4.4 Article

The Drosophila Chitinase-Like Protein IDGF3 Is Involved in Protection against Nematodes and in Wound Healing

期刊

JOURNAL OF INNATE IMMUNITY
卷 8, 期 2, 页码 199-210

出版社

KARGER
DOI: 10.1159/000442351

关键词

Chitinase-like proteins; Imaginal disc growth factor; Hemolymph clot; Wound healing; Nematode infection; Insect immunity

资金

  1. Swedish Research Council [VR-2010-5988]
  2. Swedish Foundation for International Cooperation in Research and Higher Education (STINT) [IG2011-2042]
  3. Knut and Alice Wallenberg Foundation [KAW2012.0058]
  4. Swedish Cancer Foundation [CAN 2010/553]
  5. Czech Science Foundation [GA14-27816S]

向作者/读者索取更多资源

Chitinase-like proteins (CLPs) of the 18 glycosyl hydrolase family retain structural similarity to chitinases but lack enzymatic activity. Although CLPs are upregulated in several human disorders that affect regenerative and inflammatory processes, very little is known about their normal physiological function. We show that an insect CLP (Drosophila imaginal disc growth factor 3, IDGF3) plays an immune-protective role during entomopathogenic nematode (EPN) infections. During these infections, nematodes force their entry into the host via border tissues, thus creating wounds. Whole-genome transcriptional analysis of nematode-infected wildtype and Idgf3 mutant larvae have shown that, in addition to the regulation of genes related to immunity and wound closure, IDGF3 represses Jak/STAT and Wingless signaling. Further experiments have confirmed that IDGF3 has multiple roles in innate immunity. It serves as an essential component required for the formation of hemolymph clots that seal wounds, and Idgf3 mutants display an extended developmental delay during wound healing. Altogether, our findings indicate that vertebrate and invertebrate CLP proteins function in analogous settings and have a broad impact on inflammatory reactions and infections. This opens the way to further genetic analysis of Drosophila IDGF3 and will help to elucidate the exact molecular context of CLP function. (C) 2015 The Author(s) Published by S. Karger AG, Basel

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