<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Herlea-Pana O</submitter><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><pagination>749879</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8524045</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>β-cell ER stress plays an important role in β-cell dysfunction and death during the pathogenesis of diabetes. Proinsulin misfolding is regarded as one of the primary initiating factors of ER stress and unfolded protein response (UPR) activation in β-cells. Here, we found that the ER stress sensor inositol-requiring enzyme 1α (IRE1α) was activated in the Akita mice, a mouse model of mutant insulin gene-induced diabetes of youth (MIDY), a monogenic diabetes. Normalization of IRE1α RNase hyperactivity by pharmacological inhibitors significantly ameliorated the hyperglycemic conditions and increased serum insulin levels in Akita mice. These benefits were accompanied by a concomitant protection of functional β-cell mass, as shown by the suppression of β-cell apoptosis, increase in mature insuli</pubmed_abstract><journal>Frontiers in endocrinology</journal><pubmed_title>Pharmacological Inhibition of Inositol-Requiring Enzyme 1α RNase Activity Protects Pancreatic Beta Cell and Improves Diabetic Condition in Insulin Mutation-Induced Diabetes.</pubmed_title><pmcid>PMC8524045</pmcid><funding_grant_id>DK108887, DK116017, GM103636</funding_grant_id><funding_grant_id>R01 DK116017</funding_grant_id><funding_grant_id>R56 DK108887</funding_grant_id><pubmed_authors>Herlea-Pana O</pubmed_authors><pubmed_authors>Undi RB</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Lim HY</pubmed_authors><pubmed_authors>Eeda V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacological Inhibition of Inositol-Requiring Enzyme 1α RNase Activity Protects Pancreatic Beta Cell and Improves Diabetic Condition in Insulin Mutation-Induced Diabetes.</name><description>β-cell ER stress plays an important role in β-cell dysfunction and death during the pathogenesis of diabetes. Proinsulin misfolding is regarded as one of the primary initiating factors of ER stress and unfolded protein response (UPR) activation in β-cells. Here, we found that the ER stress sensor inositol-requiring enzyme 1α (IRE1α) was activated in the Akita mice, a mouse model of mutant insulin gene-induced diabetes of youth (MIDY), a monogenic diabetes. Normalization of IRE1α RNase hyperactivity by pharmacological inhibitors significantly ameliorated the hyperglycemic conditions and increased serum insulin levels in Akita mice. These benefits were accompanied by a concomitant protection of functional β-cell mass, as shown by the suppression of β-cell apoptosis, increase in mature insuli</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-04T10:55:52.496Z</modification><creation>2025-04-04T10:55:52.496Z</creation></dates><accession>S-EPMC8524045</accession><cross_references><pubmed>34675883</pubmed><doi>10.3389/fendo.2021.749879</doi></cross_references></HashMap>