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定义和重新定义肾祖细胞群体。

Defining and redefining the nephron progenitor population.

机构信息

Institute for Molecular Bioscience, The University of Queensland, St. Lucia, 4072, Australia.

出版信息

Pediatr Nephrol. 2011 Sep;26(9):1395-406. doi: 10.1007/s00467-010-1750-4. Epub 2011 Jan 14.

Abstract

It has long been appreciated that the mammalian kidney arises via reciprocal interactions between an epithelial ureteric epithelium and the surrounding metanephric mesenchyme. More recently, lineage tracing has confirmed that the portion of the metanephric mesenchyme closest to the advancing ureteric tips, the cap mesenchyme, represents the progenitor population for the nephron epithelia. This Six2(+)Cited1(+) population undergoes self-renewal throughout nephrogenesis while retaining the potential to epithelialize. In contrast, the Foxd1(+) portion of the metanephric mesenchyme shows no epithelial potential, developing instead into the interstitial, perivascular, and possibly endothelial elements of the kidney. The cap mesenchyme rests within a nephrogenic niche, surrounded by the stroma and the ureteric tip. While the role of Wnt signaling in nephron induction is known, there remains a lack of clarity over the intrinsic and extrinsic regulation of cap mesenchyme specification, self-renewal, and nephron potential. It is also not known what regulates cessation of nephrogenesis, but there is no nephron generation in response to injury during the postnatal period. In this review, we will examine what is and is not known about this nephron progenitor population and discuss how an increased understanding of the regulation of this population may better explain the observed variation in final nephron number and potentially facilitate the reinitiation or prolongation of nephron formation.

摘要

长期以来,人们一直认为哺乳动物的肾脏是通过输尿管上皮和周围的后肾间充质之间的相互作用而产生的。最近,谱系追踪已经证实,靠近输尿管尖端的后肾间充质部分,即帽状间充质,代表了肾单位上皮的祖细胞群体。这个 Six2(+)Cited1(+)群体在整个肾发生过程中进行自我更新,同时保持上皮化的潜力。相比之下,Foxd1(+)部分的后肾间充质没有上皮潜力,而是发育成肾脏的间质、血管周围和可能的内皮成分。帽状间充质位于肾发生龛内,周围是基质和输尿管尖端。虽然 Wnt 信号在肾单位诱导中的作用是已知的,但帽状间充质的特化、自我更新和肾单位潜力的内在和外在调节仍然不清楚。也不知道是什么调节了肾发生的停止,但在出生后期间,损伤不会引起肾单位的生成。在这篇综述中,我们将探讨关于这个肾单位祖细胞群体已知和未知的方面,并讨论如何更好地理解这个群体的调节,这可能有助于更好地解释最终肾单位数量的观察到的变化,并有可能促进肾单位形成的重新启动或延长。

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本文引用的文献

1
New nephron development in fish from polluted waters: a possible biomarker.
Ecotoxicology. 1995 Jun;4(3):157-68. doi: 10.1007/BF00116479.
2
Characterization of mesonephric development and regeneration using transgenic zebrafish.
Am J Physiol Renal Physiol. 2010 Nov;299(5):F1040-7. doi: 10.1152/ajprenal.00394.2010. Epub 2010 Sep 1.
3
Redirection of renal mesenchyme to stromal and chondrocytic fates in the presence of TGF-beta2.
Differentiation. 2010 Apr-Jun;79(4-5):272-84. doi: 10.1016/j.diff.2010.01.004. Epub 2010 Feb 18.
4
A transient niche regulates the specification of Drosophila intestinal stem cells.
Science. 2010 Jan 8;327(5962):210-3. doi: 10.1126/science.1181958.
5
Overexpression of Sall1 in vivo leads to reduced body weight without affecting kidney development.
J Biochem. 2010 Mar;147(3):445-50. doi: 10.1093/jb/mvp214. Epub 2010 Jan 6.
6
Advances in early kidney specification, development and patterning.
Development. 2009 Dec;136(23):3863-74. doi: 10.1242/dev.034876.
7
A robust and highly efficient immune cell reprogramming system.
Cell Stem Cell. 2009 Nov 6;5(5):554-66. doi: 10.1016/j.stem.2009.10.004.
8
The hematopoietic stem cell niche: low in oxygen but a nice place to be.
J Cell Physiol. 2010 Jan;222(1):17-22. doi: 10.1002/jcp.21908.
9
Non-homeodomain regions of Hox proteins mediate activation versus repression of Six2 via a single enhancer site in vivo.
Dev Biol. 2009 Nov 1;335(1):156-65. doi: 10.1016/j.ydbio.2009.08.020. Epub 2009 Aug 28.
10
The murine Fgfrl1 receptor is essential for the development of the metanephric kidney.
Dev Biol. 2009 Nov 1;335(1):106-19. doi: 10.1016/j.ydbio.2009.08.019. Epub 2009 Aug 26.

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