Wolff S, Afzal V, Lindquist P B
Mutat Res. 1984 Nov;129(2):207-13. doi: 10.1016/0027-5107(84)90153-2.
When human whole blood was cultured in medium containing neither fetal calf serum nor antibiotics, more peripheral lymphocytes initiated DNA synthesis at about 24 h of culture than did lymphocytes in blood cultured in complete medium. Furthermore, the cells proliferated faster, so that by 48 h in culture approximately 20% of the metaphase cells in medium lacking fetal calf serum and antibiotics were in their second division. Such rapid cell proliferation can affect quantitative studies of chromosome aberrations, which should be observed in their first mitosis in culture, before cell death can cause a diminution in aberration yields. The rapid appearance of second-division metaphases should also be advantageous for the measurement of sister-chromatid exchanges (SCEs), which require two cell divisions for their observation. In contrast to cultures with complete medium, cells grown without fetal calf serum and antibiotics had fewer SCEs in second-division cells that divided later in the culture period.
当人全血在既不含胎牛血清也不含抗生素的培养基中培养时,与在完全培养基中培养的血液中的淋巴细胞相比,更多外周淋巴细胞在培养约24小时时开始DNA合成。此外,细胞增殖更快,因此在培养48小时时,缺乏胎牛血清和抗生素的培养基中约20%的中期细胞处于第二次分裂。这种快速的细胞增殖会影响染色体畸变的定量研究,染色体畸变应在培养的第一次有丝分裂中观察,在细胞死亡导致畸变率降低之前。第二次分裂中期的快速出现对于姐妹染色单体交换(SCE)的测量也应该是有利的,SCE的观察需要两个细胞分裂。与完全培养基培养的情况相比,在没有胎牛血清和抗生素的情况下生长的细胞在培养后期分裂的第二次分裂细胞中SCE较少。