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纤连蛋白调节肾小球系膜细胞黏附和行为。

Nephronectin Regulates Mesangial Cell Adhesion and Behavior in Glomeruli.

机构信息

Division of Nephrology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas.

Division of Nephrology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas

出版信息

J Am Soc Nephrol. 2018 Apr;29(4):1128-1140. doi: 10.1681/ASN.2017070752. Epub 2018 Jan 15.

Abstract

A critical aspect of kidney function occurs at the glomerulus, the capillary network that filters the blood. The glomerular basement membrane (GBM) is a key component of filtration, yet our understanding of GBM interactions with mesangial cells, specialized pericytes that provide structural stability to glomeruli, is limited. We investigated the role of nephronectin (), a GBM component and known ligand of 81 integrin. Immunolocalization and hybridization studies in kidneys of adult mice revealed that nephronectin is produced by podocytes and deposited into the GBM. Conditional deletion of from nephron progenitors caused a pronounced increase in mesangial cell number and mesangial sclerosis. Nephronectin colocalized with 81 integrin to novel, specialized adhesion structures that occurred at sites of mesangial cell protrusion at the base of the capillary loops. Absence of nephronectin disrupted these adhesion structures, leading to mislocalization of 81. Podocyte-specific deletion of also led to mesangial sclerosis in mice. These results demonstrate a novel role for nephronectin and 81 integrin in a newly described adhesion complex and begin to uncover the molecular interactions between the GBM and mesangial cells, which govern mesangial cell behavior and may have a role in pathologic states.

摘要

肾脏功能的一个关键方面发生在肾小球,即过滤血液的毛细血管网络。肾小球基底膜(GBM)是过滤的关键组成部分,但我们对 GBM 与系膜细胞的相互作用的理解有限,系膜细胞是为肾小球提供结构稳定性的特化周细胞。我们研究了肾络蛋白(nephronectin)的作用,它是 GBM 的一个组成部分,也是 81 整合素的已知配体。在成年小鼠肾脏的免疫定位和杂交研究中,发现肾络蛋白由足细胞产生并沉积到 GBM 中。从肾祖细胞中条件性缺失 会导致系膜细胞数量显著增加和系膜硬化。肾络蛋白与 81 整合素共定位到新型特殊粘附结构,这些结构发生在毛细血管袢底部系膜细胞突起的部位。缺乏肾络蛋白会破坏这些粘附结构,导致 81 整合素的定位错误。足细胞特异性缺失 也会导致小鼠系膜硬化。这些结果表明肾络蛋白和 81 整合素在新描述的粘附复合物中具有新的作用,并开始揭示 GBM 与系膜细胞之间的分子相互作用,这些相互作用控制系膜细胞的行为,可能在病理状态中起作用。

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