| Literature DB >> 31350199 |
Shuo Yang1, Yaya Zhao2, Junjing Yu3, Zhiqin Fan4, Si-Tang Gong5, Hong Tang6, Lei Pan7.
Abstract
Interorgan immunological communication is critical to connect the local-systemic innate immune response and orchestrate a homeostatic host defense. However, the factors and their roles in this process remain unclear. We find Drosophila IMD response in guts can sequentially trigger a systemic IMD reaction in the fat body. Sugar alcohols of the polyol pathway are essential for the spatiotemporal regulation of gut-fat body immunological communication (GFIC). IMD activation in guts causes elevated levels of sorbitol and galactitol in hemolymph. Aldose reductase (AR) in hemocytes, the rate-limiting enzyme of the polyol pathway, is necessary and sufficient for the increase of plasma sugar alcohols. Sorbitol relays GFIC by subsequent activation of Metalloprotease 2, which cleaves PGRP-LC to activate IMD response in fat bodies. Thus, this work unveils how GFIC relies on the intermediate activation of the polyol pathway in hemolymph and demonstrates that AR provides a critical metabolic checkpoint in the global inflammatory response.Entities:
Keywords: ALARMINs; DAMPs; Drosophila; IMD signaling; innate immunity; interorgan communication; polyol pathway; sorbitol
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Year: 2019 PMID: 31350199 DOI: 10.1016/j.chom.2019.07.001
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023