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代谢失调与脂肪组织纤维化:Ⅵ型胶原蛋白的作用

Metabolic dysregulation and adipose tissue fibrosis: role of collagen VI.

作者信息

Khan Tayeba, Muise Eric S, Iyengar Puneeth, Wang Zhao V, Chandalia Manisha, Abate Nicola, Zhang Bei B, Bonaldo Paolo, Chua Streamson, Scherer Philipp E

机构信息

Department of Cell Biology, Diabetes Research Center, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

Mol Cell Biol. 2009 Mar;29(6):1575-91. doi: 10.1128/MCB.01300-08. Epub 2008 Dec 29.

Abstract

Adipocytes are embedded in a unique extracellular matrix whose main function is to provide mechanical support, in addition to participating in a variety of signaling events. During adipose tissue expansion, the extracellular matrix requires remodeling to accommodate adipocyte growth. Here, we demonstrate a general upregulation of several extracellular matrix components in adipose tissue in the diabetic state, therefore implicating "adipose tissue fibrosis" as a hallmark of metabolically challenged adipocytes. Collagen VI is a highly enriched extracellular matrix component of adipose tissue. The absence of collagen VI results in the uninhibited expansion of individual adipocytes and is paradoxically associated with substantial improvements in whole-body energy homeostasis, both with high-fat diet exposure and in the ob/ob background. Collectively, our data suggest that weakening the extracellular scaffold of adipocytes enables their stress-free expansion during states of positive energy balance, which is consequently associated with an improved inflammatory profile. Therefore, the disproportionate accumulation of extracellular matrix components in adipose tissue may not be merely an epiphenomenon of metabolically challenging conditions but may also directly contribute to a failure to expand adipose tissue mass during states of excess caloric intake.

摘要

脂肪细胞嵌入在独特的细胞外基质中,其主要功能除了参与各种信号传导事件外,还提供机械支持。在脂肪组织扩张过程中,细胞外基质需要重塑以适应脂肪细胞的生长。在这里,我们证明糖尿病状态下脂肪组织中几种细胞外基质成分普遍上调,因此表明“脂肪组织纤维化”是代谢受挑战的脂肪细胞的一个标志。胶原蛋白VI是脂肪组织中高度富集的细胞外基质成分。缺乏胶原蛋白VI会导致单个脂肪细胞不受抑制地扩张,并且矛盾的是,无论是在高脂饮食暴露还是在ob/ob背景下,都与全身能量稳态的显著改善有关。总体而言,我们的数据表明,削弱脂肪细胞的细胞外支架能够使其在正能量平衡状态下无应激地扩张,这进而与改善的炎症特征相关。因此,脂肪组织中细胞外基质成分的不成比例积累可能不仅仅是代谢挑战性条件的一种附带现象,还可能直接导致在热量摄入过多状态下脂肪组织质量无法扩张。

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