Sun Wuping, Li Chen, Zhang Yonghong, Jiang Changyu, Zhai Mingzhu, Zhou Qian, Xiao Lizu, Deng Qiwen
Department of Pain Medicine and Shenzhen Municipal Key Laboratory for Pain Medicine, The Affiliated Nanshan People's Hospital of Shenzhen University, Shenzhen Municipal Sixth People's Hospital, Shenzhen, 518060, China.
Laboratory of Medicinal Plant, School of Basic Medicine; Laboratory of Chinese Herbal Pharmacology, Oncology Center, Renmin Hospital; Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine, Hubei, 442000, China.
Cell Biol Int. 2017 Aug;41(8):908-913. doi: 10.1002/cbin.10783. Epub 2017 Jun 19.
Adipose tissues play key roles in energy homeostasis. Brown adipocytes and beige adipocytes in white adipose tissue (WAT) share the similar characters of thermogenesis, both of them could be potential targets for obesity management. Several thermo-sensitive transient receptor potential channels (thermoTRPs) are shown to be involved in adipocyte biology. However, the expression pattern of thermoTRPs in adipose tissues from obese mice is still unknown. The mRNA expression of thermoTRPs in subcutaneous WAT (sWAT) and interscapular brown adipose tissue (iBAT) from lean and obese mice were measured using reverse transcriptase-quantitative PCRs (RT-qPCR). The results demonstrated that all 10 thermoTRPs are expressed in both iBAT and sWAT, and without significant difference in the mRNA expression level of thermoTRPs between these two tissues. Moreover, Trpv1 and Trpv3 mRNA expression levels in both iBAT and sWAT were significantly decreased in high fat diet (HFD)-induced obese mice and db/db (leptin receptor deficient) mice. Trpm2 mRNA expression level was significantly decreased only in sWAT from HFD-induced obese mice and db/db mice. On the other hand, Trpv2 and Trpv4 mRNA expression levels in iBAT and sWAT were significantly increased in HFD-induced obese mice and db/db mice. Taken together, we conclude that all 10 thermoTRPs are expressed in iBAT and sWAT. And several thermoTRPs differentially expressed in adipose tissues from HFD-induced obese mice and db/db mice, suggesting a potential involvement in anti-obesity regulations.
脂肪组织在能量稳态中发挥着关键作用。白色脂肪组织(WAT)中的棕色脂肪细胞和米色脂肪细胞具有相似的产热特性,它们都可能是肥胖管理的潜在靶点。几种热敏性瞬时受体电位通道(thermoTRPs)已被证明参与脂肪细胞生物学过程。然而,肥胖小鼠脂肪组织中thermoTRPs的表达模式仍不清楚。使用逆转录定量PCR(RT-qPCR)测量了瘦小鼠和肥胖小鼠皮下WAT(sWAT)和肩胛间棕色脂肪组织(iBAT)中thermoTRPs的mRNA表达。结果表明,所有10种thermoTRPs在iBAT和sWAT中均有表达,且这两种组织中thermoTRPs的mRNA表达水平无显著差异。此外,在高脂饮食(HFD)诱导的肥胖小鼠和db/db(瘦素受体缺陷)小鼠中,iBAT和sWAT中Trpv1和Trpv3的mRNA表达水平均显著降低。Trpm2的mRNA表达水平仅在HFD诱导的肥胖小鼠和db/db小鼠的sWAT中显著降低。另一方面,在HFD诱导的肥胖小鼠和db/db小鼠中,iBAT和sWAT中Trpv2和Trpv4的mRNA表达水平显著升高。综上所述,我们得出结论,所有10种thermoTRPs在iBAT和sWAT中均有表达。并且几种thermoTRPs在HFD诱导的肥胖小鼠和db/db小鼠的脂肪组织中差异表达,表明其可能参与抗肥胖调节。