Shroom regulates epithelial cell shape via the apical positioning of an actomyosin network

被引:204
作者
Hildebrand, JD [1 ]
机构
[1] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
关键词
Shroom; neural tube; myosin II; epithelial; constriction;
D O I
10.1242/jcs.02626
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The actin-binding protein Shroom is essential for neural tube morphogenesis in multiple vertebrate organisms, indicating its function is evolutionarily conserved. Shroom facilitates neurulation by regulating the morphology of neurepithelial cells. Shroom localizes to the apical tip of adherens junctions of neural ectoderm cells in vivo and to the apical junctional complex (AJC) in MDCK cells. Induced expression of Shroom in polarized epithelia elicits apical constriction and dramatic reorganization of the apical arrangement and packing of cells without altering apical-basal polarity. These events likely mimic the cell shape changes and cellular movements required for neurulation in vivo. The observed phenotypes depend on the ability of Shroom to alter F-actin distribution and regulate the formation of a previously uncharacterized contractile actomyosin network associated with the AJC. Targeting the C-terminal domain. of Shroorn to the apical plasma membrane elicits constriction and reorganization of the actomyosin network, indicting that this domain mediates Shroom's activity. In vivo, Shroom-mutant neural epithelia show a marked reduction in apically positioned myosin. Thus, Shroom likely facilitates neural tube closure by regulating cell shape changes via the apical positioning of an actomyosin network in the neurepithelium.
引用
收藏
页码:5191 / 5203
页数:13
相关论文
共 39 条
[1]   RECEPTOR-MEDIATED TRANSCYTOSIS OF IGA IN MDCK CELLS IS VIA APICAL RECYCLING ENDOSOMES [J].
APODACA, G ;
KATZ, LA ;
MOSTOV, KE .
JOURNAL OF CELL BIOLOGY, 1994, 125 (01) :67-86
[2]   NH2-terminal deletion of beta-catenin results in stable colocalization of mutant beta-catenin with adenomatous polyposis coli protein and altered MDCK cell adhesion [J].
Barth, AIM ;
Pollack, AL ;
Altschuler, Y ;
Mostov, KE ;
Nelson, WJ .
JOURNAL OF CELL BIOLOGY, 1997, 136 (03) :693-706
[3]   Myosin-dependent junction remodelling controls planar cell intercalation and axis elongation [J].
Bertet, C ;
Sulak, L ;
Lecuit, T .
NATURE, 2004, 429 (6992) :667-671
[4]   Molecular mechanisms of nonmuscle myosin-II regulation [J].
Bresnick, AR .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (01) :26-33
[5]  
Brouns MR, 2000, DEVELOPMENT, V127, P4891
[6]   NEURAL-TUBE DEFECTS - A REVIEW OF HUMAN AND ANIMAL STUDIES ON THE ETIOLOGY OF NEURAL-TUBE DEFECTS [J].
CAMPBELL, LR ;
DAYTON, DH ;
SOHAL, GS .
TERATOLOGY, 1986, 34 (02) :171-187
[7]   Endotoxin inhibits intestinal epithelial restitution through activation of Rho-GTPase and increased focal adhesions [J].
Cetin, S ;
Ford, HR ;
Sysko, LR ;
Agarwal, C ;
Wang, J ;
Neal, MD ;
Baty, C ;
Apodaca, G ;
Hackam, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24592-24600
[8]   Rho-stimulated contractility drives the formation of stress fibers and focal adhesions [J].
ChrzanowskaWodnicka, M ;
Burridge, K .
JOURNAL OF CELL BIOLOGY, 1996, 133 (06) :1403-1415
[9]   Towards a cellular and molecular understanding of neurulation [J].
Colas, JF ;
Schoenwolf, GC .
DEVELOPMENTAL DYNAMICS, 2001, 221 (02) :117-145
[10]   THE EMBRYONIC-DEVELOPMENT OF MAMMALIAN NEURAL-TUBE DEFECTS [J].
COPP, AJ ;
BROOK, FA ;
ESTIBEIRO, JP ;
SHUM, ASW ;
COCKROFT, DL .
PROGRESS IN NEUROBIOLOGY, 1990, 35 (05) :363-+