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甲基乙二醛对人白血病60细胞体外增殖的抑制作用。

Inhibition of proliferation of human leukaemia 60 cells by methylglyoxal in vitro.

作者信息

Ayoub F M, Allen R E, Thornalley P J

机构信息

Department of Chemistry and Biological Chemistry, University of Essex, Colchester, U.K.

出版信息

Leuk Res. 1993 May;17(5):397-401. doi: 10.1016/0145-2126(93)90094-2.

Abstract

Methylglyoxal (2-oxopropanal) is the physiological substrate of the glyoxalase system. When exogenous methylglyoxal (50 microM-1 mM) was added to human leukaemia 60 (HL60) cells in culture (5 x 10(4) cells/ml), inhibition of growth and toxicity was induced. The median growth inhibitory concentration IC50 value was 238 +/- 2 microM. There was little differentiation of HL60 cells induced by methylglyoxal (a maximum of 2% differentiation with 500 microM methylglyoxal). There was no similar toxicity induced by methylglyoxal in corresponding differentiated cells, neutrophils, under the same culture conditions. Cell growth and toxicity induced by methylglyoxal (250 microM) in HL60 cells occurred in the initial 24 h of culture, after which residual surviving cells exhibited normal growth kinetics. It could also be prevented by replacing the culture medium in the initial 6 h of culture; thereafter, irreversible toxicity developed, reaching the maximum value after 24 h of culture. Growth arrest and toxicity induced by methylglyoxal increased with increasing serum composition of the medium. The mechanism of toxicity is unknown.

摘要

甲基乙二醛(2-氧代丙醛)是乙二醛酶系统的生理底物。当向培养的人白血病60(HL60)细胞(5×10⁴个细胞/毫升)中加入外源性甲基乙二醛(50微摩尔/升 - 1毫摩尔/升)时,会诱导生长抑制和毒性。生长抑制浓度中位数IC50值为238±2微摩尔/升。甲基乙二醛诱导的HL60细胞分化很少(500微摩尔/升甲基乙二醛时最大分化率为2%)。在相同培养条件下,甲基乙二醛在相应的分化细胞中性粒细胞中未诱导出类似毒性。甲基乙二醛(250微摩尔/升)在HL60细胞中诱导的细胞生长和毒性发生在培养的最初24小时内,之后存活的残余细胞表现出正常的生长动力学。在培养的最初6小时内更换培养基也可以预防这种情况;此后,会产生不可逆的毒性,在培养24小时后达到最大值。甲基乙二醛诱导的生长停滞和毒性随着培养基中血清成分的增加而增加。毒性机制尚不清楚。

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