Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2000;2(2):185-203.

Signaling through the B cell antigen receptor in developing B cells

Affiliations
  • PMID: 11258417
Review

Signaling through the B cell antigen receptor in developing B cells

T M Yankee et al. Rev Immunogenet. 2000.

Abstract

Signaling events arising from the B cell antigen receptor (BCR) complex are critical for the normal progression of a B cell through its stages of maturation. These stages are characterized by the generation and expression of BCR components. Initially, the heavy chain is formed and expressed along with the surrogate light chain and VpreB. This pre-BCR may initiate events that induce the cell to generate the light chain molecules. Proper expression of these molecules triggers the cell to develop into a mature B cell. If a key signal is absent at any stage of B cell development, maturation ceases, and either the defects are corrected or the cell undergoes apoptosis. A deficiency in the expression of several intracellular proteins required for these signaling events leads to the arrest of B cell development. Advancement to specific stages of maturation relies on a particular intensity of signal through pathways leading to the activation of a set of transcription factors. These pathways include the calcium and MAPK family pathways. Factors such as the concentration and avidity of the antigen, the coligation of co-receptors, and the formation of signaling complexes dictate the intensity of these signals and thereby the fate of the B cell at each stage of development.

PubMed Disclaimer

Similar articles

Cited by

LinkOut - more resources