Suppr超能文献

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.

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。

相似文献

引用本文的文献

5
Metabolic programming of nephron progenitor cell fate.肾单位祖细胞命运的代谢编程。
Pediatr Nephrol. 2021 Aug;36(8):2155-2164. doi: 10.1007/s00467-020-04752-8. Epub 2020 Oct 21.
8
Epigenetic regulation of kidney progenitor cells.肾祖细胞的表观遗传调控
Stem Cells Transl Med. 2020 Jun;9(6):655-660. doi: 10.1002/sctm.19-0289. Epub 2020 Mar 12.
9
The tale of two (distal nephron) cell types.两种(远端肾单位)细胞类型的故事。
Am J Physiol Renal Physiol. 2018 May 1;314(5):F930-F931. doi: 10.1152/ajprenal.00044.2018. Epub 2018 Jan 24.
10
Advances in Renal Cell Imaging.肾脏细胞成像技术的进展。
Semin Nephrol. 2018 Jan;38(1):52-62. doi: 10.1016/j.semnephrol.2017.09.004.

本文引用的文献

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.
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.
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.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验