Flotillins in intercellular adhesion - from cellular physiology to human diseases

被引:55
作者
Bodin, Stephane [1 ]
Planchon, Damien
Morris, Eduardo Rios
Comunale, Franck
Gauthier-Rouviere, Cecile
机构
[1] Univ Montpellier 2, Equipe Labellisee Ligue Canc, F-34293 Montpellier, France
关键词
Flotillin; Microdomain; Cadherin; Adhesion; CADHERIN-MEDIATED ADHESIONS; LIPID-RAFT PROTEINS; MEMBRANE MICRODOMAINS; N-CADHERIN; IN-VIVO; ADHERENS JUNCTIONS; AXON REGENERATION; AMYLOID-BETA; SPFH DOMAIN; REGGIE/FLOTILLIN PROTEINS;
D O I
10.1242/jcs.159764
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Flotillin 1 and 2 are ubiquitous and highly conserved proteins. They were initially discovered in 1997 as being associated with specific caveolin-independent cholesterol-and glycosphingolipid-enriched membrane microdomains and as being expressed during axon regeneration. Flotillins have a role in a large number of physiopathological processes, mainly through their function in membrane receptor clustering and in the regulation of clathrin-independent endocytosis. In this Commentary, we summarize the research performed so far on the role of flotillins in cell-cell adhesion. Recent studies have demonstrated that flotillins directly regulate the formation of cadherin complexes. Indeed, flotillin microdomains are required for the dynamic association and stabilization of cadherins at cell-cell junctions and also for cadherin signaling. Moreover, because flotillins regulate endocytosis and also the actin cytoskeleton, they could have an indirect role in the assembly and stabilization of cadherin complexes. Because it has also recently been shown that flotillins are overexpressed during neurodegenerative diseases and in human cancers, where their upregulation is associated with metastasis formation and poor prognosis, understanding to what extent flotillin upregulation participates in the development of such pathologies is thus of particular interest, as well as how, at the molecular level, it might affect cell adhesion processes.
引用
收藏
页码:5139 / 5147
页数:9
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