NHR-8 and P-glycoproteins uncouple xenobiotic resistance from longevity in chemosensory C. elegans mutants

Author:

Guerrero Gabriel A1,Derisbourg Maxime J1ORCID,Mayr Felix AMC1,Wester Laura E1,Giorda Marco1,Dinort J Eike1,Hartman Matías D1,Schilling Klara1,Alonso-De Gennaro María José1,Lu Ryan J2,Benayoun Bérénice A2ORCID,Denzel Martin S134ORCID

Affiliation:

1. Max Planck Institute for Biology of Ageing

2. Leonard Davis School of Gerontology, University of Southern California, Los Angeles

3. CECAD - Cluster of Excellence University of Cologne

4. Center for Molecular Medicine Cologne (CMMC), University of Cologne

Abstract

Longevity is often associated with stress resistance, but whether they are causally linked is incompletely understood. Here we investigate chemosensory-defective Caenorhabditis elegans mutants that are long-lived and stress resistant. We find that mutants in the intraflagellar transport protein gene osm-3 were significantly protected from tunicamycin-induced ER stress. While osm-3 lifespan extension is dependent on the key longevity factor DAF-16/FOXO, tunicamycin resistance was not. osm-3 mutants are protected from bacterial pathogens, which is pmk-1 p38 MAP kinase dependent, while TM resistance was pmk-1 independent. Expression of P-glycoprotein (PGP) xenobiotic detoxification genes was elevated in osm-3 mutants and their knockdown or inhibition with verapamil suppressed tunicamycin resistance. The nuclear hormone receptor nhr-8 was necessary to regulate a subset of PGPs. We thus identify a cell-nonautonomous regulation of xenobiotic detoxification and show that separate pathways are engaged to mediate longevity, pathogen resistance, and xenobiotic detoxification in osm-3 mutants.

Funder

H2020 European Research Council

Max-Planck-Gesellschaft

German Research Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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