<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5</volume><submitter>Fabre O</submitter><pubmed_abstract>Obesity is associated with chronic low-grade inflammation and oxidative stress that blunt insulin response in its target tissues, leading to insulin resistance (IR). IR is a characteristic feature of type 2 diabetes. Skeletal muscle is responsible for 75% of total insulin-dependent glucose uptake; consequently, skeletal muscle IR is considered to be the primary defect of systemic IR development. Interestingly, some obese people stay insulin-sensitive and metabolically healthy. With the aim of understanding this difference and identifying the mechanisms responsible for insulin sensitivity maintenance/IR development during obesity, we explored the role of the latent endoribonuclease (RNase L) in skeletal muscle cells. RNase L is a regulator of innate immunity, of double-stranded RNA sensors </pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>e1136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3973244</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Defects in TLR3 expression and RNase L activation lead to decreased MnSOD expression and insulin resistance in muscle cells of obese people.</pubmed_title><pmcid>PMC3973244</pmcid><pubmed_authors>Breuker C</pubmed_authors><pubmed_authors>Kitzmann M</pubmed_authors><pubmed_authors>Salehzada T</pubmed_authors><pubmed_authors>Amouzou C</pubmed_authors><pubmed_authors>Fabre O</pubmed_authors><pubmed_authors>Mercier J</pubmed_authors><pubmed_authors>Bisbal C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Defects in TLR3 expression and RNase L activation lead to decreased MnSOD expression and insulin resistance in muscle cells of obese people.</name><description>Obesity is associated with chronic low-grade inflammation and oxidative stress that blunt insulin response in its target tissues, leading to insulin resistance (IR). IR is a characteristic feature of type 2 diabetes. Skeletal muscle is responsible for 75% of total insulin-dependent glucose uptake; consequently, skeletal muscle IR is considered to be the primary defect of systemic IR development. Interestingly, some obese people stay insulin-sensitive and metabolically healthy. With the aim of understanding this difference and identifying the mechanisms responsible for insulin sensitivity maintenance/IR development during obesity, we explored the role of the latent endoribonuclease (RNase L) in skeletal muscle cells. RNase L is a regulator of innate immunity, of double-stranded RNA sensors </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Mar</publication><modification>2025-04-20T02:48:58.456Z</modification><creation>2019-03-27T01:24:19Z</creation></dates><accession>S-EPMC3973244</accession><cross_references><pubmed>24651439</pubmed><doi>10.1038/cddis.2014.104</doi></cross_references></HashMap>