Title : The low-expression programming of 11β-HSD2 mediates osteoporosis susceptibility induced by prenatal caffeine exposure in male offspring rats.

Pub. Date : 2020 Oct

PMID : 32757222






3 Functional Relationships(s)
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1 Moreover, the high level of CORT induced by PCE downregulated the H3K9ac and expression levels of 11beta-HSD2 through promoting glucocorticoid receptor (GR) into the nucleus of bone marrow mesenchymal stem cells (BMSCs) and recruiting histone deacetylase 11 (HDAC11) binding to 11beta-HSD2 promoter region, which further enhanced the effect of CORT on suppressing osteogenic function of BMSCs. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus
2 Moreover, the high level of CORT induced by PCE downregulated the H3K9ac and expression levels of 11beta-HSD2 through promoting glucocorticoid receptor (GR) into the nucleus of bone marrow mesenchymal stem cells (BMSCs) and recruiting histone deacetylase 11 (HDAC11) binding to 11beta-HSD2 promoter region, which further enhanced the effect of CORT on suppressing osteogenic function of BMSCs. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus
3 Moreover, the high level of CORT induced by PCE downregulated the H3K9ac and expression levels of 11beta-HSD2 through promoting glucocorticoid receptor (GR) into the nucleus of bone marrow mesenchymal stem cells (BMSCs) and recruiting histone deacetylase 11 (HDAC11) binding to 11beta-HSD2 promoter region, which further enhanced the effect of CORT on suppressing osteogenic function of BMSCs. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus