Plasma Membrane Integrates Biophysical and Biochemical Regulation to Trigger Immune Receptor Functions

Front Immunol. 2021 Feb 19:12:613185. doi: 10.3389/fimmu.2021.613185. eCollection 2021.

Abstract

Plasma membrane provides a biophysical and biochemical platform for immune cells to trigger signaling cascades and immune responses against attacks from foreign pathogens or tumor cells. Mounting evidence suggests that the biophysical-chemical properties of this platform, including complex compositions of lipids and cholesterols, membrane tension, and electrical potential, could cooperatively regulate the immune receptor functions. However, the molecular mechanism is still unclear because of the tremendous compositional complexity and spatio-temporal dynamics of the plasma membrane. Here, we review the recent significant progress of dynamical regulation of plasma membrane on immune receptors, including T cell receptor, B cell receptor, Fc receptor, and other important immune receptors, to proceed mechano-chemical sensing and transmembrane signal transduction. We also discuss how biophysical-chemical cues couple together to dynamically tune the receptor's structural conformation or orientation, distribution, and organization, thereby possibly impacting their in-situ ligand binding and related signal transduction. Moreover, we propose that electrical potential could potentially induce the biophysical-chemical coupling change, such as lipid distribution and membrane tension, to inevitably regulate immune receptor activation.

Keywords: biophysical-chemical coupling; electrical potential; immune receptor; mechanical force; plasma membrane.

Publication types

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

MeSH terms

  • Animals
  • Binding Sites
  • Cell Membrane / chemistry*
  • Cell Membrane / metabolism*
  • Chemical Phenomena*
  • Electrophysiological Phenomena
  • Humans
  • Mechanical Phenomena
  • Membrane Lipids / chemistry
  • Membrane Lipids / metabolism
  • Protein Binding
  • Receptors, Immunologic / chemistry*
  • Receptors, Immunologic / metabolism*
  • Signal Transduction*

Substances

  • Membrane Lipids
  • Receptors, Immunologic