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Signalling crosstalk in B cells: managing worth and need
1284 John Morgan Building, University of Pennsylvania School of Medicine, 36th and Hamilton Walk, Philadelphia, Pennsylvania 19104, USA. cancro@mail.med.upenn.edu
B cell receptor (BCR) and B cell-activating factor receptor (BAFFR) signaling are crucial for B cell survival. Crosstalk between BCR and BAFFR pathways integrates selective and homeostatic signals, with BCR generating a limiting substrate for BAFFR signaling.
Area of Science:
- Immunology
- Cell Biology
Background:
- B cell receptor (BCR) and B cell-activating factor receptor (BAFFR) signaling are essential for B cell survival.
- BCR provides cell-intrinsic selection signals, while BAFFR responds to extrinsic homeostatic demands.
- Integration mechanisms likely exist to reconcile these distinct signaling inputs.
Approach:
- This opinion article reviews recent evidence on the interdependence of BCR and BAFFR signaling pathways.
- Focuses on the biochemical crosstalk mediating signal integration.
Key Points:
- BCR and BAFFR signaling pathways are interdependent for maintaining B cell survival.
- Crosstalk between downstream pathways integrates cell-intrinsic (BCR) and cell-extrinsic (BAFFR) signals.
- BCR signaling generates a limiting substrate essential for effective BAFFR signal propagation.
Conclusions:
- The interdependence of BCR and BAFFR signaling is mediated by biochemical crosstalk.
- This crosstalk ensures B cell survival by integrating selection and homeostatic signals.
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