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Published on: October 25, 2016
CD5 is associated with the human B cell antigen receptor complex
A C Lankester1, G M van Schijndel, J L Cordell
1Department of Clinical Viro-Immunology, The Netherlands Red Cross Blood Transfusion Service, Amsterdam.
Insights
CD5 associates with the B cell receptor (BCR) complex on human B cells, influencing signaling pathways. This finding reveals a unique role for CD5+ B cells in modulating BCR signals and immune responses.
Area of Science:
- Immunology
- Cell Biology
Background:
- The B cell receptor (BCR) complex, crucial for B cell activation, consists of membrane immunoglobulin and the Ig alpha/beta heterodimer.
- A subset of B cells, including those in chronic lymphocytic leukemia, express CD5, a molecule also found on T cells.
- CD5+ B cells are implicated in autoimmunity and possess distinct signaling properties compared to conventional B cells.
Purpose of the Study:
- To investigate the association of CD5 with the BCR complex in human B cells.
- To determine the functional role of CD5 in BCR-mediated signaling.
Main Methods:
- Co-immunoprecipitation assays to assess CD5 association with the BCR complex.
- Analysis of tyrosine kinase activity following BCR stimulation in CD5+ B cells.
Main Results:
- CD5 is demonstrated to be physically associated with the BCR complex on human B cells.
- CD5 functions as a substrate for BCR-induced tyrosine kinase activity.
- These findings suggest CD5+ B cells possess a distinct capacity to modulate BCR signals.
Conclusions:
- CD5 plays a direct role in BCR complex signaling, acting as a substrate for associated kinases.
- The association of CD5 with the BCR complex provides a molecular basis for the unique signaling characteristics of CD5+ B cells.
- This interaction offers potential therapeutic targets for conditions involving aberrant B cell signaling.
Abstract:
On human B cells the antigen receptor complex is composed of the membrane form of the immunoglobulin molecule and the non-covalently associated Ig alpha/beta heterodimer. A small subpopulation of normal B cells and chronic lymphocytic leukemia B cells express (analogous to T cells) the transmembrane molecule CD5, a counterstructure of B cell-specific CD72. Numbers of CD5+ B cells are increased in several physiological and pathological conditions. Moreover, CD5+ B cells are being held responsible for the production of autoreactive antibodies and seem to have signaling characteristics distinct from conventional B cells. On T cells, CD5 associates with the T cell receptor CD3 complex and ligation of CD5 leads to the generation of co-stimulatory signals, that act on T cell activation. We here demonstrate that CD5 is associated with the B cell receptor (BCR) complex and serves as substrate for BCR-induced tyrosine kinase activity. Hence, CD5+ B cells have a unique potential to modulate BCR signals.
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