|  Help  |  About  |  Contact Us

Publication : Critical role for cytosolic group IVA phospholipase A2 in early adipocyte differentiation and obesity.

First Author  Peña L Year  2016
Journal  Biochim Biophys Acta Volume  1861
Issue  9 Pt A Pages  1083-1095
PubMed ID  27317983 Mgi Jnum  J:251181
Mgi Id  MGI:6105356 Doi  10.1016/j.bbalip.2016.06.004
Citation  Pena L, et al. (2016) Critical role for cytosolic group IVA phospholipase A2 in early adipocyte differentiation and obesity. Biochim Biophys Acta 1861(9 Pt A):1083-1095
abstractText  Adipogenesis is the process of differentiation of immature mesenchymal stem cells into adipocytes. Elucidation of the mechanisms that regulate adipocyte differentiation is key for the development of novel therapies for the control of obesity and related comorbidities. Cytosolic group IVA phospholipase A2 (cPLA2alpha) is the pivotal enzyme in receptor-mediated arachidonic acid (AA) mobilization and attendant eicosanoid production. Using primary multipotent cells and cell lines predetermined to become adipocytes, we show here that cPLA2alpha displays a proadipogenic function that occurs very early in the adipogenic process. Interestingly, cPLA2alpha levels decrease during adipogenesis, but cPLA2alpha-deficient preadipocytes exhibit a reduced capacity to differentiate into adipocytes, which affects early and terminal adipogenic transcription factors. Additionally, the absence of the phospholipase alters proliferation and cell-cycle progression that takes place during adipogenesis. Preconditioning of preadipocytes with AA increases the adipogenic capacity of these cells. Moreover, animals deficient in cPLA2alpha show resistance to obesity when fed a high fat diet that parallels changes in the expression of adipogenic transcription factors of the adipose tissue. Collectively, these results show that preadipocyte cPLA2alpha activation is a hitherto unrecognized factor for adipogenesis in vitro and in vivo.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

3 Bio Entities

Trail: Publication

0 Expression