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Brain control of humoral immune responses amenable to behavioural modulation

机译:运动免疫应答的脑控制适用于行为调节

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It has been speculated that brain activities might directly control adaptive immune responses in lymphoid organs, although there is little evidence for this. Here we show that splenic denervation in mice specifically compromises the formation of plasma cells during a T cell-dependent but not T cell-independent immune response. Splenic nerve activity enhances plasma cell production in a manner that requires B-cell responsiveness to acetylcholine mediated by the alpha 9 nicotinic receptor, and T cells that express choline acetyl transferase(1,2) probably act as a relay between the noradrenergic nerve and acetylcholine-responding B cells. We show that neurons in the central nucleus of the amygdala (CeA) and the paraventricular nucleus (PVN) that express corticotropin-releasing hormone (CRH) are connected to the splenic nerve; ablation or pharmacogenetic inhibition of these neurons reduces plasma cell formation, whereas pharmacogenetic activation of these neurons increases plasma cell abundance after immunization. In a newly developed behaviour regimen, mice are made to stand on an elevated platform, leading to activation of CeA and PVN CRH neurons and increased plasma cell formation. In immunized mice, the elevated platform regimen induces an increase in antigen-specific IgG antibodies in a manner that depends on CRH neurons in the CeA and PVN, an intact splenic nerve, and B cell expression of the alpha 9 acetylcholine receptor. By identifying a specific brain-spleen neural connection that autonomically enhances humoral responses and demonstrating immune stimulation by a bodily behaviour, our study reveals brain control of adaptive immunity and suggests the possibility to enhance immunocompetency by behavioural intervention.Neuronal activities in the central amygdala and paraventricular nucleus are transmitted via the splenic nerve to increase plasma cell formation after immunization, and this process can be behaviourally enhanced in mice.
机译:据推测,脑活动可能直接控制淋巴机关中的适应性免疫反应,尽管这几乎没有证据。在这里,我们表明小鼠中的脾脏剥削者特异性地损害了在T细胞依赖性而不是T细胞无关的免疫应答期间形成血浆细胞的形成。脾脏神经活性以需要对由α9烟碱受体介导的乙酰胆碱的乙酰胆碱的方式增强血浆细胞产生,以及表达胆碱乙酰转移酶(1,2)的T细胞可能在去甲肾上腺神经和乙酰胆碱之间作为继电器 - 相应的B细胞。我们展示杏仁核(CEA)中央核中的神经元和表达CorticoTropin释放激素(CRH)的椎间盘(CEA)和旁注细胞核(PVN)与脾脏连接;这些神经元的消融或药物发生抑制减少了血浆细胞形成,而这些神经元的药物发生活化会增加免疫后的血浆细胞丰度。在新开发的行为方案中,使小鼠站在升高的平台上,导致CEA和PVN CRH神经元的激活和增加的血浆细胞形成。在免疫小鼠中,升高的平台方案以取决于CEA和PVN的CRH神经元,完整的脾脏神经和α9乙酰胆碱受体的B细胞表达,诱导抗原特异性IgG抗体增加。通过鉴定特定的脑脾脏神经连接,即通过身体行为自主增强体液反应并证明免疫刺激,我们的研究揭示了对适应症的脑控制,并提出了通过行为干预来增强免疫活性的可能性。中部杏仁菌和椎间盘中的活性活性通过脾脏神经传播核,以在免疫后增加血浆细胞形成,并且在小鼠中可以表现该方法。

著录项

  • 来源
    《Nature》 |2020年第7807期|204-208|共5页
  • 作者单位

    Tsinghua Univ Tsinghua Peking Ctr Life Sci Beijing Peoples R China|Tsinghua Univ Inst Immunol Lab Dynam Immunobiol Beijing Peoples R China|Tsinghua Univ Sch Med Dept Basic Med Sci Beijing Peoples R China|Tsinghua Univ Sch Life Sci Beijing Peoples R China;

    Tsinghua Univ Sch Life Sci Beijing Peoples R China|McGovern Inst Brain Res Beijing Peoples R China;

    ShanghaiTech Univ Sch Life Sci & Technol Shanghai Peoples R China;

    Tsinghua Univ Tsinghua Peking Ctr Life Sci Beijing Peoples R China|Tsinghua Univ Inst Immunol Lab Dynam Immunobiol Beijing Peoples R China|Tsinghua Univ Sch Med Dept Basic Med Sci Beijing Peoples R China|Tsinghua Univ Sch Life Sci Beijing Peoples R China;

    Tsinghua Univ Sch Pharmacol Sci Beijing Peoples R China;

    Chinese Acad Sci Shenzhen Inst Adv Technol Shenzhen Peoples R China;

    Tsinghua Univ Sch Life Sci Beijing Peoples R China|McGovern Inst Brain Res Beijing Peoples R China;

    Tsinghua Univ Sch Pharmacol Sci Beijing Peoples R China;

    Capital Med Univ Sch Basic Med Sci Beijing Peoples R China|Chinese Inst Brain Res Beijing Peoples R China;

    Chinese Acad Sci Shenzhen Inst Adv Technol Shenzhen Peoples R China|Wuhan Inst Phys & Math Key Lab Magnet Resonance Biol Syst State Key Lab Magnet Resonance & Atom Mol Phys Ctr Brain Sci Wuhan Peoples R China|Chinese Acad Sci Ctr Excellence Brain Sci & Intelligent Technol Wuhan Peoples R China;

    Tsinghua Univ Sch Life Sci Beijing Peoples R China|McGovern Inst Brain Res Beijing Peoples R China;

    ShanghaiTech Univ Sch Life Sci & Technol Shanghai Peoples R China|Nantong Univ Coinnovat Ctr Neuroregenerat Nantong Peoples R China;

    Tsinghua Univ Tsinghua Peking Ctr Life Sci Beijing Peoples R China|Tsinghua Univ Inst Immunol Lab Dynam Immunobiol Beijing Peoples R China|Tsinghua Univ Sch Med Dept Basic Med Sci Beijing Peoples R China|Tsinghua Univ Sch Life Sci Beijing Peoples R China|Tsinghua Univ Beijing Key Lab Immunol Res Chron Dis Beijing Peoples R China|Tsinghua Univ Beijing Frontier Res Ctr Biol Struct Beijing Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 22:15:24

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