B cell mechanosensing: A mechanistic overview

Adv Immunol. 2019:144:23-63. doi: 10.1016/bs.ai.2019.08.003.

Abstract

B cells are essential to the adaptive immune system for providing the humoral immunity against cohorts of pathogens. The presentation of antigen to the B cell receptor (BCR) leads to the initiation of B cell activation, which is a process sensitive to the stiffness features of the substrates presenting the antigens. Mechanosensing of the B cells, potentiated through BCR signaling and the adhesion molecules, efficiently regulates B cell activation, proliferation and subsequent antibody responses. Defects in sensing of the antigen-presenting substrates can lead to the activation of autoreactive B cells in autoimmune diseases. The use of high-resolution, high-speed live-cell imaging along with the sophisticated biophysical materials, has uncovered the mechanisms underlying the initiation of B cell activation within seconds of its engagement with the antigen presenting substrates. In this chapter, we reviewed studies that have contributed to uncover the molecular mechanisms of B cell mechanosensing during the initiation of B cell activation.

Keywords: B cells; FAK; Integrin; Mechanosensing; Substrate stiffness.

Publication types

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

MeSH terms

  • Animals
  • Antibody Formation*
  • Antigen Presentation*
  • Autoimmune Diseases / metabolism
  • B-Lymphocytes / immunology*
  • Focal Adhesion Protein-Tyrosine Kinases / genetics
  • Focal Adhesion Protein-Tyrosine Kinases / immunology
  • Humans
  • Immunological Synapses / chemistry
  • Immunological Synapses / genetics
  • Immunological Synapses / pathology
  • Integrins / immunology
  • Mechanotransduction, Cellular / immunology*
  • Molecular Motor Proteins / immunology
  • Neoplasms / immunology
  • Neoplasms / metabolism
  • Receptors, Antigen, B-Cell / immunology*
  • Receptors, Antigen, B-Cell / metabolism
  • Signal Transduction / immunology*

Substances

  • Integrins
  • Molecular Motor Proteins
  • Receptors, Antigen, B-Cell
  • Focal Adhesion Protein-Tyrosine Kinases