Ising Christina, Brinkkoetter Paul T
Department II of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Robert-Koch-Street 21, 50931, Cologne, Germany.
Department of Neurology, Hope Center for Neurological Disorders, Charles F. and Joanne Knight Alzheimer's Disease Research Center, Washington University School of Medicine, 660 S. Euclid Ave, St. Louis, MO, 63110, USA.
Adv Exp Med Biol. 2017;982:563-575. doi: 10.1007/978-3-319-55330-6_29.
The kidney filtration barrier consists of three well-defined anatomic layers comprising a fenestrated endothelium, the glomerular basement membrane (GBM) and glomerular epithelial cells, the podocytes. Podocytes are post-mitotic and terminally differentiated cells with primary and secondary processes. The latter are connected by a unique cell-cell contact, the slit diaphragm. Podocytes maintain the GBM and seal the kidney filtration barrier to prevent the onset of proteinuria. Loss of prohibitin-1/2 (PHB1/2) in podocytes results not only in a disturbed mitochondrial structure but also in an increased insulin/IGF-1 signaling leading to mTOR activation and a detrimental metabolic switch. As a consequence, PHB-knockout podocytes develop proteinuria and glomerulosclerosis and eventually loss of renal function. In addition, experimental evidence suggests that PHB1/2 confer additional, extra-mitochondrial functions in podocytes as they localize to the slit diaphragm and thereby stabilize the unique intercellular contact between podocytes required to maintain an effective filtration barrier.
肾脏滤过屏障由三个界限分明的解剖层组成,包括有窗孔的内皮细胞、肾小球基底膜(GBM)和肾小球上皮细胞(足细胞)。足细胞是有丝分裂后终末分化的细胞,具有初级和次级突起。后者通过独特的细胞间接触——裂孔隔膜相连。足细胞维持GBM并封闭肾脏滤过屏障以防止蛋白尿的发生。足细胞中抑制素-1/2(PHB1/2)的缺失不仅会导致线粒体结构紊乱,还会导致胰岛素/IGF-1信号增强,从而导致mTOR激活和有害的代谢转换。因此,敲除PHB的足细胞会出现蛋白尿和肾小球硬化,最终导致肾功能丧失。此外,实验证据表明,PHB1/2在足细胞中具有额外的线粒体以外的功能,因为它们定位于裂孔隔膜,从而稳定维持有效滤过屏障所需的足细胞之间独特的细胞间接触。