首页> 外文期刊>Journal of the American Society of Nephrology: JASN >Parietal epithelial cells participate in the formation of sclerotic lesions in focal segmental glomerulosclerosis.
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Parietal epithelial cells participate in the formation of sclerotic lesions in focal segmental glomerulosclerosis.

机译:顶叶上皮细胞参与局灶节段性肾小球硬化症中硬化病变的形成。

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摘要

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-sa 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.
机译:局灶性节段性肾小球硬化症(FSGS)的硬化性病变发展的发病机制仍然未知。在这里,我们选择性标记足细胞或顶上皮细胞(PECs),以确定PEC是否有助于硬化。在FSGS的三个不同模型(5/6肾切除术+ DOCA盐;鼠类转基因慢性Thy1.1模型;或MWF大鼠)中和在人体活检中,诱导FSGS的主要损伤与PECs的局部活化有关。形成与毛簇的细胞粘附。从该进入部位,活化的PEC侵入肾小球簇的受影响部分并沉积细胞外基质。在受影响的部分内,足细胞丢失,并且在毛细血管内腔内形成了肾小球膜硬化。总之,这些结果表明,PEC有助于定义FSGS的硬化性病变的发展和进展,但是这种发病机制可能与所有肾小球硬化病因有关。

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