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将成熟巨核细胞输注到小鼠体内可产生有功能的血小板。

Infusion of mature megakaryocytes into mice yields functional platelets.

机构信息

Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

出版信息

J Clin Invest. 2010 Nov;120(11):3917-22. doi: 10.1172/JCI43326. Epub 2010 Oct 25.

Abstract

Thrombopoiesis, the process by which circulating platelets arise from megakaryocytes, remains incompletely understood. Prior studies suggest that megakaryocytes shed platelets in the pulmonary vasculature. To better understand thrombopoiesis and to develop a potential platelet transfusion strategy that is not dependent upon donors, of which there remains a shortage, we examined whether megakaryocytes infused into mice shed platelets. Infused megakaryocytes led to clinically relevant increases in platelet numbers. The released platelets were normal in size, displayed appropriate surface markers, and had a near-normal circulating half-life. The functionality of the donor-derived platelets was also demonstrated in vivo. The infused megakaryocytes mostly localized to the pulmonary vasculature, where they appeared to shed platelets. These data suggest that it may be unnecessary to generate platelets from ex vivo grown megakaryocytes to achieve clinically relevant increases in platelet numbers.

摘要

血小板生成,即循环血小板由巨核细胞产生的过程,仍不完全清楚。先前的研究表明,巨核细胞在肺血管中释放血小板。为了更好地理解血小板生成,并开发一种不依赖于供体的潜在血小板输血策略,因为供体仍然短缺,我们检查了输注到小鼠体内的巨核细胞是否会释放血小板。输注的巨核细胞导致血小板数量出现临床相关的增加。释放的血小板大小正常,表面标记物合适,循环半衰期接近正常。供体来源的血小板的功能也在体内得到了证明。输注的巨核细胞主要定位于肺血管系统,在那里它们似乎释放血小板。这些数据表明,为了达到临床上相关的血小板数量增加,可能不需要从体外培养的巨核细胞中生成血小板。

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