首页> 美国卫生研究院文献>Journal of Toxicologic Pathology >Thy-1 Expressing Mesenchymal Cells in Rat Nephrogenesis in Correlation with Cells Immunoreactive for α-Smooth Muscle Actin and Vimentin
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Thy-1 Expressing Mesenchymal Cells in Rat Nephrogenesis in Correlation with Cells Immunoreactive for α-Smooth Muscle Actin and Vimentin

机译:大鼠肾生成中表达Thy-1的间质细胞。 与α-平滑肌肌动蛋白和 波形蛋白

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摘要

Thy-1 expression may influence myofibroblast development. Through the epithelial-mesenchymal transition (EMT), injured renal epithelial cells undergo regression to the metanephric mesenchymal phenotype and then acquire a myofibroblastic nature (expressing α-smooth muscle actin; α-SMA). Because the metanephric blastema differentiates into mesenchymal and renal epithelial cells, we investigated Thy-1 immunoexpression during nephrogenesis in F344 rats in correlation with vimentin and α-SMA expressions. Kidney samples were obtained from fetuses on gestation days 18 and 21, neonates on days 1-18 and adults at 6 weeks of age. Mesangial cells in S-shaped bodies and immature and mature glomeruli continuously expressed both Thy-1 and α-SMA during early nephrogenesis (fetuses and neonates on days 1-9). During early nephrogenesis, loosely-arranged blastemal cell-derived mesenchymal cells in the cortex and medulla also exhibited Thy-1 and α-SMA, although the α-SMA expression was weaker than that of Thy-1. Vimentin expression coincided with that of Thy-1. These findings indicate that the derivation of α-SMA-expressing myofibroblastic cells may be related to mesangial or blastemal cells expressing both Thy-1 and α-SMA. Interestingly, there was a difference in Thy-1 expression between cortical and medullary tubulointerstitial cells from late nephrogenesis (neonates on days 12-18) and those from adults in that the cortical cells reacted faintly or negatively to Thy-1, whereas the medullary cells reacted strongly to Thy-1; additionally, bundle-arranged mesenchymal cells that were only observed in the neonates on days 1-12 reacted strongly to α-SMA, but faintly to Thy-1. Blastemal cell-derived mesenchymal cells seem to alter the immunoexpressions of Thy-1 and α-SMA, depending on the conditions which they develop. Thy-1 immunoexpression would be useful for investigation of reverse embryogenesis, which might occur in fibrotic kidneys.
机译:Thy-1的表达可能会影响成肌纤维细胞的发育。通过上皮-间质转化(EMT),受损的肾上皮细胞经历退变至后肾间充质表型,然后获得肌成纤维细胞特性(表达α-平滑肌肌动蛋白;α-SMA)。因为后肾母细胞分化为间充质和肾上皮细胞,所以我们研究了波形蛋白和α-SMA表达与F344大鼠肾生成过程中Thy-1免疫表达的关系。在妊娠第18和21天从胎儿,在1-18天从新生儿和6周大的成年人中获取肾脏样品。在早期肾生成过程中(胎儿和新生儿在第1-9天),S形体以及未成熟和成熟肾小球的肾小球系膜细胞连续表达Thy-1和α-SMA。在早期肾生成过程中,尽管α-SMA表达弱于Thy-1,但在皮质和​​髓质中松散排列的胚细胞来源的间充质细胞也表现出Thy-1和α-SMA。波形蛋白的表达与Thy-1一致。这些发现表明表达α-SMA的肌成纤维细胞的衍生可能与同时表达Thy-1和α-SMA的肾小球系膜细胞或胚系细胞有关。有趣的是,皮质和髓质之间的Thy-1表达有所不同 晚期肾生成的肾小管间质细胞(在第​​12-18天发生新生)和 来自成年人的皮层细胞对 Thy-1,而髓样细胞对Thy-1强烈反应;另外, 束排列的间充质细胞仅在新生儿 第1-12天对α-SMA反应强烈,但对Thy-1反应较弱。恶臭的 细胞来源的间充质细胞似乎改变了Thy-1和 α-SMA,取决于它们形成的条件。 Thy-1免疫表达 对于研究反向胚胎发生很有用,可能发生在 纤维化肾脏。

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