Secreted microRNAs: a new form of intercellular communication

被引:629
作者
Chen, Xi [1 ]
Liang, Hongwei [1 ]
Zhang, Junfeng [1 ]
Zen, Ke [1 ]
Zhang, Chen-Yu [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Jiangsu Engn Res Ctr microRNA Biol & Biotechnol, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
secreted microRNA; circulating microRNA; microvesicle; exosome; high-density lipoprotein; RISC; Argonaute2; intercellular communication; CIRCULATING MICRORNAS; MICROVESICLES; EXOSOMES; BIOGENESIS; BIOMARKERS; CANCER; COMPLEXES; PLASMA; SERUM; RNAS;
D O I
10.1016/j.tcb.2011.12.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In multicellular organisms, cell-to-cell communication is of particular importance for the proper development and function of the organism as a whole. Intensive studies over the past three years suggesting horizontal transfer of secreted microRNAs (miRNAs) between cells point to a potentially novel role for these molecules in intercellular communication. Using a microvesicle-dependent, or RNA-binding protein-associated, active trafficking system, secreted miRNAs can be delivered into recipient cells where they function as endogenous miRNAs, simultaneously regulating multiple target genes or signaling events. In this Opinion, we summarize recent literature on the biogenesis and uptake of secreted miRNAs, propose a possible working model for how secreted miRNAs might be sorted and transferred between cells and speculate on their biological significance.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 58 条
[51]   Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells [J].
Valadi, Hadi ;
Ekstrom, Karin ;
Bossios, Apostolos ;
Sjostrand, Margareta ;
Lee, James J. ;
Lotvall, Jan O. .
NATURE CELL BIOLOGY, 2007, 9 (06) :654-U72
[52]   MicroRNAs are transported in plasma and delivered to recipient cells by high-density lipoproteins [J].
Vickers, Kasey C. ;
Palmisano, Brian T. ;
Shoucri, Bassem M. ;
Shamburek, Robert D. ;
Remaley, Alan T. .
NATURE CELL BIOLOGY, 2011, 13 (04) :423-U182
[53]   ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data [J].
Wang, Kai ;
Li, Mingyao ;
Hakonarson, Hakon .
NUCLEIC ACIDS RESEARCH, 2010, 38 (16) :e164
[54]   Circulating microRNAs, potential biomarkers for drug-induced liver injury [J].
Wang, Kai ;
Zhang, Shile ;
Marzolf, Bruz ;
Troisch, Pamela ;
Brightman, Amy ;
Hu, Zhiyuan ;
Hood, Leroy E. ;
Galas, David J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (11) :4402-4407
[55]   The emerging shape of the ESCRT machinery [J].
Williams, Roger L. ;
Urbe, Sylvie .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (05) :355-368
[56]   MiR-150 controls B cell differentiation by targeting the transcription factor c-myb [J].
Xiao, Changchun ;
Calado, Dinis Pedro ;
Galler, Gunther ;
Thai, To-Ha ;
Patterson, Heide Christine ;
Wang, Jing ;
Rajewsky, Nikolaus ;
Bender, Timothy P. ;
Rajewsky, Klaus .
CELL, 2007, 131 (01) :146-159
[57]   Transfer of MicroRNAs by Embryonic Stem Cell Microvesicles [J].
Yuan, Alex ;
Farber, Erica L. ;
Rapoport, Ana Lia ;
Tejada, Desiree ;
Deniskin, Roman ;
Akhmedov, Novrouz B. ;
Farber, Debora B. .
PLOS ONE, 2009, 4 (03)
[58]   Secreted Monocytic miR-150 Enhances Targeted Endothelial Cell Migration [J].
Zhang, Yujing ;
Liu, Danqing ;
Chen, Xi ;
Li, Jing ;
Li, Limin ;
Bian, Zhen ;
Sun, Fei ;
Lu, Jiuwei ;
Yin, Yuan ;
Cai, Xing ;
Sun, Qi ;
Wang, Kehui ;
Ba, Yi ;
Wang, Qiang ;
Wang, Dongjin ;
Yang, Junwei ;
Liu, Pingsheng ;
Xu, Tao ;
Yan, Qiao ;
Zhang, Junfeng ;
Zen, Ke ;
Zhang, Chen-Yu .
MOLECULAR CELL, 2010, 39 (01) :133-144