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在肾小球形成过程中,基质细胞需要Pod1。

Pod1 is required in stromal cells for glomerulogenesis.

作者信息

Cui Shiying, Schwartz Lois, Quaggin Susan E

机构信息

The Samuel Lunenfeld Research Institute, Mt Sinai Hospital, Toronto, Ontario, Canada.

出版信息

Dev Dyn. 2003 Mar;226(3):512-22. doi: 10.1002/dvdy.10244.

Abstract

Pod1 (capsulin/epicardin/Tcf21) is a basic-helix-loop-helix transcription factor that is highly expressed in the mesenchyme of developing organs that include the kidney, lung, gut, and heart. Null Pod1 mice are born but die shortly after birth due to a lack of alveoli in the lungs and cardiac defects. In addition, the kidneys are hypoplastic and demonstrate disrupted branching morphogenesis of the ureteric bud epithelium, a marked reduction in the number of nephrons, a delay in glomerulogenesis, and blood vessel abnormalities. To further dissect the cellular function of Pod1 during kidney development, chimeric mice were generated through aggregations of null Pod1 embryonic stem cells and murine embryos ubiquitously expressing enhanced green fluorescent protein (GFP). Histologic, immunohistochemical, and in situ hybridization analysis of the resulting chimeric offspring demonstrated both cell autonomous and non-cell autonomous roles for Pod1 in the differentiation of specific renal cell lineages that include peritubular interstitial cells and pericytes. Most strikingly, the glomerulogenesis defect was rescued by the presence of wild-type stromal cells, suggesting a non-cell autonomous role for Pod1 in this cell population.

摘要

Pod1(capsulin/epicardin/Tcf21)是一种碱性螺旋-环-螺旋转录因子,在包括肾脏、肺、肠道和心脏在内的发育器官间充质中高度表达。Pod1基因敲除小鼠能够出生,但由于肺部缺乏肺泡和心脏缺陷,出生后不久便死亡。此外,肾脏发育不全,输尿管芽上皮的分支形态发生受到破坏,肾单位数量显著减少,肾小球发生延迟,且存在血管异常。为了进一步剖析Pod1在肾脏发育过程中的细胞功能,通过将Pod1基因敲除胚胎干细胞与普遍表达增强型绿色荧光蛋白(GFP)的小鼠胚胎聚集,培育出了嵌合小鼠。对所得嵌合后代进行的组织学、免疫组织化学和原位杂交分析表明,Pod1在包括肾小管周间质细胞和周细胞在内的特定肾细胞谱系分化中具有细胞自主和非细胞自主作用。最引人注目的是,野生型基质细胞的存在挽救了肾小球发生缺陷,这表明Pod1在该细胞群体中具有非细胞自主作用。

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