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BMC Cardiovasc Disord ; 21(1): 395, 2021 08 16.
Artigo em Inglês | MEDLINE | ID: mdl-34399692

RESUMO

BACKGROUND: Knowledge of stenosis in coronary arteries requires an understanding of the cellular and molecular processes that occur throughout the leukocyte rolling process. In this study, the roles of miR-125a-5p and miR-495-3p were investigated on the adhesion of endothelial cells (ECs) isolated from the human aorta. METHODS: Human primary endothelial cells were obtained from the aorta of people who had died of brain death. Whole blood was used to isolate the monocytes. The miR-125 and miR-495 were predicted and transfected into ECs using Poly Ethylene Imine (PEI). The expression levels of adhesion molecules and monocyte recruitment were identified by the RT-qPCR technique and Leukocyte-Endothelial Adhesion Assay kit, respectively. RESULTS: The ICAM-1, ICAM-2 and VCAM-1 expression levels decreased significantly in the miR-495/PEI-transfected ECs (P < 0.05) while in the miR-125/PEI-transfected ECs only the ICAM-2 and ITGB-2 expression levels decreased significantly (P < 0.05) as compared to the miR-synthetic/PEI-transfected ECs. Furthermore, the monocyte adhesion was decreased in the miR-125 and miR-mix/PEI-transfected ECs as compared to the miR-synthetic/PEI-transfected ECs (P = 0.01 and P = 0.04, respectively). CONCLUSION: According to the findings, the efficient relations between miR-125 and adhesion molecules may be responsible for the inhibition of monocyte rolling.


Assuntos
Aorta/metabolismo , Moléculas de Adesão Celular/metabolismo , Adesão Celular , Células Endoteliais/metabolismo , MicroRNAs/metabolismo , Monócitos/metabolismo , Antígenos CD/genética , Antígenos CD/metabolismo , Aorta/citologia , Antígenos CD18/genética , Antígenos CD18/metabolismo , Moléculas de Adesão Celular/genética , Células Cultivadas , Regulação da Expressão Gênica , Humanos , Iminas/química , Molécula 1 de Adesão Intercelular/genética , Molécula 1 de Adesão Intercelular/metabolismo , Migração e Rolagem de Leucócitos , MicroRNAs/genética , Polietilenos/química , Transdução de Sinais , Transfecção , Molécula 1 de Adesão de Célula Vascular/genética , Molécula 1 de Adesão de Célula Vascular/metabolismo
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