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The conserved p38 MAPK family is activated by phosphorylation during stress responses and inactivated by phosphatases. C. elegans PMK-1 p38 MAPK initiates innate immune responses and blocks development when hyperactivated. Here we show that PMK-1 signaling is enhanced during early aging by modulating the stoichiometry of non-phospho-PMK-1 to promote tissue integrity and longevity. Loss of pmk-1 function accelerates progressive declines in neuronal integrity and lysosome function compromising longevity which has both cell autonomous and cell non-autonomous contributions. CED-3 caspase cleavage limits phosphorylated PMK-1. Enhancing p38 signaling with caspase cleavage-resistant PMK-1 protects lysosomal and neuronal integrity extending a youthful phase. PMK-1 works through a complex transcriptional program to regulate lysosome formation. During early aging, the absolute phospho-p38 amount is maintained but the reservoir of non-phospho-p38 diminishes to enhance signaling without hyperactivation. Our findings show that modulating the stoichiometry of non-phospho-p38 dynamically supports tissue-homeostasis during aging without hyper-activation of stress response.
Pubmed ID: 37507441
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Software package as distribution of ImageJ and ImageJ2 together with Java, Java3D and plugins organized into coherent menu structure. Used to assist research in life sciences.
View all literature mentionsAmerican chemical, life science and biotechnology company owned by Merck KGaA. Merger of Sigma Chemical Company and Aldrich Chemical Company. Provides organic and inorganic chemicals, building blocks, reagents, advanced materials and stable isotopes for chemical synthesis, medicinal chemistry and materials science, antibiotics, buffers, carbohydrates, enzymes, forensic tools, hematology and histology, nucleotides, proteins, peptides, amino acids and their derivatives.
View all literature mentionsCenter that acquires, maintains, and distributes genetic stocks and information about stocks of the small free-living nematode Caenorhabditis elegans for use by investigators initiating or continuing research on this genetic model organism. A searchable strain database, general information about C. elegans, and links to key Web sites of use to scientists, including WormBase, WormAtlas, and WormBook are available.
View all literature mentionsCaenorhabditis elegans with name unc-119(ed3) III; wgIs304. from WB.
View all literature mentionsCaenorhabditis elegans with name otIs412 X. from WB.
View all literature mentionsCaenorhabditis elegans with name daf-2(e1370) from WB.
View all literature mentionsCaenorhabditis elegans with name wgIs600. from WB.
View all literature mentionsCaenorhabditis elegans with name daf-16(m26) I. from WB.
View all literature mentionsCaenorhabditis elegans with name wdIs52. from WB.
View all literature mentionsCaenorhabditis elegans with name ieSi61 II; unc-119(ed3) III. from WB.
View all literature mentionsCaenorhabditis elegans with name daf-16(mgDf50) from WB.
View all literature mentionsCaenorhabditis elegans with name ieSi57 [eft-3p::TIR1::mRuby::unc-54 3'UTR + Cbr-unc-119(+)] II. from WB.
View all literature mentionsCaenorhabditis elegans with name pmk-1(km25) IV. from WB.
View all literature mentionsCaenorhabditis elegans with name unc-119(ed3) III; wgIs234. from WB.
View all literature mentionsCaenorhabditis elegans with name agIs219 III. from WB.
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