<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chandrasekaran R</submitter><funding>George Mason University</funding><funding>Canadian Institutes of Health Research</funding><funding>CIHR</funding><pagination>e0274420</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9477357</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(9)</volume><pubmed_abstract>UDP-glucose dehydrogenase (UGDH) generates essential precursors of hyaluronic acid (HA) synthesis, however mechanisms regulating its activity are unclear. We used enzyme histostaining and quantitative image analysis to test whether cytokines that stimulate HA synthesis upregulate UGDH activity. Fibroblast-like synoviocytes (FLS, from N = 6 human donors with knee pain) were cultured, freeze-thawed, and incubated for 1 hour with UDP-glucose, NAD+ and nitroblue tetrazolium (NBT) which allows UGDH to generate NADH, and NADH to reduce NBT to a blue stain. Compared to serum-free medium, FLS treated with PDGF showed 3-fold higher UGDH activity and 6-fold higher HA release, but IL-1beta/TGF-beta1 induced 27-fold higher HA release without enhancing UGDH activity. In selected proliferating cells, UG</pubmed_abstract><journal>PloS one</journal><pubmed_title>UDP-glucose dehydrogenase (UGDH) activity is suppressed by peroxide and promoted by PDGF in fibroblast-like synoviocytes: Evidence of a redox control mechanism.</pubmed_title><pmcid>PMC9477357</pmcid><funding_grant_id>MOP-133729</funding_grant_id><funding_grant_id>162921</funding_grant_id><funding_grant_id>133729</funding_grant_id><pubmed_authors>El-Gabalawy H</pubmed_authors><pubmed_authors>Paige M</pubmed_authors><pubmed_authors>Sheth R</pubmed_authors><pubmed_authors>Fong D</pubmed_authors><pubmed_authors>McCormack R</pubmed_authors><pubmed_authors>Hoemann CD</pubmed_authors><pubmed_authors>Chandrasekaran R</pubmed_authors><pubmed_authors>Alishetty S</pubmed_authors><pubmed_authors>Cheng AP</pubmed_authors><pubmed_authors>Mathieu C</pubmed_authors></additional><is_claimable>false</is_claimable><name>UDP-glucose dehydrogenase (UGDH) activity is suppressed by peroxide and promoted by PDGF in fibroblast-like synoviocytes: Evidence of a redox control mechanism.</name><description>UDP-glucose dehydrogenase (UGDH) generates essential precursors of hyaluronic acid (HA) synthesis, however mechanisms regulating its activity are unclear. We used enzyme histostaining and quantitative image analysis to test whether cytokines that stimulate HA synthesis upregulate UGDH activity. Fibroblast-like synoviocytes (FLS, from N = 6 human donors with knee pain) were cultured, freeze-thawed, and incubated for 1 hour with UDP-glucose, NAD+ and nitroblue tetrazolium (NBT) which allows UGDH to generate NADH, and NADH to reduce NBT to a blue stain. Compared to serum-free medium, FLS treated with PDGF showed 3-fold higher UGDH activity and 6-fold higher HA release, but IL-1beta/TGF-beta1 induced 27-fold higher HA release without enhancing UGDH activity. In selected proliferating cells, UG</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T00:30:42.829Z</modification><creation>2024-12-03T19:32:25.964Z</creation></dates><accession>S-EPMC9477357</accession><cross_references><pubmed>36107941</pubmed><doi>10.1371/journal.pone.0274420</doi></cross_references></HashMap>