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Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response
Biochemical and Biophysical Research Communications xxx (2017) 1e6
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Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response Qian Guo a, 1, Sanli Jin a, 1, Hailong Hu a, Ying Zhou a, Yuheng Yan a, He Zong a, Yu Wang a, Hongjuan He a, Yuri Oh b, Chuanpeng Liu a, Ning Gu a, * a b
School of Life Science and Technology, Harbin Institute of Technology, Harbin, China Faculty of Education, Wakayama University, Wakayama, Japan
a r t i c l e i n f o
a b s t r a c t
Article history: Received 1 September 2017 Accepted 6 September 2017 Available online xxx
Adiponectin, an adipocytokine produced by adipocytes, functions as an anti-inflammatory and antiapoptotic substance, while also enhancing insulin sensitivity. Patients or model animals with obesity or diabetes typically present attenuated expression of adiponectin. Moreover, obesity and diabetes are often accompanied with hypoxia in adipose tissue, which may result in endoplasmic reticulum (ER) stress as well as low expression of adiponectin. The purpose of this study was to investigate the specific role of the unfolded protein response (UPR) involved in the low expression of adiponectin induced by hypoxia. Subjecting 3T3-L1 adipocytes to hypoxia significantly reduced adiponectin expression and activated the PERK and IRE1 signaling pathways in a time-dependent manner. The ATF6 signaling pathway showed no obvious changes with hypoxia treatment under a similar time course. Moreover, the down-regulated expression of adiponectin induced by hypoxia was relieved once the PERK and IRE1 signaling pathways were suppressed by the inhibitors GSK2656157 and 4m8C, respectively. Overall, these data demonstrate that hypoxia can suppress adiponectin expression and activate the PERK and IRE1 signaling pathways in differentiated adipocytes, and this two pathways are involved in the suppression of adiponectin expression induced by hypoxia. © 2017 Elsevier Inc. All rights reserved.
Keywords: Hypoxia Adiponectin ER stress Unfolded protein response (UPR) PERK IRE1
1. Introduction Adiponectin is a 30 kDa adipocytokine synthesized and excreted by adipose tissue. This important biomarker structurally contains a globular C-terminal domain and a collagenous N-terminal domain. And it typically exerts insulin sensitizing, anti-inflammatory, and anti-apoptotic functions [1]. Adiponectin has been shown to lower blood glucose levels through suppression of hepatic glucose levels, while also effectuating insulin-sensitizing effects via reduction of hepatic lipids [2,3]. Previous studies have demonstrated that adiponectin activates the AMPK pathway thus regulating fat metabolism and increasing glucose uptake. As such, adiponectin might be an effective agent for treating diabetes [4]. In Type 2 diabetes, lower plasma adiponectin levels have been reported, possibly triggered by metabolically unfavorable conditions such as hypoxia [5,6].
* Corresponding author. School of Life Science and Technology, Harbin Institute of Technology, No. 92 West Da-zhi Street, Harbin, 150001, Heilongjiang, China. E-mail address: [email protected] (N. Gu). 1 These authors are thought to have equal contributions.
Recent studies showed that adipocyte cell volume measurements in obese patients and model animals were significantly increased. This phenomenon caused a deficiency of O2 in the center of the enlarged adipose cells resulting in cytoplasmic hypoxia [7]. In addition, other studies showed that continuously high levels of blood glucose in diabetes patients might also contribute to the hypoxia state in adipose tissue [8]. Hypoxia can affect a number of biological functions such as angiogenesis, cell proliferation, apoptosis and inflammation [9]. It has been reported that prolonged exposure to hypoxia induces insulin resistance in adipose tissue. In addition, adipose tissue exposed to hypoxia, caused by obesity, has been associated with the development of Type 2 diabetes by interfering with the insulin signaling pathway [9,10]. Recent research suggests that hypoxia may also cause accumulation of unfolded proteins in the endoplasmic reticulum (ER) thus resulting in ER stress [11]. To deal with ER stress, cells initiate an adaptive response known as the unfolded protein response (UPR), which is mediated by three transmembrane proteins: PKR-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE1), and activating transcription factor 6 (ATF6) [12]. To date,
http://dx.doi.org/10.1016/j.bbrc.2017.09.020 0006-291X/© 2017 Elsevier Inc. All rights reserved.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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Fig. 1. Hypoxia inhibited the expression of adiponectin in differentiated 3T3-L1 adipocytes. A and B. Lipid accumulation was determined by Oil Red O staining and quantified by measuring absorbance at 510 nm. C and D. The mRNA and protein levels of adiponectin in 3T3-L1 adipocytes were analyzed on day 8 of differentiation by qRT-PCR and Western blot respectively with hypoxia treatment at different time points. The data shown represent the means ± S.E. values of 3e4 independent experiments. **p < 0.01, ***p < 0.001.
little is known about the involvement of the three URP signaling pathways in the observed decrease of adiponectin expression under hypoxia conditions. In this study, we verified that hypoxia activates the PERK and IRE1 signaling pathways but inhibits the expression of adiponectin in 3T3-L1 cells under hypoxia treatment. Furthermore, the present findings demonstrate that the PERK and IRE1 signaling pathways participated in the hypoxia-induced down-regulation of adiponectin expression in 3T3-L1 cells.
2. Materials and methods 2.1. Material and reagents Fetal bovine serum (FBS) and Dulbecco's Modification of Eagle's Medium (DMEM) were obtained from Corning (Herndon, Virginia, USA). Pancreatin was purchased from Invitrogen-Gibco (Grand Island, NY). 3-Isobutyl-1-methylxanthine (IBMX) and insulin were purchased from Sigma-Aldrich (St Louis, MO, USA). Dexamethaone (DEX) was purchased from Nacalai Tesque (Tokyo, Japan). 4m8C and GSK2656157 were purchased from Selleck Chemicals (Houston, Texas, USA). RNAiso Plus was purchased from TaKaRa (Tokyo, Japan). Antibody against adiponectin was obtained from Affinity BioReagents (Colorado, USA). Antibodies against phosphorylated eIF2a (Ser 51), CHOP and tubulin were purchased from Cell Signaling Technology (Danvers, MA, USA). Antibodies against XBP1 and ATF6 were separately from Abcam (Cambridge, MA, USA) and Novus (Colorado, USA). Antibody against b-actin was obtained from Sigma-Aldrich (St Louis, MO, USA).
2.2. Cell culture and hypoxia treatment 3T3-L1 cells were maintained in DMEM supplemented with 10% FBS in a humidified atmosphere (5% CO2, 95% air) at a temperature of 37 C. Two days post-confluence, differentiation of 3T3-L1 preadipocyte was induced by replacing the media with DMEM supplemented with 10% FBS which also contained 0.5 mmol/L IBMX, 2.0 mmol/L DEX and 10 mg/mL insulin. Forty-eight hours later, the media was replaced with DMEM supplemented with 10% FBS and 10 mg/mL insulin once again. With the differentiation, some oil droplets would be secreted. After differentiating for 8 days, differentiated adipocytes were used for the experiments. For hypoxia treatment, the cells were cultured in 5% O2 in a gas-impermeable chamber (Billups-Rothenberg, Inc., Del Mar, CA, USA) at 37 C. For normoxia controls, cells remained to be cultured in the humidified atmosphere (5% CO2, 95% air) at a temperature of 37 C. 2.3. RNA isolation and real-time RT-PCR Total RNA was isolated using RNAiso Plus according to the manufacturer's instructions. Briefly, 1 mg RNA was used to perform reverse transcription using PrimeScript™ RT reagent Kit with gDNA Eraser purchased from TaKaRa (Tokyo, Japan). Real-time polymerase chain reaction amplification of the transcribed cDNA was performed with the SYBR Premix Ex Taq™ Ⅱ purchased from TaKaRa (Tokyo, Japan). The sequences of the primer sets were as follows: 36B4 forward, 50 -GTAGTCAGTCTCCACAGACAAAG C-30 and reverse, 50 eCCGTGTGAGGTCACAGTACC-3’; adiponectin forward, 50 -GTTCT ACTGCAACATTCCGG-30 and reverse, 50 -TACACCTGGAGCCAGACT TG-3’; CHOP forward, 50 -GGGAAACAGCGCATGAAGGA-30 and reverse, 50 -GCGTGATGGTGCTGGGTACA-3’; ATF4 forward, 50 -GAGC
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
Q. Guo et al. / Biochemical and Biophysical Research Communications xxx (2017) 1e6
TTCCTGAACAGCGAAGTG-30 and reverse, 50 -TGGCCACCTCCAGATAGTCATC-3’; XBP1-s forward, 50 -TGAGAACCAGGAGTTAAGAACACGC-30 and reverse, 50 eCCTGCACCTGCTGCGGAC-3’; XBP1-u forward, 50 -TGAGAACCAGGAGTTAAGAACACGC-30 and reverse, 50 CACATAGTCTGAGTGCTGCGG-3’; ATF6 forward, 50 -TGGGCAGGACTATGAAGTAATG-30 and reverse, 50 -CAACGACTCAGGGATGGTGCTG3’. Quantification of gene expression was determined by comparative quantity, using 36B4 gene expression as an internal control. 2.4. Western blot analysis Cells were treated with RIPA lysis buffer supplemented with protease inhibitor cocktail and protein phosphatase inhibitor. Protein concentration was quantified by using a DC protein kit (BioRad Laboratories, Hercules, CA, USA). Samples then were separated and transferred to PVDF membranes. Then, membranes were incubated with primary antibodies overnight at 4 C. Primary antibodies used were against Adiponectin, p-eIF2a, CHOP, XBP1-s, XBP1-u, ATF6, b-actin and tubulin. In the following day, the membranes were incubated with secondary antibody for 2 h at room temperature. Expression levels of the respective proteins were determined by enhanced chemiluminescence reagent. 2.5. Oil Red O staining The cellular lipid content was assessed by Oil Red O staining. Cells were washed twice with phosphate-buffered saline (PBS) and then fixed with 4% paraformaldehyde for 10 min at room temperature. Cells were washed twice with PBS and treated with 60% isopropyl alcohol. Cells were stained with Oil Red O Solution for
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20 min at room temperature followed by incubation in 60% isopropyl alcohol. Cells were fully washed with PBS, visualized by light microscopy, and photographed. In order to obtain quantitative data, 100% isopropyl alcohol was used to extract the Oil Red O absorbed by the cells into a 96-well plate. Absorbance of extracted stain was measured at 510 nm.
2.6. Statistical analysis Results are expressed as the mean ± S.E. values. The significance of difference among all groups were tested by one-way analysis of variance (ANOVA) test, and the comparison between each two groups was carried out using student's t-test.
3. Results 3.1. Hypoxia inhibits the expression of adiponectin in differentiated adipocytes Given that hypoxia is implicated in adipose tissue dysfunction in obesity, differentiated adipocytes were subject to hypoxia for 24 h, and then stained with Oil Red O to test for lipid droplet accumulation. The results showed that there were no significant differences between normoxia and hypoxia groups (Fig. 1A and B). Next, the role of hypoxia was investigated in the expression of adiponectin. The results showed that with increasing time of hypoxia, the expression of adiponectin gradually decreased (Fig. 1C and D).
Fig. 2. Hypoxia activated the PERK and IRE1 signaling pathways in differentiated 3T3-L1 adipocytes. A, C and E. The mRNA levels of ATF4, CHOP, XBP1-u, XBP1-s, and ATF6 in differentiated 3T3-L1 adipocytes treated with hypoxia for 0, 12, 16, 20, 24 h. B, D and F. Western blot analysis of the protein expression of p-eIF2a, CHOP, XBP1-u, XBP1-s, and ATF6 (50 kD and 90 kD) under the same conditions as A (B), C (D) or E (F). The data shown represent the means ± S.E. values of 3e4 independent experiments. *p < 0.05, **p < 0.01, ***p < 0.001.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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3.2. Hypoxia activates the PERK and IRE1 signaling pathways in differentiated adipocytes
3.4. The IRE1 pathway participates in the inhibition of adiponectin expression induced by hypoxia
Effects of ER stress were examined in differentiated adipocytes under hypoxia conditions. The results showed that expression of the activating transcription factor-4 (ATF4) and CCAAT/enhancer binding protein [C/EBP] homologous protein (CHOP), which are constituents of the PERK signaling pathway, was significantly increased in a dose-dependent manner (Fig. 2A and B). Similarly, the mRNA expression of spliced X-box binding protein 1 (XBP1-s) was also markedly increased. This was accompanied by a decrease of unspliced X-box binding protein 1 (XBP1-u) which resulted in the increase of XBP1-s/total XBP1 (Fig. 2C). Protein expression changes were consistent with mRNA data (Fig. 2D). However, the activating transcription factor-6 (ATF6) showed no obvious change (Fig. 2E and F).
Similar to the PERK signaling pathway, the role of the IRE1 pathway in the down-regulation of adiponectin expression was examined. In this study, 4m8C was used to inhibit the IER1 pathway. The results showed that the expression of XBP1-s and the ratio of XBP1-s/total XBP1 were both decreased, indicating that the IRE1 pathway was successfully suppressed (Fig. 4A and B). Similarly, the expression of adiponectin increased in the inhibitor group compared with the hypoxia group (Fig. 4C and D).
3.3. The PERK pathway participates in the inhibition of adiponectin expression induced by hypoxia To determine the role of the PERK signaling pathway in the inhibition of adiponectin expression induced by hypoxia, signaling pathway inhibitor GSK2656157 was used. The results showed that both 1 mmol/L and 5 mmol/L effectively inhibited the mRNA expression of ATF4 and CHOP (Fig. 3A). Western blot analysis showed that the protein level of eukaryotic translation initiation factor 2a (eIF2a) was also decreased in response to the inhibitor (Fig. 3B). Furthermore, the expression of adiponectin was recovered (Fig. 3C and D).
4. Discussion Adiponectin, an adipocytokine produced almost exclusively by adipocytes, has a multifarious biological functions such as antiinflammatory, anti-atherogenic, and anti-proliferative [13]. Previous studies showed that patients or model animals with obesity or diabetes typically have a low expression of adiponectin; however, the underlying mechanism is not known [14,15]. Additional studies inferred that hypoxia might be one of the factors inhibiting the expression of adiponectin [16]. In the case of obesity, excessive adipocyte hypertrophy and the relative lack of blood flow induces hypoxia in adipose tissue, which may lead to alterations in expression of adipocytokines [17]. Results in the present study showed that in differentiated adipocytes, hypoxia treatment decreased the expression of adiponectin in a time-dependent manner (Fig. 1C and D). This observation was consistent with previous reports. In addition, it has been shown that the expression of
Fig. 3. Role of the PERK pathway in the low-expression of adiponectin induced by hypoxia treatment in differentiated 3T3-L1 adipocytes. A. The gene expression of ATF4 and CHOP at the mRNA level in differentiated 3T3-L1 adipocytes with GSK2656157 pretreatment for 2 h and hypoxia treatment for 12 h. B. Western blot analysis of CHOP and the phosphorylation of eIF2a in adipocytes with the same treatment conditions as in A. C. Gene expression of adiponectin at the mRNA level in differentiated 3T3-L1 adipocytes with the same treatment conditions as in A. D. Western blot analysis of adiponectin with the same treatment conditions in A. The data shown represent the means ± S.E. values of 3e4 independent experiments. *p < 0.05 vs. normoxia; **p < 0.01 vs. normoxia; ***p < 0.001 vs. normoxia; #p < 0.05 vs. hypoxia; ##p < 0.01 vs. hypoxia; ###p < 0.001 vs. hypoxia.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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Fig. 4. Role of the IRE1 pathway in the low-expression of adiponectin induced by hypoxia treatment in differentiated 3T3-L1 adipocytes. A. The gene expression of XBP1-s and XBP1-u at the mRNA level in differentiated 3T3-L1 adipocytes with the 4m8C pretreatment for 2 h and hypoxia treatment for 12 h. B. Western blot analysis of XBP1-s and XBP1-u in adipocytes with the same treatment conditions as in A. C. The gene expression of adiponectin at mRNA levels in differentiated 3T3-L1 adipocytes with the same treatment conditions as in A. D. Western blot analysis of adiponectin with the same treatment conditions in A. The data shown represent the means ± S.E. values of 3e4 independent experiments. **p < 0.01 vs. normoxia; ***p < 0.001 vs. normoxia; ##p < 0.01 vs. hypoxia; ###p < 0.001 vs. hypoxia.
adiponectin is influenced by the degree of cell differentiation in 3T3-L1 cells [18]. Therefore, in the present study, the differentiation degree of 3T3-L1 cells treated with hypoxia was determined by measuring cellular lipid accumulation. Results showed that compared with the control group, hypoxia treatment for 24h had no influence on adipocyte differentiation (Fig. 1A and B). This indicated that the degree of differentiation did not impact adiponectin expression in response to hypoxia. Therefore, additional research is needed to determine the mechanism of adiponectin down-regulation induced by hypoxia. Several studies have reported that cellular disturbances including hypoxia, oxidative stress and calcium dysregulation can cause accumulation of unfolded proteins. This results in ER stress also known as the unfolded protein response (UPR) [19]. UPR is known to be mediated by three transmembrane proteins: PKR-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE1), and activating transcription factor 6 (ATF6) [12]. Increasing evidence suggests that ER stress might induce lipogenesis and promote obesityrelated insulin resistance, Type 2 diabetes, and hepatic steatosis. In addition, studies have showed that ER stress reduces the adiponectin levels in both serum and adipose tissue [20]. Although ER stress is involved in the down-regulation of adiponectin induced by hypoxia, little is known about the role of PERK, IRE1, and ATF6. PERK is transmembrane serine/threonine protein kinase. Activated PERK undergoes dimerization and trans-autophosphorylation to activate eIF2a which is located downstream of PERK
[21,22]. Active eIF2a inhibits the general initiation of translation. However, ATF4 was activated upon the PERK-mediated phosphorylation of eIF2a due to selective translation [23]. Increased ATF4 upregulates the pro-apoptotic transcription factor CHOP. Once activated, CHOP regulates the expression of several apoptotic genes in the nucleus. Particularly, it downregulates Bcl-2 expression for the proapoptotic phenotype [24]. In this study, we explored whether hypoxia activated the PERK signaling pathway. The results showed that the expression of p-eIF2a, ATF4, and CHOP increased significantly in differentiated adipocytes under hypoxia. This suggested that hypoxia successfully activated the PERK signaling pathway (Fig. 2A and B). IRE1 is a bifunctional enzyme with serine/ threonine kinase and endoribonuclease activities in its C-terminal domain and an ER stress-sensing domain in the N-terminus [25]. Activated IRE1 likewise undergoes dimerization and autophosphorylation. These post-translational modifications induce activation of site-specific endoribonuclease activity and initiate splicing of a 26-base intron from XBP1 mRNA to form XBP1-s. This activity promotes the expression of genes involved in the degradation of misfolded or unfolded proteins [26]. In this study, adipocytes treated by hypoxia for 24 h showed an increase in spliced XBP1, implying that hypoxia also activated the IRE1 signaling pathway (Fig. 2C and D). Similar to the PERK and IRE1 pathways, once the pathway is activated, ATF6, as a type II transmembrane protein, migrates to the Golgi apparatus where it is cleaved by site-1 protease (S1P) and site-2 protease (S2P) to yield a 50 kD-cleaved ATF6.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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The 50 kD ATF6 then is translocated to the cell nucleus and binds to a response element in genes encoding ER chaperone proteins. This, in turn, increases protein folding activity [25]. In this study, no changes in the 50 kD ATF6 subunit were observed in adipocytes with hypoxia treatment (Fig. 2E and F). These results indicated that hypoxia failed to activate the ATF6 signaling pathway in a timedependent manner. Given that hypoxia could activate the PERK and IRE1 signaling pathways as well as suppress adiponectin expression, we sought to investigate whether the PERK and IRE1 pathways had an impact on the regulation of adiponectin expression. GSK2656157 and 4m8C were used to inhibit the PERK and IRE1 pathways, respectively. GSK2656157 is an ATP-competitive and highly selective inhibitor of PERK activation and decreases the levels of downstream substrates including phosphorylated p-eIF2a, ATF4, and CHOP [27]. 4m8C is a potent and selective IRE1 RNase inhibitor used as a platform for developing new locally acting drugs. Results in this study showed that GSK2656157 successfully inhibited the level of ATF4, CHOP, and p-eIF2a under hypoxia conditions in differentiated adipocytes (Fig. 3A and B). Likewise, we applied the ratio of XBP1-s/total XBP1 as an indicator to test the splicing of XBP1, which was effectively inhibited by 4m8C. (Fig. 4A and B). Likewise, the expression of adiponectin was subsequently tested. Results showed that either the PERK or the IRE1 pathway being inhibited, the suppression of adiponectin by hypoxia was then recovered (Fig. 3C/D and 4C/D). Thus, it can be concluded that the PERK and IRE1 signaling pathways participated in the suppression of adiponectin induced by hypoxia in differentiated adipocytes. In summary, the present study demonstrated that hypoxia suppressed adiponectin expression and activated the PERK and IRE1 signaling pathways in differentiated adipocytes. Furthermore, the two pathways were involved in the suppression of adiponectin expression by hypoxia. Further studies are needed to fully elucidate the specific underlying molecular mechanisms. Acknowledgments This work was supported by funds of the National Natural Science Foundation of China (Grant No. 21677044, 31271593), the Open Project of State Key Laboratory of Urban Water Resource and Environment of Harbin Institute of Technology (Grant No. ES201115, ES201512), the National Funds for Creative Research Group of China (Grant No. 51121062), the Fundamental Research Funds for the Central Universities (Grant No. HIT. NSRIF. 201669).
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Transparency document related to this article can be found online at https://doi.org/10.1016/j.bbrc.2017.09.020.
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Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response Qian Guo a, 1, Sanli Jin a, 1, Hailong Hu a, Ying Zhou a, Yuheng Yan a, He Zong a, Yu Wang a, Hongjuan He a, Yuri Oh b, Chuanpeng Liu a, Ning Gu a, * a b
School of Life Science and Technology, Harbin Institute of Technology, Harbin, China Faculty of Education, Wakayama University, Wakayama, Japan
a r t i c l e i n f o
a b s t r a c t
Article history: Received 1 September 2017 Accepted 6 September 2017 Available online xxx
Adiponectin, an adipocytokine produced by adipocytes, functions as an anti-inflammatory and antiapoptotic substance, while also enhancing insulin sensitivity. Patients or model animals with obesity or diabetes typically present attenuated expression of adiponectin. Moreover, obesity and diabetes are often accompanied with hypoxia in adipose tissue, which may result in endoplasmic reticulum (ER) stress as well as low expression of adiponectin. The purpose of this study was to investigate the specific role of the unfolded protein response (UPR) involved in the low expression of adiponectin induced by hypoxia. Subjecting 3T3-L1 adipocytes to hypoxia significantly reduced adiponectin expression and activated the PERK and IRE1 signaling pathways in a time-dependent manner. The ATF6 signaling pathway showed no obvious changes with hypoxia treatment under a similar time course. Moreover, the down-regulated expression of adiponectin induced by hypoxia was relieved once the PERK and IRE1 signaling pathways were suppressed by the inhibitors GSK2656157 and 4m8C, respectively. Overall, these data demonstrate that hypoxia can suppress adiponectin expression and activate the PERK and IRE1 signaling pathways in differentiated adipocytes, and this two pathways are involved in the suppression of adiponectin expression induced by hypoxia. © 2017 Elsevier Inc. All rights reserved.
Keywords: Hypoxia Adiponectin ER stress Unfolded protein response (UPR) PERK IRE1
1. Introduction Adiponectin is a 30 kDa adipocytokine synthesized and excreted by adipose tissue. This important biomarker structurally contains a globular C-terminal domain and a collagenous N-terminal domain. And it typically exerts insulin sensitizing, anti-inflammatory, and anti-apoptotic functions [1]. Adiponectin has been shown to lower blood glucose levels through suppression of hepatic glucose levels, while also effectuating insulin-sensitizing effects via reduction of hepatic lipids [2,3]. Previous studies have demonstrated that adiponectin activates the AMPK pathway thus regulating fat metabolism and increasing glucose uptake. As such, adiponectin might be an effective agent for treating diabetes [4]. In Type 2 diabetes, lower plasma adiponectin levels have been reported, possibly triggered by metabolically unfavorable conditions such as hypoxia [5,6].
* Corresponding author. School of Life Science and Technology, Harbin Institute of Technology, No. 92 West Da-zhi Street, Harbin, 150001, Heilongjiang, China. E-mail address: [email protected] (N. Gu). 1 These authors are thought to have equal contributions.
Recent studies showed that adipocyte cell volume measurements in obese patients and model animals were significantly increased. This phenomenon caused a deficiency of O2 in the center of the enlarged adipose cells resulting in cytoplasmic hypoxia [7]. In addition, other studies showed that continuously high levels of blood glucose in diabetes patients might also contribute to the hypoxia state in adipose tissue [8]. Hypoxia can affect a number of biological functions such as angiogenesis, cell proliferation, apoptosis and inflammation [9]. It has been reported that prolonged exposure to hypoxia induces insulin resistance in adipose tissue. In addition, adipose tissue exposed to hypoxia, caused by obesity, has been associated with the development of Type 2 diabetes by interfering with the insulin signaling pathway [9,10]. Recent research suggests that hypoxia may also cause accumulation of unfolded proteins in the endoplasmic reticulum (ER) thus resulting in ER stress [11]. To deal with ER stress, cells initiate an adaptive response known as the unfolded protein response (UPR), which is mediated by three transmembrane proteins: PKR-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE1), and activating transcription factor 6 (ATF6) [12]. To date,
http://dx.doi.org/10.1016/j.bbrc.2017.09.020 0006-291X/© 2017 Elsevier Inc. All rights reserved.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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Fig. 1. Hypoxia inhibited the expression of adiponectin in differentiated 3T3-L1 adipocytes. A and B. Lipid accumulation was determined by Oil Red O staining and quantified by measuring absorbance at 510 nm. C and D. The mRNA and protein levels of adiponectin in 3T3-L1 adipocytes were analyzed on day 8 of differentiation by qRT-PCR and Western blot respectively with hypoxia treatment at different time points. The data shown represent the means ± S.E. values of 3e4 independent experiments. **p < 0.01, ***p < 0.001.
little is known about the involvement of the three URP signaling pathways in the observed decrease of adiponectin expression under hypoxia conditions. In this study, we verified that hypoxia activates the PERK and IRE1 signaling pathways but inhibits the expression of adiponectin in 3T3-L1 cells under hypoxia treatment. Furthermore, the present findings demonstrate that the PERK and IRE1 signaling pathways participated in the hypoxia-induced down-regulation of adiponectin expression in 3T3-L1 cells.
2. Materials and methods 2.1. Material and reagents Fetal bovine serum (FBS) and Dulbecco's Modification of Eagle's Medium (DMEM) were obtained from Corning (Herndon, Virginia, USA). Pancreatin was purchased from Invitrogen-Gibco (Grand Island, NY). 3-Isobutyl-1-methylxanthine (IBMX) and insulin were purchased from Sigma-Aldrich (St Louis, MO, USA). Dexamethaone (DEX) was purchased from Nacalai Tesque (Tokyo, Japan). 4m8C and GSK2656157 were purchased from Selleck Chemicals (Houston, Texas, USA). RNAiso Plus was purchased from TaKaRa (Tokyo, Japan). Antibody against adiponectin was obtained from Affinity BioReagents (Colorado, USA). Antibodies against phosphorylated eIF2a (Ser 51), CHOP and tubulin were purchased from Cell Signaling Technology (Danvers, MA, USA). Antibodies against XBP1 and ATF6 were separately from Abcam (Cambridge, MA, USA) and Novus (Colorado, USA). Antibody against b-actin was obtained from Sigma-Aldrich (St Louis, MO, USA).
2.2. Cell culture and hypoxia treatment 3T3-L1 cells were maintained in DMEM supplemented with 10% FBS in a humidified atmosphere (5% CO2, 95% air) at a temperature of 37 C. Two days post-confluence, differentiation of 3T3-L1 preadipocyte was induced by replacing the media with DMEM supplemented with 10% FBS which also contained 0.5 mmol/L IBMX, 2.0 mmol/L DEX and 10 mg/mL insulin. Forty-eight hours later, the media was replaced with DMEM supplemented with 10% FBS and 10 mg/mL insulin once again. With the differentiation, some oil droplets would be secreted. After differentiating for 8 days, differentiated adipocytes were used for the experiments. For hypoxia treatment, the cells were cultured in 5% O2 in a gas-impermeable chamber (Billups-Rothenberg, Inc., Del Mar, CA, USA) at 37 C. For normoxia controls, cells remained to be cultured in the humidified atmosphere (5% CO2, 95% air) at a temperature of 37 C. 2.3. RNA isolation and real-time RT-PCR Total RNA was isolated using RNAiso Plus according to the manufacturer's instructions. Briefly, 1 mg RNA was used to perform reverse transcription using PrimeScript™ RT reagent Kit with gDNA Eraser purchased from TaKaRa (Tokyo, Japan). Real-time polymerase chain reaction amplification of the transcribed cDNA was performed with the SYBR Premix Ex Taq™ Ⅱ purchased from TaKaRa (Tokyo, Japan). The sequences of the primer sets were as follows: 36B4 forward, 50 -GTAGTCAGTCTCCACAGACAAAG C-30 and reverse, 50 eCCGTGTGAGGTCACAGTACC-3’; adiponectin forward, 50 -GTTCT ACTGCAACATTCCGG-30 and reverse, 50 -TACACCTGGAGCCAGACT TG-3’; CHOP forward, 50 -GGGAAACAGCGCATGAAGGA-30 and reverse, 50 -GCGTGATGGTGCTGGGTACA-3’; ATF4 forward, 50 -GAGC
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
Q. Guo et al. / Biochemical and Biophysical Research Communications xxx (2017) 1e6
TTCCTGAACAGCGAAGTG-30 and reverse, 50 -TGGCCACCTCCAGATAGTCATC-3’; XBP1-s forward, 50 -TGAGAACCAGGAGTTAAGAACACGC-30 and reverse, 50 eCCTGCACCTGCTGCGGAC-3’; XBP1-u forward, 50 -TGAGAACCAGGAGTTAAGAACACGC-30 and reverse, 50 CACATAGTCTGAGTGCTGCGG-3’; ATF6 forward, 50 -TGGGCAGGACTATGAAGTAATG-30 and reverse, 50 -CAACGACTCAGGGATGGTGCTG3’. Quantification of gene expression was determined by comparative quantity, using 36B4 gene expression as an internal control. 2.4. Western blot analysis Cells were treated with RIPA lysis buffer supplemented with protease inhibitor cocktail and protein phosphatase inhibitor. Protein concentration was quantified by using a DC protein kit (BioRad Laboratories, Hercules, CA, USA). Samples then were separated and transferred to PVDF membranes. Then, membranes were incubated with primary antibodies overnight at 4 C. Primary antibodies used were against Adiponectin, p-eIF2a, CHOP, XBP1-s, XBP1-u, ATF6, b-actin and tubulin. In the following day, the membranes were incubated with secondary antibody for 2 h at room temperature. Expression levels of the respective proteins were determined by enhanced chemiluminescence reagent. 2.5. Oil Red O staining The cellular lipid content was assessed by Oil Red O staining. Cells were washed twice with phosphate-buffered saline (PBS) and then fixed with 4% paraformaldehyde for 10 min at room temperature. Cells were washed twice with PBS and treated with 60% isopropyl alcohol. Cells were stained with Oil Red O Solution for
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20 min at room temperature followed by incubation in 60% isopropyl alcohol. Cells were fully washed with PBS, visualized by light microscopy, and photographed. In order to obtain quantitative data, 100% isopropyl alcohol was used to extract the Oil Red O absorbed by the cells into a 96-well plate. Absorbance of extracted stain was measured at 510 nm.
2.6. Statistical analysis Results are expressed as the mean ± S.E. values. The significance of difference among all groups were tested by one-way analysis of variance (ANOVA) test, and the comparison between each two groups was carried out using student's t-test.
3. Results 3.1. Hypoxia inhibits the expression of adiponectin in differentiated adipocytes Given that hypoxia is implicated in adipose tissue dysfunction in obesity, differentiated adipocytes were subject to hypoxia for 24 h, and then stained with Oil Red O to test for lipid droplet accumulation. The results showed that there were no significant differences between normoxia and hypoxia groups (Fig. 1A and B). Next, the role of hypoxia was investigated in the expression of adiponectin. The results showed that with increasing time of hypoxia, the expression of adiponectin gradually decreased (Fig. 1C and D).
Fig. 2. Hypoxia activated the PERK and IRE1 signaling pathways in differentiated 3T3-L1 adipocytes. A, C and E. The mRNA levels of ATF4, CHOP, XBP1-u, XBP1-s, and ATF6 in differentiated 3T3-L1 adipocytes treated with hypoxia for 0, 12, 16, 20, 24 h. B, D and F. Western blot analysis of the protein expression of p-eIF2a, CHOP, XBP1-u, XBP1-s, and ATF6 (50 kD and 90 kD) under the same conditions as A (B), C (D) or E (F). The data shown represent the means ± S.E. values of 3e4 independent experiments. *p < 0.05, **p < 0.01, ***p < 0.001.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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3.2. Hypoxia activates the PERK and IRE1 signaling pathways in differentiated adipocytes
3.4. The IRE1 pathway participates in the inhibition of adiponectin expression induced by hypoxia
Effects of ER stress were examined in differentiated adipocytes under hypoxia conditions. The results showed that expression of the activating transcription factor-4 (ATF4) and CCAAT/enhancer binding protein [C/EBP] homologous protein (CHOP), which are constituents of the PERK signaling pathway, was significantly increased in a dose-dependent manner (Fig. 2A and B). Similarly, the mRNA expression of spliced X-box binding protein 1 (XBP1-s) was also markedly increased. This was accompanied by a decrease of unspliced X-box binding protein 1 (XBP1-u) which resulted in the increase of XBP1-s/total XBP1 (Fig. 2C). Protein expression changes were consistent with mRNA data (Fig. 2D). However, the activating transcription factor-6 (ATF6) showed no obvious change (Fig. 2E and F).
Similar to the PERK signaling pathway, the role of the IRE1 pathway in the down-regulation of adiponectin expression was examined. In this study, 4m8C was used to inhibit the IER1 pathway. The results showed that the expression of XBP1-s and the ratio of XBP1-s/total XBP1 were both decreased, indicating that the IRE1 pathway was successfully suppressed (Fig. 4A and B). Similarly, the expression of adiponectin increased in the inhibitor group compared with the hypoxia group (Fig. 4C and D).
3.3. The PERK pathway participates in the inhibition of adiponectin expression induced by hypoxia To determine the role of the PERK signaling pathway in the inhibition of adiponectin expression induced by hypoxia, signaling pathway inhibitor GSK2656157 was used. The results showed that both 1 mmol/L and 5 mmol/L effectively inhibited the mRNA expression of ATF4 and CHOP (Fig. 3A). Western blot analysis showed that the protein level of eukaryotic translation initiation factor 2a (eIF2a) was also decreased in response to the inhibitor (Fig. 3B). Furthermore, the expression of adiponectin was recovered (Fig. 3C and D).
4. Discussion Adiponectin, an adipocytokine produced almost exclusively by adipocytes, has a multifarious biological functions such as antiinflammatory, anti-atherogenic, and anti-proliferative [13]. Previous studies showed that patients or model animals with obesity or diabetes typically have a low expression of adiponectin; however, the underlying mechanism is not known [14,15]. Additional studies inferred that hypoxia might be one of the factors inhibiting the expression of adiponectin [16]. In the case of obesity, excessive adipocyte hypertrophy and the relative lack of blood flow induces hypoxia in adipose tissue, which may lead to alterations in expression of adipocytokines [17]. Results in the present study showed that in differentiated adipocytes, hypoxia treatment decreased the expression of adiponectin in a time-dependent manner (Fig. 1C and D). This observation was consistent with previous reports. In addition, it has been shown that the expression of
Fig. 3. Role of the PERK pathway in the low-expression of adiponectin induced by hypoxia treatment in differentiated 3T3-L1 adipocytes. A. The gene expression of ATF4 and CHOP at the mRNA level in differentiated 3T3-L1 adipocytes with GSK2656157 pretreatment for 2 h and hypoxia treatment for 12 h. B. Western blot analysis of CHOP and the phosphorylation of eIF2a in adipocytes with the same treatment conditions as in A. C. Gene expression of adiponectin at the mRNA level in differentiated 3T3-L1 adipocytes with the same treatment conditions as in A. D. Western blot analysis of adiponectin with the same treatment conditions in A. The data shown represent the means ± S.E. values of 3e4 independent experiments. *p < 0.05 vs. normoxia; **p < 0.01 vs. normoxia; ***p < 0.001 vs. normoxia; #p < 0.05 vs. hypoxia; ##p < 0.01 vs. hypoxia; ###p < 0.001 vs. hypoxia.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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Fig. 4. Role of the IRE1 pathway in the low-expression of adiponectin induced by hypoxia treatment in differentiated 3T3-L1 adipocytes. A. The gene expression of XBP1-s and XBP1-u at the mRNA level in differentiated 3T3-L1 adipocytes with the 4m8C pretreatment for 2 h and hypoxia treatment for 12 h. B. Western blot analysis of XBP1-s and XBP1-u in adipocytes with the same treatment conditions as in A. C. The gene expression of adiponectin at mRNA levels in differentiated 3T3-L1 adipocytes with the same treatment conditions as in A. D. Western blot analysis of adiponectin with the same treatment conditions in A. The data shown represent the means ± S.E. values of 3e4 independent experiments. **p < 0.01 vs. normoxia; ***p < 0.001 vs. normoxia; ##p < 0.01 vs. hypoxia; ###p < 0.001 vs. hypoxia.
adiponectin is influenced by the degree of cell differentiation in 3T3-L1 cells [18]. Therefore, in the present study, the differentiation degree of 3T3-L1 cells treated with hypoxia was determined by measuring cellular lipid accumulation. Results showed that compared with the control group, hypoxia treatment for 24h had no influence on adipocyte differentiation (Fig. 1A and B). This indicated that the degree of differentiation did not impact adiponectin expression in response to hypoxia. Therefore, additional research is needed to determine the mechanism of adiponectin down-regulation induced by hypoxia. Several studies have reported that cellular disturbances including hypoxia, oxidative stress and calcium dysregulation can cause accumulation of unfolded proteins. This results in ER stress also known as the unfolded protein response (UPR) [19]. UPR is known to be mediated by three transmembrane proteins: PKR-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE1), and activating transcription factor 6 (ATF6) [12]. Increasing evidence suggests that ER stress might induce lipogenesis and promote obesityrelated insulin resistance, Type 2 diabetes, and hepatic steatosis. In addition, studies have showed that ER stress reduces the adiponectin levels in both serum and adipose tissue [20]. Although ER stress is involved in the down-regulation of adiponectin induced by hypoxia, little is known about the role of PERK, IRE1, and ATF6. PERK is transmembrane serine/threonine protein kinase. Activated PERK undergoes dimerization and trans-autophosphorylation to activate eIF2a which is located downstream of PERK
[21,22]. Active eIF2a inhibits the general initiation of translation. However, ATF4 was activated upon the PERK-mediated phosphorylation of eIF2a due to selective translation [23]. Increased ATF4 upregulates the pro-apoptotic transcription factor CHOP. Once activated, CHOP regulates the expression of several apoptotic genes in the nucleus. Particularly, it downregulates Bcl-2 expression for the proapoptotic phenotype [24]. In this study, we explored whether hypoxia activated the PERK signaling pathway. The results showed that the expression of p-eIF2a, ATF4, and CHOP increased significantly in differentiated adipocytes under hypoxia. This suggested that hypoxia successfully activated the PERK signaling pathway (Fig. 2A and B). IRE1 is a bifunctional enzyme with serine/ threonine kinase and endoribonuclease activities in its C-terminal domain and an ER stress-sensing domain in the N-terminus [25]. Activated IRE1 likewise undergoes dimerization and autophosphorylation. These post-translational modifications induce activation of site-specific endoribonuclease activity and initiate splicing of a 26-base intron from XBP1 mRNA to form XBP1-s. This activity promotes the expression of genes involved in the degradation of misfolded or unfolded proteins [26]. In this study, adipocytes treated by hypoxia for 24 h showed an increase in spliced XBP1, implying that hypoxia also activated the IRE1 signaling pathway (Fig. 2C and D). Similar to the PERK and IRE1 pathways, once the pathway is activated, ATF6, as a type II transmembrane protein, migrates to the Golgi apparatus where it is cleaved by site-1 protease (S1P) and site-2 protease (S2P) to yield a 50 kD-cleaved ATF6.
Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020
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The 50 kD ATF6 then is translocated to the cell nucleus and binds to a response element in genes encoding ER chaperone proteins. This, in turn, increases protein folding activity [25]. In this study, no changes in the 50 kD ATF6 subunit were observed in adipocytes with hypoxia treatment (Fig. 2E and F). These results indicated that hypoxia failed to activate the ATF6 signaling pathway in a timedependent manner. Given that hypoxia could activate the PERK and IRE1 signaling pathways as well as suppress adiponectin expression, we sought to investigate whether the PERK and IRE1 pathways had an impact on the regulation of adiponectin expression. GSK2656157 and 4m8C were used to inhibit the PERK and IRE1 pathways, respectively. GSK2656157 is an ATP-competitive and highly selective inhibitor of PERK activation and decreases the levels of downstream substrates including phosphorylated p-eIF2a, ATF4, and CHOP [27]. 4m8C is a potent and selective IRE1 RNase inhibitor used as a platform for developing new locally acting drugs. Results in this study showed that GSK2656157 successfully inhibited the level of ATF4, CHOP, and p-eIF2a under hypoxia conditions in differentiated adipocytes (Fig. 3A and B). Likewise, we applied the ratio of XBP1-s/total XBP1 as an indicator to test the splicing of XBP1, which was effectively inhibited by 4m8C. (Fig. 4A and B). Likewise, the expression of adiponectin was subsequently tested. Results showed that either the PERK or the IRE1 pathway being inhibited, the suppression of adiponectin by hypoxia was then recovered (Fig. 3C/D and 4C/D). Thus, it can be concluded that the PERK and IRE1 signaling pathways participated in the suppression of adiponectin induced by hypoxia in differentiated adipocytes. In summary, the present study demonstrated that hypoxia suppressed adiponectin expression and activated the PERK and IRE1 signaling pathways in differentiated adipocytes. Furthermore, the two pathways were involved in the suppression of adiponectin expression by hypoxia. Further studies are needed to fully elucidate the specific underlying molecular mechanisms. Acknowledgments This work was supported by funds of the National Natural Science Foundation of China (Grant No. 21677044, 31271593), the Open Project of State Key Laboratory of Urban Water Resource and Environment of Harbin Institute of Technology (Grant No. ES201115, ES201512), the National Funds for Creative Research Group of China (Grant No. 51121062), the Fundamental Research Funds for the Central Universities (Grant No. HIT. NSRIF. 201669).
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Transparency document related to this article can be found online at https://doi.org/10.1016/j.bbrc.2017.09.020.
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Please cite this article in press as: Q. Guo, et al., Hypoxia in 3T3-L1 adipocytes suppresses adiponectin expression via the PERK and IRE1 unfolded protein response, Biochemical and Biophysical Research Communications (2017), http://dx.doi.org/10.1016/j.bbrc.2017.09.020