Plakophilin 3 mediates Rap1-dependent desmosome assembly and adherens junction maturation

被引:28
|
作者
Todorovic, Viktor [1 ]
Koetsier, Jennifer L. [1 ]
Godsel, Lisa M. [1 ,2 ]
Green, Kathleen J. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pathol, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, Chicago, IL 60611 USA
[3] Northwestern Univ, Feinberg Sch Med, RH Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
CIRCULATING TUMOR-CELLS; E-CADHERIN; EPITHELIAL-CELLS; AREA-COMPOSITA; MESSENGER-RNA; PKC-ALPHA; RAP1; PROTEINS; ADHESION; DESMOPLAKIN;
D O I
10.1091/mbc.E14-05-0968
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pathways driving desmosome and adherens junction assembly are temporally and spatially coordinated, but how they are functionally coupled is poorly understood. Here we show that the Armadillo protein plakophilin 3 (Pkp3) mediates both desmosome assembly and E-cadherin maturation through Rap1 GTPase, thus functioning in a manner distinct from the closely related plakophilin 2 (Pkp2). Whereas Pkp2 and Pkp3 share the ability to mediate the initial phase of desmoplakin (DP) accumulation at sites of cell-cell contact, they play distinct roles in later steps: Pkp3 is required for assembly of a cytoplasmic population of DP-enriched junction precursors, whereas Pkp2 is required for transfer of the precursors to the membrane. Moreover, Pkp3 forms a complex with Rap1 GTPase, promoting its activation and facilitating desmosome assembly. We show further that Pkp3 deficiency causes disruption of an E-cadherin/Rap1 complex required for adherens junction sealing. These findings reveal Pkp3 as a coordinator of desmosome and adherens junction assembly and maturation through its functional association with Rap1.
引用
收藏
页码:3749 / 3764
页数:16
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