Suppr超能文献

大鼠体内巨核细胞倍性的调控。

Regulation of megakaryocyte ploidy in vivo in the rat.

作者信息

Kuter D J, Rosenberg R D

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Blood. 1990 Jan 1;75(1):74-81.

PMID:2294997
Abstract

The relationship between the bone marrow (BM) megakaryocyte and the circulating platelet was explored. Incremental changes in platelet count were made in rats by infusion of antiplatelet antibody or by platelet transfusion, and the response of megakaryocytes was measured by flow cytometry. Proportional changes in megakaryocyte ploidy were demonstrated: As the platelet count declined, ploidy increased; as the platelet count increased, ploidy decreased. Even moderate degrees of thrombocytopenia and thrombocytosis (48% and 177% of the normal platelet count) were associated with changes in ploidy. These changes were not the results of the technique used to alter the platelet count because reinfusion of platelets after 3 hours of thrombocytopenia prevented any ploidy change. These studies proved that the circulating platelet and the megakaryocyte constitute a classic feedback loop whose activity can be measured by the degree of ploidization of the megakaryocyte. The minimal duration of thrombocytopenia necessary to promote megakaryocyte ploidy changes was approximately 10 hours. Using a BM culture assay, we identified a plasma factor which induced alterations in megakaryocyte ploidy and whose level is inversely proportional to the platelet count.

摘要

研究了骨髓巨核细胞与循环血小板之间的关系。通过输注抗血小板抗体或进行血小板输血使大鼠血小板计数发生递增变化,并通过流式细胞术检测巨核细胞的反应。结果表明巨核细胞倍性存在比例变化:随着血小板计数下降,倍性增加;随着血小板计数增加,倍性降低。即使是中度血小板减少和血小板增多(分别为正常血小板计数的48%和177%)也与倍性变化有关。这些变化并非用于改变血小板计数的技术所致,因为血小板减少3小时后再输注血小板可防止任何倍性变化。这些研究证明,循环血小板和巨核细胞构成一个经典的反馈回路,其活性可通过巨核细胞的倍化程度来衡量。促进巨核细胞倍性变化所需的血小板减少最短持续时间约为10小时。通过骨髓培养试验,我们鉴定出一种血浆因子,它可诱导巨核细胞倍性改变,且其水平与血小板计数呈负相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验