Differential requirement for β-catenin in epithelial and fiber cells during lens development

被引:75
作者
Cain, Sarah [1 ]
Martinez, Gemma [1 ]
Kokkinos, Maria I. [1 ]
Turner, Kirsty [1 ]
Richardson, Robert J. [1 ]
Abud, Helen E. [2 ]
Huelsken, Joerg [3 ]
Robinson, Michael L. [4 ]
de Iongh, Robb U. [1 ]
机构
[1] Univ Melbourne, Dept Anat & Cell Biol, Ocular Dev Lab, Melbourne, Vic 3010, Australia
[2] Monash Univ, Dept Anat & Cell Biol, Clayton, Vic 38000, Australia
[3] Swiss Inst Expt Canc Res, ISREC, EPFL, Swiss Fed Inst Technol, CH-1066 Epalinges, Switzerland
[4] Miami Univ, Dept Zool, Oxford, OH 45056 USA
基金
英国医学研究理事会;
关键词
lens development; Wnt signaling; adherens junctions; beta-catenin;
D O I
10.1016/j.ydbio.2008.07.002
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Recent studies implicate Wnt/beta-catenin signaling in lens differentiation (Stump, R. J. et aL 2003 A role for,,. Wnt/beta-catenin signaling in lens epithelial differentiation. Dev Biol;259:48-61). beta-catenin is a component of adherens junctions and functions as a transcriptional activator in canonical Wnt signaling. We investigated the effects of Cre/LoxP-mediated deletion of beta-catenin during lens development using two Cre lines that specifically deleted beta-catenin whole lens or only in differentiated fibers, from E13.5. We found that beta-catenin was required in lens epithelium and during early fiber differentiation but appeared to be redundant in differentiated fiber cells. Complete loss of beta-catenin resulted in an abnormal and deficient epithelial layer with loss of E-cadherin and Pax6 expression as well as abnormal expression of c-Maf and p57(ki)p(2) but not Prox]. There was also disrupted fiber cell differentiation, characterized by poor cell elongation, decreased beta-crystallin expression, epithelial cell cycle arrest at G(1)-S transition and premature cell cycle exit. Despite cell cycle arrest there was no induction of apoptosis. Mutant fiber cells displayed altered apical-basal polarity as evidenced by altered distribution of the tight junction protein, ZO1, disruption of apical actin filaments and abnormal deposition of extracellular matrix, resulting in a deficient lens Capsule. Loss of beta-catenin also affected the formation of adhesion junctions as evidenced by dissociation of N-cadherin and F-actin localization in differentiating fiber cells. However, loss of beta-catenin from terminally differentiating fibers had no apparent effects on adhesion junctions between adjacent embryonic fibers. These data indicate that beta-catenin plays distinct functions during lens fiber differentiation and is involved in both Wnt signaling and adhesion-related mechanisms that regulate lens epithelium and early fiber differentiation. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:420 / 433
页数:14
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