A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways

被引:42
|
作者
Kuriyama, Sei [1 ]
Mayor, Roberto [1 ]
机构
[1] UCL, Fac Life Sci, Dept Cell & Dev Biol, London WC1E 6BT, England
来源
DEVELOPMENT | 2009年 / 136卷 / 04期
基金
英国生物技术与生命科学研究理事会;
关键词
Neural induction; Syndecan-4; FGF; PKC; Rac; JNK; AP-1; c-Fos; PROTEIN-KINASE-C; FIBROBLAST-GROWTH-FACTOR; CONVERGENT EXTENSION MOVEMENTS; EARLY XENOPUS EMBRYO; DIRECT BINDING; CHICK-EMBRYO; DIRECTIONAL MIGRATION; CYTOPLASMIC DOMAIN; SPEMANN ORGANIZER; BMP INHIBITION;
D O I
10.1242/dev.027334
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Syndecan-4 (Syn4) is a heparan sulphate proteoglycan that is able to bind to some growth factors, including FGF, and can control cell migration. Here we describe a new role for Syn4 in neural induction in Xenopus. Syn4 is expressed in dorsal ectoderm and becomes restricted to the neural plate. Knockdown with antisense morpholino oligonucleotides reveals that Syn4 is required for the expression of neural markers in the neural plate and in neuralised animal caps. Injection of Syn4 mRNA induces the cell-autonomous expression of neural, but not mesodermal, markers. We show that two parallel pathways are involved in the neuralising activity of Syn4: FGF/ERK, which is sensitive to dominant-negative FGF receptor and to the inhibitors SU5402 and U0126, and a PKC pathway, which is dependent on the intracellular domain of Syn4. Neural induction by Syn4 through the PKC pathway requires inhibition of PKC delta and activation of PKC alpha. We show that PKC alpha inhibits Rac GTPase and that c-Jun is a target of Rac. These findings might account for previous reports implicating PKC in neural induction and allow us to propose a link between FGF and PKC signalling pathways during neural induction.
引用
收藏
页码:575 / 584
页数:10
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