Kuriya S, Murphy M J
Blood Cells. 1986;12(1):233-47.
We examined the effects of the urinary extracts from aplastic anemia (AA) patients, idiopathic thrombocytopenic purpura (ITP) patients, and normal subjects on murine megakaryocyte/platelet production in vivo and in vitro. In the first study, single doses of AA urinary protein (65%-90% ethanol precipitate) were individually injected intraperitoneally into rats and mice. Blood platelet counts in rats increased significantly 24 hours after the injection. Total megakaryocyte colony-forming units (CFU-Meg) in mouse spleens increased by 24 hours postinjection, peaked at 48 hours and returned to normal levels at 96 hours. Changes in the number of megakaryocyte colonies showed similar patterns of increasing, peaking and returning to normal levels postinjection. In the second study, we compared the effects of some urinary extracts on murine megakaryocyte/platelet production. These observations provided the evidence that AA urinary extracts contain a factor that directly stimulates megakaryocyte progenitor cell proliferation in mouse spleen in vivo as well as the release of platelets from megakaryocytes, and ITP urinary extracts do not contain increased levels of Meg-CSF and/or some other factor that directly stimulates CFU-Meg in vivo, and the decreased blood platelet mass that is clinically characteristic of ITP is not a primary in vivo determinant of the elaboration of these factors.
我们研究了再生障碍性贫血(AA)患者、特发性血小板减少性紫癜(ITP)患者及正常受试者的尿液提取物对小鼠体内及体外巨核细胞/血小板生成的影响。在第一项研究中,将单剂量的AA尿蛋白(65%-90%乙醇沉淀)分别腹腔注射到大鼠和小鼠体内。注射后24小时,大鼠的血小板计数显著增加。小鼠脾脏中的巨核细胞集落形成单位(CFU-Meg)总数在注射后24小时增加,在48小时达到峰值,并在96小时恢复到正常水平。巨核细胞集落数量的变化在注射后呈现出类似的增加、达到峰值和恢复到正常水平的模式。在第二项研究中,我们比较了一些尿液提取物对小鼠巨核细胞/血小板生成的影响。这些观察结果证明,AA尿液提取物含有一种因子,该因子可直接刺激小鼠脾脏中的巨核细胞祖细胞增殖以及巨核细胞释放血小板,而ITP尿液提取物中Meg-CSF和/或其他直接刺激体内CFU-Meg的因子水平并未升高,并且ITP临床上特征性的血小板量减少并非这些因子产生的主要体内决定因素。