精选类固醇生物碱诱导唐氏利什曼原虫细胞死亡的分子机制

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Naveena Menpadi, Pranjal Chandra, Vikash Kumar Dubey
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引用次数: 0

摘要

我们早些时候曾报道过新型抗利什曼病分子--veratramine 和 hupehenine,它们以寄生虫的脱磷辅酶 A 激酶为靶标。在目前的研究中,我们评估了这两种甾体生物碱(veratramine 和 hupehenine)在抗击寄生虫方面的功效。与预期相反,我们的研究没有发现线粒体膜电位丧失和磷脂酰丝氨酸外化等典型的细胞凋亡迹象。相反,我们观察到酸性细胞器的形成明显增加,这表明原核中存在一种有利于生存的反应。通过各种流式细胞分析和成像方法,我们得出结论,这些天然化合物诱导的寄生虫死亡并不遵循细胞凋亡途径,而很可能涉及自噬。这一发现标志着自噬介导的细胞死亡首次在唐氏利什曼原虫中由维拉曲明和胡贝宁引发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Mechanisms of Cell Death in Leishmania donovani Induced by Selected Steroidal Alkaloids.

We have earlier reported novel anti-leishmanial molecules, veratramine and hupehenine, targeting dephospho-coenzyme A kinase of the parasite. In our current investigation, we assessed the efficacy of these two steroidal alkaloids, veratramine and hupehenine, in combating the parasite. Contrary to expectations, our study did not detect the typical signs of apoptosis such as mitochondrial membrane potential loss and phosphatidylserine externalization. Instead, we observed a notable increase in acidic organelle formation, suggesting a pro-survival response in promastigotes. Through diverse flow cytometric analyses and imaging methods, we conclude that the parasitic death induced by these natural compounds does not follow the apoptosis pathway but likely involves autophagy. This discovery marks the first instance of autophagy-mediated cell death in Leishmania donovani triggered by veratramine and hupehenine.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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