MicroRNAs in platelet biogenesis and function

被引:46
作者
Dangwal, Seema [1 ]
Thum, Thomas [1 ,2 ]
机构
[1] Hannover Med Sch, Inst Mol & Translat Therapeut Strategies IMTTS, D-30625 Hannover, Germany
[2] IRCCS San Raffaele, Ctr Clin & Basic Res, Rome, Italy
关键词
Platelet reactivity; megakaryocytopoiesis; platelet miRNA; P2Y12; PROTEIN-SYNTHESIS; P2Y(12) RECEPTOR; EXPRESSION; DIFFERENTIATION; CELLS; MICROPARTICLES; IDENTIFICATION; INFLAMMATION; PROGENITOR; PATHWAY;
D O I
10.1160/TH12-03-0211
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelets are important to maintain primary haemostasis and play a key role in pathology of thrombotic and occlusive vascular disorders such as acute coronary syndrome or stroke. Despite of lacking a nucleus and genomic DNA, platelets possess diverse types of RNAs, ranging from protein coding messenger RNAs to small non-coding RNAs inherited from their parent megakaryocytes. Indeed, platelets are capable of using their own translational machinery to synthesise proteins upon their activation suggesting the possibility of post-transcriptional gene regulation in platelets. MicroRNAs (miRNAs) are highly conserved, tiny non-coding RNAs exhibiting a fine-tune control of protein expression by complementary sequence recognition, binding and translational repression of protein coding mRNA transcripts. Multiple functional aspects of miRNAs as well as their expression in platelets or megakaryocytes underscore a role in platelet biology. Changes in miRNA expression patterns have been noted during platelet genesis and activation. In the present review we highlight recently identified megakaryocytic/platelet miRNAs and discuss their role in platelet biogenesis and functions essential to maintain haemostasis in the body.
引用
收藏
页码:599 / 604
页数:6
相关论文
共 59 条
[1]  
Amisten S, 2012, METHODS MOL BIOL, V788, P155, DOI 10.1007/978-1-61779-307-3_12
[2]   Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis [J].
Avecilla, ST ;
Hattori, K ;
Heissig, B ;
Tejada, R ;
Liao, F ;
Shido, K ;
Jin, DK ;
Dias, S ;
Zhang, F ;
Hartman, TE ;
Hackett, NR ;
Crystal, RG ;
Witte, L ;
Hicklin, DJ ;
Bohlen, P ;
Eaton, D ;
Lyden, D ;
de Sauvage, F ;
Rafii, S .
NATURE MEDICINE, 2004, 10 (01) :64-71
[3]   Thrombopoietin regulates c-Myb expression by modulating micro RNA 150 expression [J].
Barroga, Charlene F. ;
Pham, Hang ;
Kaushansky, Kenneth .
EXPERIMENTAL HEMATOLOGY, 2008, 36 (12) :1585-1592
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   Biogenesis and Regulation of Cardiovascular MicroRNAs [J].
Bauersachs, Johann ;
Thum, Thomas .
CIRCULATION RESEARCH, 2011, 109 (03) :334-347
[6]   Platelets Amplify Inflammation in Arthritis via Collagen-Dependent Microparticle Production [J].
Boilard, Eric ;
Nigrovic, Peter A. ;
Larabee, Katherine ;
Watts, Gerald F. M. ;
Coblyn, Jonathan S. ;
Weinblatt, Michael E. ;
Massarotti, Elena M. ;
Remold-O'Donnell, Eileen ;
Farndale, Richard W. ;
Ware, Jerry ;
Lee, David M. .
SCIENCE, 2010, 327 (5965) :580-583
[7]   Platelets at work in primary hemostasis [J].
Broos, Katleen ;
Feys, Hendrik B. ;
De Meyer, Simon F. ;
Vanhoorelbeke, Karen ;
Deckmyn, Hans .
BLOOD REVIEWS, 2011, 25 (04) :155-167
[8]   Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[9]   TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing [J].
Chendrimada, TP ;
Gregory, RI ;
Kumaraswamy, E ;
Norman, J ;
Cooch, N ;
Nishikura, K ;
Shiekhattar, R .
NATURE, 2005, 436 (7051) :740-744
[10]   Novel techniques and targets in cardiovascular microRNA research [J].
Dangwal, S. ;
Bang, C. ;
Thum, T. .
CARDIOVASCULAR RESEARCH, 2012, 93 (04) :545-554