Dr Rebecca Clark rebecca.clark2@durham.ac.uk
Associate Professor
Multiple TGF-β superfamily signals modulate the adult Drosophila immune response
Clark, R.I.; Woodcock, K.J.; Geissmann, F.; Trouillet, C.; Dionne, M.S.
Authors
K.J. Woodcock
F. Geissmann
C. Trouillet
M.S. Dionne
Abstract
TGF-β superfamily signals play complex roles in regulation of tissue repair and inflammation in mammals [1]. Drosophila melanogaster is a well-established model for the study of innate immune function [2, 3] and wound healing [4–7]. Here, we explore the role and regulation of two TGF-β superfamily members, dawdle and decapentaplegic (dpp), in response to wounding and infection in adult Drosophila. We find that both TGF-β signals exhibit complex regulation in response to wounding and infection, each is expressed in a subset of phagocytes, and each inhibits a specific arm of the immune response. dpp is rapidly activated by wounds and represses the production of antimicrobial peptides; flies lacking dpp function display persistent, strong antimicrobial peptide expression after even a small wound. dawdle, in contrast, is activated by Gram-positive bacterial infection but repressed by Gram-negative infection or wounding; its role is to limit infection-induced melanization. Flies lacking dawdle function exhibit melanization even when uninfected. Together, these data imply a model in which the bone morphogenetic protein (BMP) dpp is an important inhibitor of inflammation following sterile injury whereas the activin-like dawdle determines the nature of the induced immune response.
Citation
Clark, R., Woodcock, K., Geissmann, F., Trouillet, C., & Dionne, M. (2011). Multiple TGF-β superfamily signals modulate the adult Drosophila immune response. Current Biology, 21(19), 1672-1677. https://doi.org/10.1016/j.cub.2011.08.048
Journal Article Type | Article |
---|---|
Acceptance Date | Aug 19, 2011 |
Online Publication Date | Sep 29, 2011 |
Publication Date | Oct 11, 2011 |
Deposit Date | Aug 13, 2015 |
Publicly Available Date | Jun 15, 2018 |
Journal | Current Biology |
Print ISSN | 0960-9822 |
Electronic ISSN | 1879-0445 |
Publisher | Cell Press |
Peer Reviewed | Peer Reviewed |
Volume | 21 |
Issue | 19 |
Pages | 1672-1677 |
DOI | https://doi.org/10.1016/j.cub.2011.08.048 |
Public URL | https://durham-repository.worktribe.com/output/1433883 |
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Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/
Copyright Statement
© 2011 Elsevier Ltd. Open access under CC BY license.
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