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KRT14 marks a subpopulation of bladder basal cells with pivotal role in regeneration and tumorigenesis.KRT14 标记了一个具有在再生和肿瘤发生中关键作用的膀胱基底细胞亚群。
Nat Commun. 2016 Jun 20;7:11914. doi: 10.1038/ncomms11914.
2
Ureter growth and differentiation.输尿管的生长与分化。
Semin Cell Dev Biol. 2014 Dec;36:21-30. doi: 10.1016/j.semcdb.2014.07.014. Epub 2014 Aug 1.
3
Retinoid signaling in progenitors controls specification and regeneration of the urothelium.视黄酸信号在祖细胞中控制尿路上皮的特化和再生。
Dev Cell. 2013 Sep 16;26(5):469-482. doi: 10.1016/j.devcel.2013.07.017. Epub 2013 Aug 29.
4
Tbx18 expression demarcates multipotent precursor populations in the developing urogenital system but is exclusively required within the ureteric mesenchymal lineage to suppress a renal stromal fate.Tbx18 的表达划定了发育中泌尿生殖系统中多能前体细胞群的范围,但在输尿管间质谱系中是唯一需要的,以抑制肾脏基质命运。
Dev Biol. 2013 Aug 1;380(1):25-36. doi: 10.1016/j.ydbio.2013.04.036. Epub 2013 May 15.
5
Brg1 determines urothelial cell fate during ureter development.Brg1 决定输尿管发育过程中的尿路上皮细胞命运。
J Am Soc Nephrol. 2013 Mar;24(4):618-26. doi: 10.1681/ASN.2012090902. Epub 2013 Feb 28.
6
Developmental stage and time dictate the fate of Wnt/β-catenin-responsive stem cells in the mammary gland.发育阶段和时间决定了乳腺中 Wnt/β-连环蛋白反应性干细胞的命运。
Cell Stem Cell. 2012 Sep 7;11(3):387-400. doi: 10.1016/j.stem.2012.05.023. Epub 2012 Aug 2.
7
Canonical Wnt signaling regulates smooth muscle precursor development in the mouse ureter.经典 Wnt 信号通路调控小鼠输尿管平滑肌前体细胞的发育。
Development. 2012 Sep;139(17):3099-108. doi: 10.1242/dev.077388. Epub 2012 Jul 25.
8
Distinct stem cells contribute to mammary gland development and maintenance.不同的干细胞对乳腺的发育和维持起着重要作用。
Nature. 2011 Oct 9;479(7372):189-93. doi: 10.1038/nature10573.
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Impaired stria vascularis integrity upon loss of E-cadherin in basal cells.基底细胞中 E-钙黏蛋白缺失导致血管纹完整性受损。
Dev Biol. 2011 Nov 1;359(1):95-107. doi: 10.1016/j.ydbio.2011.08.030. Epub 2011 Sep 9.
10
Expression patterns and roles of periostin during kidney and ureter development.骨膜蛋白在肾脏和输尿管发育过程中的表达模式和作用。
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输尿管发育中细胞谱系的多样化

Diversification of Cell Lineages in Ureter Development.

作者信息

Bohnenpoll Tobias, Feraric Sarah, Nattkemper Marvin, Weiss Anna-Carina, Rudat Carsten, Meuser Max, Trowe Mark-Oliver, Kispert Andreas

机构信息

Institut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany.

Institut für Molekularbiologie, Medizinische Hochschule Hannover, Hannover, Germany

出版信息

J Am Soc Nephrol. 2017 Jun;28(6):1792-1801. doi: 10.1681/ASN.2016080849. Epub 2016 Dec 27.

DOI:10.1681/ASN.2016080849
PMID:28028137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5461796/
Abstract

The mammalian ureter consists of a mesenchymal wall composed of smooth muscle cells and surrounding fibrocytes of the tunica adventitia and the lamina propria and an inner epithelial lining composed of layers of basal, intermediate, and superficial cells. How these cell types arise from multipotent progenitors is poorly understood. Here, we performed marker analysis, cell proliferation assays, and genetic lineage tracing to define the lineage relations and restrictions of the mesenchymal and epithelial cell types in the developing and mature mouse ureter. At embryonic day (E) 12.5, the mesenchymal precursor pool began to subdivide into an inner and outer compartment that began to express markers of smooth muscle precursors and adventitial fibrocytes, respectively, by E13.5. Smooth muscle precursors further diversified into lamina propria cells directly adjacent to the ureteric epithelium and differentiated smooth muscle cells from E16.5 onwards. Uncommitted epithelial progenitors of the ureter differentiated into intermediate cells at E14.5. After stratification into two layers at E15.5 and three cell layers at E18.5, intermediate cells differentiated into basal cells and superficial cells. In homeostasis, proliferation of all epithelial and mesenchymal cell types remained low but intermediate cells still gave rise to basal cells, whereas basal cells divided only into basal cells. These studies provide a framework to further determine the molecular mechanisms of cell differentiation in the tissues of the developing ureter.

摘要

哺乳动物的输尿管由间充质壁和内层上皮衬里组成。间充质壁由平滑肌细胞以及外膜和固有层周围的纤维细胞构成,内层上皮衬里由基底细胞层、中间细胞层和表层细胞层组成。目前人们对这些细胞类型如何从多能祖细胞分化而来知之甚少。在此,我们进行了标志物分析、细胞增殖试验和遗传谱系追踪,以确定发育中和成熟小鼠输尿管中间充质细胞和上皮细胞类型的谱系关系及限制。在胚胎第12.5天(E12.5),间充质前体细胞池开始分为内、外两个部分,到E13.5时,这两个部分分别开始表达平滑肌前体细胞和外膜纤维细胞的标志物。从E16.5开始,平滑肌前体细胞进一步分化为紧邻输尿管上皮的固有层细胞和分化型平滑肌细胞。输尿管未分化的上皮祖细胞在E14.5时分化为中间细胞。在E15.5分层为两层、E18.5分层为三层细胞层后,中间细胞分化为基底细胞和表层细胞。在稳态下,所有上皮和间充质细胞类型的增殖率都很低,但中间细胞仍可分化为基底细胞,而基底细胞仅分裂形成基底细胞。这些研究为进一步确定发育中输尿管组织细胞分化的分子机制提供了一个框架。