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MicroRNA-142 promotes the expression of eNOS in human peripheral blood-derived endothelial progenitor cells in vitro
被引:2
|作者:
Zhang, H. -W.
[1
]
Li, H.
[1
]
Yan, H.
[2
]
Liu, B. -L.
[2
]
机构:
[1] Tianjin Med Univ, Hosp 2, Dept Neurosurg, Tianjin, Peoples R China
[2] Tianjin Huanhu Hosp, Dept Neurosurg, Tianjin, Peoples R China
关键词:
microRNA-142;
ADAMTS-1;
VEGF;
eNOS;
NO;
OXIDE SYNTHASE EXPRESSION;
DISINTEGRIN;
PROTEINS;
FAMILY;
GROWTH;
ATHEROSCLEROSIS;
ADAMTS-1;
GENE;
BMPS;
D O I:
暂无
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
OBJECTIVE: MicroRNAs (miRNAs) are small non-coding RNAs (18-25nt) that regulate gene expression mainly through affecting post-transcriptional modification. In this research, the human peripheral blood-derived endothelial progenitor cells were isolated to research the inter-coordination of miR-142, ADAMTS-1, VEGF and eNOS through gene over-expressed in EPCs. MATERIALS AND METHODS: Endothelial progenitor cells (EPCs) were isolated from human peripheral blood, and demonstrate the interaction of miR-142 and targets (ADAMTS-1) in vitro. RESULTS: The results showed that miR-142 could promote the productivity of NO through inhibited ADAMTS-1 expression (inhibitor of VEGF), activated function of VEGF and eNOS in human EPCs. This finding suggests that miR-142 and eNOS may have cooperative effect in vessel tone and play an important role in the angiogenesis. CONCLUSIONS: In our research, we demonstrated that the miR-142 can promote eNOS expression through down-regulated ADAMTS-1 expression (inhibitor of VEGF) in human EPCs, these results provide a new insight in microRNA regulation of vessel tone and angiogenesis.
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页码:4167 / 4175
页数:9
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