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Epigenetic Control of Autophagy Related Genes Transcription in Pulpitis via JMJD3.
Yin, Bei; Ma, Qingge; Zhao, Lingyi; Song, Chenghao; Wang, Chenglin; Yu, Fanyuan; Shi, Yu; Ye, Ling.
Afiliação
  • Yin B; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Ma Q; West China School of Stomatology, Sichuan University, Chengdu, China.
  • Zhao L; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Song C; West China School of Stomatology, Sichuan University, Chengdu, China.
  • Wang C; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Yu F; West China School of Stomatology, Sichuan University, Chengdu, China.
  • Shi Y; State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  • Ye L; West China School of Stomatology, Sichuan University, Chengdu, China.
Front Cell Dev Biol ; 9: 654958, 2021.
Article em En | MEDLINE | ID: mdl-34434926
ABSTRACT
Autophagy is an intracellular self-cannibalization process delivering cytoplasmic components to lysosomes for digestion. Autophagy has been reported to be involved in pulpitis, but the regulation of autophagy during pulpitis progression is largely unknown. To figure out the epigenetic regulation of autophagy during pulpitis, we screened several groups of histone methyltransferases and demethylases in response to TNFα treatment. It was found JMJD3, a histone demethylase reducing di- and tri-methylation of H3K27, regulated the expression of several key autophagy genes via demethylation of H3K27me3 at the gene promoters. Our study highlighted the epigenetic regulation of autophagy genes during pulpitis, which will potentially provide a novel therapeutic strategy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China
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