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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Comparative analysis of human ex vivo-generated platelets vs megakaryocyte-generated platelets in mice: a cautionary tale
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Comparative analysis of human ex vivo-generated platelets vs megakaryocyte-generated platelets in mice: a cautionary tale

机译:小鼠中人离体产生的血小板与巨核细胞产生的血小板的比较分析:一个警示故事

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摘要

Thrombopoiesis is the process by which megakaryocytes release platelets that circulate as uniform small, disc-shaped anucleate cytoplasmic fragments with critical roles in hemostasis and related biology. The exact mechanism of thrombopoiesis and the maturation pathways of platelets released into the circulation remain incompletely understood. We showed that ex vivo-generated murine megakaryocytes infused into mice release platelets within the pulmonary vasculature. Here we now show that infused human megakaryocytes also release platelets within the lungs of recipient mice. In addition, we observed a population of platelet-like particles (PLPs) in the infusate, which include platelets released during ex vivo growth conditions. By comparing these 2 platelet populations to human donor platelets, we found marked differences: platelets derived from infused megakaryocytes closely resembled infused donor platelets in morphology, size, and function. On the other hand, the PLP was a mixture of nonplatelet cellular fragments and nonuniform-sized, preactivated platelets mostly lacking surface CD42b that were rapidly cleared by macrophages. These data raise a cautionary note for the clinical use of human platelets released under standard ex vivo conditions. In contrast, human platelets released by intrapulmonary-entrapped megakaryocytes appear more physiologic in nature and nearly comparable to donor platelets for clinical application.
机译:血小板生成是巨核细胞释放血小板的过程,血小板以均匀的小盘状无核细胞质碎片形式循环,在止血和相关生物学中起关键作用。血小板生成的确切机制和释放到循环中的血小板成熟途径尚不完全清楚。我们表明,注入小鼠体内的离体产生的鼠巨核细胞释放出肺血管内的血小板。现在,我们在这里显示,注入的人巨核细胞还会在受体小鼠的肺内释放血小板。此外,我们在输注液中观察到血小板样颗粒(PLP)的数量,其中包括离体生长条件下释放的血小板。通过将这两个血小板种群与人类供体血小板进行比较,我们发现了显着差异:从注入的巨核细胞衍生的血小板在形态,大小和功能上与注入的供体血小板非常相似。另一方面,PLP是非血小板细胞片段和大小不一的预活化血小板的混合物,大部分缺乏表面CD42b,这些表面可被巨噬细胞迅速清除。这些数据为在标准离体条件下释放的人血小板的临床使用提出了警告。相反,由肺内包裹的巨核细胞释放的人血小板在本质上似乎更具生理学性质,几乎与临床应用的供体血小板相当。

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