دورية أكاديمية

miR-223-3p suppresses inflammation to protect cardiomyocytes by targeting NLRP3 in acute myocardial infarction patients

التفاصيل البيبلوغرافية
العنوان: miR-223-3p suppresses inflammation to protect cardiomyocytes by targeting NLRP3 in acute myocardial infarction patients
المؤلفون: WANG, Fangfang, CHEN, Xin, SONG, Ying, HUANG, Shenglan, ZHOU, Changle, HUANG, Changgen, CHEN, Zengguang, ZHANG, Liangfeng, JI, Yuan
المصدر: Food Science and Technology. January 2021 41(2)
بيانات النشر: Sociedade Brasileira de Ciência e Tecnologia de Alimentos, 2021.
سنة النشر: 2021
مصطلحات موضوعية: miR-223-3p, NLRP3, acute myocardial infarction, inflammation
الوصف: microRNA (miRNA) had been found played an important role in occurrence and development of acute myocardial infarction (AMI) disease. In this paper, we found that the circulating miR-223-3p in AMI patients was significantly higher than that in unstable angina (UA) patients and healthy people. Univariate and logistic regression analysis showed the circulating miR-223-3p was a protective factor in the occurrence of AMI. We also found that the circulating miR-223-3p was negatively correlated with the serum CK-MB, cTnI, AST, LDH, TNF-α, IL-6, IL-1β and IL-8. The luciferase reporter gene system confirmed that miR-223-3p targeted inhibition of NLRP3 expression in THP-1 and human peripheral blood mononuclear cell (PBMC), and miR-223-3p was negatively correlated with the expression of NLRP3 in the PBMC of AMI patients. In PBMC of healthy people, miR-146a-mimic could increase the expression of NLRP3, but decreased the level of TNF-α secretion. Moreover, H2C9 cells apoptosis by TNF-α in a dose-dependent. In conclusion, these results suggested that miR-223-3p suppressed inflammation to protect cardiomyocytes by targeting NLRP3 in AMI patients.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 0101-2061
DOI: 10.1590/fst.25020
URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612021000600514
حقوق: info:eu-repo/semantics/openAccess
رقم الأكسشن: edssci.S0101.20612021000600514
قاعدة البيانات: SciELO
الوصف
تدمد:01012061
DOI:10.1590/fst.25020