The desmosome as a model for lipid raft driven membrane domain organization

被引:25
|
作者
Zimmer, Stephanie E. [1 ,2 ]
Kowalczyk, Andrew P. [2 ,3 ]
机构
[1] Emory Univ, Grad Program Biochem Cell & Dev Biol, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Cell Biol, Whitehead Biomed Res Bldg,615 Michael St, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Dermatol, Atlanta, GA 30322 USA
来源
基金
美国国家卫生研究院;
关键词
Desmosome; Intercellular junction; Lipid raft; Cadherin; Keratin; Skin disease; PROTEIN-KINASE-C; PLASMA-MEMBRANE; PLAKOGLOBIN-BINDING; TIGHT JUNCTIONS; ALPHA-CATENIN; CELL-ADHESION; MICE LACKING; TRANSMEMBRANE DOMAIN; CYTOPLASMIC DOMAIN; BILAYER THICKNESS;
D O I
10.1016/j.bbamem.2020.183329
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
Desmosomes are cadherin-based adhesion structures that mechanically couple the intermediate filament cytoskeleton of adjacent cells to confer mechanical stress resistance to tissues. We have recently described desmosomes as mesoscale lipid raft membrane domains that depend on raft dynamics for assembly, function, and disassembly. Lipid raft microdomains are regions of the plasma membrane enriched in sphingolipids and cholesterol. These domains participate in membrane domain heterogeneity, signaling and membrane trafficking. Cellular structures known to be dependent on raft dynamics include the post-synaptic density in neurons, the immunological synapse, and intercellular junctions, including desmosomes. In this review, we discuss the current state of the desmosome field and put forward new hypotheses for the role of lipid rafts in desmosome adhesion, signaling and epidermal homeostasis. Furthermore, we propose that differential lipid raft affinity of intercellular junction proteins is a central driving force in the organization of the epithelial apical junctional complex.
引用
收藏
页数:10
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