Lennon Rachel, Randles Michael J, Humphries Martin J
Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, The University of Manchester , Manchester , UK ; Institute of Human Development, Faculty of Medical and Human Sciences, The University of Manchester , Manchester , UK ; Department of Paediatric Nephrology, Manchester Academic Health Science Centre, Central Manchester University Hospitals NHS Foundation Trust , Manchester , UK.
Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, The University of Manchester , Manchester , UK ; Institute of Human Development, Faculty of Medical and Human Sciences, The University of Manchester , Manchester , UK.
Front Endocrinol (Lausanne). 2014 Oct 14;5:160. doi: 10.3389/fendo.2014.00160. eCollection 2014.
Podocytes are specialized epithelial cells that cover the outer surfaces of glomerular capillaries. Unique cell junctions, known as slit diaphragms, which feature nephrin and Neph family proteins in addition to components of adherens, tight, and gap junctions, connect adjacent podocyte foot processes. Single gene disorders affecting the slit diaphragm result in nephrotic syndrome in humans, characterized by massive loss of protein across the capillary wall. In addition to specialized cell junctions, interconnecting podocytes also adhere to the glomerular basement membrane (GBM) of the capillary wall. The GBM is a dense network of secreted, extracellular matrix (ECM) components and contains tissue-restricted isoforms of collagen IV and laminin in addition to other structural proteins and ECM regulators such as proteases and growth factors. The specialized niche of the GBM provides a scaffold for endothelial cells and podocytes to support their unique functions and human genetic mutations in GBM components lead to renal failure, thus highlighting the importance of cell-matrix interactions in the glomerulus. Cells adhere to ECM via adhesion receptors, including integrins, syndecans, and dystroglycan and in particular the integrin heterodimer α3β1 is required to maintain barrier integrity. Therefore, the sophisticated function of glomerular filtration relies on podocyte adhesion both at cell junctions and at the interface with the ECM. In health, the podocyte coordinates signals from cell junctions and cell-matrix interactions, in response to environmental cues in order to regulate filtration and as our understanding of mechanisms that control cell adhesion in the glomerulus develops, then insight into the effects of disease will improve. The ultimate goal will be to develop targeted therapies to prevent or repair defects in the filtration barrier and to restore glomerular function.
足细胞是覆盖肾小球毛细血管外表面的特殊上皮细胞。独特的细胞连接,即裂孔隔膜,除了黏附连接、紧密连接和缝隙连接的成分外,还以nephrin和Neph家族蛋白为特征,连接相邻的足细胞足突。影响裂孔隔膜的单基因疾病会导致人类肾病综合征,其特征是毛细血管壁大量蛋白质流失。除了特殊的细胞连接外,相互连接的足细胞还黏附于毛细血管壁的肾小球基底膜(GBM)。GBM是由分泌的细胞外基质(ECM)成分组成的致密网络,除了其他结构蛋白和ECM调节因子(如蛋白酶和生长因子)外,还含有IV型胶原蛋白和层粘连蛋白的组织限制性异构体。GBM的特殊微环境为内皮细胞和足细胞提供了一个支架,以支持它们的独特功能,GBM成分中的人类基因突变会导致肾衰竭,从而突出了肾小球中细胞-基质相互作用的重要性。细胞通过黏附受体(包括整合素、多配体聚糖和肌营养不良蛋白聚糖)黏附于ECM,特别是整合素异二聚体α3β1是维持屏障完整性所必需的。因此,肾小球滤过的复杂功能依赖于足细胞在细胞连接处和与ECM界面处的黏附。在健康状态下,足细胞会根据环境线索协调来自细胞连接和细胞-基质相互作用的信号,以调节滤过,随着我们对控制肾小球细胞黏附机制的理解不断发展,对疾病影响的认识也将得到提高。最终目标将是开发靶向疗法,以预防或修复滤过屏障的缺陷并恢复肾小球功能。