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Updated: Aug 12, 2026

Murine Model of CD40-activation of B cells
Published on: March 6, 2010
Regulation of lymphocyte activation by the cell-surface molecule CD22
C L Law1, S P Sidorenko, E A Clark
1Dept of Microbiology, University of Washington, Seattle 98195.
Insights
Accessory molecules like CD22 regulate B-cell antigen receptor (BCR) activation. This review explores CD22
Area of Science:
- Immunology
- Molecular Biology
Background:
- Accessory molecules are crucial for lymphocyte activation.
- The B-cell antigen receptor (BCR) pathway is central to adaptive immunity.
- CD22 is an accessory molecule expressed on B-lineage cells.
Purpose of the Study:
- To review the structure-function relationship between CD22 and the BCR.
- To discuss the role of CD22 as a cell-adhesion molecule.
- To propose models for the in vivo functions of CD22.
Main Methods:
- Literature review of current knowledge.
- Analysis of structural and functional data.
- Development of theoretical models.
Main Results:
- CD22 interacts with the BCR, influencing its signaling.
- CD22 functions as a cell-adhesion molecule.
- Potential in vivo roles for CD22 are proposed.
Conclusions:
- Understanding the CD22-BCR interaction is key to B-cell regulation.
- CD22's dual role as a signaling modulator and adhesion molecule is highlighted.
- Further research into CD22's in vivo functions is warranted.
Abstract:
Accessory molecules play an important role in the regulation of lymphocyte activation mediated by the B-cell antigen receptor (BCR). CD22 is one such accessory molecule expressed on B-lineage cells. Here, Che-Leung Law and colleagues review current knowledge on the structure-function relationship between CD22 and the BCR, discuss the role of CD22 as a cell-adhesion molecule and suggest models for potential in vivo functions of CD22.
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