Division of Kidney and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
Nephrol Dial Transplant. 2014 May;29(5):1005-12. doi: 10.1093/ndt/gft413. Epub 2013 Dec 8.
Recent studies have reported that podocytes are postnatally generated from progenitor cells localized in Bowman's capsule or in the bone marrow. In the present study, we investigated whether or not podocyte regeneration is important in the repair of injured glomeruli after mild podocyte injury in mice.
Mild podocyte injury was induced in NEP25 mice (n = 8) by injecting an immunotoxin, LMB2 (0.625 ng/g body weight). Control mice, not injured by LMB2 injection (n = 7) was used as a comparison. Proliferating cells were labeled by continuous infusion of bromodeoxyuridine (BrdU). Podocytes, identified by nephrin, WT1 or podocin staining, that had incorporated BrdU were enumerated 4 weeks later.
A total of 742 corpuscles were inspected in serial sections stained for BrdU and nephrin; 19% showed sclerosis. BrdU(+) cells were observed in both the glomeruli and Bowman's capsules, averaging 2.5 ± 3.1 in non-sclerotic corpuscles and 7.0 ± 5.8 in sclerotic corpuscles. Only one BrdU(+) cell was also positive for nephrin. Another cell, localized at a position consistent with its potential identification as a podocyte, was nephrin negative but had incorporated BrdU. WT1 staining similarly revealed that only two nuclei were doubly positive for BrdU and WT1. Additional 1676 corpuscles were inspected by double staining for BrdU and podocin; none were doubly positive.
Podocytes are not replenished by proliferation of endogenous progenitor cells in mice with glomerular injury.
最近的研究报告称,足细胞是由位于鲍曼囊或骨髓中的祖细胞在出生后产生的。本研究旨在探讨在轻度足细胞损伤后,小鼠肾小球损伤修复过程中足细胞再生是否重要。
通过注射免疫毒素 LMB2(0.625ng/g 体重),在 NEP25 小鼠(n=8)中诱导轻度足细胞损伤。对照组(n=7)未注射 LMB2 作为对照。通过连续灌注溴脱氧尿苷(BrdU)标记增殖细胞。4 周后,通过肾小囊蛋白、WT1 或足突蛋白染色来计数已摄取 BrdU 的足细胞。
在连续切片中对 BrdU 和肾小囊蛋白进行染色,共检查了 742 个小球;19%的小球出现硬化。肾小球和鲍曼囊中均观察到 BrdU(+)细胞,非硬化小球中平均为 2.5±3.1 个,硬化小球中平均为 7.0±5.8 个。只有一个 BrdU(+)细胞也为肾小囊蛋白阳性。另一个细胞位于与潜在足细胞鉴定一致的位置,但其肾小囊蛋白为阴性,但已摄取 BrdU。WT1 染色同样显示,只有两个核对 BrdU 和 WT1 双重阳性。另外还检查了 1676 个小球的 BrdU 和 podocin 双重染色;均未发现双重阳性。
在肾小球损伤的小鼠中,足细胞不会通过内源性祖细胞的增殖来补充。