课题基金 / 基金详情

Role of TGF-B signaling molecules as regulators of host immune and metabolic response to parasitic nematode infection factors

Role of TGF-B signaling molecules as regulators of host immune and metabolic response to parasitic nematode infection factors
TGF-B信号分子作为寄生线虫感染因子宿主免疫和代谢反应调节剂的作用
批准号:
2019869
负责人:
Ioannis Eleftherianos
金额:
$80.97万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-01 至 2024-07-31

项目摘要

项目成果

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中文摘要
翻译
寄生虫感染是全世界人类健康的一大威胁。目前,还没有针对人类寄生虫感染的疫苗。开发新的药物和疫苗将需要更好地了解参与对寄生线虫感染分子的免疫反应的宿主因素。对合适宿主的要求和缺乏良好的动物模型限制了对动物激活防御寄生虫攻击的防御机制的研究。该项目将采用一个由两种模式生物组成的系统:昆虫,果蝇和昆虫寄生线虫Heterorhabditis,以提供寄生感染过程及其对宿主免疫影响的机制见解。我们将把注意力集中在异habditis线虫感染过程中产生的一种致病性因子的活性上,以研究其与宿主抗线虫免疫功能的相互作用。这项研究的结果将产生新的信息,宿主成分在协调对寄生线虫的有效反应中的作用。这些发现预计将大大有助于开发限制人类寄生虫感染的创新策略。来自托马斯·杰斐逊科技高中(TJHSST; Alexandria, VA)的高中生将接受动手实验培训,他们将积极参与研究。尽管在先天免疫领域取得了重要进展,但宿主对寄生线虫感染的免疫反应目前还没有得到充分的研究。果蝇和虫源性线虫形成了一个阐明宿主先天抗线虫免疫的杰出系统。转化生长因子-β (TGF-β)信号参与了几个重要的生物过程。本研究的假设是宿主TGF-β信号活性调节了针对寄生线虫感染因子的组织特异性免疫和代谢机制。本项目旨在探讨异habditis丝氨酸肽酶(Heterorhabditis serine peptide ase, SP)对果蝇TGF-β信号调节及免疫代谢功能的影响。我们将分析注射异habditis重组丝氨酸肽酶(Heterorhabditis recombinant serine peptide ase, rSP)后激活素信号的果蝇组织特异性转录调控,以及TGF-β信号与NF-κB先天免疫信号的相互关系。此外,我们将研究激活素信号是否在果蝇中调节细胞免疫,以及后者是否与体液免疫相互作用以应对异虫性嗜好炎。最后,我们将研究激活素信号与果蝇脂质代谢在异habditis rSP侵袭下的相互作用。本研究结果将为激活素在宿主抗虫源性线虫免疫代谢反应中的作用提供新的信息。这些发现可能揭示了宿主先天抗线虫免疫系统的一个未知调节因子,因此有望有助于开发控制有害害虫的创新方法。来自托马斯·杰斐逊科技高中(TJHSST; Alexandria, VA)的高中生将在实验室接受培训,参与研究的各个方面。该奖项反映了美国国家科学基金会的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
Parasitic nematode infections represent a major threat to human health worldwide. Currently, there are no vaccines available for parasitic nematode infections in humans. Development of new drugs and vaccines will require a better understanding of host factors that participate in the immune response to parasitic nematode infection molecules. The requirement of a suitable host and the lack of good animal models have limited investigations into the defense mechanisms that animals activate to oppose parasitic nematode attacks. This project will employ a system consisting of two model organisms: an insect, Drosophila and the insect parasitic nematode Heterorhabditis to provide mechanistic insight into parasitic infection processes and their effect on host immunity. We will focus our attention to the activity of a pathogenicity factor that is produced in Heterorhabditis nematodes during infection to investigate its interaction with host anti-nematode immune functions. Results from this research will generate novel information on the role of host components in orchestrating an effective response against parasitic nematodes. Such findings are expected to contribute considerably to the development of innovative tactics to restrict parasitic nematode infections in humans. High school students from Thomas Jefferson High School for Science and Technology (TJHSST; Alexandria, VA) will receive hands-on lab training and they will be actively involved in the research. Despite important progress in the innate immunity field, host immune responses to parasitic nematode infection are currently understudied. Drosophila and the entomopathogenic nematode Heterorhabditis form an outstanding system to elucidate host innate anti-nematode immunity. Transforming Growth Factor-beta (TGF-β) signaling participates in several important biological processes. The hypothesis of this proposal is that host TGF-β signaling activity regulates tissue-specific immune and metabolic mechanisms against parasitic nematode infection factors. The goal of this project is to explore the effect of Heterorhabditis serine peptidase (SP) on TGF-β signaling regulation and immunometabolic function in Drosophila. We will analyze the Drosophila tissue-specific transcriptional regulation of Activin signaling upon injection with Heterorhabditis recombinant serine peptidase (rSP) and the interrelationship between TGF-β signaling and NF-κB innate immune signaling. Also, we will examine whether Activin signaling in Drosophila modulates cellular immunity and whether the latter interacts with humoral immunity in response to Heterorhabditis rSP. Finally, we will investigate the interaction between Activin signaling and lipid metabolism in Drosophila upon challenge with Heterorhabditis rSP. Results from this research will generate novel information on the role of Activin in the host immunometabolic response against entomopathogenic nematodes. Such findings may expose a previously unknown regulator of the host innate anti-nematode immune system and therefore are expected to contribute to the development of innovative approaches for controlling harmful insect pests. High school students from Thomas Jefferson High School for Science and Technology (TJHSST; Alexandria, VA) will be trained in the lab to participate in all aspects of the research.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
    2026
  • 负责人:
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