Secreted Monocytic miR-150 Enhances Targeted Endothelial Cell Migration

被引:1135
作者
Zhang, Yujing [2 ]
Liu, Danqing [3 ]
Chen, Xi [1 ]
Li, Jing [2 ]
Li, Limin [3 ]
Bian, Zhen [3 ]
Sun, Fei [4 ,5 ]
Lu, Jiuwei [4 ,5 ]
Yin, Yuan [1 ]
Cai, Xing [1 ]
Sun, Qi [2 ]
Wang, Kehui [2 ]
Ba, Yi [6 ]
Wang, Qiang [7 ]
Wang, Dongjin [7 ]
Yang, Junwei [8 ]
Liu, Pingsheng [4 ,5 ]
Xu, Tao [4 ,5 ]
Yan, Qiao [2 ]
Zhang, Junfeng [1 ]
Zen, Ke [3 ]
Zhang, Chen-Yu [2 ]
机构
[1] Nanjing Univ, Sch Life Sci, Biomat & Drug Delivery Div, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Jiangsu Diabet Ctr, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Lab Mol Metab, Nanjing 210093, Jiangsu, Peoples R China
[4] Chinese Acad Sci, Lab Biol Elect Microscopy, Beijing 100101, Peoples R China
[5] Chinese Acad Sci, Struct Biol Ctr Biol Imaging, Inst Biophys, Beijing 100101, Peoples R China
[6] Tianjin Med Univ, Canc Inst & Hosp, Tianjin 300060, Peoples R China
[7] Nanjing Univ, Affiliated Drum Tower Hosp, Dept Thorac Surg, Sch Med, Nanjing 210008, Jiangsu, Peoples R China
[8] Nanjing Med Univ, Affiliated Hosp 2, Res Ctr Nephrol, Nanjing 210011, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
C-MYB; CIRCULATING MICRORNAS; TUMOR-GROWTH; CANCER; SERUM; BIOGENESIS; EXPRESSION; BIOMARKERS; MECHANISM; EXOSOMES;
D O I
10.1016/j.molcel.2010.06.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are a class of noncoding RNAs that regulate target gene expression at the posttran-scriptional level. Here, we report that secreted miRNAs can serve as signaling molecules mediating intercellular communication. In human blood cells and cultured THP-1 cells, miR-150 was selectively packaged into microvesicles (MVs) and actively secreted. THP-1-derived MVs can enter and deliver miR-150 into human HMEC-1 cells, and elevated exogenous miR-150 effectively reduced c-Myb expression and enhanced cell migration in HMEC-1 cells. In vivo studies confirmed that intravenous injection of THP-1 MVs significantly increased the level of miR-150 in mouse blood vessels. MVs isolated from the plasma of patients with atherosclerosis contained higher levels of miR-150, and they more effectively promoted HMEC-1 cell migration than MVs from healthy donors. These results demonstrate that cells can secrete miRNAs and deliver them into recipient cells where the exogenous miRNAs can regulate target gene expression and recipient cell function.
引用
收藏
页码:133 / 144
页数:12
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