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乳酸的积累及其对同步培养物中恶性疟原虫生长的影响。

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

作者信息

Zolg J W, Macleod A J, Scaife J G, Beaudoin R L

出版信息

In Vitro. 1984 Mar;20(3 Pt 1):205-15. doi: 10.1007/BF02618189.

DOI:10.1007/BF02618189
PMID:6370836
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.

摘要

体外培养的恶性疟原虫同步化会产生单步生长模式,这有助于研究疟原虫特定阶段的代谢活动。选择乳酸(LA)作为代谢标志物,在废弃培养基中发现的这种终产物浓度与疟原虫不同的红细胞内阶段相关。当每隔12小时更换培养基时,主要含有滋养体的培养物每12小时每10⁷个被寄生细胞产生3.66±0.55 μmol LA(n = 26),该LA量比主要含有环状体的相应培养物中发现的量高约8至20倍。根据发育阶段,在相同条件下培养时,被寄生的红细胞产生的LA比未感染的红细胞多5至100倍(每12小时每10⁹个红细胞产生3.72±0.62 μmol LA)(n = 41)。在12小时内暴露于高达12 mM的细胞外LA浓度下,疟原虫的红细胞内发育未受损害。这种培养物中的生长被描述为不受抑制,其特征是增殖指数为10或更高。高于12 mM的LA阈值时,疟原虫发育逐渐受到抑制。所报道的特定阶段LA产生可用于预测在恶性疟原虫体外同步生长的后续12小时孵育期结束时积累的LA量。利用这些值,可以建立最佳的培养基更换时间表,从而确保不受抑制的生长和相应高的疟原虫产量。

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