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锑通过宿主和寄生虫中的非选择性阳离子通道诱导细胞内钙离子增加,这是细胞内杜氏利什曼原虫无鞭毛体凋亡的原因。

Antimonial-induced increase in intracellular Ca2+ through non-selective cation channels in the host and the parasite is responsible for apoptosis of intracellular Leishmania donovani amastigotes.

作者信息

Sudhandiran G, Shaha Chandrima

机构信息

National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.

出版信息

J Biol Chem. 2003 Jul 4;278(27):25120-32. doi: 10.1074/jbc.M301975200. Epub 2003 Apr 21.

Abstract

The capability of the obligate intracellular parasites like Leishmania donovani to survive within the host cell parasitophorous vacuoles as nonmotile amastigotes determines disease pathogenesis, but the mechanism of elimination of the parasites from these vacuoles are not well understood. By using the anti-leishmanial drug potassium antimony tartrate, we demonstrate that, upon drug exposure, intracellular L. donovani amastigotes undergo apoptotic death characterized by nuclear DNA fragmentation and externalization of phosphatidylserine. Changes upstream of DNA fragmentation included generation of reactive oxygen species like superoxide, nitric oxide, and hydrogen peroxide that were primarily concentrated in the parasitophorous vacuoles. In the presence of antioxidants like N-acetylcysteine or Mn(III) tetrakis(4-benzoic acid)porphyrin chloride, an inhibitor of inducible nitric-oxide synthase, a diminution of reactive oxygen species generation and improvement of amastigote survival were observed, suggesting a close link between drug-induced oxidative stress and amastigote death. Changes downstream to reactive oxygen species increase involved elevation of intracellular Ca2+ concentrations in both the parasite and the host that was preventable by antioxidants. Flufenamic acid, a non-selective cation channel blocker, decreased the elevation of Ca2+ in both the cell types and reduced amastigote death, thus establishing a central role of Ca2+ in intracellular parasite clearance. This influx of Ca2+ was preceded by a fall in the amastigote mitochondrial membrane potential. Therefore, this study projects the importance of flufenamic acid-sensitive non-selective cation channels as important modulators of antimonial efficacy and lends credence to the suggestion that, within the host cell, apoptosis is the preferred mode of death for the parasites.

摘要

像杜氏利什曼原虫这样的专性细胞内寄生虫,能够以无运动能力的无鞭毛体形式在宿主细胞的寄生泡内存活,这决定了疾病的发病机制,但目前对这些寄生虫从这些泡中清除的机制还了解甚少。通过使用抗利什曼原虫药物酒石酸锑钾,我们证明,在药物暴露后,细胞内的杜氏利什曼原虫无鞭毛体发生凋亡死亡,其特征为核DNA片段化和磷脂酰丝氨酸外翻。DNA片段化上游的变化包括超氧化物、一氧化氮和过氧化氢等活性氧的产生,这些活性氧主要集中在寄生泡中。在存在抗氧化剂如N - 乙酰半胱氨酸或氯化锰(III)四(4 - 苯甲酸)卟啉(一种诱导型一氧化氮合酶抑制剂)的情况下,观察到活性氧产生减少且无鞭毛体存活率提高,这表明药物诱导的氧化应激与无鞭毛体死亡之间存在密切联系。活性氧增加下游的变化包括寄生虫和宿主细胞内Ca2 + 浓度升高,而抗氧化剂可预防这种升高。氟芬那酸是一种非选择性阳离子通道阻滞剂,它降低了两种细胞类型中Ca2 + 的升高并减少了无鞭毛体死亡,从而确立了Ca2 + 在细胞内寄生虫清除中的核心作用。这种Ca2 + 的内流之前是无鞭毛体线粒体膜电位的下降。因此,本研究突出了氟芬那酸敏感的非选择性阳离子通道作为锑剂疗效重要调节剂的重要性,并支持了这样一种观点,即在宿主细胞内,凋亡是寄生虫首选的死亡方式。

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