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本文引用的文献

1
Mosaic analysis of cell rearrangements during ureteric bud branching in dissociated/reaggregated kidney cultures and in vivo.在解离/重聚集的肾脏培养物和体内对输尿管芽分支过程中细胞重排的镶嵌分析。
Dev Dyn. 2016 Apr;245(4):483-96. doi: 10.1002/dvdy.24387. Epub 2016 Feb 17.
2
Maintaining epithelial stemness with p63.维持上皮干细胞干性的 p63。
Sci Signal. 2015 Jul 28;8(387):re9. doi: 10.1126/scisignal.aaa1033.
3
Transcription factor p63 bookmarks and regulates dynamic enhancers during epidermal differentiation.转录因子p63在表皮分化过程中标记并调控动态增强子。
EMBO Rep. 2015 Jul;16(7):863-78. doi: 10.15252/embr.201439941. Epub 2015 Jun 1.
4
Histone deacetylase 1 and 2 regulate Wnt and p53 pathways in the ureteric bud epithelium.组蛋白去乙酰化酶1和2调节输尿管芽上皮中的Wnt和p53信号通路。
Development. 2015 Mar 15;142(6):1180-92. doi: 10.1242/dev.113506.
5
p63(+)Krt5(+) distal airway stem cells are essential for lung regeneration.p63(阳性)Krt5(阳性)的远端气道干细胞对肺再生至关重要。
Nature. 2015 Jan 29;517(7536):616-20. doi: 10.1038/nature13903. Epub 2014 Nov 12.
6
p53/p63/p73 in the epidermis in health and disease.健康与疾病状态下表皮中的p53/p63/p73
Cold Spring Harb Perspect Med. 2014 Aug 1;4(8):a015248. doi: 10.1101/cshperspect.a015248.
7
SOX2 and p63 colocalize at genetic loci in squamous cell carcinomas.SOX2 和 p63 在鳞状细胞癌的遗传基因座上共定位。
J Clin Invest. 2014 Apr;124(4):1636-45. doi: 10.1172/JCI71545. Epub 2014 Mar 3.
8
Basal cell signaling by p63 controls luminal progenitor function and lactation via NRG1.p63 通过 NRG1 控制基底细胞信号传导,从而控制腔前体细胞功能和泌乳。
Dev Cell. 2014 Jan 27;28(2):147-60. doi: 10.1016/j.devcel.2013.11.019. Epub 2014 Jan 9.
9
Luminal mitosis drives epithelial cell dispersal within the branching ureteric bud.管腔有丝分裂驱动分支输尿管芽内的上皮细胞离散。
Dev Cell. 2013 Nov 11;27(3):319-30. doi: 10.1016/j.devcel.2013.09.001. Epub 2013 Oct 31.
10
To bud or not to bud: the RET perspective in CAKUT.萌芽与否:CAKUT中RET的视角
Pediatr Nephrol. 2014 Apr;29(4):597-608. doi: 10.1007/s00467-013-2606-5.

p63+输尿管芽尖细胞是闰细胞的祖细胞。

p63+ ureteric bud tip cells are progenitors of intercalated cells.

作者信息

El-Dahr Samir S, Li Yuwen, Liu Jiao, Gutierrez Elleny, Hering-Smith Kathleen S, Signoretti Sabina, Pignon Jean-Christophe, Sinha Satrajit, Saifudeen Zubaida

机构信息

Department of Pediatrics and.

Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana, USA.

出版信息

JCI Insight. 2017 May 4;2(9). doi: 10.1172/jci.insight.89996.

DOI:10.1172/jci.insight.89996
PMID:28469077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5414549/
Abstract

During renal branching morphogenesis, ureteric bud tip cells (UBTC) serve as the progenitor epithelium for all cell types of the collecting duct. While the transcriptional circuitry of ureteric bud (UB) branching has been intensively studied, the transcriptional control of UBTC differentiation has been difficult to ascertain. This is partly due to limited knowledge of UBTC-specific transcription factors that mark the progenitor state. Here, we identify the transcription factor p63 (also known as TP63), a master regulator of basal stem cells in stratified epithelia, as a specific marker of mouse and human UBTC. Nuclear p63 marks Ret+ UBTC transiently and is silenced by the end of nephrogenesis. Lineage tracing revealed that a subset of UBTC expressing the ΔNp63 isoform (N-terminus truncated p63) is dedicated to generating cortical intercalated cells. Germline targeting of ΔNp63 in mice caused a marked reduction in intercalated cells near the time of birth, indicating that p63 not only marks UBTC, but also is essential for their differentiation. We conclude that the choice of UBTC progenitors to differentiate is determined earlier than previously recognized and that UBTC progenitors are prepatterned and fate restricted. These findings prompt the rethinking of current paradigms of collecting duct differentiation and may have implications for regenerative renal medicine.

摘要

在肾脏分支形态发生过程中,输尿管芽尖细胞(UBTC)作为集合管所有细胞类型的祖上皮细胞。虽然对输尿管芽(UB)分支的转录调控机制已进行了深入研究,但UBTC分化的转录调控机制却难以确定。部分原因是对标记祖细胞状态的UBTC特异性转录因子了解有限。在此,我们鉴定出转录因子p63(也称为TP63),它是复层上皮中基底干细胞的主要调节因子,是小鼠和人类UBTC的特异性标记物。核p63短暂标记Ret+ UBTC,并在肾发生结束时沉默。谱系追踪显示,表达ΔNp63异构体(N端截短的p63)的一部分UBTC专门生成皮质闰细胞。在小鼠中对ΔNp63进行种系靶向导致出生时附近闰细胞显著减少,表明p63不仅标记UBTC,而且对其分化至关重要。我们得出结论,UBTC祖细胞分化的选择比之前认为的要早,并且UBTC祖细胞是预先模式化且命运受限的。这些发现促使人们重新思考当前集合管分化的范式,可能对再生肾脏医学产生影响。