The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila
Immune and metabolic pathways collectively influence host responses to microbial invaders, and mutations in one pathway frequently disrupt activity in another. We used the model to characterize metabolic homeostasis in flies with modified immune deficiency (IMD) pathway activity. The IMD pathway is...
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Veröffentlicht in: | The Journal of immunology (1950) 2019-05, Vol.202 (9), p.2747-2759 |
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container_title | The Journal of immunology (1950) |
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creator | Davoodi, Saeideh Galenza, Anthony Panteluk, Andrew Deshpande, Rujuta Ferguson, Meghan Grewal, Savraj Foley, Edan |
description | Immune and metabolic pathways collectively influence host responses to microbial invaders, and mutations in one pathway frequently disrupt activity in another. We used the
model to characterize metabolic homeostasis in flies with modified immune deficiency (IMD) pathway activity. The IMD pathway is very similar to the mammalian TNF-α pathway, a key regulator of vertebrate immunity and metabolism. We found that persistent activation of IMD resulted in hyperglycemia, depleted fat reserves, and developmental delays, implicating IMD in metabolic regulation. Consistent with this hypothesis, we found that
mutants weigh more, are hyperlipidemic, and have impaired glucose tolerance. To test the importance of metabolic regulation for host responses to bacterial infection, we challenged insulin pathway mutants with lethal doses of several
pathogens. We found that loss-of-function mutations in the insulin pathway impacted host responses to infection in a manner that depends on the route of infection and the identity of the infectious microbe. Combined, our results support a role for coordinated regulation of immune and metabolic pathways in host containment of microbial invaders. |
doi_str_mv | 10.4049/jimmunol.1801632 |
format | Article |
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model to characterize metabolic homeostasis in flies with modified immune deficiency (IMD) pathway activity. The IMD pathway is very similar to the mammalian TNF-α pathway, a key regulator of vertebrate immunity and metabolism. We found that persistent activation of IMD resulted in hyperglycemia, depleted fat reserves, and developmental delays, implicating IMD in metabolic regulation. Consistent with this hypothesis, we found that
mutants weigh more, are hyperlipidemic, and have impaired glucose tolerance. To test the importance of metabolic regulation for host responses to bacterial infection, we challenged insulin pathway mutants with lethal doses of several
pathogens. We found that loss-of-function mutations in the insulin pathway impacted host responses to infection in a manner that depends on the route of infection and the identity of the infectious microbe. Combined, our results support a role for coordinated regulation of immune and metabolic pathways in host containment of microbial invaders.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.1801632</identifier><identifier>PMID: 30902902</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Drosophila melanogaster ; Homeostasis - genetics ; Homeostasis - immunology ; Immunity, Innate ; Mutation ; Signal Transduction - genetics ; Signal Transduction - immunology</subject><ispartof>The Journal of immunology (1950), 2019-05, Vol.202 (9), p.2747-2759</ispartof><rights>Copyright © 2019 by The American Association of Immunologists, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-392cc9f577b8b7906bb9c5de87b60d9e7a9ac61f36d7504fd016dd4115cb92ab3</citedby><cites>FETCH-LOGICAL-c407t-392cc9f577b8b7906bb9c5de87b60d9e7a9ac61f36d7504fd016dd4115cb92ab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30902902$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Davoodi, Saeideh</creatorcontrib><creatorcontrib>Galenza, Anthony</creatorcontrib><creatorcontrib>Panteluk, Andrew</creatorcontrib><creatorcontrib>Deshpande, Rujuta</creatorcontrib><creatorcontrib>Ferguson, Meghan</creatorcontrib><creatorcontrib>Grewal, Savraj</creatorcontrib><creatorcontrib>Foley, Edan</creatorcontrib><title>The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Immune and metabolic pathways collectively influence host responses to microbial invaders, and mutations in one pathway frequently disrupt activity in another. We used the
model to characterize metabolic homeostasis in flies with modified immune deficiency (IMD) pathway activity. The IMD pathway is very similar to the mammalian TNF-α pathway, a key regulator of vertebrate immunity and metabolism. We found that persistent activation of IMD resulted in hyperglycemia, depleted fat reserves, and developmental delays, implicating IMD in metabolic regulation. Consistent with this hypothesis, we found that
mutants weigh more, are hyperlipidemic, and have impaired glucose tolerance. To test the importance of metabolic regulation for host responses to bacterial infection, we challenged insulin pathway mutants with lethal doses of several
pathogens. We found that loss-of-function mutations in the insulin pathway impacted host responses to infection in a manner that depends on the route of infection and the identity of the infectious microbe. Combined, our results support a role for coordinated regulation of immune and metabolic pathways in host containment of microbial invaders.</description><subject>Animals</subject><subject>Drosophila melanogaster</subject><subject>Homeostasis - genetics</subject><subject>Homeostasis - immunology</subject><subject>Immunity, Innate</subject><subject>Mutation</subject><subject>Signal Transduction - genetics</subject><subject>Signal Transduction - immunology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMFPwjAUhxujEUTvnkyPXoav3dbSowEVIkZj8Ly03ZuUbCuuWwz_vSOAyUve5ff78t5HyC2DcQKJeti4qupqX47ZBJiI-RkZsjSFSAgQ52QIwHnEpJADchXCBgAE8OSSDGJQwPsZktfVGuliT0E6w8JZh7Xd0Q_drn_1jn7id1fqFgN9w1YbXzpL575CH1odXKCuprPGB79du1Jfk4tClwFvjntEvp6fVtN5tHx_WUwfl5FNQLZRrLi1qkilNBMjFQhjlE1znEgjIFcotdJWsCIWuUwhKfL-tTxPGEutUVybeETuD9xt4386DG1WuWCxLHWNvgsZZ0qkPGEK-igcora_MjRYZNvGVbrZZQyyvcLspDA7Kuwrd0d6ZyrM_wsnZ_EfkHZvDA</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Davoodi, Saeideh</creator><creator>Galenza, Anthony</creator><creator>Panteluk, Andrew</creator><creator>Deshpande, Rujuta</creator><creator>Ferguson, Meghan</creator><creator>Grewal, Savraj</creator><creator>Foley, Edan</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190501</creationdate><title>The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila</title><author>Davoodi, Saeideh ; Galenza, Anthony ; Panteluk, Andrew ; Deshpande, Rujuta ; Ferguson, Meghan ; Grewal, Savraj ; Foley, Edan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-392cc9f577b8b7906bb9c5de87b60d9e7a9ac61f36d7504fd016dd4115cb92ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Drosophila melanogaster</topic><topic>Homeostasis - genetics</topic><topic>Homeostasis - immunology</topic><topic>Immunity, Innate</topic><topic>Mutation</topic><topic>Signal Transduction - genetics</topic><topic>Signal Transduction - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Davoodi, Saeideh</creatorcontrib><creatorcontrib>Galenza, Anthony</creatorcontrib><creatorcontrib>Panteluk, Andrew</creatorcontrib><creatorcontrib>Deshpande, Rujuta</creatorcontrib><creatorcontrib>Ferguson, Meghan</creatorcontrib><creatorcontrib>Grewal, Savraj</creatorcontrib><creatorcontrib>Foley, Edan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Davoodi, Saeideh</au><au>Galenza, Anthony</au><au>Panteluk, Andrew</au><au>Deshpande, Rujuta</au><au>Ferguson, Meghan</au><au>Grewal, Savraj</au><au>Foley, Edan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>202</volume><issue>9</issue><spage>2747</spage><epage>2759</epage><pages>2747-2759</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Immune and metabolic pathways collectively influence host responses to microbial invaders, and mutations in one pathway frequently disrupt activity in another. We used the
model to characterize metabolic homeostasis in flies with modified immune deficiency (IMD) pathway activity. The IMD pathway is very similar to the mammalian TNF-α pathway, a key regulator of vertebrate immunity and metabolism. We found that persistent activation of IMD resulted in hyperglycemia, depleted fat reserves, and developmental delays, implicating IMD in metabolic regulation. Consistent with this hypothesis, we found that
mutants weigh more, are hyperlipidemic, and have impaired glucose tolerance. To test the importance of metabolic regulation for host responses to bacterial infection, we challenged insulin pathway mutants with lethal doses of several
pathogens. We found that loss-of-function mutations in the insulin pathway impacted host responses to infection in a manner that depends on the route of infection and the identity of the infectious microbe. Combined, our results support a role for coordinated regulation of immune and metabolic pathways in host containment of microbial invaders.</abstract><cop>United States</cop><pmid>30902902</pmid><doi>10.4049/jimmunol.1801632</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Drosophila melanogaster Homeostasis - genetics Homeostasis - immunology Immunity, Innate Mutation Signal Transduction - genetics Signal Transduction - immunology |
title | The Immune Deficiency Pathway Regulates Metabolic Homeostasis in Drosophila |
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