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昆虫病原真菌(Entomopthorales)感染对(鳞翅目)幼虫中十八种细胞因子样蛋白的影响。

The effect of infection with the entomopathogenic fungus (Entomopthorales) on eighteen cytokine-like proteins in (Lepidoptera) larvae.

机构信息

Museum and Institute of Zoology, Polish Academy of Science, Warsaw, Poland.

Dioscuri Centre for RNA-Protein Interactions in Human Health and Disease, International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.

出版信息

Front Immunol. 2024 May 7;15:1385863. doi: 10.3389/fimmu.2024.1385863. eCollection 2024.

DOI:10.3389/fimmu.2024.1385863
PMID:38774871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11106378/
Abstract

BACKGROUND

In response to the replace mammal research models with insects in preliminary immunological studies, interest has grown in invertebrate defense systems. The immunological response is regulated by cytokines; however, while their role in mammals is well understood, little is known of their function in insects. A suitable target for studies into insect immunology is (Lepidoptera), the wax moth: a common host for human fungal and bacterial pathogens. is also a perfect subject for studies into the presence of cytokine-like proteins.

SPECIFIC OBJECTIVES

The main goal of present research was detection in insect immunocompetent cells the 18 mammalian cytokines (IL-1α, IL-1β, IL-2, IL-3, IL-6, IL-7, IL-8, IL-12, IL-13, IL-15, IL-17, IL-19, IFN-γ, TNF-α, TNF-β, GM-CSF, M-CSF, G-CSF), which play important role in immunological response and indication how their level change after fungal infection.

METHODOLOGY

The changes of cytokine-like proteins level were detected in hemocytes taken from G larvae infected with entomopathogenic fungus, . The presence of cytokine-proteins was confirmed with using fluorescence microscopy (in cultured hemocytes) and flow cytometry (in freshly collected hemolymph). The ELISA test was used to detect changes in concentration of examined cytokine-like proteins.

RESULTS

Our findings indicated the presence of eighteen cytokine-like molecules in hemocytes during infection with . The hemocytes taken from infected larvae demonstrated higher fluorescence intensity for six cytokine-like proteins (GM-CSF, M-CSF, IL-3, IL-15, IL-1β and IL-19) compared to untreated controls. ELISA test indicated significantly higher IL-3 and IL-15. M-CSF, IL-1α and IL-19 concentration in the hemolymph after fungal infection, and significantly lower TNF-β and G-CSF.

CONCLUSIONS

Our findings confirm that the selected cytokine-like molecules are present in insect hemocytes and that their concentrations change after fungal infection, which might suggest that they play a role in the anti-fungal immunological response.

摘要

背景

为了在初步免疫研究中用昆虫替代哺乳动物研究模型,人们对无脊椎动物防御系统的兴趣日益浓厚。细胞因子调节免疫反应;然而,尽管它们在哺乳动物中的作用已被充分了解,但对它们在昆虫中的功能知之甚少。(鳞翅目)的黄粉虫是一种常见的人类真菌和细菌病原体宿主,是昆虫免疫学研究的理想对象。黄粉虫也是研究细胞因子样蛋白存在的理想对象。

具体目标

本研究的主要目的是在昆虫免疫活性细胞中检测 18 种哺乳动物细胞因子(IL-1α、IL-1β、IL-2、IL-3、IL-6、IL-7、IL-8、IL-12、IL-13、IL-15、IL-17、IL-19、IFN-γ、TNF-α、TNF-β、GM-CSF、M-CSF、G-CSF),这些细胞因子在免疫反应中发挥重要作用,并表明它们在真菌感染后的水平变化。

方法

用昆虫病原真菌感染 G 期幼虫的血淋巴检测细胞因子样蛋白水平的变化。用荧光显微镜(在培养的血淋巴细胞中)和流式细胞术(在新鲜采集的血淋巴中)证实细胞因子蛋白的存在。用 ELISA 试验检测检测到的细胞因子样蛋白浓度的变化。

结果

我们的研究结果表明,在感染 时,十八种细胞因子样分子存在于 血淋巴中。与未处理的对照相比,从感染幼虫中提取的血淋巴中,六种细胞因子样蛋白(GM-CSF、M-CSF、IL-3、IL-15、IL-1β和 IL-19)的荧光强度更高。ELISA 试验表明,感染真菌后,IL-3 和 IL-15 的浓度显著升高,M-CSF、IL-1α 和 IL-19 的浓度在血淋巴中显著降低,而 TNF-β 和 G-CSF 的浓度则显著降低。

结论

我们的研究结果证实,所选细胞因子样分子存在于昆虫血淋巴中,并且在真菌感染后其浓度发生变化,这可能表明它们在抗真菌免疫反应中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/4acfccc502f7/fimmu-15-1385863-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/99949198a952/fimmu-15-1385863-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/98a7563acd00/fimmu-15-1385863-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/c5bcc9e6fd8e/fimmu-15-1385863-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/9db99050e41f/fimmu-15-1385863-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/e996836b3ad8/fimmu-15-1385863-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/4acfccc502f7/fimmu-15-1385863-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/99949198a952/fimmu-15-1385863-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/98a7563acd00/fimmu-15-1385863-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/c5bcc9e6fd8e/fimmu-15-1385863-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/9db99050e41f/fimmu-15-1385863-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/e996836b3ad8/fimmu-15-1385863-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24db/11106378/4acfccc502f7/fimmu-15-1385863-g006.jpg

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