The accumulation of lactic acid and its influence on the growth of Plasmodium falciparum in synchronized cultures.

In Vitro Pub Date : 1984-03-01 DOI:10.1007/BF02618189
J W Zolg, A J Macleod, J G Scaife, R L Beaudoin
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引用次数: 29

Abstract

Synchronization of Plasmodium falciparum cultured in vitro results in a one-step growth pattern that allows the study of stage-specific metabolic activities of the parasites. Lactic acid (LA) was selected as a metabolic marker, and the concentration of this end product found in spent media was correlated with the different erythrocytic stages of the parasites. When the medium was changed at 12 h intervals, cultures containing predominantly trophozoites produced 3.66 +/- 0.55 mumol LA per 12 h per 10(7) parasitized cells (n = 26), an amount of LA that is about 8 to 20 times higher than that found in corresponding cultures containing predominantly ring forms. Depending on the stage of development, parasitized red blood cells produced between 5 and 100 times more LA than uninfected erythrocytes (3.72 +/- 0.62 mumol LA per 12 hours per 10(9) red blood cells) (n = 41) when cultured under identical conditions. The intraerythrocytic development of the parasites was not impaired by exposure to extracellular concentrations of LA up to 12 mM over a 12 h period. The growth resulting in such cultures was described as uninhibited and was characterized by a multiplication index of 10 or higher. Above the threshold of 12 mM of LA, progressive inhibition of parasite development occurred. The stage-specific LA production reported can be used to predict the amount of LA that will have accumulated at the end of a subsequent 12 h incubation period during synchronized in vitro growth of Plasmodium falciparum. Using these values, it is possible to establish an optimal medium exchange schedule, thereby assuring uninhibited growth and a correspondingly high parasite yield.

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同步培养中乳酸积累及其对恶性疟原虫生长的影响。
体外培养的恶性疟原虫同步导致一步生长模式,允许研究寄生虫的阶段特异性代谢活动。选择乳酸(LA)作为代谢标志物,在废培养基中发现的终产物浓度与寄生虫的不同红细胞阶段相关。当每隔12小时更换一次培养基时,每10(7)个寄生细胞(n = 26)中以滋养体为主的培养物每12小时产生3.66 +/- 0.55 mumol LA,其LA量比以环状形式为主的相应培养物的LA量高出约8至20倍。根据发育阶段的不同,在相同条件下培养时,被寄生的红细胞产生的LA是未感染红细胞的5至100倍(每10(9)个红细胞每12小时3.72 +/- 0.62 μ mol LA) (n = 41)。暴露于细胞外浓度高达12 mM的LA 12小时内,寄生虫的红细胞内发育未受到损害。在这种培养中产生的生长被描述为不受抑制的,其特征是增殖指数为10或更高。超过12 mM的LA阈值,寄生虫发育发生渐进式抑制。报告的阶段特异性LA产量可用于预测恶性疟原虫同步体外生长期间随后12小时孵育期结束时积累的LA量。利用这些值,可以建立一个最佳的培养基交换计划,从而确保不受抑制的生长和相应的高寄生虫产量。
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