暴露于大利什曼原虫和Phlebotomus papatasi唾液腺匀浆的Rhombomys opimus、BALB/c和C57BL/6小鼠巨噬细胞中ARG1和iNOS基因的表达模式。

IF 1.4 4区 医学 Q3 PARASITOLOGY Experimental parasitology Pub Date : 2024-11-22 DOI:10.1016/j.exppara.2024.108863
Maryam Shirazian, Niloofar Taghipour, Amir Ahmad Akhavan, Seyyed Javad Seyyed Tabaei, Mohammad Reza Abaei, Fahimeh Firouzjaie, Mahboubeh Fatemi, Nariman Mosaffa, Vahideh Moin Vaziri
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引用次数: 0

摘要

利什曼病宿主的巨噬细胞(MQ)与沙蝇唾液之间的早期相互作用对利什曼病的结果至关重要。巨噬细胞可以杀死寄生虫,也可以作为寄生虫的长期宿主,这取决于宿主的免疫力。事实证明,沙蝇唾液中的免疫原蛋白大多会通过上调细胞因子来加重利什曼病的病情。我们研究了 BALB/c(易感性)、C57BL/6(抵抗性)和 Rhombomys opimus(R. opimus,天然储库)三种不同啮齿类动物的巨噬细胞在利什曼原虫(L. major)、Phlebotomus papatasi(Ph. papatasi)唾液腺匀浆(SGH)以及 L. major + SGH 存在下精氨酸酶 1(ARG1)和诱导性一氧化氮合成酶(iNOS)基因的表达情况。使用的是静止期原虫;唾液腺提取自雌性 Papatasi(3 至 5 日龄/不喂血)。超声制备 SGH。从每只啮齿动物的腹腔采集巨噬细胞,并分组如下:1)巨噬细胞(对照组);2)MQ+L.major;3)MQ+SGH;4)MQ+L.major+SGH。培养 6 小时后,收集培养基上清,提取 RNA 并合成 cDNA,用 Real-time PCR 检测所需基因的表达水平。MQ+SGH和MQ+L.major组中ARG1的表达模式在BALB/c和C57BL/6中分别显示出最高和最低的表达水平。但在MQ+L.major+SGH组中,虽然ARG1在BALB/c中的表达量最高,但在R. opimus中的表达量最低。另一方面,iNOS 的表达在所有处理组的 C57BL/6 巨噬细胞中都有显著增加。有趣的是,与其他啮齿动物相比,MQ+L.major 组的 C57BL/6 巨噬细胞中 iNOS 的表达有显著差异。ARG1和iNOS在BALB/c和C57BL/6以及R. opimus的巨噬细胞中的表达是不同的,这可以证明它们的临床疾病结果。基因表达模式的差异与宿主的遗传有关,表明即使是同种沙蝇,宿主之间的遗传差异也会影响唾液蛋白引起的免疫反应。
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Expression pattern of ARG1 and iNOS genes in macrophages of Rhombomys opimus, BALB/c and C57BL/6 mice exposed to Leishmania major and salivary gland homogenates of Phlebotomus papatasi.

Early interactions between Leishmania-macrophages (MQ) of host and effect of sand fly saliva are central to leishmaniasis outcome. Macrophages are able to kill or act as long-term hosts of parasite depending on host immunity. It proved that immunogenic proteins in sand fly saliva mostly have an exacerbating effect on leishmaniasis by up-regulating cytokines. We have explored expression of Arginase 1 (ARG1) and inducible Nitric Oxide Synthase (iNOS) genes in macrophages of three different rodents, BALB/c (susceptible), C57BL/6 (resistant) and Rhombomys opimus (R. opimus, natural reservoir) in presence of Leishmania major (L. major), salivary gland homogenate (SGH) of Phlebotomus papatasi ( Ph. papatasi) and finally L. major + SGH. Stationary phase of promastigotes was used; salivary glands were extracted from female of Ph. papatasi (3 to 5 day-old/non-blood fed). SGH prepared by sonication. Macrophages harvested from the peritoneal cavity of each rodent and grouped as follow; 1) macrophage (control group), 2) MQ+L.major 3) MQ+SGH 4) MQ+L.major+SGH. After 6 hours of incubation, culture medium supernatant collected, RNA extraction and cDNA synthesis performed, expression level of desired genes checked by Real-time PCR. ARG1 expression pattern in MQ+SGH and MQ+L.major group showed the highest and lowest expressions level respectively in BALB/c and C57BL/6. But, in MQ+L.major+SGH, although the highest ARG1 expression happened in BALB/c again, the lowest one observed in R. opimus. On the other hand, iNOS expression showed significant increase in all treated group of C57BL/6 macrophages. Interestingly, iNOS expression showed significant differences in MQ+L.major group of C57BL/6 in comparison to other rodents. Expression of ARG1 and iNOS in macrophages of BALB/c and C57BL/6 and R. opimus are different and can justify their clinical outcome of disease. The difference in gene expression pattern is related to the genetics of host and shows that genetic differences between hosts can affect the immune responses caused by saliva proteins even of the same species of sand fly.

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来源期刊
Experimental parasitology
Experimental parasitology 医学-寄生虫学
CiteScore
3.10
自引率
4.80%
发文量
160
审稿时长
3 months
期刊介绍: Experimental Parasitology emphasizes modern approaches to parasitology, including molecular biology and immunology. The journal features original research papers on the physiological, metabolic, immunologic, biochemical, nutritional, and chemotherapeutic aspects of parasites and host-parasite relationships.
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