Singer J W, Fialkow P J, Adamson J W, Steinmann L, Ernst C, Murphy S, Kopecky K J
J Clin Invest. 1979 Nov;64(5):1320-4. doi: 10.1172/JCI109588.
In previous studies of two patients with polycythemia vera (PV) and heterozygous at the X-linked locus for glucose-6-phosphate dehydrogenase (G-6-PD), only type A isoenzyme was found in non-lymphoid hematopoietic cells. However, some granulocytic and erythrocytic colonies grown in vitro had type B G-6-PD and therefore arose from presumably normal progenitors. In this study we exposed marrow cells from these same two patients to high-specific activity tritiated thymidine (3HTdR) before culture to kill cells actively synthesizing DNA. Individual granulocytic colonies were plucked and tested for G-6-PD after 14 d of culture. The frequency of type B colonies rose after exposure to 3HTdR from 8/101 to 11/36 in patient 1 and from 0/32 to 6/31 in patient 2 (P less than 0.003). No increase in the frequency of normal erythroid bursts after 3HTdR exposure was seen, implying that in PV, early granulopoiesis, and erythropoiesis are regulated differently. The results demonstrated that only type A granulocytic colonies, arising from the abnormal clone, were removed by the 3HTdR. In addition, for patient 2, statistical analysis indicated there was an absolute increase in normal granulocytic colonies detected in culture. Thus, PV clonal colony-forming units in culture (CFU-C) cycle more rapidly than do normal CFU-C and may suppress proliferation of normal CFU-C in vitro.
在先前对两名真性红细胞增多症(PV)患者的研究中,这两名患者在X连锁的葡萄糖-6-磷酸脱氢酶(G-6-PD)位点为杂合子,在非淋巴细胞造血细胞中仅发现了A型同工酶。然而,一些体外培养生长的粒细胞和红细胞集落具有B型G-6-PD,因此可能来自正常祖细胞。在本研究中,我们在培养前将来自这两名相同患者的骨髓细胞暴露于高比活度的氚标记胸腺嘧啶核苷(3HTdR),以杀死正在活跃合成DNA的细胞。培养14天后,挑选单个粒细胞集落并检测G-6-PD。在患者1中,暴露于3HTdR后B型集落的频率从8/101升至11/36,在患者2中从0/32升至6/31(P小于0.003)。暴露于3HTdR后正常红系爆式集落的频率未见增加,这意味着在PV中,早期粒细胞生成和红细胞生成的调节方式不同。结果表明,只有来自异常克隆的A型粒细胞集落被3HTdR清除。此外,对于患者2,统计分析表明培养中检测到的正常粒细胞集落有绝对增加。因此,PV培养中的克隆集落形成单位(CFU-C)比正常CFU-C的周期更快,并且可能在体外抑制正常CFU-C的增殖。