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器官培养中小鼠肾发生过程中WT1基因表达的分析。

Analysis of WT1 gene expression during mouse nephrogenesis in organ culture.

作者信息

Yeger H, Forget D, Alami J, Williams B R

机构信息

Department of Pathology, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

In Vitro Cell Dev Biol Anim. 1996 Sep;32(8):496-504. doi: 10.1007/BF02723053.

Abstract

The temporal and spatial expression patterns of the Wilms tumor gene, WT1, were studied during the organogenesis of the mouse kidney in vitro. In situ hybridization and immunocytochemistry localized cellular expression of WT1 in whole kidney organ cultures to the induced metanephric mesenchyme and developing podocytes. Organ cultures were further characterized immunocytochemically with antibodies that specifically labeled the different tubular epithelial components and supporting mesenchyme of the developing nephrons. In organ cultures, the WT1 expression pattern could be visualized in induced metanephric mesenchyme and entire cell cohorts of differentiating podocytes. Expression of WT1 and cell specific markers were retained in short-term monolayer cultures of dissociated kidneys. The development of the metanephric kidney in vitro involves a highly restricted temporal and spatial cellular expression pattern of WT1 which closely follows that observed in tissue sections from gestational kidney isolated during organogenesis in the mouse.

摘要

在体外小鼠肾脏器官发生过程中,对肾母细胞瘤基因WT1的时空表达模式进行了研究。原位杂交和免疫细胞化学将WT1在全肾器官培养物中的细胞表达定位到诱导的后肾间充质和发育中的足细胞。用特异性标记发育中肾单位不同肾小管上皮成分和支持性间充质的抗体对器官培养物进行进一步的免疫细胞化学特征分析。在器官培养物中,WT1表达模式可在诱导的后肾间充质和分化足细胞的整个细胞群体中观察到。WT1和细胞特异性标志物的表达在解离肾脏的短期单层培养物中得以保留。体外后肾的发育涉及WT1高度受限的时空细胞表达模式,这与在小鼠器官发生期间分离的妊娠肾脏组织切片中观察到的模式密切相关。

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