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克氏锥虫感染细胞的转录组概况:增殖抑制剂和促进剂的同时上调和下调。

Transcriptome profile of Trypanosoma cruzi-infected cells: simultaneous up- and down-regulation of proliferation inhibitors and promoters.

作者信息

Shigihara Takako, Hashimoto Muneaki, Shindo Noriko, Aoki Takashi

机构信息

Division of Molecular and Biochemical Research, Biomedical Research Center, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.

出版信息

Parasitol Res. 2008 Mar;102(4):715-22. doi: 10.1007/s00436-007-0819-x. Epub 2007 Dec 5.

Abstract

As Trypanosoma cruzi, the etiological agent of Chagas disease, multiplies in the cytoplasm of nucleated host cells, infection with this parasite is highly likely to affect host cells. We performed an exhaustive transcriptome analysis of T. cruzi-infected HeLa cells using an oligonucleotide microarray containing probes for greater than 47,000 human gene transcripts. In comparison with uninfected cells, those infected with T. cruzi showed greater than threefold up-regulation of 41 genes and greater than threefold down-regulation of 23 genes. Real-time reverse transcriptase-polymerase chain reaction (RT-PCR) of selected, differentially expressed genes confirmed the microarray data. Many of these up- and down-regulated genes were related to cellular proliferation, including seven up-regulated genes encoding proliferation inhibitors and three down-regulated genes encoding proliferation promoters, strongly suggesting that T. cruzi infection inhibits host cell proliferation, which may allow more time for T. cruzi to replicate and produce its intracellular nests. These findings provide new insight into the molecular mechanisms by which intracellular T. cruzi infection influences the host cell, leading to pathogenicity.

摘要

作为恰加斯病的病原体克氏锥虫在有核宿主细胞的细胞质中繁殖,感染这种寄生虫极有可能影响宿主细胞。我们使用包含超过47,000个人类基因转录本探针的寡核苷酸微阵列对克氏锥虫感染的HeLa细胞进行了详尽的转录组分析。与未感染细胞相比,感染克氏锥虫的细胞中41个基因上调超过三倍,23个基因下调超过三倍。对选定的差异表达基因进行实时逆转录聚合酶链反应(RT-PCR)证实了微阵列数据。这些上调和下调的基因中有许多与细胞增殖相关,包括七个编码增殖抑制剂的上调基因和三个编码增殖促进剂的下调基因,这强烈表明克氏锥虫感染会抑制宿主细胞增殖,这可能会为克氏锥虫的复制和产生其细胞内巢留出更多时间。这些发现为细胞内克氏锥虫感染影响宿主细胞并导致致病性的分子机制提供了新的见解。

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