Subcellular localization of β-catenin is regulated by cell density

被引:53
作者
Dietrich, C [1 ]
Scherwat, J [1 ]
Faust, D [1 ]
Oesch, F [1 ]
机构
[1] Univ Mainz, Inst Toxicol, D-55131 Mainz, Germany
关键词
beta-catenin; cell-cell adhesion; proliferation; contact; -inhibition; keratinocytes;
D O I
10.1006/bbrc.2002.6625
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
It is generally accepted that subcellular distribution of beta-catenin regulates its function. Membrane-bound beta-catenin mediates cell-cell adhesion, whereas elevation of the cytoplasmic and nuclear pool of the protein is associated with an oncogenic function. Although the role of beta-catenin in transformed cells is relatively well characterized, little is known about its importance in proliferation and cell-cycle control of nontransformed epithelial cells. Using different approaches we show that in human keratinocytes (HaCaT) beta-catenin is distributed throughout the cells in subconfluent, proliferating cultures. In contrast, beta-catenin is nearly exclusively located at the plasma membrane in confluent, contact-inhibited cells. Hence, we demonstrate for the first time that beta-catenin is translocated from the cytoplasm to the plasma membrane in response to high cell density. We conclude that beta-catenin plays an important role in proliferation and mediating contact-inhibition by changing intracellular localization. (C) 2002 EIsevier Science (USA).
引用
收藏
页码:195 / 199
页数:5
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