音猬因子/ patched基因以及表皮生长因子/ 表皮生长因子受体 erbB共同调节胎鼠下颌下腺的分支形态发生。

Shh/Ptch and EGF/ErbB cooperatively regulate branching morphogenesis of fetal mouse submandibular glands.

作者信息

Mizukoshi Kenji, Koyama Noriko, Hayashi Toru, Zheng Liguang, Matsuura Sachiko, Kashimata Masanori

机构信息

Department of Pharmacology, Asahi University School of Dentistry, 1851-1 Hozumi, Mizuho, Gifu 501-0296, Japan.

Department of Pharmacy, Peking University School and Hospital of Stomatology, 22 Zhongguancun Avenue South, Haidian District, Beijing 100081, PR China.

出版信息

Dev Biol. 2016 Apr 15;412(2):278-87. doi: 10.1016/j.ydbio.2016.02.018. Epub 2016 Mar 2.

Abstract

The hedgehog family includes Sonic hedgehog (Shh), Desert hedgehog, and Indian hedgehog, which are well known as a morphogens that play many important roles during development of numerous organs such as the tongue, pancreas, kidney, cartilage, teeth and salivary glands (SMG). In Shh null mice, abnormal development of the salivary gland is seen after embryonic day 14 (E14). Shh also induced lobule formation and lumen formation in acini-like structures in cultured E14 SMG. In this study, we investigated the relationship between Shh and epidermal growth factor (EGF)/ErbB signaling in developing fetal mouse SMG. Administration of Shh to cultured E13 SMG stimulated branching morphogenesis (BrM) and induced synthesis of mRNAs for EGF ligands and receptors of the ErbB family. Shh also stimulated activation of ErbB signaling system such as ERK1/2. AG1478, a specific inhibitor of ErbB receptors, completely suppressed BrM and activation of EGF/ErbB/ERK1/2 cascade in E13 SMGs cultured with Shh. The expressions of mRNA for Egf in mesenchyme and mRNA for Erbb1, Erbb2 and Erbb3 in epithelium of E13 SMG were specifically induced by administration of Shh. These results show that Shh stimulates BrM of fetal mouse SMG, at least in part, through activation of the EGF/ErbB/ERK1/2 signaling system.

摘要

刺猬家族包括音猬因子(Shh)、沙漠刺猬因子和印度刺猬因子,它们作为形态发生素广为人知,在许多器官(如舌头、胰腺、肾脏、软骨、牙齿和唾液腺(SMG))的发育过程中发挥着许多重要作用。在Shh基因敲除小鼠中,胚胎第14天(E14)后可见唾液腺发育异常。Shh还能诱导培养的E14唾液腺中腺泡样结构的小叶形成和管腔形成。在本研究中,我们研究了发育中的胎鼠唾液腺中Shh与表皮生长因子(EGF)/ErbB信号传导之间的关系。将Shh应用于培养的E13唾液腺可刺激分支形态发生(BrM),并诱导EGF配体和ErbB家族受体的mRNA合成。Shh还能刺激ErbB信号系统(如ERK1/2)的激活。AG1478是一种ErbB受体特异性抑制剂,可完全抑制与Shh共同培养的E13唾液腺中的BrM以及EGF/ErbB/ERK1/2级联反应的激活。给予Shh可特异性诱导E13唾液腺间充质中Egf的mRNA表达以及上皮中Erbb1、Erbb2和Erbb3的mRNA表达。这些结果表明,Shh至少部分通过激活EGF/ErbB/ERK1/2信号系统来刺激胎鼠唾液腺的BrM。

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