Plasma-membrane-bound macromolecules are dynamically aggregated to form non-random codistribution patterns of selected functional elements. Do pattern recognition processes govern antigen presentation and intercellular interactions?

J Mol Recognit. 1995 Jul-Aug;8(4):237-46. doi: 10.1002/jmr.300080402.

Abstract

Molecular recognition processes between cell surface elements are discussed with special reference to cell surface pattern formation of membrane-bound integral proteins. The existence, as detected by flow cytometric resonance energy transfer (Appendix), and significance of cell surface patterns involving the interleukin-2 receptor, the T-cell receptor-CD3 system, the intercellular adhesion molecule ICAM-1, and the major histocompatibility complex class I and class II molecules in the plasma membrane of lymphocytes are described. The modulation of antigen presentation by transmembrane potential changes is discussed, and a general role of transmembrane potential changes, and therefore of ion channel activities, adduced as one of the major regulatory mechanisms of cell-cell communication. A general role in the mediation and regulation of intercellular interactions is suggested for cell-surface macromolecular patterns. The dynamic pattern of protein and lipid molecules in the plasma membrane is generated by the genetic code, but has a remarkable flexibility and may be one of the major instruments of accommodation and recognition processes at the cellular level.

Publication types

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

MeSH terms

  • Animals
  • Antigens, Surface / physiology*
  • CD3 Complex
  • Cell Communication*
  • Energy Transfer
  • Flow Cytometry
  • Humans
  • Intercellular Adhesion Molecule-1 / physiology
  • Major Histocompatibility Complex
  • Membrane Potentials
  • Membrane Proteins / physiology*
  • Receptors, Antigen, T-Cell / physiology
  • Receptors, Cell Surface
  • Receptors, Interleukin-2 / physiology

Substances

  • Antigens, Surface
  • CD3 Complex
  • Membrane Proteins
  • Receptors, Antigen, T-Cell
  • Receptors, Cell Surface
  • Receptors, Interleukin-2
  • Intercellular Adhesion Molecule-1