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Gene expression changes of thermo-sensitive transient receptor potential channels in obese mice.

Authors :
Sun, Wuping
Li, Chen
Zhang, Yonghong
Jiang, Changyu
Zhai, Mingzhu
Zhou, Qian
Xiao, Lizu
Deng, Qiwen
Source :
Cell Biology International; Aug2017, Vol. 41 Issue 8, p908-913, 6p
Publication Year :
2017

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10656995
Volume :
41
Issue :
8
Database :
Complementary Index
Journal :
Cell Biology International
Publication Type :
Academic Journal
Accession number :
124277231
Full Text :
https://doi.org/10.1002/cbin.10783