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谱系示踪法绘制无小管肾小球脏层足细胞的起源。

Origin of parietal podocytes in atubular glomeruli mapped by lineage tracing.

机构信息

Department of Nephrology and Immunology, RWTH University of Aachen, Aachen, NRW, Germany;

出版信息

J Am Soc Nephrol. 2014 Jan;25(1):129-41. doi: 10.1681/ASN.2013040376. Epub 2013 Sep 26.

Abstract

Parietal podocytes are fully differentiated podocytes lining Bowman's capsule where normally only parietal epithelial cells (PECs) are found. Parietal podocytes form throughout life and are regularly observed in human biopsies, particularly in atubular glomeruli of diseased kidneys; however, the origin of parietal podocytes is unresolved. To assess the capacity of PECs to transdifferentiate into parietal podocytes, we developed and characterized a novel method for creating atubular glomeruli by electrocoagulation of the renal cortex in mice. Electrocoagulation produced multiple atubular glomeruli containing PECs as well as parietal podocytes that projected from the vascular pole and lined Bowman's capsule. Notably, induction of cell death was evident in some PECs. In contrast, Bowman's capsules of control animals and normal glomeruli of electrocoagulated kidneys rarely contained podocytes. PECs and podocytes were traced by inducible and irreversible genetic tagging using triple transgenic mice (PEC- or Pod-rtTA/LC1/R26R). Examination of serial cryosections indicated that visceral podocytes migrated onto Bowman's capsule via the vascular stalk; direct transdifferentiation from PECs to podocytes was not observed. Similar results were obtained in a unilateral ureter obstruction model and in human diseased kidney biopsies, in which overlap of PEC- or podocyte-specific antibody staining indicative of gradual differentiation did not occur. These results suggest that induction of atubular glomeruli leads to ablation of PECs and subsequent migration of visceral podocytes onto Bowman's capsule, rather than transdifferentiation from PECs to parietal podocytes.

摘要

壁细胞足细胞是完全分化的足细胞,排列在鲍曼囊内,通常只发现壁细胞(PECs)。壁细胞足细胞在整个生命过程中形成,并在人类活检中经常观察到,特别是在患病肾脏的无管状肾小球中;然而,壁细胞足细胞的起源尚未解决。为了评估 PECs 转分化为壁细胞足细胞的能力,我们开发并表征了一种通过在小鼠肾皮质电凝创建无管状肾小球的新方法。电凝产生了多个包含 PECs 以及从血管极伸出并排列在鲍曼囊内的壁细胞足细胞的无管状肾小球。值得注意的是,一些 PECs 中可见细胞死亡诱导。相比之下,对照组动物的鲍曼囊和电凝肾脏的正常肾小球很少包含足细胞。使用三重转基因小鼠(PEC 或 Pod-rtTA/LC1/R26R)通过可诱导和不可逆的基因标记追踪 PECs 和足细胞。对连续冷冻切片的检查表明,脏层足细胞通过血管干迁移到鲍曼囊上;未观察到 PECs 向足细胞的直接转分化。在单侧输尿管梗阻模型和人类患病肾脏活检中也获得了类似的结果,其中 PEC 或足细胞特异性抗体染色的重叠表明逐渐分化,但没有发生。这些结果表明,诱导无管状肾小球导致 PECs 的消融和随后的脏层足细胞迁移到鲍曼囊上,而不是 PECs 向壁细胞足细胞的转分化。

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