The p21-activated kinase Pak1 regulates induction and migration of the neural crest in Xenopus

被引:8
作者
Bisson, Nicolas [3 ]
Wedlich, Doris [4 ]
Moss, Tom [1 ,2 ]
机构
[1] Univ Laval, Fac Med, Lab Growth & Dev, Canc Res Ctr, Quebec City, PQ G1K 7P4, Canada
[2] Univ Laval, Fac Med, Dept Mol Biol Med Biochem & Pathol, Quebec City, PQ G1K 7P4, Canada
[3] Univ Laval, Fac Med, Lab Signal Network Dynam, Quebec City, PQ G1K 7P4, Canada
[4] Karlsruhe Inst Technol, Inst Zool, Karlsruhe, Germany
关键词
Pak1; neural crest; Xenopus; cell migration; Snail1; EPITHELIAL-MESENCHYMAL TRANSITIONS; TRANSCRIPTION FACTOR SNAIL; GENE-EXPRESSION; CELL-CYCLE; SPECIFICATION; INHIBITION; MESODERM; EMBRYOS; FAMILY; MEMBER;
D O I
10.4161/cc.19685
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pak1 is a member of the PAK family of serine/threonine kinases that are downstream effectors of Rac1 and Cdc42 small GTPases and that are implicated in cytoskeleton reorganization. Early expression of Pak1 in Xenopus embryos is tissue restricted, suggesting a role in organogenesis and in cranial neural crest (CNC) cell migration. By observing CNC in vivo and after transplantation, we show that a dominant-negative (DN) Pak1 inhibits its migration. DN-Pak1 also specifically modified the expression of several NC markers. Twist expression was decreased and Snail1 expression posteriorized, but Snail2 (Slug), Sox9 and AP2 were unaffected. DN-Pak1 inhibition of CNC migration could be rescued with Snail1 but not with Twist, which, in fact, cooperated with DN-Pak1 in inhibiting migration. The data confirm that neither Snail1 nor Snail2 expression alone is sufficient for Xenopus CNC migration. Furthermore, they show that, in this tissue, Snail1 and Snail2 expression is not interdependent, nor are these factors subject to obligatory co-regulation, and that their expression depends on signal transduction. Our results also represent the first evidence that Pak1 links extracellular signals to the genetic cascade of transcription factors necessary for CNC specification.
引用
收藏
页码:1316 / 1324
页数:9
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