Raskind W H, Jacobson R, Murphy S, Adamson J W, Fialkow P J
J Clin Invest. 1985 Apr;75(4):1388-90. doi: 10.1172/JCI111840.
Previous studies with the X-chromosome-linked glucose-6-phosphate dehydrogenase (G6PD) as a marker of cellular mosaicism demonstrated that polycythemia vera (PV) and essential thrombocythemia (ET) are clonal disorders of hematopoietic stem cells that can differentiate to erythrocytes, granulocytes, and platelets. To determine if the involved stem cells could also differentiate along the B-lymphoid pathway, we studied one woman with PV and one woman with ET. Of 117 Epstein-Barr virus-transformed B-lymphoblastoid lines expressing a single G6PD derived from the patient with PV, 108 expressed G6PD type A, the type characteristic of the abnormal clone. The ratio of 108:9 was significantly different from the one to one ratio predicted for this patient, which suggested that at least some circulating progenitors for B-lymphoid cell lines differentiate from the stem cell involved by the disease. Results obtained from the patient with ET were similar--104 of the 109 lymphoblastoid lines monotypic for G6PD expression displayed the enzyme type found in the abnormal clone of marrow cells. Therefore, in these patients, PV and ET, like chronic myelogenous leukemia, involve a stem cell pluripotent for the lymphoid as well as the myeloid series.
以往以X染色体连锁的葡萄糖-6-磷酸脱氢酶(G6PD)作为细胞镶嵌性标志物的研究表明,真性红细胞增多症(PV)和原发性血小板增多症(ET)是造血干细胞的克隆性疾病,可分化为红细胞、粒细胞和血小板。为了确定受累的干细胞是否也能沿着B淋巴细胞途径分化,我们研究了1例PV患者和1例ET患者。在117个由PV患者来源的、表达单一G6PD的爱泼斯坦-巴尔病毒转化的B淋巴母细胞系中,108个表达A型G6PD,即异常克隆的特征类型。108:9的比例与该患者预测的1:1比例有显著差异,这表明至少一些B淋巴细胞系的循环祖细胞是由该疾病所累及的干细胞分化而来的。从ET患者获得的结果相似——109个G6PD表达单型的淋巴母细胞系中有104个显示出骨髓细胞异常克隆中发现的酶类型。因此,在这些PV和ET患者中,与慢性粒细胞白血病一样,受累的是一种对淋巴系和髓系均具有多能性的干细胞。