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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.
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页码:2761 / 2771
页数:11
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