Reference Report
| Reference | |||
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| Citation | Clark, R.I., Woodcock, K.J., Geissmann, F., Trouillet, C., Dionne, M.S. (2011). Multiple TGF-β Superfamily Signals Modulate the Adult Drosophila Immune Response. Curr. Biol. 21(19): 1672--1677. (Export to RIS) | ||
| FlyBase ID | FBrf0216429 | ||
| Publication Type | Research paper | ||
| PubMed ID | 21962711 | ||
| PubMed 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. | ||
| DOI | 10.1016/j.cub.2011.08.048 | ||
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| Language of Publication | English | ||
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| Publication Type | Journal | ||
| Abbreviation | Curr. Biol. | ||
| Title | Current Biology | ||
| Publication Year | 1991- | ||
| ISBN/ISSN | 0960-9822 | ||
Data from Reference
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Alleles (23)
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Constructs (16)
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Genes (23)
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Insertions (2)
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Natural transposons (1)
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