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β-连环蛋白在禽类中肾血管发育和退化过程中的表达

beta-Catenin expression during vascular development and degeneration of avian mesonephros.

作者信息

Nacher Víctor, Carretero Ana, Navarro Marc, Armengol Clara, Llombart Cristina, Blasi Juan, Ruberte Jesús

机构信息

Department of Animal Health and Anatomy and Center for Animal Biotechnology and Gene Therapy (CBATEG), Autonomous University of Barcelona, Spain.

出版信息

J Anat. 2005 Feb;206(2):165-74. doi: 10.1111/j.1469-7580.2005.00382.x.

Abstract

beta-Catenin is a structural component of adherens junctions, a regulator of the Wnt signalling pathway and a transcriptional co-activator with a key role in vascular patterning. The avian mesonephros is a transitory embryonic kidney that is used in the study of vascular development and degeneration. Here we examine beta-catenin expression in this model during vascular development and degeneration. Quail embryos with developing or degenerating mesonephros were studied, on day 6 (30HH) or day 11 of incubation (40HH), respectively. QH1 whole mounts of developing mesonephros revealed numerous angioblast-like cells situated in the paramesonephric duct that seem to invade the mesonephros. Although these cells did not express beta-catenin, the surrounding periductal mesenchymal cells translocated high levels of beta-catenin into the nucleus. In contrast, degenerating mesonephros were devoid of angioblast-like cells and beta-catenin was lower than in the developing mesonephros. beta-Catenin was significantly reduced in the glomerular capillary tuffs, indicating that it was particularly down-regulated in the vascular system. No sex-related differences in beta-catenin expression were observed in degenerating mesonephros. Furthermore, two special populations of glomerular and peritubular endothelial cells were observed in degenerating mesonephros: one translocating beta-catenin into the nucleus and the other in apoptosis that did not translocate it. In conclusion, our results indicate that the paramesonephric duct is a potential new vasculogenetic pathway, and suggest that beta-catenin plays a role in the fate of mesonephric endothelial cells.

摘要

β-连环蛋白是黏着连接的结构成分、Wnt信号通路的调节因子以及在血管模式形成中起关键作用的转录共激活因子。禽中肾是一个短暂的胚胎肾脏,用于血管发育和退化的研究。在此,我们研究了该模型中血管发育和退化过程中β-连环蛋白的表达。分别对孵化第6天(30HH)或第11天(40HH)具有发育或退化中肾的鹌鹑胚胎进行了研究。发育中肾的QH1整装标本显示,位于中肾旁管中的许多成血管细胞样细胞似乎侵入了中肾。尽管这些细胞不表达β-连环蛋白,但周围的导管周围间充质细胞将高水平的β-连环蛋白转运到细胞核中。相比之下,退化的中肾没有成血管细胞样细胞,且β-连环蛋白低于发育中的中肾。肾小球毛细血管丛中的β-连环蛋白显著减少,表明其在血管系统中尤其下调。在退化的中肾中未观察到β-连环蛋白表达的性别相关差异。此外,在退化的中肾中观察到两种特殊的肾小球和肾小管周围内皮细胞群体:一种将β-连环蛋白转运到细胞核中,另一种处于凋亡状态且不转运β-连环蛋白。总之,我们的结果表明中肾旁管是一条潜在的新血管生成途径,并提示β-连环蛋白在中肾内皮细胞的命运中起作用。

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