Governing epidermal homeostasis by coupling cell-cell adhesion to integrin and growth factor signaling, proliferation, and apoptosis

被引:46
作者
Livshits, Geulah [1 ]
Kobielak, Agnieszka [1 ]
Fuchs, Elaine [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Lab Mammalian Cell Biol & Dev, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
focal adhesion kinase signaling; in utero transduction; receptor tyrosine kinase; ALPHA-CATENIN; E-CADHERIN; RAC ACTIVATION; LIVING CELLS; RECEPTOR; COMPLEX; KINASE; EGFR; SKIN; FAK;
D O I
10.1073/pnas.1202120109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cadherin/catenin-based adhesions coordinate cellular growth, survival, migration, and differentiation within a tissue by mechanically anchoring cells to their neighbors. They also intersect with diverse signaling pathways in development and cancer. Although the adhesive functions of adherens junction proteins are well characterized, their contribution to other signaling pathways is less well understood. Here, we show that ablation of alpha-catenin in the epidermis selectively induces apoptosis in suprabasal differentiating keratinocytes while sparing basal cell progenitors. This protection from death is coupled to elevated focal adhesion signaling, faster migration, and an altered distribution of growth factor receptors. We show that simultaneous depletion of alpha-catenin and focal adhesion kinase or p21-activated kinase eliminates basal cell protection as well as the elevated migration and proliferation of cells. The increased dependency of cells upon matrix interactions for their survival when cell-cell adhesions are destabilized has important implications for cancer progression and metastasis.
引用
收藏
页码:4886 / 4891
页数:6
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