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肌肉特异性 RING 型泛素 E3 连接酶(SPARC):肥胖和糖尿病相关病变的关键参与者。

SPARC: a key player in the pathologies associated with obesity and diabetes.

机构信息

Department of Diabetes and Vascular Medicine, Peninsula College of Medicine and Dentistry, University of Exeter, Exeter EX2 5DW, UK.

出版信息

Nat Rev Endocrinol. 2010 Apr;6(4):225-35. doi: 10.1038/nrendo.2010.18. Epub 2010 Mar 2.

Abstract

SPARC (secreted protein acidic and rich in cysteine, also known as osteonectin or BM-40) is a widely expressed profibrotic protein with pleiotropic roles, which have been studied in a variety of conditions. Notably, SPARC is linked to human obesity; SPARC derived from adipose tissue is associated with insulin resistance and secretion of SPARC by adipose tissue is increased by insulin and the adipokine leptin. Furthermore, SPARC is associated with diabetes complications such as diabetic retinopathy and nephropathy, conditions that are ameliorated in the Sparc-knockout mouse model. As a regulator of the extracellular matrix, SPARC also contributes to adipose-tissue fibrosis. Evidence suggests that adipose tissue becomes increasingly fibrotic in obesity. Fibrosis of subcutaneous adipose tissue may restrict accumulation of triglycerides in this type of tissue. These triglycerides are, therefore, diverted and deposited as ectopic lipids in other tissues such as the liver or as intramyocellular lipids in skeletal muscle, which predisposes to insulin resistance. Hence, SPARC may represent a novel and important link between obesity and diabetes mellitus. This Review is focused on whether SPARC could be a key player in the pathology of obesity and its related metabolic complications.

摘要

富含半胱氨酸的酸性分泌蛋白(SPARC,也称为骨粘连蛋白或 BM-40)是一种广泛表达的促纤维化蛋白,具有多种作用,已在多种情况下进行了研究。值得注意的是,SPARC 与人类肥胖有关;脂肪组织衍生的 SPARC 与胰岛素抵抗有关,而胰岛素和脂肪细胞因子瘦素会增加脂肪组织分泌的 SPARC。此外,SPARC 与糖尿病并发症有关,如糖尿病视网膜病变和肾病,在 Sparc 基因敲除小鼠模型中这些并发症得到了改善。作为细胞外基质的调节剂,SPARC 也有助于脂肪组织纤维化。有证据表明,肥胖症患者的脂肪组织纤维化程度越来越严重。皮下脂肪组织的纤维化可能会限制这种组织中甘油三酯的积累。因此,这些甘油三酯被转移并沉积在其他组织中,如肝脏或骨骼肌中的肌内脂质,从而导致胰岛素抵抗。因此,SPARC 可能是肥胖症和糖尿病之间的一个新的重要联系。本综述主要关注 SPARC 是否可能是肥胖及其相关代谢并发症病理的关键因素。

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