Premium
Micro RNA s in platelet production and activation
Author(s) -
Edelstein L. C.,
McKenzie S. E.,
Shaw C.,
Holinstat M. A.,
Kunapuli S. P.,
Bray P. F.
Publication year - 2013
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/jth.12214
Subject(s) - megakaryocytopoiesis , microrna , biology , haematopoiesis , transcriptome , microbiology and biotechnology , platelet , erythropoiesis , biogenesis , megakaryocyte , stem cell , computational biology , platelet disorder , genetics , gene expression , immunology , gene , medicine , anemia
Summary Recent work by the E ncyclopedia of DNA Elements project showed that non‐protein‐coding RNA s account for an unexpectedly large proportion of the human genome. Among these non‐coding RNA s are micro RNA s (mi RNA s), which are small RNA molecules that modulate protein expression by degrading m RNA or repressing m RNA translation. Mi RNA s have been shown to play important roles in hematopoiesis including embryonic stem cell differentiation, erythropoiesis, granulocytopoiesis/monocytopoiesis, lymphopoiesis, and megakaryocytopoiesis. Additionally, disordered mi RNA biogenesis and quantitative or qualitative alterations in mi RNA s and their targets are associated with hematological pathologies. Platelets contain machinery to process pre‐mi RNA s into mature mi RNA s, and specific platelet mi RNA levels have been found to correlate with platelet reactivity. This review summarizes the current state of knowledge of mi RNA s in megakaryocytes and platelets, and the exciting possibilities for future megakaryocyte–platelet transcriptome research.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom