The network of immune system and nerve system in host defense to bacterial infections
The network of immune system and nerve system in host defense to bacterial infections
批准号:
05670245
负责人:
NAKANE Akio
金额:
$1.41万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1995
中文摘要
免疫系统、神经系统和内分泌系统之间形成了网络。我们对细菌感染中免疫系统和神经系统之间的相互作用很感兴趣。选择P物质(SP)、血管活性肠肽(VIP)等神经肽作为神经系统参数。用免疫组织化学方法研究了单核细胞增生性李斯特氏菌和拟新陈代谢李斯特氏菌对小鼠肝脏SP和VIP的诱导作用。在感染李斯特氏菌的小鼠肝脏的血管周围和周围的浸润性细胞中均未检测到SP,而VIP则呈阳性反应。与之相反,在钩端螺旋体感染小鼠的肝脏肉芽肿样病变中检测到SP,而不是VIP。这些结果提示,SP和VIP的选择性诱导可能取决于感染的细菌,神经肽可能是由炎症细胞分泌的。在逆转录-聚合酶链式反应的研究中,PropreVIP基因的表达与李斯特氏菌在肝脏中的生长同步,这些结果表明神经肽可能参与了细菌感染的炎症过程和/或宿主防御。
英文摘要
The network is formed between immune system, nerve system, and endocrine system. We were interested in the interaction between immune system and nerve system in bacterial infections. We chose the neuropeptides such as substance P (SP) and vasoactive intestinal peptide (VIP) as the parameter of nerve system. We investigated the induction of SP and VIP en the livers of mice which were infected intravenously with Listeria monocytogenes or Tsukamullela paurometabolum.In the studies using an immunohistochemical technique, neither SP nor VIP was detected in the livers of uninfected mice. VIP,but not SP was detected around the blood vessels and in the surrounding infiltrating cells of livers obtained from Listeria-infected mice. In contrast, SP,but not VIP,was detected in the granuloma-like lesions of livers obtained from Tsukamullela-infected mice. These result suggest that the selective induction of SP and VIP might occur, depending on bacteria infected, and that the neuropeptides might be secreted by the inflammatory cells. In the studies using reverse transcription-PCR,propre VIP mRNA was induced in parallel with the growth of Listeria cells in the livers.These results demonstrate that the neuropeptides might be involved in the inflammatory process and/or the host defense in bacterial infections.
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Akio Nakane: "Vasoactive intestinal peptide in the livers of mice during Listeria monocytogenes infection" (投稿準備中).
Akio Nakane:“单核细胞增生李斯特菌感染期间小鼠肝脏中的血管活性肠肽”(准备提交)。
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通讯作者:
Akio Nakane: "Vasoactive intestinal peptide in the livers of mice during Listeria monocytogenes infection" (Manuscript in preparation).
Akio Nakane:“单核细胞增生李斯特菌感染期间小鼠肝脏中的血管活性肠肽”(手稿正在准备中)。
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Masashi Kohanawa: "CD3+/TCR-αβ-cells are important in protecting spinal cord tissues against Theiler′s virus strain GDVII infection" Microbiol.Immunol.39. 123-128 (1995)
Masashi Kohanawa:“CD3+/TCR-αβ-细胞对于保护脊髓组织免受泰勒病毒株 GDVII 感染非常重要”Microbiol.Immunol.39 (1995)。
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Akio Nakane: "A monoclonal antibody against T-cell receptor αβ induces endogenous cytokines and prevents mice from a lethal infection with Listeria monocytogenes" FEMS Immunology and Medical Microbiology. 11. 321-329 (1995)
Akio Nakane:“针对 T 细胞受体 αβ 的单克隆抗体可诱导内源性细胞因子并防止小鼠受到单核细胞增多性李斯特菌的致命感染”FEMS 免疫学和医学微生物学 11. 321-329 (1995)。
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Masashi Kohanawa: "Theiler's virus is eliminated by a gamma-interferon-independent mechanism in the brain" Journal of Neuroimmunology. 52. 79-86 (1994)
Masashi Kohanawa:“泰勒氏病毒是通过大脑中不依赖γ-干扰素的机制消除的”《神经免疫学杂志》。
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