ORIGINAL RESEARCH article
Lipoprotein Lipase Expression in Hypothalamus Is Involved in the Central Regulation of Thermogenesis and the Response to Cold Exposure
- 1Unité de Biologie Fonctionnelle et Adaptative, CNRS UMR 8251, Sorbonne Paris Cité, Université Denis Diderot, Paris, France
- 2NeurObesity Group, Department of Physiology, Centro de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), University of Santiago de Compostela-Instituto de Investigación Sanitaria, Santiago de Compostela, Spain
- 3CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Santiago de Compostela, Spain
Lipoprotein lipase (LPL) is expressed in different areas of the brain, including the hypothalamus and plays an important role in neural control of the energy balance, including feeding behavior and metabolic fluxes. This study tested the hypothesis that hypothalamic LPL participates in the control of body temperature. We first showed that cold exposure induces decreased activity and expression of LPL in the mouse hypothalamus. We then selectively deleted LPL in the mediobasal hypothalamus (MBH) through an adeno-associated virus approach in LPL-floxed mice and generated MBHΔLpl mice with 30–35% decrease in hypothalamic LPL activity. Results showed a decrease in body temperature in MBHΔLpl mice when compared with controls at 22°C. Exposure to cold (4°C for 4 h) decreased the body temperature of the control mice while that of the MBHΔLpl mice remained similar to that observed at 22°C. MBHΔLpl mice also showed increased energy expenditure during cold exposure, when compared to controls. Finally, the selective MBH deletion of LPL also increased the expression of the thermogenic PRMD16 and Dio2 in subcutaneous and perigonadal adipose tissues. Thus, the MBH LPL deletion seems to favor thermogenesis. These data demonstrate that for the first time hypothalamic LPL appears to function as a regulator of body temperature and cold-induced thermogenesis.
Adaptation to change in ambient temperature, especially cold exposure, is one of the mechanisms essential to the survival of mammals. This adaptation involves numerous signals of neural or hormonal origin and acute responses or acclimatization to prolonged cold exposures (1). Acute responses include vasoconstriction or shivering. The hypothalamus is a key area of central nervous system (CNS) involved in the adaptation to cold exposure. Indeed, afferent signals from the skin are sensed by the preoptic area of the anterior hypothalamus. The measurement of c-fos expression also suggests a role for the dorsomedial, medial, and the ventromedial hypothalamus after cold exposure in rats (2). In addition, several studies have also highlighted a role for arcuate (ARC) or ventromedial (VMH) nuclei in this adaptation (3, 4). Peripheral adaptation to cold exposure involves the activation of the sympathetic nervous system (SNS) and hypothalamic–pituitary–thyroid axis (5, 6), including an increase in type 2 iodothyronine deiodinase (Dio2) expression that activates thyroxine (T4) to 3,3′,5-triiodothyronine (T3) (7). These signals combine to activate catabolic pathways with release of energy substrates such as free fatty acids (FFA) into the bloodstream from white adipose tissue (WAT). FFA can then serve to fuel shivering thermogenesis in muscle (8). In contrast, triglycerides (TG) stored in the brown adipose tissue (BAT) are also mobilized as FFA via activation of the SNS, however, these FFA are used primarily within the BAT itself as a fuel to generate heat through uncoupling of oxidative phosphorylation (8). Furthermore, browning of WAT during cold exposure can also be an adaptive mechanism to produce thermogenesis accompanied by increased expression of beige adipocyte markers such as Dio2, PR domain containing 16 (PRDM16), cell death-inducing DNA fragmentation factor α-subunit effector 1 (Cidea), and carnitine palmitoyl transferase-1b (Cpt1b) (9–11). In Humans, short-term cooling increases serum FFA, TG, and total cholesterol concentration (12). Short-term cooling also enhances large very low-density lipoprotein, small low-density lipoprotein, and small high-density lipoprotein particle number (12). Hydrolysis of TG during cold exposure is mainly due to lipoprotein lipase (LPL) that supplies FFA for nonshivering thermogenesis. Short-term cold exposure (i.e., 4–8 h) increased LPL activity in BAT in rats (13), Djungarian hamsters (14), and mice (15). Of note, other lipases such as patatin like phospholipase domain containing 2 [Pnpla2, also known as adipose triglyceride lipase (ATGL)] and hormone-sensitive lipase (HSL) are also affected by cold exposure (16). Interestingly, this cold-induced rise of LPL activity is specific to BAT, while cold exposure decreases epididymal WAT LPL activity in rats (17). Finally, LPL is strongly expressed in the CNS especially in regions involved in the control of the energy balance (18). We have previously shown that a decrease in the expression of LPL in hippocampus (19) or hypothalamus (20) led to the development of obesity and dysregulation of energy homeostasis. Thus, it was tempting to investigate whether hypothalamic LPL was involved in regulation of body temperature depending on different ambient conditions, such as moderate hypothermia relative to thermoneutrality (22°C) or cold (4°C). The passage from 22 to 4°C represents an adaptive challenge requiring increased thermogenic needs (21). To that end, mice deficient for LPL in mediobasal (ARC + VMH) hypothalamus (MBHΔLpl) were generated by bilateral injections of adeno-associated virus (AAV)-cre in the mediobasal hypothalamus (MBH) of Lpllox/lox male mice, leading to a 30–35% decrease in hypothalamic LPL activity as previously published (20). The results obtained from these mice suggest that MBH LPL dampens cold-induced thermogenesis and its deletion promotes cold adaptation.
Materials and Methods
The experimental protocol was approved by the institutional animal care and use committee of the Paris Diderot University (CEEA40) and the agreement # 03752.02 was given to the project.
Ten-week-old Lpllox/lox male mice (Jackson laboratory, strain B6.129S4-Lpltm1Ijg/J, no. 006503) and wild-type littermates were used as controls. They were housed individually in stainless steel cages in a room maintained at 22 ± 1°C with lights on from 07:00 a.m. to 07:00 p.m. They were given a standard laboratory diet (proteins 19.4%, carbohydrates 59.5%, lipids 4.6%, vitamins, and minerals 16.5%) and water ad libitum.
An AAV Cre-GFP was used in order to induce genetic recombination within the hypothalamus in Lpllox/lox mice. The plasmid CBA.nls myc Cre.eGFP expressing the myc-nls-Cre-GFP fusion protein was kindly provided by Richard Palmiter (University of Washington, Seattle, WA, USA). Adeno-associated viruses of the serotype 2/9 (AAV2/9) (6 × 1011 vg/ml and 1.7 × 108 pi/μl) known to have a neuronal tropism (22) were produced by the viral production facility of the UMR INSERM 1089 (Nantes, France).
Surgical and Stereotactic Procedures
At 10 weeks of age, mice were anesthetized with isoflurane and received an i.p. injection of 180 µg/kg buprenorphine hydrochloride (Axiance, Pantin, France) analgesic before being placed on a stereotaxic frame. AAVs were injected bilaterally into the MBH (stereotactic coordinates are relative to bregma: x ± 0.5 mm; y −1.64 mm; z −5.7 mm) at a rate of 0.20 µl/min for a total of 0.5 µl per side, in Lpllox/lox mice (MBHΔLpl mice) and in wild-type C57Bl6/J used as controls (MBHLpl mice). At the end of surgical procedures, mice received an i.p. injection of 50 µg/kg ketoprofen (Mérial, Lyon, France). Intraperitoneal probes (Anipill, Caen, France) were placed in animals during a laparotomy, to measure their body temperature. Animals had 7 days postsurgery to recover.
Animals were individually housed in a cage with lights on from 7 a.m. to 7 p.m. and an ambient temperature of 22 ± 0.5 or 7°C (see Cold Exposure). All animals were acclimated to their cages for 48 h before experimental measurements. Data were collected every 15 min. Animals were analyzed for total energy expenditure (kcal/h), oxygen consumption and carbon dioxide production (VO2 and VCO2, where V is the volume), respiratory exchange rate (RER = VCO2/VO2), food intake (g), and locomotor activity (beam breaks/h) using calorimetric cages with bedding, food and water ad libitum (Labmaster, TSE Systems GmbH, Bad Homburg, Germany). The instrument combined a set of highly sensitive feeding and drinking sensors for automated online measurement. To allow measurement of ambulatory movements, each cage was embedded in a frame with an infrared light beam-based activity monitoring system with online measurement at 100 Hz; the detection of movement operated efficiently in both light and dark phases, allowing continuous recording. Gas ratio was determined using an indirect open-circuit calorimeter (23), which monitored O2 and CO2 concentrations by volume at the inlet ports of a tide cage with an airflow of 0.4 l/min, with regular comparisons to an empty reference cage. Total energy expenditure was calculated according to the Weir equation, using respiratory gas exchange measurements (24). The flow was previously calibrated with O2 and CO2 mixture of known concentrations (Air Liquide, S.A. France). Fatty acid oxidation was calculated from the following equation: fat ox (kcal/h) = energy expenditure × (1 − RER/0.3) according to Bruss et al. (25). Animals were monitored for body weight and composition at the beginning and end of the experiment. Data analysis was carried out with Excel XP using extracted raw values of VO2 consumption, VCO2 production (ml/h), and energy expenditure (kcal/h). Subsequently, each value was expressed either as a function of total body weight or total lean tissue mass extracted from the EchoMRI analysis.
Mice were exposed to cold at 10 days postsurgery. For the acute cold exposure, animals were exposed to 4°C for 4 h in a refrigerated bench, closed by a Plexiglas plate. Additional mice were exposed to 7°C for 24 h in the calorimetric cages described above.
Body Temperature Measurement
Body temperature was measured every 15 min by telemetry with intraperitoneal probes (Anipill, Caen, France). Data were collected by an electronic monitor and transferred to a computer with Anipill Software (Anipill, Caen, France) and were then extracted to an Excel XP file (Microsoft France, Issy-les-Moulineaux, France) before analysis.
BAT Temperature Measurement
Skin temperature surrounding BAT was recorded with an infrared camera (B335: Compact-Infrared-Thermal-Imaging-Camera; FLIR; West Malling, Kent, UK) and analyzed with a FLIR-Tools-Software (FLIR; West Malling, Kent, UK) as previously described (26, 27). For each image, the area surrounding BAT was delimited and the average temperature of the skin area was calculated as the average of two pictures/animal.
Brain tissues were dissected following the Glowinski and Iversen technique (28); hypothalamus, hippocampus, striatum, and cerebral cortex were immediately frozen. In addition, subcutaneous (WATsc) and gonadal white adipose tissue (WATgon) and intrascapular BAT were also collected and immediately frozen for further measurement of mRNA of gene of interest.
LPL Activity Assay
Heparin-releasable LPL activity was assayed in brain regions using a Roar LPL activity assay kit (RB-LPL, Roar Biomedical, Inc.). Briefly, tissues were lysed in 500 µl of assay buffer (150 mM NaCl, 10 mM Tris, 2 mM EDTA, pH 7.4) and incubated for 45 min at 37°C with an equivalent volume of heparin (100 U/ml). After incubation, samples were centrifuged for 10 min at 3,000 g, and aliquots (10 µl for mice) of the aqueous phase deposited on LPL substrate emulsion in 96-well black microplates (VWR International, # 25227-304) and incubated for 1 h at 37°C. Finally, fluorescence was read using a fluorimeter (370 nm excitation/450 nm emission), and compared to a standard curve made using known concentrations of prehydrolyzed LPL substrate. LPL activity was expressed as μmoles of FFA produced per minute per gram of tissue.
Real-Time Quantitative PCR
Total RNA was isolated from the hippocampus dissected at day 28 at the end of the experimentation using RNeasy Lipid Tissue mini kit (Qiagen, Courtaboeuf, France). Real-time quantitative PCR was carried out in a LightCycler 480 detection system (Roche, Meylan, France) using the Light-Cycler FastStart DNA Master plus SYBR Green I kit (Roche). The mRNA transcript level for each gene was normalized against the mean of 2 HKG: rpL19 and TBP, which we have previously shown to be unaffected by LPL inhibition (Table 1: primers sequences).
Data are expressed as mean ± SEM. Statistical analysis were performed using Student’s test or ANOVA followed by two-by-two Bonferroni post hoc test (GraphPad software). p < 0.05 was considered significant. Representative bar graph is expressed as mean ± SEM.
Cold Exposure Decreases Hypothalamic LPL Activity in Control Mice
There was no effect of nutritional status (i.e., fed or fasted) on hypothalamic LPL activity at either ambient temperatures of 22 or 4°C (Figure 1A). In contrast, in fed and fasted mice, exposure after 4 h at 4°C, there was a significant decrease of ~50% in hypothalamic LPL activity when compared with LPL activity at 22°C (Figure 1A). Of note, neither nutritional status nor ambient temperature exposure affected hippocampal LPL activity (Figure 1B).
Figure 1. An acute cold exposure (4 h at 4°C) decreases significantly enzymatic activity of lipoprotein lipase (LPL) in hypothalamus (A) but not in hippocampus (B). LPL activity is expressed in enzymatic units (U, μmol/min) per g of tissue. Data are mean ± SEM, n = 6–8 for each group. *p < 0.05 and ***p < 0.001 vs. mice “fed 22°C”, §p < 0.05 vs. “fasted 22°C” mice.
Cold Exposure-Induced Changes in Brain Gene Expression in Control Mice
Cold exposure induced changes in the expression of genes involved in lipid metabolism in several brains areas (Figure 2). LPL mRNA expression was decreased in response to cold exposure in the hypothalamus, as well as hormone sensitive lipase (Lipe HSL) and abhydrolase domain containing 5 (Abhd5) mRNA. Conversely, acute cold exposure significantly increased the expression of hypothalamic perilipin 5 (Plin 5). Abdh5 and Plin5 are cofactors of the Pnpla2 (also known as ATGL) which catalyzes the first step of intracellular TG hydrolysis (16). No change was observed in the expression of other hypothalamic genes involved in lipid metabolism. In the hippocampus and in the cerebral cortex, cold exposure significantly increased the expression of the perilipin 5 gene, as in the hypothalamus, but also of Pnpla2 (ATGL). No change in expression of mRNAs for lipases or their cofactors was seen in the striatum. For clock genes, the expression of hypothalamic Bmal1 and Clock and striatal Bmal1 mRNA was decreased, while hippocampal Bmal1 expression was increased after cold exposure.
Figure 2. An acute cold exposure modifies the expression of several genes involved in lipid metabolism and circadian clock. mRNA expression in (A) hypothalamus, (B) hippocampus, (C) striatum, and (D) cerebral cortex. Data are mean ± SEM and show change of expression rate relative to mRNA for mice at 22°C. n = 8–10 for each group. *p < 0.05, **p < 0.01, and ***p < 0.001 vs. “fed 22°C” group.
MBH LPL Depletion Dysregulates Body Temperature and Energy Metabolism
As shown in Table 2 and Figure 3A, MBHΔLpl mice had a significantly lower basal temperature at 22°C when compared with controls mice. However, after 4 h of exposure to 4°C, MBHΔLpl mice maintained their body temperature, whereas body temperature fell by 1.2°C during the first hour of cold exposure in control MBHLpl mice and remained lower than that in MBHΔLpl mice for the remainder of the 4 h exposure period. Figure S1 in Supplementary Material shows the temperature time courses for MBHLpl and MBHΔLpl mice with their respective controls maintained at 22°C during 4 h. The thermogenic images over intrascapular BAT pads (Figures 3B–E) and their quantification (Figure 3F) appear to correlate with comparable changes in core body temperature measured with the intraperitoneal probes: MBHΔLpl mice maintained their BAT temperature after 4 h at 4°C, whereas BAT temperature significantly dropped in controls. The expression of uncoupling protein 1 (UCP1) mRNA was upregulated by 4 h of cold exposure in both MBHLpl and MBHΔLpl mice (Figure 3G), and there was no difference in UCP2 and UCP3 expressions in MBHΔLpl mice compared to controls. In MBHLpl mice, expression of β3-adrenoreceptor mRNA was significantly downregulated by the cold exposure, whereas it remained higher in MBHΔLpl mice than their 4°C controls (Figure 3G).
Figure 3. An acute exposure to cold decreases body and skin temperature of MBHLpl mice but not of MBHΔLp (A). Thermic images of brown adipose tissue (BAT) temperature of MBHLpl at 22°C (B) and at 4°C (C) shows a decrease during the acute cold exposure whereas BAT temperature of MBHΔLpl at 22°C (D), is maintained at 4°C (E). The value of BAT temperature for MBHLpl and MBHΔLPL mice at 22°C and at 4°C is presented in a global histogram, showing a decrease of BAT temperature at 4°C for MBHLpl whereas MBHΔLpl mice present no difference at 4°C (F). Measurement of mRNA expression in BAT (G) for uncoupling proteins (UCPs) show no difference between MBHLpl and MBHΔLpl at 22 or at 4°C. mRNA expression of AdRβ3 is increased at 4°C in MBHΔLPL group compared to MBHLpl. Data are mean ± SEM (n = 6). *p < 0.05, **p < 0.01 vs. MBHLpl mice at 22°C, £p < 0.05 vs. MBHLpl mice at 4°C.
During 24 h cold exposure in metabolic cages, food intake was similar in the two groups (Figure S2 in Supplementary Material), and the locomotor activity was decreased during the daylight (cf. Figure 4A) whereas energy expenditure normalized to lean mass was significantly increased in MBHΔLpl mice (Figure 4B). A shown in Figure 4C, these mice presented a trend toward carbohydrate-oriented metabolism before the nighttime, as demonstrated by the increased RER, and consequently a lower rate of fatty acid oxidation (Figure 4D).
Figure 4. Calorimetry and locomotor activity for MBHLPL and MBHΔLPL mice during 24 h of cold exposure at 7°C. (A) Locomotor activity. (B) Energy expenditure normalized per lean body mass. (C) Respiratory exchange rate (RER, VCO2/VO2). (D) Fatty acids oxidation rate. Data are mean ± SEM (n = 5–6). *p < 0.05, **p < 0.01, and ***p < 0.001 vs. MBHLpl mice.
The Expression of “Beige” Genes Is Increased in WAT of MBHΔLpl Mice
Beige adipocytes share some common characteristics with brown adipocytes and have a thermogenic potential. In the subcutaneous adipose tissue, some genes involved in WAT thermogenic function (“beige” markers; CPT1b and PRDM16) were significantly increased in basal conditions (22°C) and remained higher compared than controls after a cold exposure. Moreover, Dio2 gene expression was higher at 22°C in MBHΔLpl mice (Figure 5A). In gonadal WAT, PRDM6 trended to be more expressed in MBHΔLpl mice compared to controls at 22°C, and DiO2 expression showed a ninefold increase following cold exposure (cf. Figure 5B).
Figure 5. Depletion of lipoprotein lipase in the mediobasal hypothalamus (MBH) increases mRNA expression of genes responsible for “beigeing” in white adipose tissues (WATs). (A) mRNA expression in subcutaneous WAT. (B) mRNA expression in gonadal WAT. Data are mean ± SEM and show change of expression rate relative to mRNA for mice at 22°C. n = 4–6 for each group. *p < 0.05, **p < 0.01 vs. MBHLpl mice at 22°C, #p < 0.05, ##p < 0.01, and ###p < 0.001 vs. MBHLpl mice at 4°C, £p < 0.05 vs. MBHΔLpl mice at 22°C.
In the present study, we first demonstrated that hypothalamic LPL mRNA expression and activity were regulated as a function of ambient temperatures between 22 and 4oC. Indeed, cold exposure induced a selective decrease in both LPL activity and gene expression in hypothalamus with no change in mRNA expression in the hippocampus, striatum, or cerebral cortex when temperature dropped from 22 to 4°C. It has already been reported that the expression of the brain LPL was regulated by the 72 h fasted or fed states (29), but to our knowledge it is the first time that a regulation as a function of the ambient temperature is described. We and others previously reported that brain LPL regulated energy balance. Wang et al. showed that neuronal LPL deficiency promoted obesity and maladaptive responses to environmental challenges (30–32). In addition, we reported that specific deletion of hypothalamic LPL induced body weight gain without hyperphagia, but with increased food efficiency in mice (20). Such increased body weight gain was partly explained by an early decrease in locomotor activity, a trend toward lower energy expenditure at night, and a preferential use of carbohydrate rather than lipid metabolism (20).
In the present study, after having shown that LPL in the hypothalamus was regulated by ambient temperature, it seemed important to investigate whether partial invalidation of LPL in the hypothalamus could therefore influence cold adaptation in mice in order to establish a cause-and-effect relationship between the expression of the enzyme and body temperature. It is well known that the control of BAT thermogenesis is regulated by the CNS (33, 34), and numerous studies have highlighted the role of the hypothalamus and the SNS in such control (4, 27, 35, 36). Besides the preoptic area of the hypothalamus, which is considered as a major coordinator of thermoregulation since it receives inputs from skin and visceral thermoreceptors, other nuclei participate in thermoregulation such as the paraventricular, the ARC and the VMH [review by Labbe et al. (4)]. Although the characterization of the neurons controlling thermogenesis remains unsolved, data pointed toward a role for the melanocortin system in stimulating BAT thermogenesis (3). In the ARC, NPY/AgRP neurons inhibit this system while POMC neurons activate it. In the VMH, steroidogenic factor 1 (SF1) neurons are known to affect BAT thermogenesis (37), by integrating both AMPK and mTOR signaling (27, 38, 39). We showed here that LPL deficiency in the hypothalamus induced a dysregulation of thermogenesis in mice at both normal vivarium temperature of 22 and at 4oC. Specifically, MBHΔLpl mice had a significant lower core body temperature compared to controls when the ambient temperature was 22°C. This result seemed to be consistent with our previous observations (i.e., sparing fatty acids and decrease of locomotor activity) (20). As mentioned above, we observed a decrease in both LPL expression and activity in the hypothalamus in normal mice during cold exposure. This result could suggest that the physiological decrease of LPL activity in the hypothalamus, in response to decreased ambient temperature plays a role in adaptive thermogenesis. In accordance with this hypothesis, when the hypothalamic LPL was permanently depleted, the animals presented higher energy expenditure and were able to defend their body temperature more successfully than controls when exposed at 4°C for 4 h. At mild temperature corresponding to their basal housing conditions (22°C), LPL depleted animals displayed a significantly lower body temperature (0.76°C), which could be interpreted as an attempt of saving energy for the long-term. The subsequent question might be to understand how a drop in hypothalamic LPL activity could induce this change in energy flow and control body temperature. It can be hypothesized that a decrease in hypothalamic LPL activity and thus a consequent local decrease in TG hydrolysis and FFA availability could be sensed by specialized neurons (18, 40) as a “thrifty” signal and a need for metabolic adaption. By specifically decreasing LPL in MBH, we therefore mimicked such a “thrifty behavior” that was observed during cold exposure (41). Because MBHΔLpl mice had already displayed some metabolic features of cold exposure, the actual exposure to cold (at least during a short period) did not induce a greater decrease in their body temperature, whereas this occurred in the control mice (decreased body temperature from 37 to 35°C). This adaption could be explained by a modulation of the circadian clock, as it has been shown that transcription of genes involved in the metabolism can be regulated by the circadian clock. For example, Clock and Bmal1 genes favor transcription of Lpl (42). Interestingly, we showed that exposure to cold decreased the expression of Bmal1 and Clock. The downregulation of Bmal1 and Clock mRNA could partly explain the decrease observed for LPL mRNA. Furthermore, a recent study suggested the existence of an independent circadian clock in the VMH (43). Exposure to cold could have an impact on hypothalamic circadian clock and thus on LPL expression. Finally, this study by Orozco-Solis et al. showed that a mouse model KO for Bmal1 in Sf1 neurons of the VMH was associated with increased BAT temperature throughout the diurnal cycle. Therefore, a decrease of Bmal1 expression during cold exposure in MBHΔLpl compared to MBHLpl could contribute to explain the preservation of BAT temperature.
Partial deletion of hypothalamic LPL also resulted in changes in mRNA expression of some marker genes of adipocyte function as well as thermogenesis-related genes. We measured some of these genes of interest in subcutaneous and gonadal adipose tissues. Interestingly, MBHΔLpl mice that were exposed to mild temperature showed a significant increase in PRDM16 expression in WATsc and a tendency in WATgon when compared with controls. PRDM16 is a critical transcriptional regulator of thermogenesis and the increase of PRDM16 in WATsc of MBHΔLpl mice could be interpreted as an attempt to adapt to their decreased body temperature at an ambient temperature of 22°C. It has been reported that adipocyte-specific deletion of PRDM16 markedly inhibited beige adipocyte function in subcutaneous fat following cold exposure or β3-agonist treatment (44). Thus, browning may occur in WATsc of MBHΔLpl mice as an adaptation to chronically lowered body temperature. However, it must be pointed out that such adaptation was not sufficient to bring the body temperature back to that observed in the control mice. This can be explained by the fact that other parameters were also affected by the hypothalamic deletion of LPL (20).
Interestingly, mRNA expression of Dio2, the enzyme that activates T4 to 3,3′,5-triiodothyronine (T3) was also significantly elevated in WATsc of MBHΔLpl mice compared to controls exposed to 22°C. Dio2 is also known as being a thermogenesis-related gene (9). As for PRDM16, the local increase in Dio2 mRNA could be interpreted as an adaptation to the decrease in body temperature through increased local production of T3. During cold exposure, mRNA expression of Dio2 in WATsc was significantly increased in controls to reach a value similar to MBHΔLp mice. As mentioned, exposure to cold induced a decrease in the body temperature of control mice (from 37 to 35°C) while that of MBHΔLPL mice remained constant compared to exposure to mild. During cold exposure, PRDM16 expression remained significantly higher in WATsc of MBHΔLPL mice compared to controls. In WATgon, Dio2 was significantly upregulated in MBHΔLp mice exposed to 4°C as compared with their controls. This could be related to the fact that they managed to maintain their body temperature: the upregulation of browning markers, already present at 22°C, may in part explain the absence of significant fluctuation in body temperature during exposure to cold. In particular, de Jesus et al. showed that increased Dio2 expression in BAT played a key role for local production of T3, even in a situation where serum concentrations of both T3 and T4 remained constant during cold stress (24 h at 4°C) (7). Such a result highlighted a key role for local production of T3 through activation of Dio2.
Finally, skin temperature surrounding BAT was recorded as an indirect index of thermogenesis and BAT function. In control mice, skin temperature decreased when mice were exposed to cold whereas it remained unchanged compared to mild temperature exposure for MBHΔLpl. This could be related to the decrease in body temperature that we also observed. However, in both groups UCP1 mRNA expression was increased during cold temperature when compared to mild exposure. Again, this difference in response between the two groups in the face of cold exposure suggests that the deficiency of LPL in the hypothalamus regulated energy homeostasis and especially thermogenesis.
In conclusion, we demonstrate here for the first time, that LPL in hypothalamus is a negative regulator of thermogenesis. Normal adaptation to a drop-in temperature involves a decrease in hypothalamic LPL activity that promotes cold-induced thermogenesis. A chronic decreased in LPL activity in hypothalamus could impair the regulation of body temperature in response to changes in ambient temperature. More generally, a defect in the central sensing of lipids could compromise the survival of individuals during winter and more particularly when a lack of food also occurred.
The experimental protocol was approved by the institutional animal care and use committee of the Paris Diderot University (CEEA40), and the agreement # 03752.02 was given to the project.
ML, SL, CC-G, and CM designed experiments. EL, RD, NK, CC, and CC-G performed experiments. EL, CC-G, and CM prepared the manuscript. RD, CC, and ML edited the manuscript. The entire study was supervised by CC-G and CM.
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.
This study was supported by grants from National Research Agency (ANR SVSE 1 2011: “lipobrain”) and ANR-16-CE14-0026 “Fat4Brain,” from the European Foundation for Study of Diabetes (EFSD/Lilly Research Fellowship Programme 2014), from Ministerio de Economía y Competitividad (MINECO cofunded by the FEDER Program of EU (ML: SAF2015-71026-R and from Xunta de Galicia (ML: 2015-CP079 and 2016-PG068. CC was recipient of Sara Borrell Contract from ISCIII. We want to warmly thank Pr Barry E. Levin for reading and editing the manuscript.
The Supplementary Material for this article can be found online at https://www.frontiersin.org/articles/10.3389/fendo.2018.00103/full#supplementary-material.
1. Castellani JW, Young AJ. Human physiological responses to cold exposure: Acute responses and acclimatization to prolonged exposure. Auton Neurosci (2016) 196:63–74. doi:10.1016/j.autneu.2016.02.009
3. De Jonghe BC, Hayes MR, Banno R, Skibicka KP, Zimmer DJ, Bowen KA, et al. Deficiency of PTP1B in POMC neurons leads to alterations in energy balance and homeostatic response to cold exposure. Am J Physiol Endocrinol Metab (2011) 300(6):E1002–11. doi:10.1152/ajpendo.00639.2010
7. de Jesus LA, Carvalho SD, Ribeiro MO, Schneider M, Kim SW, Harney JW, et al. The type 2 iodothyronine deiodinase is essential for adaptive thermogenesis in brown adipose tissue. J Clin Invest (2001) 108(9):1379–85. doi:10.1172/JCI13803
9. Kurylowicz A, Jonas M, Lisik W, Jonas M, Wicik ZA, Wierzbicki Z, et al. Obesity is associated with a decrease in expression but not with the hypermethylation of thermogenesis-related genes in adipose tissues. J Transl Med (2015) 13:31. doi:10.1186/s12967-015-0395-2
10. Lau P, Tuong ZK, Wang SC, Fitzsimmons RL, Goode JM, Thomas GP, et al. Roralpha deficiency and decreased adiposity are associated with induction of thermogenic gene expression in subcutaneous white adipose and brown adipose tissue. Am J Physiol Endocrinol Metab (2015) 308(2):E159–71. doi:10.1152/ajpendo.00056.2014
11. Velazquez-Villegas LA, Perino A, Lemos V, Zietak M, Nomura M, Pols TWH, et al. TGR5 signalling promotes mitochondrial fission and beige remodelling of white adipose tissue. Nat Commun (2018) 9(1):245. doi:10.1038/s41467-017-02068-0
12. Hoeke G, Nahon K, Bartelt A, Dinnes D, Drettwan D, Pagel P, et al. Cold exposure beneficially modulates HDL metabolism in mice and humans. Atherosclerosis (2017) 263:e95. doi:10.1016/j.atherosclerosis.2017.06.308
13. Carneheim C, Nedergaard J, Cannon B. Beta-adrenergic stimulation of lipoprotein lipase in rat brown adipose tissue during acclimation to cold. Am J Physiol (1984) 246(4 Pt 1):E327–33. doi:10.1152/ajpendo.1984.246.4.E327
14. Klingenspor M, Ebbinghaus C, Hulshorst G, Stohr S, Spiegelhalter F, Haas K, et al. Multiple regulatory steps are involved in the control of lipoprotein lipase activity in brown adipose tissue. J Lipid Res (1996) 37(8):1685–95.
15. Kuusela P, Jacobsson A, Klingenspor M, Rehnmark S, Heldmaier G, Cannon B, et al. Contrasting adrenergic effects on lipoprotein lipase gene expression in the brown adipose tissue of intact mice and in cultured brown adipocytes from mice. Biochim Biophys Acta (1997) 1345(3):327–37. doi:10.1016/S0005-2760(97)00008-8
16. Caimari A, Oliver P, Palou A. Adipose triglyceride lipase expression and fasting regulation are differently affected by cold exposure in adipose tissues of lean and obese Zucker rats. J Nutr Biochem (2012) 23(9):1041–50. doi:10.1016/j.jnutbio.2011.05.008
19. Picard A, Rouch C, Kassis N, Moulle VS, Croizier S, Denis RG, et al. Hippocampal lipoprotein lipase regulates energy balance in rodents. Mol Metab (2014) 3(2):167–76. doi:10.1016/j.molmet.2013.11.002S2212-8778(13)00120-8
20. Laperrousaz E, Moulle VS, Denis RG, Kassis N, Berland C, Colsch B, et al. Lipoprotein lipase in hypothalamus is a key regulator of body weight gain and glucose homeostasis in mice. Diabetologia (2017) 60:1314–24. doi:10.1007/s00125-017-4282-7
21. Abreu-Vieira G, Xiao C, Gavrilova O, Reitman ML. Integration of body temperature into the analysis of energy expenditure in the mouse. Mol Metab (2015) 4(6):461–70. doi:10.1016/j.molmet.2015.03.001
22. Chakrabarty P, Rosario A, Cruz P, Siemienski Z, Ceballos-Diaz C, Crosby K, et al. Capsid serotype and timing of injection determines AAV transduction in the neonatal mice brain. PLoS One (2013) 8(6):e67680. doi:10.1371/journal.pone.0067680
23. Arch JR, Hislop D, Wang SJ, Speakman JR. Some mathematical and technical issues in the measurement and interpretation of open-circuit indirect calorimetry in small animals. Int J Obes (Lond) (2006) 30(9):1322–31. doi:10.1038/sj.ijo.0803280
25. Bruss MD, Khambatta CF, Ruby MA, Aggarwal I, Hellerstein MK. Calorie restriction increases fatty acid synthesis and whole body fat oxidation rates. Am J Physiol Endocrinol Metab (2010) 298(1):E108–16. doi:10.1152/ajpendo.00524.2009
26. Contreras C, Nogueiras R, Dieguez C, Rahmouni K, Lopez M. Traveling from the hypothalamus to the adipose tissue: the thermogenic pathway. Redox Biol (2017) 12:854–63. doi:10.1016/j.redox.2017.04.019
27. Martinez-Sanchez N, Seoane-Collazo P, Contreras C, Varela L, Villarroya J, Rial-Pensado E, et al. Hypothalamic AMPK-ER stress-JNK1 axis mediates the central actions of thyroid hormones on energy balance. Cell Metab (2017) 26(1):212–29.e212. doi:10.1016/j.cmet.2017.06.014
28. Glowinski J, Iversen LL. Regional studies of catecholamines in the rat brain. I. The disposition of [3H]norepinephrine, [3H]dopamine and [3H]dopa in various regions of the brain. J Neurochem (1966) 13(8):655–69. doi:10.1111/j.1471-4159.1966.tb09873.x
29. Gavin LA, Cavalieri RR, Moeller M, McMahon FA, Castle JN, Gulli R. Brain lipoprotein lipase is responsive to nutritional and hormonal modulation. Metabolism (1987) 36(10):919–24. doi:10.1016/0026-0495(87)90124-7
30. Wang H, Astarita G, Taussig MD, Bharadwaj KG, DiPatrizio NV, Nave KA, et al. Deficiency of lipoprotein lipase in neurons modifies the regulation of energy balance and leads to obesity. Cell Metab (2011) 13(1):105–13. doi:10.1016/j.cmet.2010.12.006
32. Pellinen J, Wang H, Eckel RH. Mice with altered brain lipoprotein metabolism display maladaptive responses to environmental challenges that may predispose to weight gain. Metab Syndr Relat Disord (2014) 12(6):339–46. doi:10.1089/met.2013.0141
35. Contreras C, Gonzalez-Garcia I, Martinez-Sanchez N, Seoane-Collazo P, Jacas J, Morgan DA, et al. Central ceramide-induced hypothalamic lipotoxicity and ER stress regulate energy balance. Cell Rep (2014) 9(1):366–77. doi:10.1016/j.celrep.2014.08.057
37. Choi YH, Fujikawa T, Lee J, Reuter A, Kim KW. Revisiting the ventral medial nucleus of the hypothalamus: the roles of SF-1 neurons in energy homeostasis. Front Neurosci (2013) 7:71. doi:10.3389/fnins.2013.00071
38. Martinez de Morentin PB, Gonzalez-Garcia I, Martins L, Lage R, Fernandez-Mallo D, Martinez-Sanchez N, et al. Estradiol regulates brown adipose tissue thermogenesis via hypothalamic AMPK. Cell Metab (2014) 20(1):41–53. doi:10.1016/j.cmet.2014.03.031
39. Martinez de Morentin PB, Martinez-Sanchez N, Roa J, Ferno J, Nogueiras R, Tena-Sempere M, et al. Hypothalamic mTOR: the rookie energy sensor. Curr Mol Med (2014) 14(1):3–21. doi:10.2174/1566524013666131118103706
41. Zhao ZJ, Chi QS, Cao J, Han YD. The energy budget, thermogenic capacity and behavior in Swiss mice exposed to a consecutive decrease in temperatures. J Exp Biol (2010) 213(Pt 23):3988–97. doi:10.1242/jeb.046821
42. Delezie J, Dumont S, Dardente H, Oudart H, Grechez-Cassiau A, Klosen P, et al. The nuclear receptor REV-ERBalpha is required for the daily balance of carbohydrate and lipid metabolism. FASEB J (2012) 26(8):3321–35. doi:10.1096/fj.12-208751
43. Orozco-Solis R, Aguilar-Arnal L, Murakami M, Peruquetti R, Ramadori G, Coppari R, et al. The circadian clock in the ventromedial hypothalamus controls cyclic energy expenditure. Cell Metab (2016) 23(3):467–78. doi:10.1016/j.cmet.2016.02.003
Keywords: lipoprotein lipase, cold exposure, hypothalamus, brown adipose tissue, browning of white adipose tissue
Citation: Laperrousaz E, Denis RG, Kassis N, Contreras C, López M, Luquet S, Cruciani-Guglielmacci C and Magnan C (2018) Lipoprotein Lipase Expression in Hypothalamus Is Involved in the Central Regulation of Thermogenesis and the Response to Cold Exposure. Front. Endocrinol. 9:103. doi: 10.3389/fendo.2018.00103
Received: 07 December 2017; Accepted: 02 March 2018;
Published: 14 March 2018
Edited by:Jacques Epelbaum, Institut National de la Santé et de la Recherche Médicale (INSERM), France
Reviewed by:Denis Richard, Laval University, Canada
Mario Perello, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina
Copyright: © 2018 Laperrousaz, Denis, Kassis, Contreras, López, Luquet, Cruciani-Guglielmacci and Magnan. 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 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: Céline Cruciani-Guglielmacci, email@example.com