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一种在克氏锥虫中体外诱导无鞭毛体向锥鞭毛体转化的新方法揭示了肌醇1,4,5-三磷酸受体的重要性。

A Novel Method for Inducing Amastigote-To-Trypomastigote Transformation In Vitro in Trypanosoma cruzi Reveals the Importance of Inositol 1,4,5-Trisphosphate Receptor.

作者信息

Hashimoto Muneaki, Morales Jorge, Uemura Haruki, Mikoshiba Katsuhiko, Nara Takeshi

机构信息

Department of Molecular and Cellular Parasitology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.

Department of Protozoology, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.

出版信息

PLoS One. 2015 Aug 12;10(8):e0135726. doi: 10.1371/journal.pone.0135726. eCollection 2015.

Abstract

BACKGROUND

Trypanosoma cruzi is a parasitic protist that causes Chagas disease, which is prevalent in Latin America. Because of the unavailability of an effective drug or vaccine, and because about 8 million people are infected with the parasite worldwide, the development of novel drugs demands urgent attention. T. cruzi infects a wide variety of mammalian nucleated cells, with a preference for myocardial cells. Non-dividing trypomastigotes in the bloodstream infect host cells where they are transformed into replication-capable amastigotes. The amastigotes revert to trypomastigotes (trypomastigogenesis) before being shed out of the host cells. Although trypomastigote transformation is an essential process for the parasite, the molecular mechanisms underlying this process have not yet been clarified, mainly because of the lack of an assay system to induce trypomastigogenesis in vitro.

METHODOLOGY/PRINCIPAL FINDINGS: Cultivation of amastigotes in a transformation medium composed of 80% RPMI-1640 and 20% Grace's Insect Medium mediated their transformation into trypomastigotes. Grace's Insect Medium alone also induced trypomastigogenesis. Furthermore, trypomastigogenesis was induced more efficiently in the presence of fetal bovine serum. Trypomastigotes derived from in vitro trypomastigogenesis were able to infect mammalian host cells as efficiently as tissue-culture-derived trypomastigotes (TCT) and expressed a marker protein for TCT. Using this assay system, we demonstrated that T. cruzi inositol 1,4,5-trisphosphate receptor (TcIP3R)-an intracellular Ca2+ channel and a key molecule involved in Ca2+ signaling in the parasite-is important for the transformation process.

CONCLUSION/SIGNIFICANCE: Our findings provide a new tool to identify the molecular mechanisms of the amastigote-to-trypomastigote transformation, leading to a new strategy for drug development against Chagas disease.

摘要

背景

克氏锥虫是一种寄生原生生物,可引发恰加斯病,该病在拉丁美洲较为普遍。由于缺乏有效的药物或疫苗,且全球约有800万人感染该寄生虫,因此新型药物的研发亟待关注。克氏锥虫可感染多种哺乳动物有核细胞,尤其偏好心肌细胞。血液中不分裂的锥鞭毛体感染宿主细胞后会转化为具有复制能力的无鞭毛体。无鞭毛体在从宿主细胞中释放之前会重新转变为锥鞭毛体(锥鞭毛体生成)。尽管锥鞭毛体转化是该寄生虫的一个重要过程,但其背后的分子机制尚未阐明,主要原因是缺乏在体外诱导锥鞭毛体生成的检测系统。

方法/主要发现:在由80% RPMI - 1640和20%格雷斯昆虫培养基组成的转化培养基中培养无鞭毛体可介导其转化为锥鞭毛体。单独使用格雷斯昆虫培养基也能诱导锥鞭毛体生成。此外,在胎牛血清存在的情况下,锥鞭毛体生成的诱导效率更高。源自体外锥鞭毛体生成的锥鞭毛体能够像组织培养衍生的锥鞭毛体(TCT)一样有效地感染哺乳动物宿主细胞,并表达TCT的一种标记蛋白。利用该检测系统,我们证明克氏锥虫肌醇1,4,5 - 三磷酸受体(TcIP3R)——一种细胞内Ca2+通道以及该寄生虫Ca2+信号传导中的关键分子——对转化过程很重要。

结论/意义:我们的发现为确定无鞭毛体向锥鞭毛体转化的分子机制提供了一种新工具,从而为恰加斯病的药物研发带来了新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcca/4534300/6d0336cb4a72/pone.0135726.g001.jpg

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