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小鼠膀胱尿路上皮基底层和中间层中的一群祖细胞有助于尿路上皮的发育和再生。

A population of progenitor cells in the basal and intermediate layers of the murine bladder urothelium contributes to urothelial development and regeneration.

作者信息

Colopy Sara A, Bjorling Dale E, Mulligan William A, Bushman Wade

机构信息

Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin.

出版信息

Dev Dyn. 2014 Aug;243(8):988-98. doi: 10.1002/dvdy.24143. Epub 2014 May 19.

Abstract

BACKGROUND

Homeostatic maintenance and repair of the bladder urothelium has been attributed to proliferation of keratin 5-expressing basal cells (K5-BC) with subsequent differentiation into superficial cells. Recent evidence, however, suggests that the intermediate cell layer harbors a population of progenitor cells. We use label-retaining cell (LRC) methodology in conjunction with a clinically relevant model of uropathogenic Escherichia coli (UPEC)-induced injury to characterize urothelial ontogeny during development and in response to diffuse urothelial injury.

RESULTS

In the developing urothelium, proliferating cells were dispersed throughout the K5-BC and intermediate cells layers, becoming progressively concentrated in the K5-BC layer with age. When 5-bromo-2-deoxyuridine (BrdU) was administered during urothelial development, LRCs in the adult were found within the K5-BC, intermediate, and superficial cell layers, the location dependent upon time of labeling. UPEC inoculation resulted in loss of the superficial cell layer followed by robust proliferation of K5-BCs and intermediate cells. LRCs within the K5-BC and intermediate cell layers proliferated in response to injury.

CONCLUSIONS

Urothelial development and regeneration following injury relies on proliferation of K5-BC and intermediate cells. The existence and proliferation of LRCs within both the K5-BC and intermediate cell layers suggests the presence of two populations of urothelial progenitor cells.

摘要

背景

膀胱尿路上皮的稳态维持和修复归因于表达角蛋白5的基底细胞(K5-BC)的增殖,随后分化为表层细胞。然而,最近的证据表明,中间细胞层含有一群祖细胞。我们使用标记保留细胞(LRC)方法,结合尿路致病性大肠杆菌(UPEC)诱导损伤的临床相关模型,来表征发育过程中以及对弥漫性尿路上皮损伤反应时的尿路上皮个体发生。

结果

在发育中的尿路上皮中,增殖细胞分散在K5-BC层和中间细胞层,随着年龄增长逐渐集中在K5-BC层。在尿路上皮发育期间给予5-溴-2-脱氧尿苷(BrdU)时,在成年个体的K5-BC层、中间细胞层和表层细胞层中发现了LRC,其位置取决于标记时间。UPEC接种导致表层细胞层丧失,随后K5-BC和中间细胞大量增殖。K5-BC层和中间细胞层内的LRC对损伤作出反应而增殖。

结论

损伤后的尿路上皮发育和再生依赖于K5-BC和中间细胞的增殖。K5-BC层和中间细胞层内LRC的存在和增殖表明存在两种尿路上皮祖细胞群。

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