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OP9 Bone Marrow Stroma Cells Differentiate into Megakaryocytes and Platelets

Overview of attention for article published in PLOS ONE, March 2013
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Title
OP9 Bone Marrow Stroma Cells Differentiate into Megakaryocytes and Platelets
Published in
PLOS ONE, March 2013
DOI 10.1371/journal.pone.0058123
Pubmed ID
Authors

Yumiko Matsubara, Yukako Ono, Hidenori Suzuki, Fumio Arai, Toshio Suda, Mitsuru Murata, Yasuo Ikeda

Abstract

Platelets are essential for hemostatic plug formation and thrombosis. The mechanisms of megakaryocyte (MK) differentiation and subsequent platelet production from stem cells remain only partially understood. The manufacture of megakaryocytes (MKs) and platelets from cell sources including hematopoietic stem cells and pluripotent stem cells have been highlighted for studying the platelet production mechanisms as well as for the development of new strategies for platelet transfusion. The mouse bone marrow stroma cell line OP9 has been widely used as feeder cells for the differentiation of stem cells into MK lineages. OP9 cells are reported to be pre-adipocytes. We previously reported that 3T3-L1 pre-adipocytes differentiated into MKs and platelets. In the present study, we examined whether OP9 cells differentiate into MKs and platelets using MK lineage induction (MKLI) medium previously established to generate MKs and platelets from hematopoietic stem cells, embryonic stem cells, and pre-adipocytes. OP9 cells cultured in MKLI medium had megakaryocytic features, i.e., positivity for surface markers CD41 and CD42b, polyploidy, and distinct morphology. The OP9-derived platelets had functional characteristics, providing the first evidence for the differentiation of OP9 cells into MKs and platelets. We then analyzed gene expressions of critical factors that regulate megakaryopoiesis and thrombopoiesis. The gene expressions of p45NF-E2, FOG, Fli1, GATA2, RUNX1, thrombopoietin, and c-mpl were observed during the MK differentiation. Among the observed transcription factors of MK lineages, p45NF-E2 expression was increased during differentiation. We further studied MK and platelet generation using p45NF-E2-overexpressing OP9 cells. OP9 cells transfected with p45NF-E2 had enhanced production of MKs and platelets. Our findings revealed that OP9 cells differentiated into MKs and platelets in vitro. OP9 cells have critical factors for megakaryopoiesis and thrombopoiesis, which might be involved in a mechanism of this differentiation. p45NF-E2 might also play important roles in the differentiation of OP9 cells into MK lineages cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 59 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Japan 1 2%
India 1 2%
Germany 1 2%
Unknown 56 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 21 36%
Student > Ph. D. Student 13 22%
Other 5 8%
Student > Master 4 7%
Student > Doctoral Student 3 5%
Other 9 15%
Unknown 4 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 28 47%
Medicine and Dentistry 12 20%
Biochemistry, Genetics and Molecular Biology 8 14%
Immunology and Microbiology 2 3%
Computer Science 1 2%
Other 3 5%
Unknown 5 8%