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Updated: Aug 8, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
Positive and negative roles of CD72 in B cell function
Hsin-Jung Wu1, Subbarao Bondada
1Department of Microbiology and Immunology, The Sanders Brown Center on Aging, University of Kentucky, Lexington 40536, USA.
Insights
CD72, a B cell co-receptor, interacts with its ligand CD100. This interaction may enhance B cell responses through a dual signaling model, involving both positive and negative signal modulation.
Area of Science:
- Immunology
- Cell signaling
Background:
- B cell activation relies on B cell receptor (BCR) and co-receptor signaling.
- CD72 is a B cell co-receptor crucial for B cell development and function, except in plasma cells.
- CD100 is identified as the natural ligand for CD72.
Purpose of the Study:
- To investigate the signaling mechanisms of CD72 in B cell activation.
- To propose a dual signaling model for CD72 based on its interactions.
Main Methods:
- The study discusses the association of CD72 with signaling molecules like SHP-1, Grb2, and CD19.
- Analysis of CD72's role in B cell growth and differentiation upon CD100 ligation.
Main Results:
- CD72 ligation enhances B cell growth and differentiation.
- Evidence suggests CD72 can associate with both inhibitory (SHP-1) and potentially activating (Grb2, CD19) signaling molecules.
- These associations suggest a complex role for CD72 in modulating BCR signaling.
Conclusions:
- CD72 plays a significant role in regulating B cell responses.
- A dual signaling model for CD72 is proposed, integrating both positive and negative regulatory pathways.
- Understanding CD72 signaling is critical for B cell immunology.
Abstract:
Regulation of B cell activation depends on integration of signals transmitted by the B cell receptor (BCR) and a variety of co-receptors. CD72 is a B cell co-receptor that is expressed in all stages of B cell development except plasma cells. Ligation of CD72 enhances B cell growth and differentiation. Recently, the class IV semaphoring, CD100, has been identified as the natural ligand for CD72. Cytoplasmic domain of CD72 has been shown to be associated with SHP-1 leading to the proposal that the positive effects of CD72 on B cell response may result from sequestration of negative signals from BCR. However, association of CD72 with Grb2 and/or CD19 suggests that CD72 could transmit positive signals. Based on these data, we propose a dual signaling model of CD72.
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