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- W2166016722 abstract "Male gender and the male hormone testosterone increase susceptibility to kidney ischemia and reperfusion (I/R) injury, which is associated with inflammatory responses. Possible involvement of histone deacetylase (HDAC) in inflammatory responses has been suggested. We investigated the gender-specific role of HDACs in plasminogen activator inhibitor type-1 (PAI-1) expression and I/R injury. PAI-1 inhibition protected the kidney from I/R-induced inflammation and functional loss. Among HDACs, only HDAC11 negatively regulated PAI-1 expression in I/R-subjected kidney gender specifically and lipopolysaccharide (LPS)-stimulated mouse monocytes/macrophages. HDAC11 gene silencing increased PAI-1 expression. Chromatin immunoprecipitation assay confirmed binding of HDAC11 to the promoter region of PAI-1 and then release by I/R insult or LPS treatment. I/R-induced HDAC11 release was inhibited by orchiectomy and reversed by dihydrotestosterone treatment. Release of HDAC11 increased acetylation of histone H3. In conclusion, male gender and male hormones accelerate I/R-induced decreases in expression and binding of HDAC11, resulting in an increase in PAI-1 expression. These data provide important insight into gender dimorphism offering HDAC11 as a novel target for I/R injury." @default.
- W2166016722 created "2016-06-24" @default.
- W2166016722 creator A5013033476 @default.
- W2166016722 creator A5030182387 @default.
- W2166016722 creator A5086651935 @default.
- W2166016722 date "2013-07-01" @default.
- W2166016722 modified "2023-10-13" @default.
- W2166016722 title "Gender-specific role of HDAC11 in kidney ischemia- and reperfusion-induced PAI-1 expression and injury" @default.
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- W2166016722 doi "https://doi.org/10.1152/ajprenal.00015.2013" @default.
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