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Role of Src kinases and Syk in Fc? receptor-mediated phagocytosis and phagosome-lysosome fusion
Linköping University, Faculty of Health Sciences. Linköping University, Department of Molecular and Clinical Medicine, Medical Microbiology.
2001 (English)In: Journal of Leukocyte Biology, ISSN 0741-5400, E-ISSN 1938-3673, Vol. 70, no 5, 801-811 p.Article in journal (Refereed) Published
Abstract [en]

Phagocytosis is increased by Fc? receptors (Fc?Rs), and studies with syk-1- macrophages demonstrated that Syk kinase is required for Fc?TR phagocytosis. Similar studies with macrophages lacking the Src family kinases Hck, Fgr, and Lyn showed that these kinases are not required for phagocytosis but that they enhance the rate of particle engulfment. In this report we show that both wild-type and hck-1- fgr-1- macrophages expressed Fyn, Src, and Yes and that these kinases were activated on ingestion of immunoglobulin G (IgG)-coated particles and redistributed, together with Syk, to actin-rich phagocytic cups and the phagosomal membrane. At doses blocking IgG-dependent phagocytosis, the tyrosine kinase inhibitors PP1 and piceatannol inhibited both Src family kinase and Syk activities, as well as their redistribution to actin-rich phagocytic cups. Hck, Fgr, and Lyn were dispensable for lysosome-phagosome fusion (PLF) induced by IgG-coated particles. However, PP1 or piceatannol hampered unopsonized yeast-induced PLF despite the fact that they did not block yeast internalization.

Place, publisher, year, edition, pages
2001. Vol. 70, no 5, 801-811 p.
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:liu:diva-26057Local ID: 10516OAI: oai:DiVA.org:liu-26057DiVA: diva2:246605
Available from: 2009-10-08 Created: 2009-10-08 Last updated: 2017-12-13

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