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pubmed-article:9923451pubmed:abstractTextWe examined withdrawal effects of recombinant mouse Tpo (rm-Tpo) on the apoptosis of mature and immature megakaryocytes in in vitro experiments. Apoptotic megakaryocytes were detected by double staining for acetylcholinesterase and by the TdT-mediated dUTP-biotin nick end labeling (TUNEL) method. When the purified mature megakaryocytes were cultured with or without rm-Tpo, the numbers of viable megakaryocytes, apoptotic megakaryocytes, and megakaryocytes with cytoplasmic processes were not significantly different between the two groups. In contrast, purified immature megakaryocytes underwent apoptosis when rm-Tpo was absent from the culture system. Murine bone marrow cells were cultured with rm-Tpo (50 U/mL) on days 1-7 to generate immature megakaryocytes and subsequently were cultured with different concentrations of rm-Tpo (0-50 U/mL) on days 8-14. The number of viable megakaryocytes was decreased and that of apoptotic megakaryocytes was increased by rm-Tpo in a dose-dependent manner. These results indicated a clear relation between the rm-Tpo level and the apoptosis of immature megakaryocytes.lld:pubmed
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pubmed-article:9923451pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:9923451pubmed:articleTitleImmature megakaryocytes undergo apoptosis in the absence of thrombopoietin.lld:pubmed
pubmed-article:9923451pubmed:affiliationDivision of Hematology, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.lld:pubmed
pubmed-article:9923451pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9923451pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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