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      Cholinergic receptor-Wnt pathway controls immune activation by sensing intestinal dysfunction

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      1 , 2 , 1 , 2 , 1 , 3 , *
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          SUMMARY

          Alterations in the intestinal physiology caused by pathogen colonization result in immune activation. To provide insights into the mechanisms underlying the control of immune activation by changes in intestinal homeostasis, we conducted a forward genetic screen for suppressors of immune activation by intestinal distension in Caenorhabditis elegans. Our results indicate that C. elegans ACC-4, a member of a family of acetylcholine receptors, is required in immune activation by defects in the defecation motor program or by pathogen infection. ACC-4 acts postsynaptically in non-cholinergic RIM neurons to regulate several immune genes and a Wnt-mediated host immune response. These findings uncover a gut-brain-microbial axis that uses neural cholinergic signaling and the Wnt pathway to control immune activation in response to alterations in intestinal homeostasis.

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          In brief

          Ren et al. show that C. elegans ACC-4, a member of a family of acetylcholine receptors, is required in immune activation by intestinal distension or pathogen infection. ACC-4 functions in non-cholinergic RIM neurons to regulate immune genes, including Wnt-regulated genes.

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          Microbiota-generated metabolites promote metabolic benefits via gut-brain neural circuits.

          Soluble dietary fibers promote metabolic benefits on body weight and glucose control, but underlying mechanisms are poorly understood. Recent evidence indicates that intestinal gluconeogenesis (IGN) has beneficial effects on glucose and energy homeostasis. Here, we show that the short-chain fatty acids (SCFAs) propionate and butyrate, which are generated by fermentation of soluble fiber by the gut microbiota, activate IGN via complementary mechanisms. Butyrate activates IGN gene expression through a cAMP-dependent mechanism, while propionate, itself a substrate of IGN, activates IGN gene expression via a gut-brain neural circuit involving the fatty acid receptor FFAR3. The metabolic benefits on body weight and glucose control induced by SCFAs or dietary fiber in normal mice are absent in mice deficient for IGN, despite similar modifications in gut microbiota composition. Thus, the regulation of IGN is necessary for the metabolic benefits associated with SCFAs and soluble fiber. Copyright © 2014 Elsevier Inc. All rights reserved.
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            Specific interference by ingested dsRNA.

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              Functional genomic analysis of C. elegans chromosome I by systematic RNA interference.

              Complete genomic sequence is known for two multicellular eukaryotes, the nematode Caenorhabditis elegans and the fruit fly Drosophila melanogaster, and it will soon be known for humans. However, biological function has been assigned to only a small proportion of the predicted genes in any animal. Here we have used RNA-mediated interference (RNAi) to target nearly 90% of predicted genes on C. elegans chromosome I by feeding worms with bacteria that express double-stranded RNA. We have assigned function to 13.9% of the genes analysed, increasing the number of sequenced genes with known phenotypes on chromosome I from 70 to 378. Although most genes with sterile or embryonic lethal RNAi phenotypes are involved in basal cell metabolism, many genes giving post-embryonic phenotypes have conserved sequences but unknown function. In addition, conserved genes are significantly more likely to have an RNAi phenotype than are genes with no conservation. We have constructed a reusable library of bacterial clones that will permit unlimited RNAi screens in the future; this should help develop a more complete view of the relationships between the genome, gene function and the environment.
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                Author and article information

                Journal
                101573691
                39703
                Cell Rep
                Cell Rep
                Cell reports
                2211-1247
                9 November 2022
                01 November 2022
                25 November 2022
                : 41
                : 5
                : 111575
                Affiliations
                [1 ]Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, OR, USA
                [2 ]These authors contributed equally
                [3 ]Lead contact
                Author notes
                [* ]Correspondence: aballay@ 123456ohsu.edu

                AUTHOR CONTRIBUTIONS

                J.R. and A.A. conceived and designed the experiments. J.S. and Y.S. performed the experiments. J.S., Y.S., and A.A. analyzed the data and wrote the paper.

                Article
                NIHMS1846960
                10.1016/j.celrep.2022.111575
                9699718
                36323254
                41f6f519-5fd9-4455-9377-f6c1ca664469

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Cell biology
                Cell biology

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