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原发性血小板增多症中巨核细胞祖细胞的集落形成

Colony formation by megakaryocytic progenitors in essential thrombocythaemia.

作者信息

Juvonen E, Partanen S, Ruutu T

出版信息

Br J Haematol. 1987 Jun;66(2):161-4. doi: 10.1111/j.1365-2141.1987.tb01293.x.

Abstract

Colony formation by megakaryocytic progenitors (CFU-M) from the blood or bone marrow of 12 patients with essential thrombocythaemia was studied in vitro with the methyl cellulose assay. When the cultures were stimulated with plasma from a patient with aplastic anaemia and with phytohaemagglutinin stimulated conditioned medium (PHA-LCM), the patients showed a significant trend towards higher circulating CFU-M numbers when compared with the controls; three of the patients exceeded our normal range. In the bone marrow cultures there were no differences in the number or morphology of megakaryocytic colonies between the patients and the controls. When normal human plasma was the only source of colony stimulating activity, 11 out of 12 patients, but none of the controls, showed megakaryocytic colony formation. The same patients also had 'spontaneous' erythroid colony growth without the addition of exogenous erythropoietin into the cultures. Only one of the patients with essential thrombocythaemia (ET) had normal megakaryocytic and erythroid colony formation. The present study shows that, in most patients with ET 'spontaneous' CFU-M colony formation occurs in suboptimal culture conditions, a phenomenon obviously analogous to the spontaneous erythroid colony formation seen in the myeloproliferative disorders.

摘要

采用甲基纤维素法对12例原发性血小板增多症患者血液或骨髓中的巨核细胞祖细胞(CFU-M)进行体外集落形成研究。当用再生障碍性贫血患者的血浆和植物血凝素刺激的条件培养基(PHA-LCM)刺激培养物时,与对照组相比,这些患者的循环CFU-M数量有显著升高趋势;其中3例患者超过了我们的正常范围。在骨髓培养中,患者与对照组之间巨核细胞集落的数量或形态没有差异。当正常人血浆是集落刺激活性的唯一来源时,12例患者中有11例出现巨核细胞集落形成,而对照组无一例出现。同样这些患者在未向培养物中添加外源性促红细胞生成素的情况下也有“自发”的红系集落生长。仅1例原发性血小板增多症(ET)患者的巨核细胞和红系集落形成正常。本研究表明,在大多数ET患者中,“自发”的CFU-M集落在次优培养条件下发生,这一现象明显类似于骨髓增殖性疾病中所见的自发红系集落形成。

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