Down-regulation of Tissue Inhibitor of Metalloproteinase-3 (TIMP-3) Expression Is Necessary for Adipocyte Differentiation

被引:42
作者
Bernot, Denis [1 ]
Barruet, Emilie [1 ]
Poggi, Marjorie [1 ]
Bonardo, Bernadette [1 ]
Alessi, Marie-Christine [1 ]
Peiretti, Franck [1 ]
机构
[1] Univ Aix Marseille 2, Fac Med, INSERM, U626, F-13385 Marseille 5, France
关键词
NUTRITIONALLY INDUCED OBESITY; SP1 TRANSCRIPTION FACTOR; WHITE ADIPOSE-TISSUE; MATRIX METALLOPROTEINASES; GENE-TRANSCRIPTION; FUNCTIONAL-ROLE; MICE; ADIPOGENESIS; APOPTOSIS; PROMOTER;
D O I
10.1074/jbc.M109.078444
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
Matrix metalloproteinase activity is essential for proper extracellular matrix remodeling that takes place during adipose tissue formation. Four tissue inhibitors of matrix metalloproteinases (TIMPs) regulate their activity. However, the role of TIMPs in adipocyte differentiation is poorly understood. We found that the expression of all TIMPs was modified during adipocyte differentiation, but that of TIMP-3 was distinguished by its extreme down-regulation. TIMP-3 expression was closely linked to the differentiation process. Indeed, it remained low during the adipocyte differentiation but increased when cell differentiation was prevented. We identified the transcription factor Sp1 as being responsible for the regulation of TIMP-3 expression during adipocyte differentiation. Overexpression of TIMP-3 reduced adipocyte differentiation, underlining its active role in this process. TIMP-3 overexpression decreased the expression of the early and obligate key inductors of adipogenesis Kruppel-like factor 4 (Klf4), early growth response 2 (Egr2/Krox20), and CAAT/enhancer-binding protein beta (C/EBP beta). Our results indicate that during preadipocyte differentiation, the Sp1-dependent decrease in TIMP-3 expression is required for the successful implementation of the adipocyte differentiation program.
引用
收藏
页码:6508 / 6514
页数:7
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