Hypoxia-mimetic effects in the secretome of human preadipocytes and adipocytes

被引:15
|
作者
Rosenow, Anja [1 ]
Noben, Jean-Paul [2 ,3 ]
Bouwman, Freek G. [1 ]
Mariman, Edwin C. M. [1 ]
Renes, Johan [1 ]
机构
[1] Maastricht Univ, Dept Human Biol, NUTRIM Sch Nutr Toxicol & Metab, NL-6200 MD Maastricht, Netherlands
[2] Hasselt Univ, Biomed Res Inst, Diepenbeek, Belgium
[3] Transnatl Univ Limburg, Sch Life Sci, Diepenbeek, Belgium
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2013年 / 1834卷 / 12期
关键词
Human (pre)adipocyte; Hypoxia-mimetic; Secretome; Turnover; INDUCIBLE FACTOR 1-ALPHA; ADIPOSE-TISSUE; EXTRACELLULAR-MATRIX; ADIPOKINE EXPRESSION; DIFFERENTIATION; PROTEIN; METABOLISM; GLUCOSE; DYSREGULATION; INFLAMMATION;
D O I
10.1016/j.bbapap.2013.10.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
White adipose tissue (WAT) regulates energy metabolism by secretion of proteins with endocrine and paracrine effects. Dysregulation of the secretome of obesity-associated enlarged WAT may lead to obesity-related disorders. This can be caused by hypoxia as a result of poorly vascularized WAT. The effect of hypoxia on the secretome of human (pre)adipocytes is largely unknown. Therefore, we investigated the effect of CoCl2, a hypoxia mimetic, on the secretome of human SGBS (pre)adipocytes by a proteomics approach combined with bioinformatic analysis. In addition, regulation of protein secretion was examined by protein turnover experiments. As such, secretome changes were particularly associated with protein down-regulation and extracellular matrix protein dysregulation. The observed up-regulation of collagens in adipocytes may be essential for cell survival while down-regulation of collagens in preadipocytes may indicate a disturbed differentiation process. These CoCl2-induced changes reflect WAT dysfunction that ultimately may lead to obesity-associated complications. In addition, 9 novel adipocyte secreted proteins were identified from which 6 were regulated by CoCl2. Mass spectrometry data have been deposited to the ProteomeXchange with identifier PXD000162. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:2761 / 2771
页数:11
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