Literature DB >> 15211580

Hemolymph-dependent and -independent responses in Drosophila immune tissue.

Raul Bettencourt1, H Asha, Charles Dearolf, Y Tony Ip.   

Abstract

Insects possess an antimicrobial defense response that is similar to the mammalian innate immune response. The innate immune system is designed to recognize conserved components of microorganisms called pathogen-associated molecular patterns (PAMPs). How host receptors detect PAMPs and transmit the signals to mount the immune response is being elucidated. Using GFP-Dorsal, -Dif, and -Relish reporter proteins in ex vivo assays, we demonstrate that Drosophila fat bodies, a major immune tissue, have both hemolymph-dependent and -independent responses. Microbial preparations such as lipoteichoic acid (LTA) and peptidoglycan (PGN) can stimulate some responses from dissected and rinsed larval fat bodies. Therefore, at least some aspects of recognition can occur on fat body cell surfaces, bypassing the requirement of hemolymph. Our results also show that supernatants from bacterial cultures can stimulate the nuclear translocation of Dorsal in dissected fat bodies, but this stimulation is strictly hemolymph-dependent. Various biochemical assays suggest that the factors from bacterial supernatants that stimulate the hemolymph-dependent nuclear translocation are likely made up of proteins. We further show that Dorsal mutant larvae have much lower phenoloxidase activity, consistent with a more important role of Dorsal in innate immunity than previously shown. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15211580     DOI: 10.1002/jcb.20123

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  18 in total

1.  Heterodimers of NF-kappaB transcription factors DIF and Relish regulate antimicrobial peptide genes in Drosophila.

Authors:  Takahiro Tanji; Eun-Young Yun; Y Tony Ip
Journal:  Proc Natl Acad Sci U S A       Date:  2010-08-02       Impact factor: 11.205

2.  Melanotic mutants in Drosophila: pathways and phenotypes.

Authors:  Svetlana Minakhina; Ruth Steward
Journal:  Genetics       Date:  2006-07-02       Impact factor: 4.562

3.  Toll and IMD pathways synergistically activate an innate immune response in Drosophila melanogaster.

Authors:  Takahiro Tanji; Xiaodi Hu; Alexander N R Weber; Y Tony Ip
Journal:  Mol Cell Biol       Date:  2007-04-16       Impact factor: 4.272

4.  Alcohol resistance in Drosophila is modulated by the Toll innate immune pathway.

Authors:  B R Troutwine; A Ghezzi; A Z Pietrzykowski; N S Atkinson
Journal:  Genes Brain Behav       Date:  2016-04       Impact factor: 3.449

5.  Helicase89B is a Mot1p/BTAF1 homologue that mediates an antimicrobial response in Drosophila.

Authors:  Yoshimasa Yagi; Y Tony Ip
Journal:  EMBO Rep       Date:  2005-09-30       Impact factor: 8.807

6.  Intestinal FoxO signaling is required to survive oral infection in Drosophila.

Authors:  C Fink; J Hoffmann; M Knop; Y Li; K Isermann; T Roeder
Journal:  Mucosal Immunol       Date:  2015-12-02       Impact factor: 7.313

7.  WntD is a feedback inhibitor of Dorsal/NF-kappaB in Drosophila development and immunity.

Authors:  Michael D Gordon; Marc S Dionne; David S Schneider; Roel Nusse
Journal:  Nature       Date:  2005-08-17       Impact factor: 49.962

8.  Effect of pre-incubation temperature on susceptibility of Galleria mellonella larvae to infection by Candida albicans.

Authors:  Peter Mowlds; Kevin Kavanagh
Journal:  Mycopathologia       Date:  2007-10-06       Impact factor: 2.574

9.  Microarray analyses reveal distinct roles for Rel proteins in the Drosophila immune response.

Authors:  Subhamoy Pal; Junlin Wu; Louisa P Wu
Journal:  Dev Comp Immunol       Date:  2007-05-15       Impact factor: 3.636

10.  An introduction to parasitic wasps of Drosophila and the antiparasite immune response.

Authors:  Chiyedza Small; Indira Paddibhatla; Roma Rajwani; Shubha Govind
Journal:  J Vis Exp       Date:  2012-05-07       Impact factor: 1.355

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.