PMID- 32897801 OWN - NLM STAT- MEDLINE DCOM- 20211207 LR - 20211214 IS - 1551-4005 (Electronic) IS - 1538-4101 (Print) IS - 1551-4005 (Linking) VI - 19 IP - 20 DP - 2020 Oct TI - Knockdown of circular RNA circMAT2B reduces oxygen-glucose deprivation-induced inflammatory injury in H9c2 cells through up-regulating miR-133. PG - 2622-2630 LID - 10.1080/15384101.2020.1814025 [doi] AB - Myocardial infarction (MI) is the main cause of morbidity and mortality. Reperfusion ways can cause damage to cardiomyocytes. CircMAT2B, a novel circRNA, takes positive roles in regulating glucose metabolism under hypoxia. Therefore, we aimed to explore the effects of circMAT2B on MI. Oxygen-glucose deprivation (OGD)-induced H9c2 cell model was employed to stimulate MI. Ex-circMAT2B, si-circMAT2B, miR-133 inhibitor and relative control were transfected into H9c2 cells. qRT-PCR was employed to examine levels of circMAT2B and miR-133. Cell activity, apoptosis, ROS generation and release of inflammatory factors were assessed by CCK-8, flow cytometry, ROS species assay kit and ELISA, respectively. Moreover, the expression of apoptosis-related and pathway-related factors was detected through western blot analysis. The results showed that circMAT2B expression was notably up-regulated by OGD treatment. Moreover, circMAT2B knockdown could effectively decrease OGD-induced the increasing of apoptosis, ROS generation and the expression of IL-1beta, IL-6 and TNF-alpha. Besides, miR-133 was positively regulated by si-circMAT2B. CircMAT2B knockdown attenuated OGD-induced H9c2 cell damage and alleviated OGD-induced the inhibition of PI3K/AKT and Raf/MEK/ERK pathways through up-regulating miR-133. In brief, circMAT2B knockdown works as an inflammatory inhibitor in OGD-induced H9c2 cells inflammatory injury through up-regulating miR-133. FAU - Zhu, Yanhui AU - Zhu Y AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University , Jinan, Shandong, China. FAU - Zou, Chengwei AU - Zou C AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University , Jinan, Shandong, China. FAU - Jia, Yanting AU - Jia Y AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University , Jinan, Shandong, China. FAU - Zhang, Haizhou AU - Zhang H AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University , Jinan, Shandong, China. FAU - Ma, Xiaochun AU - Ma X AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University , Jinan, Shandong, China. FAU - Zhang, Jun AU - Zhang J AUID- ORCID: 0000-0002-2267-0182 AD - Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University , Jinan, Shandong, China. LA - eng PT - Journal Article DEP - 20200908 PL - United States TA - Cell Cycle JT - Cell cycle (Georgetown, Tex.) JID - 101137841 RN - 0 (MIRN133 microRNA, rat) RN - 0 (MicroRNAs) RN - 0 (RNA, Circular) RN - 0 (RNA, Long Noncoding) RN - IY9XDZ35W2 (Glucose) RN - S88TT14065 (Oxygen) SB - IM MH - Animals MH - Apoptosis/genetics MH - Cell Line MH - Glucose/*metabolism MH - Inflammation/*genetics/*metabolism MH - MicroRNAs/*genetics MH - Myocardial Infarction/genetics/metabolism MH - Myocytes, Cardiac/metabolism MH - Oxygen/*metabolism MH - RNA, Circular/*genetics MH - RNA, Long Noncoding/genetics MH - Rats MH - Transcriptional Activation/genetics MH - Up-Regulation/*genetics PMC - PMC7644149 OTO - NOTNLM OT - Circular RNA circMAT2B OT - inflammatory injury OT - miR-133 OT - oxygen-glucose deprivation COIS- The authors declare that they have no conflict of interest. EDAT- 2020/09/09 06:00 MHDA- 2021/12/15 06:00 PMCR- 2021/09/08 CRDT- 2020/09/08 17:11 PHST- 2020/09/09 06:00 [pubmed] PHST- 2021/12/15 06:00 [medline] PHST- 2020/09/08 17:11 [entrez] PHST- 2021/09/08 00:00 [pmc-release] AID - 1814025 [pii] AID - 10.1080/15384101.2020.1814025 [doi] PST - ppublish SO - Cell Cycle. 2020 Oct;19(20):2622-2630. doi: 10.1080/15384101.2020.1814025. Epub 2020 Sep 8.