Regulation of Dihydropyrimidinase-like 3 Gene Expression by MicroRNAs in PC12 Cells with Induced Ischaemia and Hypothermia
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
Grantová podpora
NRF-2020R1I1A3074228
National Research Foundation of Korea
2013
Chungnam National University Hospital
PubMed
38063003
DOI
10.14712/fb2023069020069
PII: fb_2023069020069
Knihovny.cz E-zdroje
- Klíčová slova
- PC12 cells, dihydropyrimidinase like 3 (Dpysl3), hypothermia, ischaemia, microRNAs,
- MeSH
- buňky PC12 MeSH
- exprese genu MeSH
- hypotermie * genetika MeSH
- ischemie chemicky indukované genetika MeSH
- krysa rodu Rattus MeSH
- lidé MeSH
- mikro RNA * genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- dihydropyrimidinase MeSH Prohlížeč
- Dpysl3 protein, rat MeSH Prohlížeč
- mikro RNA * MeSH
- MIRN326 microRNA, human MeSH Prohlížeč
- MIRN326 microRNA, rat MeSH Prohlížeč
- MIRN497 microRNA, human MeSH Prohlížeč
- MIRN497 microRNA, rat MeSH Prohlížeč
Although hypothermic treatment has been reported to have some beneficial effects on ischaemia at the clinical level, the mechanism of ischaemia suppression by hypothermia remains unclear due to a lack of mechanism understanding and insufficient data. The aim of this study was to isolate and characterize microRNAs specifically expressed in ischaemia-hypothermia for the dihydropyrimidinase-like 3 (Dpysl3) gene. PC12 cells were induced with CoCl2 for chemical ischaemia and incubated at 32 ℃ for hypothermia. In ischaemia-hypothermia, four types of microRNAs (miR-106b-5p, miR-194-5p, miR-326-5p, and miR-497-5p) were highly related to the Dpysl3 gene based on exosomal microRNA analysis. Dpysl3 gene expression was up-regulated by miR-497-5p but down-regulated by miR-106b-5p, miR-194-5p and miR-326-5p. Our results suggest that these four microRNAs are involved in the regulation of Dpysl3 gene expression. These findings provide valuable clues that exosomal microRNAs could be used as therapeutic targets for effective treatment of ischaemia.
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