Title : Decreased H3K9ac level of KLF4 mediates podocyte developmental toxicity induced by prenatal caffeine exposure in male offspring rats.

Pub. Date : 2019 Oct 10

PMID : 31306741






3 Functional Relationships(s)
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1 In vitro, corticosterone increased GR and HDAC7 whereas reduced the H3K9ac level of KLF4 and KLF4/Nephrin expression. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus
2 KLF4 over-expression reversed the reduction of Nephrin expression, knockdown of HDAC7 and GR antagonist RU486 partially reversed the inhibitory effects of corticosterone on H3K9ac level and KLF4 expression. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus
3 In conclusion, PCE caused podocyte developmental toxicity in male offspring, which was associated with corticosterone-induced low-functional programming of KLF4 through GR/HDAC7/H3K9ac pathway. Corticosterone nuclear receptor subfamily 3, group C, member 1 Rattus norvegicus