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


Journal

Journal of cellular physiology
ISSN: 1097-4652
Titre abrégé: J Cell Physiol
Pays: United States
ID NLM: 0050222

Informations de publication

Date de publication:
02 2020
Historique:
received: 18 01 2019
accepted: 27 06 2019
pubmed: 23 8 2019
medline: 21 10 2020
entrez: 22 8 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31432516
doi: 10.1002/jcp.29100
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
Cell Cycle Proteins 0
Collagen Type I 0
YAP-Signaling Proteins 0
Yap1 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1821-1837

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Xiaoling Liu (X)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.

Xinyu Long (X)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.

Yanfang Gao (Y)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.

Weiwei Liu (W)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.

Toshihiko Hayashi (T)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.
Department of Chemistry and Life Science, School of Advan ced Engineering, Kogakuin University, Nakanomachi, Hachioji, Tokyo, Japan.

Kazunori Mizuno (K)

Nippi Research Institute of Biomatrix, Ibaraki, Japan.

Shunji Hattori (S)

Nippi Research Institute of Biomatrix, Ibaraki, Japan.

Hitomi Fujisaki (H)

Nippi Research Institute of Biomatrix, Ibaraki, Japan.

Takayuki Ogura (T)

Nippi Research Institute of Biomatrix, Ibaraki, Japan.

Satoshi Onodera (S)

Medical Research Institute of Curing Mibyo, Narusedai, Machida, Tokyo, Japan.

Dan Ohtan Wang (DO)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.

Takashi Ikejima (T)

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, China.
Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research & Development, Shenyang Pharmaceutical University, Shenyang, Liaoning, China.

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Classifications MeSH