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墨西哥利什曼原虫无鞭毛体对鼠树突状细胞一氧化氮合酶表达的调控。

Regulation of the expression of nitric oxide synthase by Leishmania mexicana amastigotes in murine dendritic cells.

机构信息

Departamento de Medicina Experimental, Facultad de Medicina, Universidad Nacional Autónoma de México, Dr. Balmis 148, Col. Doctores, México 06726, D.F., Mexico.

出版信息

Exp Parasitol. 2010 Nov;126(3):426-34. doi: 10.1016/j.exppara.2010.07.014. Epub 2010 Jul 24.

Abstract

In mammalian hosts, Leishmania parasites are obligatory intracellular organisms that invade macrophages (M phi) and dendritic cells (DC). In M phi, the production of nitric oxide (NO) catalyzed by the inducible nitric oxide synthase (iNOS) has been implicated as a major defense against Leishmania infection. The modulation of this microbicidal mechanism by different species of Leishmania has been well studied in M phi. Although DC are permissive for infection with Leishmania both in vivo and in vitro, the effect of this parasite in the expression of iNOS and NO production in these cells has not been established. To address this issue, we analyzed the regulation of iNOS by Leishmania mexicana amastigotes in murine bone marrow-derived dendritic cells (BMDC) stimulated with LPS and IFN-gamma. We show that the infection of BMDC with amastigotes down regulated NO production and diminished iNOS protein levels in cells stimulated with LPS alone or in combination with IFN-gamma. The reduction in iNOS protein levels and NO production did not correlate with a decrease in iNOS mRNA expression, suggesting that the parasite affects post-transcriptional events of NO synthesis. Although amastigotes were able to reduce NO production in BMDC, the interference with this cytotoxic mechanism was not sufficient to permit the survival of L. mexicana. At 48 h post-infection, BMDC stimulated with LPS+IFN-gamma were able to eliminate the parasites. These results are the first to identify the regulation of iNOS by L. mexicana amastigotes in DC.

摘要

在哺乳动物宿主体内,利什曼原虫寄生虫是一种必需的细胞内生物,它会入侵巨噬细胞(M phi)和树突状细胞(DC)。在巨噬细胞中,诱导型一氧化氮合酶(iNOS)催化生成的一氧化氮(NO)被认为是抵抗利什曼原虫感染的主要防御机制。不同种类的利什曼原虫对这种杀菌机制的调节在巨噬细胞中得到了很好的研究。虽然 DC 在体内和体外都允许利什曼原虫感染,但尚未确定该寄生虫对这些细胞中 iNOS 的表达和 NO 产生的影响。为了解决这个问题,我们分析了利什曼墨西哥变种的无鞭毛体对 LPS 和 IFN-γ刺激的鼠骨髓来源树突状细胞(BMDC)中 iNOS 的调节作用。我们发现,无鞭毛体感染 BMDC 会下调单独或与 IFN-γ联合刺激 LPS 时的 NO 产生和 iNOS 蛋白水平。iNOS 蛋白水平和 NO 产生的减少与 iNOS mRNA 表达的减少无关,这表明寄生虫影响了 NO 合成的转录后事件。尽管无鞭毛体能够减少 BMDC 中的 NO 产生,但这种细胞毒性机制的干扰不足以允许利什曼墨西哥变种的存活。在感染后 48 小时,用 LPS+IFN-γ刺激的 BMDC 能够消除寄生虫。这些结果首次确定了利什曼墨西哥变种的无鞭毛体对 DC 中 iNOS 的调节作用。

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