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内源性巨核细胞集落形成及巨核细胞祖细胞对血小板生成素的敏感性,有助于鉴别原发性血小板增多症和反应性血小板增多症。

Endogenous megakaryocytic colony formation and thrombopoietin sensitivity of megakaryocytic progenitor cells are useful to distinguish between essential thrombocythemia and reactive thrombocytosis.

作者信息

Mi J Q, Blanc-Jouvan F, Wang J, Sotto M F, Cousin F, Castinel A, Chauvet M, Sotto J J, Polack B, Mossuz P

机构信息

Department of Hematology, CHU Grenoble, BP217-38043 Grenoble cedex, France.

出版信息

J Hematother Stem Cell Res. 2001 Jun;10(3):405-9. doi: 10.1089/152581601750289000.

Abstract

Diagnosis of essential thrombocythemia (ET) is controversial and remains mainly an exclusion diagnosis. Endogenous megakaryocyte colony (EMC) formation have been largely evaluated to identify specific criteria for ET, but results are impeded by the lack of medium standardization. We evaluated megakaryocyte (MK) colony formation in a serum-free collagen-based medium, without cytokine and in the presence of various concentrations of thrombopoietin (TPO). Thirty-six bone marrows from patients diagnosed with ET (n = 11), polycythemia vera (PV; n = 12), reactive thrombocytosis (RT; n = 6) and healthy donors (n = 7) were assessed. We demonstrate that 11 out 11 of the ET patients had spontaneous megakaryocyte colony-forming unit (CFU-MK) formation, in contrast to none of the RT patients and healthy donors. MK progenitors from ET patients remained responsive to TPO, because exogenous addition of TPO significantly increased cloning efficiency. Moreover, at low doses of TPO (0.5 ng/ml and 5 ng/ml), the number of positive cultures and mean number of TPO stimulated CFU-MK were significantly higher in cultures of cells from patients with ET than in patients with RT. In summary, we have described a standardized serum-free, collagen-based assay that allows differential diagnosis of ET and RT, according to endogenous CFU-MK formation and sensitivity to TPO.

摘要

原发性血小板增多症(ET)的诊断存在争议,目前主要仍是排除性诊断。内源性巨核细胞集落(EMC)形成已得到广泛评估,以确定ET的特定标准,但由于缺乏培养基标准化,结果受到影响。我们在无细胞因子的无血清胶原基培养基中,以及在存在不同浓度血小板生成素(TPO)的情况下,评估了巨核细胞(MK)集落形成。对36例诊断为ET(n = 11)、真性红细胞增多症(PV;n = 12)、反应性血小板增多症(RT;n = 6)的患者及健康供者(n = 7)的骨髓进行了评估。我们发现,11例ET患者中有11例出现自发巨核细胞集落形成单位(CFU-MK)形成,而RT患者和健康供者均未出现。ET患者的MK祖细胞对TPO仍有反应,因为外源性添加TPO可显著提高克隆效率。此外,在低剂量TPO(0.5 ng/ml和5 ng/ml)时,ET患者细胞培养物中的阳性培养物数量和TPO刺激的CFU-MK平均数显著高于RT患者。总之,我们描述了一种标准化的无血清、胶原基检测方法,可根据内源性CFU-MK形成和对TPO的敏感性对ET和RT进行鉴别诊断。

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