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胚胎肾中的干细胞。

Stem cells in the embryonic kidney.

作者信息

Nishinakamura R

机构信息

Division of Integrative Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, 2-2-1 Honjo, Kumamoto, Japan.

出版信息

Kidney Int. 2008 Apr;73(8):913-7. doi: 10.1038/sj.ki.5002784. Epub 2008 Jan 16.

DOI:10.1038/sj.ki.5002784
PMID:18200005
Abstract

The mammalian kidney, the metanephros, is formed by a reciprocally inductive interaction between two precursor tissues, the metanephric mesenchyme and the ureteric bud. The ureteric bud induces the metanephric mesenchyme to differentiate into the epithelia of glomeruli and renal tubules. Multipotent renal progenitors that form colonies upon Wnt4 stimulation and strongly express Sall1 exist in the metanephric mesenchyme; these cells can partially reconstitute a three-dimensional structure in an organ culture setting. Six2 maintains this mesenchymal progenitor population by opposing Wnt4-mediated epithelialization. Upon epithelial tube formation, Notch2 is required for the differentiation of proximal nephron structures (podocyte and proximal tubules). In addition, the induction methods of the intermediate mesoderm, the precursor of the metanephric mesenchyme, begin to be elucidated. If derivation of metanephric mesenchyme becomes possible, we will be closer to the generation and manipulation of multiple cell lineages in the kidney.

摘要

哺乳动物的肾脏,即后肾,由两个前体组织——后肾间充质和输尿管芽之间相互诱导的相互作用形成。输尿管芽诱导后肾间充质分化为肾小球和肾小管的上皮细胞。后肾间充质中存在多能肾祖细胞,这些细胞在Wnt4刺激下形成集落并强烈表达Sall1;这些细胞能够在器官培养环境中部分重建三维结构。Six2通过对抗Wnt4介导的上皮化来维持这种间充质祖细胞群体。在上皮管形成时,Notch2是近端肾单位结构(足细胞和近端小管)分化所必需的。此外,后肾间充质的前体——中间中胚层的诱导方法也开始得到阐明。如果后肾间充质的衍生成为可能,我们将更接近肾脏中多种细胞谱系的生成和操控。

相似文献

1
Stem cells in the embryonic kidney.胚胎肾中的干细胞。
Kidney Int. 2008 Apr;73(8):913-7. doi: 10.1038/sj.ki.5002784. Epub 2008 Jan 16.
2
Notch2 activation in the embryonic kidney depletes nephron progenitors.Notch2 激活导致胚胎肾中肾祖细胞耗竭。
J Am Soc Nephrol. 2010 May;21(5):803-10. doi: 10.1681/ASN.2009040353. Epub 2010 Mar 18.
3
Nephron progenitors in the metanephric mesenchyme.后肾原基在中肾间充质中。
Pediatr Nephrol. 2011 Sep;26(9):1463-7. doi: 10.1007/s00467-011-1806-0. Epub 2011 Feb 19.
4
Identification of multipotent progenitors in the embryonic mouse kidney by a novel colony-forming assay.通过一种新型集落形成试验鉴定胚胎小鼠肾脏中的多能祖细胞。
Development. 2006 Jan;133(1):151-61. doi: 10.1242/dev.02174. Epub 2005 Nov 30.
5
Essential roles of Sall family genes in kidney development.Sall家族基因在肾脏发育中的重要作用。
J Physiol Sci. 2006 Apr;56(2):131-6. doi: 10.2170/physiolsci.M95. Epub 2006 Apr 22.
6
Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney.Six2对于发育中的肾脏中肾发生的抑制和祖细胞更新是必需的。
EMBO J. 2006 Nov 1;25(21):5214-28. doi: 10.1038/sj.emboj.7601381. Epub 2006 Oct 12.
7
Osr1 expression demarcates a multi-potent population of intermediate mesoderm that undergoes progressive restriction to an Osr1-dependent nephron progenitor compartment within the mammalian kidney.Osr1的表达界定了中肾间充质的一个多能细胞群体,该群体在哺乳动物肾脏内逐渐局限于一个依赖Osr1的肾单位祖细胞区室。
Dev Biol. 2008 Dec 1;324(1):88-98. doi: 10.1016/j.ydbio.2008.09.010. Epub 2008 Sep 19.
8
Redefining the in vivo origin of metanephric nephron progenitors enables generation of complex kidney structures from pluripotent stem cells.重新定义后肾原基祖细胞的体内起源,使多能干细胞能够生成复杂的肾组织结构。
Cell Stem Cell. 2014 Jan 2;14(1):53-67. doi: 10.1016/j.stem.2013.11.010. Epub 2013 Dec 12.
9
Metanephric mesenchyme contains embryonic renal stem cells.后肾间充质包含胚胎肾干细胞。
Am J Physiol Renal Physiol. 2002 Oct;283(4):F799-809. doi: 10.1152/ajprenal.00375.2001.
10
An epithelial precursor is regulated by the ureteric bud and by the renal stroma.上皮前体细胞受输尿管芽和肾间质的调控。
Dev Biol. 2002 Jun 15;246(2):296-310. doi: 10.1006/dbio.2002.0646.

引用本文的文献

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Renal regenerative capacity related to stem cell reserve in nephrectomized rats.肾切除大鼠与干细胞储备相关的肾再生能力。
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2
Diabetic Kidney Disease Represents a Locus of Opportunity.糖尿病肾病是一个机会点。
Front Physiol. 2021 Mar 8;12:650503. doi: 10.3389/fphys.2021.650503. eCollection 2021.
3
PAX2 is dispensable for in vitro nephron formation from human induced pluripotent stem cells.PAX2 在人诱导多能干细胞体外肾单位形成中可有可无。
Sci Rep. 2017 Jul 3;7(1):4554. doi: 10.1038/s41598-017-04813-3.
4
Advances in the Knowledge about Kidney Decellularization and Repopulation.肾脏去细胞化与再细胞化知识的进展
Front Bioeng Biotechnol. 2017 Jun 1;5:34. doi: 10.3389/fbioe.2017.00034. eCollection 2017.
5
Induction of nephron progenitors and glomeruli from human pluripotent stem cells.从人多能干细胞诱导生成肾单位祖细胞和肾小球。
Pediatr Nephrol. 2017 Feb;32(2):195-200. doi: 10.1007/s00467-016-3339-z. Epub 2016 Feb 11.
6
Special Morphological Features at the Interface of the Renal Stem/Progenitor Cell Niche Force to Reinvestigate Transport of Morphogens During Nephron Induction.肾干细胞/祖细胞龛界面的特殊形态学特征促使我们重新研究肾单位诱导过程中形态发生素的转运。
Biores Open Access. 2016 Jan 1;5(1):49-60. doi: 10.1089/biores.2015.0039. eCollection 2016.
7
When morphogenetic proteins encounter special extracellular matrix and cell-cell connections at the interface of the renal stem/progenitor cell niche.当形态发生蛋白在肾干/祖细胞生态位的界面遇到特殊的细胞外基质和细胞间连接时。
Anat Cell Biol. 2015 Mar;48(1):1-9. doi: 10.5115/acb.2015.48.1.1. Epub 2015 Mar 20.
8
Sall1 maintains nephron progenitors and nascent nephrons by acting as both an activator and a repressor.Sall1通过作为激活剂和抑制剂来维持肾单位祖细胞和新生肾单位。
J Am Soc Nephrol. 2014 Nov;25(11):2584-95. doi: 10.1681/ASN.2013080896. Epub 2014 Apr 17.
9
Bmp7 maintains undifferentiated kidney progenitor population and determines nephron numbers at birth.Bmp7 维持未分化的肾祖细胞群体,并决定出生时的肾单位数量。
PLoS One. 2013 Aug 26;8(8):e73554. doi: 10.1371/journal.pone.0073554. eCollection 2013.
10
Chromatin-modifying agents reactivate embryonic renal stem/progenitor genes in human adult kidney epithelial cells but abrogate dedifferentiation and stemness.染色质修饰剂可重新激活人类成年肾上皮细胞中的胚胎肾干/祖基因,但会消除去分化和干性。
Cell Reprogram. 2013 Aug;15(4):281-92. doi: 10.1089/cell.2012.0087. Epub 2013 Jul 10.