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在中肾管发育过程中,成纤维细胞生长因子受体信号对细胞增殖的区域特异性调控。

Region-specific regulation of cell proliferation by FGF receptor signaling during the Wolffian duct development.

作者信息

Okazawa Mika, Murashima Aki, Harada Masayo, Nakagata Naomi, Noguchi Masafumi, Morimoto Mitsuru, Kimura Tadashi, Ornitz David M, Yamada Gen

机构信息

Department of Developmental Genetics, Institute of Advanced Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-8509, Japan; Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita 565-0871, Osaka, Japan.

Department of Developmental Genetics, Institute of Advanced Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-8509, Japan.

出版信息

Dev Biol. 2015 Apr 1;400(1):139-47. doi: 10.1016/j.ydbio.2015.01.023. Epub 2015 Feb 9.

Abstract

The Wolffian duct (WD) is a primordium of the male reproductive tract and kidney collecting duct system. Fibroblast growth factor receptors (FGFRs), members of the receptor tyrosine kinase (RTK) family, are essential for kidney development. Although the functions of FGFR signaling in kidney morphogenesis have been analyzed, their function in WD development has not been comprehensively investigated. Here, we demonstrate that Fgfr2 is the major Fgfr gene expressed throughout the WD epithelia and that it is essential for the maintenance of the WD, specifically in the caudal part of the WD. Hoxb7-Cre mediated inactivation of Fgfr2 in the mouse WD epithelia resulted in the regression of the caudal part of the WD and abnormal male reproductive tract development. Cell proliferation and expression of the downstream target genes of RTK signaling (Etv4 and Etv5) were decreased in the caudal part of the WD epithelia in the mutant embryos. Cranial (rostral) WD formation and ureteric budding were not affected. Ret, Etv4, and Etv5 expression were sustained in the ureteric bud of the mutant embryos. Taken together, these data suggest region-specific requirements for FGFR2 signaling in the developing caudal WD epithelia.

摘要

沃尔夫管(WD)是雄性生殖道和肾集合管系统的原基。成纤维细胞生长因子受体(FGFRs)属于受体酪氨酸激酶(RTK)家族成员,对肾脏发育至关重要。尽管FGFR信号通路在肾脏形态发生中的功能已得到分析,但其在WD发育中的功能尚未得到全面研究。在此,我们证明Fgfr2是在整个WD上皮中表达的主要Fgfr基因,并且它对WD的维持至关重要,特别是在WD的尾部。Hoxb7-Cre介导的小鼠WD上皮中Fgfr2的失活导致WD尾部的退化和雄性生殖道发育异常。在突变胚胎的WD上皮尾部,细胞增殖以及RTK信号通路下游靶基因(Etv4和Etv5)的表达均降低。头部( Rostral)WD的形成和输尿管芽生未受影响。突变胚胎输尿管芽中Ret、Etv4和Etv5的表达得以维持。综上所述,这些数据表明发育中的尾部WD上皮对FGFR2信号通路有区域特异性需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/029a/4382079/4fa568ecca7a/nihms668372f1.jpg

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