Journal article

The tyrosine kinase Lyn limits the cytokine responsiveness of plasma cells to restrict their accumulation in mice

S Infantino, SA Jones, JA Walker, MJ Maxwell, A Light, K O'Donnell, E Tsantikos, V Peperzak, T Phesse, M Ernst, F Mackay, ML Hibbs, KA Fairfax, DM Tarlinton

Science Signaling | AMER ASSOC ADVANCEMENT SCIENCE | Published : 2014

Abstract

Maintenance of an appropriate number of plasma cells, long-lived antibody-producing cells that are derived from B cells, is essential formaintaining immunological memory while limiting disease. Plasma cell survival relies on extrinsic factors, the limited availability of which determines the size of the plasma cell population. Mice deficient in the nonreceptor tyrosine kinase Lyn are prone to an autoimmune disease that is characterized by inflammation and an excess of plasma cells (plasmacytosis). Wedemonstrated that the plasmacytosis was intrinsic to B cells and independent of inflammation. We also showed that Lyn attenuated signaling by signal transducer and activator of transcription 3 (S..

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University of Melbourne Researchers

Grants

Awarded by NHMRC, Australia


Awarded by Lupus Research Institute, DFG (Deutsche Forschungsgemeinschaft)


Awarded by National Health and Medical Research Council of Australia


Funding Acknowledgements

This work was made possible through Victorian State Government Operational Infrastructure Support and Australian Government NHMRC Independent Research Institute Infrastructure Support Scheme (IRIISS). This work was supported by NHMRC, Australia (Program Grant 575500, Project Grants 1008288 and 1025239, Fellowships 516786, 1060675, 603112, 603124); The Lupus Research Institute, DFG (Deutsche Forschungsgemeinschaft) Project IN175/1-1; the Multiple Myeloma Research Foundation USA; Ludwig Institute for Cancer; and the European Molecular Biology Organization.