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Acute Csk inhibition hinders B cell activation by constraining the PI3 kinase pathway

Wen Lu, Katarzyna M. Skrzypczynska, Arthur Weiss

2021Proceedings of the National Academy of Sciences19 citationsDOIOpen Access PDF

Abstract

Significance B lymphocytes recognize pathogenic antigens and become activated via their B cell receptors (BCR). This BCR-dependent activation is controlled by Src-family kinases (SFKs). It is unclear how B cells tolerate the fluctuations of SFK activities and maintain unresponsiveness in the absence of foreign antigens. Using a chemical-genetic system, we acutely inhibited C-terminal Src kinase to enhance the SFK activity in mouse B cells. Surprisingly, we observed marked inhibition of BCR-downstream signaling due to associated impairment of the phosphatidylinositol-trisphosphate pathway. These results reveal the critical importance of maintaining a proper amount of SFK activity in quiescent B cells for appropriate BCR-dependent responses, which may be critical for naïve B cell unresponsiveness to self-antigens to maintain peripheral tolerance.

Topics & Concepts

Tyrosine-protein kinase CSKCell biologySrc family kinaseProto-oncogene tyrosine-protein kinase SrcSignal transductionTyrosine kinaseKinaseT-cell receptorBiologyMAPK/ERK pathwayChemistryT cellSH3 domainImmunologyImmune systemT-cell and B-cell ImmunologyImmune Cell Function and InteractionChronic Lymphocytic Leukemia Research
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