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Model membrane systems to reconstitute immune cell signaling

期刊

FEBS JOURNAL
卷 288, 期 4, 页码 1070-1090

出版社

WILEY
DOI: 10.1111/febs.15488

关键词

giant vesicles; immune synapse; model membranes; reconstitution; supported lipid bilayers

资金

  1. Newton-Katip Celebi Institutional Links grant [352333122]
  2. SciLifeLab fellowship
  3. Wellcome Institutional Strategic Support Fund (ISSF)
  4. Medical Research Council (MRC) [MC_UU_12010, G0902418, MC_UU_12025]
  5. MRC/BBSRC/EPSRC [MR/K01577X/1]
  6. EPSRC/MRC [EP/L016052/1]
  7. Wellcome Trust [104924/14/Z/14, PRF 100262]
  8. Oxford-Bristol Meyer Squibb translational research funding program
  9. European Molecular Biology Organization [ALTF 1420-2015]
  10. European Commission [AdG 670930]
  11. Marie Sklodowska-Curie Actions (LTFCOFUND2013) [GA2013-609409]
  12. Kennedy Trust for Rheumatology
  13. MRC [G0902418, MR/K01577X/1] Funding Source: UKRI

向作者/读者索取更多资源

The importance of understanding cellular membrane functions through experimental systems mimicking their biochemical composition and biophysical properties is emphasized. The interplay between membrane components and physical properties of the plasma membrane is discussed, highlighting the significance for biomimetic studies. The advantages and considerations of different model membrane systems are reviewed, with an emphasis on their contributions to understanding immune cell signaling, particularly the immunological synapse.
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.

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