Wickramasinghe S N, Olsen I, Saunders J E
Scand J Haematol. 1975 Sep;15(2):139-44. doi: 10.1111/j.1600-0609.1975.tb01065.x.
The thymidine kinase activity per 10(6) DNA-synthesising marrow cells and the rate of incorporation of tritiated thymidine into the DNA of 10(3) DNA-synthesising marrow cells were estimated in 9 haematologically normal patients and 49 patients suffering from a variety of haematological disorders. Slight increases in thymidine kinase activity were found in 6 of the 31 patients with haematological diseases associated with normoblastic erythropoiesis and greater increases were found in 3 of the 18 patients with megaloblastic haemopoiesis due to vitamin B12 or folate deficiency. In the latter group, there was a statistically significant inverse correlation between haemoglobin levels and thymidine kinase activity. No correlation was found between thymidine kinase activity and the rate of incorporation of tritiated thymidine in either the normoblastic or megaloblastic group, suggesting that the level of thymidine kinase activity does not limit the rate of incorporation of exogenously supplied thymidine into the DNA of human bone marrow cells.
在9名血液学正常的患者和49名患有各种血液系统疾病的患者中,估算了每10⁶个进行DNA合成的骨髓细胞中的胸苷激酶活性,以及³H标记的胸苷掺入10³个进行DNA合成的骨髓细胞DNA中的速率。在31例伴有正成红细胞性红细胞生成的血液系统疾病患者中,有6例胸苷激酶活性略有升高;在18例因维生素B12或叶酸缺乏导致巨幼细胞性造血的患者中,有3例升高更为明显。在后一组中,血红蛋白水平与胸苷激酶活性之间存在统计学上的显著负相关。在正成红细胞性或巨幼细胞性组中,均未发现胸苷激酶活性与³H标记的胸苷掺入速率之间存在相关性,这表明胸苷激酶活性水平并不限制外源性供应的胸苷掺入人骨髓细胞DNA的速率。