Hussain J I, Smith C J, Allen J C
Cell Tissue Kinet. 1983 Nov;16(6):583-91.
The influence of acrolein or spermine on the viability and growth of phytohaemagglutinin-stimulated rat thymic lymphocytes in cultures supplemented with foetal calf serum have been investigated. Acrolein (greater than 20 microM) was cytotoxic; spermine had little effect on viability, but inhibited [3H]TdR incorporation at low concentrations (approximately 10 microM). Cells treated with greater than 8 microM acrolein 3 hr before stimulation exhibited irreversible inhibition of protein synthesis, whereas 50 microM spermine had no effect, even when cells were treated for 24 hr before stimulation. However, addition of 25 microM spermine after stimulation did inhibit both [3H]-uridine incorporation and protein synthesis: this was reversible if cells were freed of polyamine within 4 hr, but not if washed after 24 hr. These results show that, contrary to several previous reports, in-vitro inhibition of cell proliferation by spermine is not due to the formation and action of acrolein.
研究了在补充有胎牛血清的培养物中,丙烯醛或精胺对植物血凝素刺激的大鼠胸腺淋巴细胞活力和生长的影响。丙烯醛(大于20微摩尔)具有细胞毒性;精胺对活力影响很小,但在低浓度(约10微摩尔)时抑制[3H]TdR掺入。在刺激前3小时用大于8微摩尔丙烯醛处理的细胞表现出蛋白质合成的不可逆抑制,而50微摩尔精胺即使在刺激前处理细胞24小时也没有影响。然而,刺激后添加25微摩尔精胺确实抑制了[3H]-尿苷掺入和蛋白质合成:如果在4小时内使细胞去除多胺,这是可逆的,但如果在24小时后洗涤则不可逆。这些结果表明,与先前的几份报告相反,精胺在体外对细胞增殖的抑制不是由于丙烯醛的形成和作用。