Hooton J W, Hoffbrand A V
Biochim Biophys Acta. 1977 Aug 2;477(3):250-63. doi: 10.1016/0005-2787(77)90050-8.
DNA synthesis has been studied in nuclei isolated from phytohaemagglutinin-stimulated lymphocytes from normal subjects and patients with megaloblastic anaemia. Lymphocytes were incubated for 72 h, nuclei isolated and incorporation of tritiated deoxythymidine triphosphate ([3H]TTP) into DNA measured, usually over a 10 min incubation period. Preincubation of normal phytohaemagglutinin-stimulated lymphocytes with methotrexate (1 - 10(-5) M, 48--72 h), 5-fluorouracil (1 - 10(-6) M, 70--72 h), and 1-beta-D-arabinofuranosyl cytosine (cytosine arabinoside) (4 - 10(-5) M, 71--72 h) caused a mean rise in [3H]TTP incorporation of 1.7 (P less than 0.01), 1.7 (P less than 0.05) and 2.4 (P less than 0.0025) fold, respectively. Hydroxyurea (3 - 10(-4) M, 48--72 h) in two experiments caused a mean increase of 1.6 fold. Untreated vitamin B-12- and folate-deficient cells showed a 2.0-fold (P less than 0.05) increase above the incorporation when the deficiencies were corrected by addition of vitamin B-12 and folic acid between 0 and 72 h in vitro. The mean percentages of the incorporation due to ATP-independent synthesis in nuclei from normal untreated cells, 5-fluorouracil-treated, cytosine arabinoside treated and vitamin B-12- or folate-deficient cells were 56 +/- 7% S.E., 41 +/- 7%, 84 +/- 3% and 28 +/- 6%, respectively. 5-Fluorouracil caused a two-fold increase in the cytoplasmic fraction of DNA polymerase when added to phytohaemagglutinin-stimulated lymphocytes between 48 and 72 h of culture but had no significant effect when added between 70 and 72 h.
对从正常受试者和巨幼细胞贫血患者的植物血凝素刺激淋巴细胞中分离出的细胞核中的DNA合成进行了研究。淋巴细胞孵育72小时,分离细胞核,并测量氚标记的三磷酸脱氧胸苷([3H]TTP)掺入DNA的情况,通常在10分钟的孵育期内进行测量。用甲氨蝶呤(1 - 10(-5)M,48 - 72小时)、5-氟尿嘧啶(1 - 10(-6)M,70 - 72小时)和1-β-D-阿拉伯呋喃糖基胞嘧啶(阿糖胞苷)(4 - 10(-5)M,71 - 72小时)对正常的植物血凝素刺激淋巴细胞进行预孵育,导致[3H]TTP掺入量平均分别增加1.7倍(P小于0.01)、1.7倍(P小于0.05)和2.4倍(P小于0.0025)。在两个实验中,羟基脲(3 - 10(-4)M,48 - 72小时)使[3H]TTP掺入量平均增加1.6倍。未经处理的维生素B12和叶酸缺乏细胞在体外0至72小时之间添加维生素B12和叶酸纠正缺乏后,其掺入量比缺乏时增加了2.0倍(P小于0.05)。来自正常未处理细胞、5-氟尿嘧啶处理细胞、阿糖胞苷处理细胞以及维生素B12或叶酸缺乏细胞的细胞核中,不依赖ATP的合成所导致的掺入量的平均百分比分别为56±7%(标准误)、41±7%、84±3%和28±6%。在培养48至72小时之间向植物血凝素刺激的淋巴细胞中添加5-氟尿嘧啶时,DNA聚合酶的细胞质部分增加了两倍,但在70至72小时之间添加时没有显著影响。