隐tolepine诱导的多诺瓦利什曼原虫原生体细胞死亡通过抑制自噬而增强。

Molecular biology international Pub Date : 2011-01-01 Epub Date: 2011-03-03 DOI:10.4061/2011/187850
Souvik Sengupta, Sayan Chowdhury, Somdeb Bosedasgupta, Colin W Wright, Hemanta K Majumder
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引用次数: 27

摘要

多诺瓦利什曼原虫是全世界内脏利什曼病的病原体。缺乏疫苗和耐药性的出现证明需要改进针对利什曼病的药物治疗和更新的治疗干预策略。本研究研究了天然吲哚喹啉类生物碱隐tolepine对L. donovani AG83 promastigotes的影响。我们的研究结果表明,隐tolepine诱导L. donovani promastigotes细胞功能障碍,导致这种单细胞寄生虫死亡。有趣的是,我们的研究表明隐tolepine诱导的L. donovani细胞死亡被细胞引发的初始自噬特征所抵消。我们首次表明,自噬是L. donovani promastigotes对隐tolepine治疗反应的一种生存机制,抑制自噬会导致细胞死亡数量的早期增加。本研究可为今后设计更好的利什曼病药物和治疗策略提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cryptolepine-Induced Cell Death of Leishmania donovani Promastigotes Is Augmented by Inhibition of Autophagy.

Leishmania donovani are the causative agents of visceral leishmaniasis worldwide. Lack of vaccines and emergence of drug resistance warrants the need for improved drug therapy and newer therapeutic intervention strategies against leishmaniasis. In the present study, we have investigated the effect of the natural indoloquinoline alkaloid cryptolepine on L. donovani AG83 promastigotes. Our results show that cryptolepine induces cellular dysfunction in L. donovani promastigotes, which leads to the death of this unicellular parasite. Interestingly, our study suggest that cryptolepine-induced cell death of L. donovani is counteracted by initial autophagic features elicited by the cells. For the first time, we show that autophagy serves as a survival mechanism in response to cryptolepine treatment in L. donovani promastigotes and inhibition of autophagy causes an early increase in the amount of cell death. This study can be exploited for designing better drugs and better therapeutic strategies against leishmaniasis in future.

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