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视黄酸信号在祖细胞中控制尿路上皮的特化和再生。

Retinoid signaling in progenitors controls specification and regeneration of the urothelium.

机构信息

Columbia University, Depts. of Urology, Genetics & Development and Pathology 1130 St. Nicholas Avenue, New York NY, USA.

Columbia University, Department of Pathology, 630 West 168th Street, New York, NY, USA.

出版信息

Dev Cell. 2013 Sep 16;26(5):469-482. doi: 10.1016/j.devcel.2013.07.017. Epub 2013 Aug 29.

DOI:10.1016/j.devcel.2013.07.017
PMID:23993789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4024836/
Abstract

The urothelium is a multilayered epithelium that serves as a barrier between the urinary tract and blood, preventing the exchange of water and toxic substances. It consists of superficial cells specialized for synthesis and transport of uroplakins that assemble into a tough apical plaque, one or more layers of intermediate cells, and keratin 5-expressing basal cells (K5-BCs), which are considered to be progenitors in the urothelium and other specialized epithelia. Fate mapping, however, reveals that intermediate cells rather than K5-BCs are progenitors in the adult regenerating urothelium, that P cells, a transient population, are progenitors in the embryo, and that retinoids are critical in P cells and intermediate cells, respectively, for their specification during development and regeneration. These observations have important implications for tissue engineering and repair and, ultimately, may lead to treatments that prevent loss of the urothelial barrier, a major cause of voiding dysfunction and bladder pain syndrome.

摘要

尿路上皮是一种多层上皮组织,作为尿路和血液之间的屏障,防止水和有毒物质的交换。它由专门用于合成和运输尿路上皮蛋白的浅层细胞组成,这些蛋白组装成坚韧的顶端斑块,还有一层或多层中间细胞,以及表达角蛋白 5 的基底细胞(K5-BC),这些细胞被认为是尿路上皮和其他特化上皮的祖细胞。然而,通过命运图谱分析发现,在成年再生尿路上皮中,中间细胞而不是 K5-BC 是祖细胞,在胚胎中 P 细胞是短暂的祖细胞,视黄酸分别在 P 细胞和中间细胞中对于它们在发育和再生过程中的特化是至关重要的。这些观察结果对组织工程和修复具有重要意义,最终可能导致预防尿路上皮屏障丧失的治疗方法,这是排尿功能障碍和膀胱疼痛综合征的主要原因。

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本文引用的文献

1
p63-expressing cells are the stem cells of developing prostate, bladder, and colorectal epithelia.p63 表达细胞是前列腺、膀胱和结直肠上皮发育中的干细胞。
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Differentiation of human pluripotent stem cells into urothelial organoids via transient activation of WNT signaling.通过短暂激活WNT信号通路将人类多能干细胞分化为尿路上皮类器官
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PPARG contributes to urothelial integrity in the murine ureter by activating the expression of Shh and superficial cell-specific genes.PPARG通过激活Shh和表层细胞特异性基因的表达,对小鼠输尿管的尿路上皮完整性有促进作用。
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