Model membrane systems to reconstitute immune cell signaling

FEBS J. 2021 Feb;288(4):1070-1090. doi: 10.1111/febs.15488. Epub 2020 Aug 3.

Abstract

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.

Keywords: giant vesicles; immune synapse; model membranes; reconstitution; supported lipid bilayers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • B-Lymphocytes / metabolism
  • Cell Membrane / metabolism*
  • Humans
  • Immunological Synapses / metabolism*
  • Lipid Bilayers / metabolism*
  • Membrane Proteins / metabolism*
  • Phagocytes / metabolism
  • Signal Transduction*
  • T-Lymphocytes / metabolism

Substances

  • Lipid Bilayers
  • Membrane Proteins