表皮生长因子信号传导与皮肤附属器发育。

EDA signaling and skin appendage development.

作者信息

Cui Chang-Yi, Schlessinger David

机构信息

Laboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.

出版信息

Cell Cycle. 2006 Nov 1;5(21):2477-83. doi: 10.4161/cc.5.21.3403. Epub 2006 Sep 14.

Abstract

The same morphogenetic signals are often involved in the development of different organs. For developing skin appendages, a model for tissue-specific regulation of signaling is provided by the EDA pathway, which accesses the otherwise ubiquitous NFkappaB transcription factors. EDA signaling is mediated by ectodysplasin, EDAR and EDARADD, which form a new TNF ligand-receptor-adaptor family that is restricted to skin appendages in vertebrates from fish to human. The critical function of the pathway was demonstrated in the hereditary genetic disorder Anhidrotic Ectodermal Dysplasia (EDA), which is characterized by defective formation of hair follicles, sweat glands and teeth. The pathway does not appear to initiate the development of the appendages, but is regulated by and regulates the course of further morphogenesis. In mice, transgenic and knockout strains have increasingly revealed features of the mechanism, and suggest possible non-invasive interventions to alleviate EDA deficiency, especially in sweat glands and eyes.

摘要

相同的形态发生信号通常参与不同器官的发育。对于皮肤附属器的发育,EDA信号通路提供了一种信号组织特异性调节模型,该通路可作用于原本普遍存在的NFκB转录因子。EDA信号由外胚层发育不良蛋白、EDAR和EDARADD介导,它们形成了一个新的TNF配体-受体-衔接蛋白家族,该家族在从鱼类到人类的脊椎动物中仅限于皮肤附属器。该信号通路的关键功能在遗传性疾病无汗性外胚层发育不良(EDA)中得到了证实,其特征是毛囊、汗腺和牙齿形成缺陷。该信号通路似乎并不启动附属器的发育,而是受进一步形态发生过程的调节并对其进行调控。在小鼠中,转基因和基因敲除品系越来越多地揭示了该机制的特征,并提出了减轻EDA缺陷的可能的非侵入性干预措施,尤其是在汗腺和眼睛方面。

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