21 juin 2022
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info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.2201129119
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info:eu-repo/semantics/altIdentifier/pmid/35696562
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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_8C01245BEAE47
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A.T. Linder et al., « Sialic acids on B cells are crucial for their survival and provide protection against apoptosis. », Serveur académique Lausannois, ID : 10.1073/pnas.2201129119
Sialic acids (Sias) on the B cell membrane are involved in cell migration, in the control of the complement system and, as sialic acid-binding immunoglobulin-like lectin (Siglec) ligands, in the regulation of cellular signaling. We studied the role of sialoglycans on B cells in a mouse model with B cell-specific deletion of cytidine monophosphate sialic acid synthase (CMAS), the enzyme essential for the synthesis of sialoglycans. Surprisingly, these mice showed a severe B cell deficiency in secondary lymphoid organs. Additional depletion of the complement factor C3 rescued the phenotype only marginally, demonstrating a complement-independent mechanism. The B cell survival receptor BAFF receptor was not up-regulated, and levels of activated caspase 3 and processed caspase 8 were high in B cells of Cmas-deficient mice, indicating ongoing apoptosis. Overexpressed Bcl-2 could not rescue this phenotype, pointing to extrinsic apoptosis. These results show that sialoglycans on the B cell surface are crucial for B cell survival by counteracting several death-inducing pathways.