Matthews J H, Wickramasinghe S N
Br J Haematol. 1986 Jun;63(2):281-91. doi: 10.1111/j.1365-2141.1986.tb05551.x.
3H-thymidine (3H-TdR) incorporation, deoxyuridine (dU)-suppressed values, modal cell volume and the relative DNA content of individual cells have been determined in phytohaemagglutinin (PHA)-stimulated normal human lymphocytes cultured for varying periods in folate-free medium and media supplemented with various concentrations of folic acid. The results indicate that when the intracellular folate content falls below 400-600 pg/10(6) cells, lymphocytes exhibit increased 3H-TdR incorporation into DNA, raised dU-suppressed values, an increase in cell volume and abnormal DNA synthesis. This critical concentration of folate is just present in resting lymphocytes, but falls on stimulation by PHA, and the effects of folate deficiency become increasingly evident beyond a culture period of 24 h unless the folic acid concentration in the medium is at least 0.32 microgram/ml. Thus human lymphocytes cultured in folate-free medium provide a model for folate-deficient DNA synthesis, but their usefulness for the performance of dU suppression tests in the diagnosis of clinical folate deficiency is likely to be limited.
在无叶酸培养基以及添加了不同浓度叶酸的培养基中培养不同时间的植物血凝素(PHA)刺激的正常人淋巴细胞,已测定其3H-胸腺嘧啶核苷(3H-TdR)掺入量、脱氧尿苷(dU)抑制值、细胞平均体积以及单个细胞的相对DNA含量。结果表明,当细胞内叶酸含量降至400 - 600 pg/10(6)细胞以下时,淋巴细胞表现出3H-TdR掺入DNA增加、dU抑制值升高、细胞体积增大以及DNA合成异常。这种叶酸临界浓度仅存在于静息淋巴细胞中,但在PHA刺激后会下降,除非培养基中叶酸浓度至少为0.32微克/毫升,否则在培养24小时后叶酸缺乏的影响会越来越明显。因此,在无叶酸培养基中培养的人淋巴细胞为叶酸缺乏性DNA合成提供了一个模型,但它们在临床叶酸缺乏诊断中进行dU抑制试验的实用性可能有限。