Phosphoinositide 3-kinase is required for process outgrowth and cell polarization of gastrulating mesendodermal cells

被引:102
作者
Montero, JA
Kilian, B
Chan, J
Bayliss, PE
Heisenberg, CP
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
关键词
D O I
10.1016/S0960-9822(03)00505-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: During vertebrate gastrulation, cell polarization and migration are core components in the cellular rearrangements that lead to the formation of the three germ layers, ectoderm, mesoderm, and endoderm. Previous studies have implicated the Wnt/planar cell polarity (PCP) signaling pathway in controlling cell morphology and movement during gastrulation. However, cell polarization and directed cell migration are reduced but not completely abolished in the absence of Wnt/PCP signals; this observation indicates that other signaling pathways must be involved. Results: We show that Phosphoinositide 3-Kinases (PI3Ks) are required at the onset of zebrafish gastrulation in mesendodermal cells for process formation and cell polarization. Platelet Derived Growth Factor (PDGF) functions upstream of PI3K, while Protein Kinase B (PKB), a downstream effector of PI3K activity, localizes to the leading edge of migrating mesendodermal cells. In the absence of PI3K activity, PKB localization and cell polarization are strongly reduced in mesendodermal cells and are followed by slower but still highly coordinated and directed movements of these cells. Conclusions: We have identified a novel role of a signaling pathway comprised of PDGF, PI3K, and PKB in the control of morphogenetic cell movements during gastrulation. Furthermore, our findings provide insight into the relationship between cell polarization and directed cell migration at the onset of zebrafish gastrulation.
引用
收藏
页码:1279 / 1289
页数:11
相关论文
共 39 条
[1]  
ATALIOTIS P, 1995, DEVELOPMENT, V121, P3099
[2]   Integration of signaling networks that regulate Dictyostelium differentiation [J].
Aubry, L ;
Firtel, R .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :469-517
[3]   PDGF-receptor tyrosine kinase blocker AG1295 selectively attenuates smooth muscle cell growth in vitro and reduces neointimal formation after balloon angioplasty in swine [J].
Banai, S ;
Wolf, Y ;
Golomb, G ;
Pearle, A ;
Waltenberger, J ;
Fishbein, I ;
Schneider, A ;
Gazit, A ;
Perez, L ;
Huber, R ;
Lazarovichi, G ;
Rabinovich, L ;
Levitzki, A ;
Gertz, SD .
CIRCULATION, 1998, 97 (19) :1960-1969
[4]  
BARTH KA, 1995, DEVELOPMENT, V121, P1755
[5]  
Carballada R, 2001, DEVELOPMENT, V128, P35
[6]   Single-cell internalization during zebrafish gastrulation [J].
Carmany-Rampey, A ;
Schier, AF .
CURRENT BIOLOGY, 2001, 11 (16) :1261-1265
[7]   Control of cell polarity and chemotaxis by Akt/PKB and PI3 kinase through the regulation of PAKa [J].
Chung, CY ;
Potikyan, G ;
Firtel, RA .
MOLECULAR CELL, 2001, 7 (05) :937-947
[8]   Role of phosphatidylinositol 3′ kinase and a downstream pleckstrin homology domain-containing protein in controlling chemotaxis in Dictyostelium [J].
Funamoto, S ;
Milan, K ;
Meili, R ;
Firtel, RA .
JOURNAL OF CELL BIOLOGY, 2001, 153 (04) :795-809
[9]  
Ghil JS, 1999, INT J DEV BIOL, V43, P329
[10]   Role of the PI3K regulatory subunit in the control of actin organization and cell migration [J].
Jiménez, C ;
Portela, RA ;
Mellado, M ;
Rodríguez-Frade, JM ;
Collard, J ;
Serrano, A ;
Martínez-A, C ;
Avila, J ;
Carrera, AC .
JOURNAL OF CELL BIOLOGY, 2000, 151 (02) :249-261