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牛中肾和后肾的干细胞因子和 KIT 免疫定位的相似发育模式。

Similar developmental patterns in immunolocalisation of stem cell factor and KIT in bovine meso- and metanephros.

机构信息

Institute of Anatomy, Medical Faculty, University of Leipzig, Liebigstrasse 13, 04103, Leipzig, Germany.

出版信息

Histochem Cell Biol. 2010 Apr;133(4):417-24. doi: 10.1007/s00418-010-0677-y. Epub 2010 Feb 18.

Abstract

The mesonephros is often regarded as a simplified version of the terminal renal organ, the metanephros. Both renal organs result from an epithelio-mesenchymal interaction between the Wolffian duct and the nephrogenic ridge. It appears that the epithelio-mesenchymal interaction makes use of similar signal cascades for both renal organs and that key events required for the development of the metanephros occur at earlier stages. In murine metanephroi, the stem cell factor (SCF)/-KIT-signal transduction pathway has recently been shown to regulate ureteric bud branching and epithelial cell differentiation. We immunohistochemically defined the time-sequence of KIT and SCF presence in both renal organs using bovine embryos/foetuses with crown rump length (CRL) of 1.7-24 cm. In the mesonephroi, epithelial cells with strong KIT staining were scattered in distal tubules, and SCF was expressed in the epithelial wall of corpuscles and proximal tubules. KIT positivity occurred in the metanephroi of embryos prior to SCF; KIT was predominantly localised at the ureteric bud tips in the nephrogenic zone. In foetuses of 13 cm and more CRL, the SCF/KIT profile of developmentally advanced nephrons mirrored the situation in the mesonephros. Epithelial cells with strong KIT staining were scattered in the cortical areas of distal tubules, while SCF was expressed in the epithelial wall of corpuscles and proximal tubules. Our morphological findings agree with a potential role of KIT at the ureteric bud tips and demonstrate a similar expression of KIT and SCF along the areas of developmentally advanced mesonephric and metanephric nephrons.

摘要

中肾通常被认为是终末肾器官——后肾的简化版。这两种肾器官都是由沃尔夫管和肾嵴之间的上皮-间充质相互作用产生的。似乎上皮-间充质相互作用利用了类似的信号级联来产生这两种肾器官,并且后肾发育所需的关键事件发生在更早的阶段。在鼠类后肾中,最近已经表明,干细胞因子 (SCF)/-KIT 信号转导途径调节输尿管芽分支和上皮细胞分化。我们使用具有头臀长 (CRL) 为 1.7-24 厘米的牛胚胎/胎儿,通过免疫组织化学方法定义了这两种肾器官中 KIT 和 SCF 存在的时间顺序。在中肾中,具有强烈 KIT 染色的上皮细胞散布在远曲小管中,而 SCF 则在肾小球和近曲小管的上皮壁中表达。在 SCF 之前,KIT 在胚胎的后肾中呈阳性;KIT 主要定位于肾发生区的输尿管芽尖端。在 CRL 为 13 厘米及以上的胎儿中,发育成熟的肾单位的 SCF/KIT 特征与中肾的情况相似。具有强烈 KIT 染色的上皮细胞散布在皮质区的远曲小管中,而 SCF 则在肾小球和近曲小管的上皮壁中表达。我们的形态学发现与 KIT 在输尿管芽尖端的潜在作用一致,并证明了 KIT 和 SCF 在发育成熟的中肾和后肾单位的区域具有相似的表达。

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