| Literature DB >> 28322447 |
Jiaqi Liu1,2,3, Ziye Xu1,2,3, Weiche Wu1,2,3, Yizhen Wang1,2,3, Tizhong Shan1,2,3.
Abstract
The cyclic adenosine monophosphate (cAMP)-protein kinase A (PKA) signaling pathway plays important role in regulating energy homeostasis. Many of the effects of the cAMP-PKA signaling is mediated through the cAMP responsive element binding protein (CREB) and its coactivator CREB-regulated transcription coactivators (CRTCs). CRTC3 is a member of CRTCs family proteins and plays important roles in glucose and energy metabolism. Previous studies show that global knockout of CRTC3 enhances oxygen consumption and energy expenditure and subsequently protects the knockout animal against obesity. In skeletal muscle, CRTC3 affects lipid and glycogen metabolism and mitochondrial biogenesis. In white adipocytes, CRTC3 regulates GLUT4 expression and glucose uptake. More recently, the localization and function of CRTC3 in brown fat have been reported. In this review, we mainly discuss the regulatory role of CRTC3 in skeletal muscle and adipose tissues.Entities:
Keywords: CRTC3; adipose tissue; glucose and lipid metabolism; skeletal muscle
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Year: 2017 PMID: 28322447 DOI: 10.1002/jcp.25917
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384