Model membrane systems to reconstitute immune cell signaling

被引:25
|
作者
Cespedes, Pablo F. [1 ]
Beckers, Daniel [2 ]
Dustin, Michael L. [1 ]
Sezgin, Erdinc [2 ,3 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthoped Rheumatol & Musculoskeleta, Oxford OX3 9DS, England
[2] Univ Oxford, MRC Weatherall Inst Mol Med, MRC Human Immunol Unit, Oxford, England
[3] Karolinska Inst, Dept Womens & Childrens Hlth, Sci Life Lab, Stockholm, Sweden
基金
英国工程与自然科学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
giant vesicles; immune synapse; model membranes; reconstitution; supported lipid bilayers; SUPRAMOLECULAR ACTIVATION CLUSTERS; SUPPORTED PLANAR BILAYERS; PLASMA-MEMBRANE; IMMUNOLOGICAL SYNAPSE; T-CELLS; PHOSPHOLIPID-BILAYERS; ASYMMETRIC DISTRIBUTION; MULTIVESICULAR BODIES; PHASE-SEPARATION; LIPID DIFFUSION;
D O I
10.1111/febs.15488
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
Understanding the broad variety of functions encoded in cellular membranes requires experimental systems mimicking both their biochemical composition and biophysical properties. Here, we review the interplay between membrane components and the physical properties of the plasma membrane worth considering for biomimetic studies. Later, we discuss the main advantages and caveats of different model membrane systems. We further expand on how the use of model systems has contributed to the understanding of immune cell signaling, with a specific focus on the immunological synapse. We discuss the similarities of immune synapses observed for innate and adaptive immune cells and focus on the physical principles underlying these similarities.
引用
收藏
页码:1070 / 1090
页数:21
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