4.4 Article

The c-src Homologue Src64B Is Sufficient to Activate the Drosophila Cellular Immune Response

Journal

JOURNAL OF INNATE IMMUNITY
Volume 1, Issue 4, Pages 335-339

Publisher

KARGER
DOI: 10.1159/000191216

Keywords

Innate immunity; Tyrosine kinase; Haemocyte; Src

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Funding

  1. Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK

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The Drosophila larval cellular immune response involves cells (haemocytes) that can be recruited from a haematopoietic organ known as the lymph gland, as well as a sessile population of cells found just underneath the larval cuticle arranged in a segmental pattern. Overexpression of the Drosophila c-src homologue Src64B disrupts the sessile-haemocyte banding pattern. Though Src64B overexpression induced the formation of specialized haemocytes known as lamellocytes, its hyperactivation had no effect on circulating plasmatocyte concentration. Also, there is evidence of non-autonomous regulation as Src64B activity was observed in non-overexpressing plasmatocytes. Finally, Src64B overexpression induced F-actin formation and Jun kinase activation in plasmatocytes. Copyright (C) 2009 S. Karger AG, Basel

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