Department of Nephrology and Clinical Immunology, RWTH University Hospital Aachen, Pauwelsstr. 30, 52074 Aachen, Germany.
J Am Soc Nephrol. 2011 Jul;22(7):1262-74. doi: 10.1681/ASN.2010090970. Epub 2011 Jun 30.
The pathogenesis of the development of sclerotic lesions in focal segmental glomerulosclerosis (FSGS) remains unknown. Here, we selectively tagged podocytes or parietal epithelial cells (PECs) to determine whether PECs contribute to sclerosis. In three distinct models of FSGS (5/6-nephrectomy + DOCA-salt; the murine transgenic chronic Thy1.1 model; or the MWF rat) and in human biopsies, the primary injury to induce FSGS associated with focal activation of PECs and the formation of cellular adhesions to the capillary tuft. From this entry site, activated PECs invaded the affected segment of the glomerular tuft and deposited extracellular matrix. Within the affected segment, podocytes were lost and mesangial sclerosis developed within the endocapillary compartment. In conclusion, these results demonstrate that PECs contribute to the development and progression of the sclerotic lesions that define FSGS, but this pathogenesis may be relevant to all etiologies of glomerulosclerosis.
局灶节段性肾小球硬化症(FSGS)中硬化病变发展的发病机制尚不清楚。在这里,我们选择性地标记足细胞或壁细胞(PEC),以确定 PEC 是否有助于硬化。在三种不同的 FSGS 模型(5/6 肾切除+DOCA-盐;慢性 Thy1.1 转基因小鼠模型;或 MWF 大鼠)和人类活检中,引起 FSGS 的主要损伤与 PEC 的局灶性激活以及与毛细血管丛的细胞黏附的形成有关。从这个进入部位,激活的 PEC 侵入肾小球丛的受影响节段,并沉积细胞外基质。在受影响的节段内,足细胞丢失,毛细血管内的系膜硬化发展。总之,这些结果表明 PEC 有助于定义 FSGS 的硬化病变的发展和进展,但这种发病机制可能与肾小球硬化的所有病因都有关。