increases STAT3 phosphorylation (Zhang et al., 2005), and we also found that LIF is able to completely overcome the effects of BX795, PF4708671, or KU0063794. This exemplifies, the strength of the STAT3 activating pathway and confirms the overall dominance of STAT3 signaling as a major determinant of rod fate specification. In spite of this, it will be important to understand how mTORC2 and P70-S6K can influence the formation of rod photoreceptors, and possibly other retinal cell types.
It will also be important to fully define the developmental role of PDPK-1. There is strong evidence that both its activity and its subcellular localization are highly regulated. Further knowledge concerning the identity of the PDPK-1 regulators, their impact on PDPK-1 localization, and the consequences of PDPK-1 localization on downstream signaling will substantially expand our understanding of how multiple signals trigger or inhibit rod photoreceptor development.
TX and DH performed the statistical analysis and wrote the sections of the manuscript. TX wrote the first draft of the manuscript. All authors contributed to conception and design of the study and manuscript revision, read, and approved the submitted version.
This work was supported by grants from the NIH and the Macula Vision Research Foundation.
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.
The authors thank Evgenya Popova for her critical review and intellectual contribution to this manuscript.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcell.2018.00134/full#supplementary-material
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Keywords: photoreceptor, retina, development, IGF-1, PDPK-1, PKC, STAT3, mTORC2
Citation: Xing T, Hass DT, Zhang SS and Barnstable CJ (2018) The 3-Phosphoinositide-Dependent Protein Kinase 1 Inhibits Rod Photoreceptor Development. Front. Cell Dev. Biol. 6:134. doi: 10.3389/fcell.2018.00134
Received: 17 July 2018; Accepted: 24 September 2018;
Published: 10 October 2018.
Edited by:Jiri Novotny, Charles University, Czechia
Reviewed by:Manoj B. Menon, Hannover Medical School, Germany
José A. Armengol, Universidad Pablo de Olavide, Spain
Copyright © 2018 Xing, Hass, Zhang and Barnstable. 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: Colin J. Barnstable, firstname.lastname@example.org
†These authors have contributed equally to this work