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早期肾单位模式分析揭示了远端肾小囊增殖在通过帽状间充质衍生的连接段与输尿管芽顶端融合中的作用。

Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment.

作者信息

Georgas Kylie, Rumballe Bree, Valerius M Todd, Chiu Han Sheng, Thiagarajan Rathi D, Lesieur Emmanuelle, Aronow Bruce J, Brunskill Eric W, Combes Alexander N, Tang Dave, Taylor Darrin, Grimmond Sean M, Potter S Steven, McMahon Andrew P, Little Melissa H

机构信息

NHMRC Principal Research Fellow, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.

出版信息

Dev Biol. 2009 Aug 15;332(2):273-86. doi: 10.1016/j.ydbio.2009.05.578. Epub 2009 Jun 6.

Abstract

While nephron formation is known to be initiated by a mesenchyme-to-epithelial transition of the cap mesenchyme to form a renal vesicle (RV), the subsequent patterning of the nephron and fusion with the ureteric component of the kidney to form a patent contiguous uriniferous tubule has not been fully characterized. Using dual section in situ hybridization (SISH)/immunohistochemistry (IHC) we have revealed distinct distal/proximal patterning of Notch, BMP and Wnt pathway components within the RV stage nephron. Quantitation of mitoses and Cyclin D1 expression indicated that cell proliferation was higher in the distal RV, reflecting the differential developmental programs of the proximal and distal populations. A small number of RV genes were also expressed in the early connecting segment of the nephron. Dual ISH/IHC combined with serial section immunofluorescence and 3D reconstruction revealed that fusion occurs between the late RV and adjacent ureteric tip via a process that involves loss of the intervening ureteric epithelial basement membrane and insertion of cells expressing RV markers into the ureteric tip. Using Six2-eGFPCre x R26R-lacZ mice, we demonstrate that these cells are derived from the cap mesenchyme and not the ureteric epithelium. Hence, both nephron patterning and patency are evident at the late renal vesicle stage.

摘要

虽然已知肾单位的形成始于帽状间充质的间充质-上皮转化以形成肾小囊(RV),但肾单位随后的模式形成以及与肾脏输尿管成分融合以形成通畅连续的泌尿小管尚未得到充分表征。通过双切片原位杂交(SISH)/免疫组织化学(IHC),我们揭示了RV期肾单位内Notch、BMP和Wnt信号通路成分明显的远端/近端模式。有丝分裂和细胞周期蛋白D1表达的定量分析表明,远端RV中的细胞增殖更高,这反映了近端和远端群体不同的发育程序。少数RV基因也在肾单位的早期连接段表达。双ISH/IHC结合连续切片免疫荧光和三维重建显示,晚期RV与相邻输尿管尖端之间通过一个过程发生融合,该过程涉及中间输尿管上皮基底膜的消失以及表达RV标记物的细胞插入输尿管尖端。使用Six2-eGFPCre x R26R-lacZ小鼠,我们证明这些细胞来源于帽状间充质而非输尿管上皮。因此,在晚期肾小囊阶段,肾单位的模式形成和通畅性均很明显。

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