Literature DB >> 17060622

Rel/NF-kappaB double mutants reveal that cellular immunity is central to Drosophila host defense.

Nina Matova1, Kathryn V Anderson.   

Abstract

Studies on Drosophila immunity have focused on the humoral response, whereas less is known about the Drosophila cellular immunity. Here we show that mutants that lack the Drosophila Rel/NF-kappaB proteins Dorsal and Dif have very few blood cells, are constitutively infected by opportunistic microbes, and die from infection as larvae. When the double mutants are grown in microbe-free conditions, the animals are rescued from chronic infection and many survive to adult stages. Thus, Dif and Dorsal are required for survival because they protect the animal from infection by microbes from the environment. Specific expression of Dif or dorsal in the blood cell lineage is sufficient to restore blood cell number, clear microbes, and allow survival to the adult stage. These findings demonstrate that the cellular immune response is essential for the ability of Drosophila to survive in their standard laboratory environment, and that Dif and Dorsal control crucial aspects of the cellular immune response, including blood cell survival and the ability to fight off microbial infection.

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Year:  2006        PMID: 17060622      PMCID: PMC1637598          DOI: 10.1073/pnas.0605721103

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

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Journal:  Curr Biol       Date:  1999-11-04       Impact factor: 10.834

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  41 in total

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Authors:  Nina Matova; Kathryn V Anderson
Journal:  J Cell Sci       Date:  2010-02-15       Impact factor: 5.285

4.  The Toll/NF-κB signaling pathway is required for epidermal wound repair in Drosophila.

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7.  Nuclear translocation of immulectin-3 stimulates hemocyte proliferation.

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8.  Toll-dependent antimicrobial responses in Drosophila larval fat body require Spätzle secreted by haemocytes.

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Journal:  J Cell Sci       Date:  2009-11-24       Impact factor: 5.285

9.  Genome-wide transcriptomic profiling of Anopheles gambiae hemocytes reveals pathogen-specific signatures upon bacterial challenge and Plasmodium berghei infection.

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