通道反射:器官特异性疾病发展的神经免疫串扰

D. Kamimura, Yuki Tanaka, Takuto Ohki, Masaaki Murakami
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引用次数: 1

摘要

中枢神经系统(CNS)的内稳态是由一种独特的血管结构——血脑屏障(BBB)严格调节的。实验和临床证据表明,血脑屏障异常在慢性炎症性疾病,如多发性硬化症(MS)。通过使用多发性硬化症的动物模型,我们发现了新的神经免疫串扰来解释致病性免疫细胞如何进入中枢神经系统破坏其稳态,我们将这种现象命名为通道反射。区域性的神经输入,如重力、电、疼痛或慢性压力,会引起特定的神经激活,从而在特定的血管上形成免疫细胞(尤其是致病细胞)的通道。此外,最近发现的压力诱导的通道反射揭示了大脑、胃肠道和心脏之间压力诱导的神经联系。因此,通道反射对各种器官的内稳态至关重要,通道反射异常激活的神经通路破坏了正常的器官内稳态。炎症反射是局部神经免疫相互作用的另一种机制。它对多种疾病具有胆碱能抗炎作用。在本节中,我们讨论局部神经免疫相互作用的新角色,特别关注门户反射。并诱导交感神经的激活(5),导致L5背血管分泌去甲肾上腺素(NE)(6)。NE增强L5背侧血管中的炎症放大器,导致趋化因子上调,并从血管中募集致病性CD4+ T细胞(7)。
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Gateway Reflex: A Neuro-Immune Crosstalk for Organ-Specific Disease Development
Homeostasis of the central nervous system (CNS) is strictly regulated by a unique struc- ture of blood vessels, the blood-brain barrier (BBB). Experimental and clinical evidence has revealed that abnormalities in the BBB in chronic inflammatory diseases such as mul - tiple sclerosis (MS). By using an animal model of MS, we identified novel neuro-immune crosstalk to explain how pathogenic immune cells enter the CNS to disrupt its homeosta- sis, a phenomenon we named the gateway reflex. Regional neural inputs such as grav ity, electricity, pain or chronic stress cause specific neural activation to create a gateway of immune cells, particularly pathogenic ones, at specific blood vessels. Moreover, the recently discovered stress-induced gateway reflex uncovered a stress-induced neural link between the brain, gastrointestine, and heart. Thus, the gateway reflex is critical for the homeostasis of various organs, and aberrant activation of neural pathways by the gateway reflex disrupts normal organ homeostasis. The inflammatory reflex is another mechanism for local neuro-immune interactions. It potently exerts a cholinergic anti- inflammatory effect on various disease conditions. In this section, we discuss emerging roles for local neuro-immune interactions, with a special focus on the gateway reflex. sympathetic ganglion (4) and induces the activation of sympathetic nerves (5), which results in norepinephrine (NE) secretion (6) at the L5 dorsal vessels. NE enhances the inflammation amplifier in the L5 dorsal vessels, causing an upregulation of chemokines and recruiting pathogenic CD4+ T cells from the vessels (7).
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