Ploidy distribution of CFU-Meg progeny.
نویسنده
چکیده
In their study of the DNA levels (ploidy) of murine megakaryocyte colonies, Chatelain and Burstein evaluated the effects of acute thrombocytopenia upon the ploidy of megakaryocyte colonies derived from mice that had received platelet antiserum.’ They reported that colonies derived from bone marrow, obtained 24 hours after the administration of platelet antiserum, demonstrated the same ploidy distribution as did control colonies, in agreement with our observations when marrow or spleen was cultured 48 hours after the administration of platelet antiserum.2 However, the authors’ sweeping conclusion that “An acute thrombocytopenic environment does not influence the ultimate ploidy of the progeny of CFU-M” is not justified. While they are correct in stating that a similar result was described by us two days following thrombocytopenia,2 they also should have indicated that when colonies were derived from bone marrow or spleen four orfive days
منابع مشابه
Thrombopoietin (c-mpl ligand) acts synergistically with erythropoietin, stem cell factor, and interleukin-11 to enhance murine megakaryocyte colony growth and increases megakaryocyte ploidy in vitro.
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Thrombopoietin (Tpo), the ligand for the ompl receptor, is a major regulator of platelet production in vivo. Treatment of mice with purified recombinant Tpo increases platelet count fourfold and expands colony-forming unit-megakaryocyte (CFU-Meg) numbers. Other cytokines including interleukin-3 (IL-3). IL-6, IL-11, erythropoietin (Epo), and stem cell factor (SCF) can stimulate megakaryopoiesis....
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ورودعنوان ژورنال:
- Blood
دوره 65 6 شماره
صفحات -
تاریخ انتشار 1985