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Type I collagen inhibits adipogenic differentiation via YAP activation in vitro.

Authors :
Liu, Xiaoling
Long, Xinyu
Gao, Yanfang
Liu, Weiwei
Hayashi, Toshihiko
Mizuno, Kazunori
Hattori, Shunji
Fujisaki, Hitomi
Ogura, Takayuki
Onodera, Satoshi
Wang, Dan Ohtan
Ikejima, Takashi
Source :
Journal of Cellular Physiology. Feb2020, Vol. 235 Issue 2, p1821-1837. 17p.
Publication Year :
2020

Abstract

Extracellular matrix (ECM) has a marked influence on adipose tissue development. Adipose tissue formation is initiated with proliferation of preadipocytes and migration before undergoing further differentiation into mature adipocytes. Previous studies showed that collagen I (col I) provides a good substratum for 3T3‐L1 preadipocytes to grow and migrate. However, it remains unclear whether and how col I regulates adipogenic differentiation of preadipocytes. This study reports that lipid accumulation, representing in vitro adipogenesis of the 3T3‐L1 preadipocytes or the mouse primary adipocyte precursor cells derived from subcutaneous adipose tissue in the inguinal region is inhibited by the culture on col I, owing to downregulation of adipogenic factors. Previous study shows that col I enhances 3T3‐L1 cell migration via stimulating the nuclear translocation of yes‐associated protein (YAP). In this study, we report that downregulation of YAP is associated with in vitro adipogenesis of preadipocytes as well as with in vivo adipose tissue of high‐fat diet fed mice. Increased expression of YAP in the cells cultured on col I‐coated dishes is correlated with repression of adipogenic differentiation processes. The inactivation of YAP using YAP inhibitor, verteporfin, or YAP small‐interfering RNA enhanced adipogenic differentiation and reversed the inhibitory effect of col I. Activation of YAP either by the transfection of YAP plasmid or the silence of large tumor suppressor 1 (LATS1), an inhibitory kinase of YAP, inhibited adipogenic differentiation. The results indicate that col I inhibits adipogenic differentiation via YAP activation in vitro. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219541
Volume :
235
Issue :
2
Database :
Academic Search Index
Journal :
Journal of Cellular Physiology
Publication Type :
Academic Journal
Accession number :
139842619
Full Text :
https://doi.org/10.1002/jcp.29100