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中枢神经系统和神经内分泌系统中的白细胞介素-1受体。在感染和应激中的作用。

Receptors for interleukin-1 in the central nervous and neuroendocrine systems. Role in infection and stress.

作者信息

Haour F, Marquette C, Ban E, Crumeyrolle-Arias M, Rostene W, Tsiang H, Fillion G

机构信息

Pharmacologie Neuro-Immuno-Endocrinienne, Institut Pasteur, Paris.

出版信息

Ann Endocrinol (Paris). 1995;56(3):173-9.

PMID:7677401
Abstract

The functional interactions between the Immune (IS) and the Central Nervous Systems (CNS) are clearly indicated by the fact these systems are sharing mediators and receptors. Interleukins and more specifically Interleukin-1 (IL-1) have been shown to be powerful regulators of both system activity which suggested IL-1 receptors in the CNS. IL-1 receptors, similar to type I lymphocyte receptors, have been characterized in murine nervous structures (dentate gyrus of the hippocampus and frontal cortex), in vascular structures (vessels, choroid plexus) and in a neuroendocrine structure (anterior pituitary). Stimulation of the immune system and of IL-1 synthesis by bacterial product (intra peritoneal injection of LPS) induced a marked decrease of IL-1 receptor levels in the CNS. Under the same conditions pituitary receptors were unaffected indicating the autonomy of brain functioning. This decrease is in relation with an increase in local IL-1 synthesis as indicated by the increase of IL-1 mRNA in the brain tissue. During viral infection (rabies virus) very similar results are observed. Brain receptors are decreasing in the brain at day 4 post infection while IL-1 concentration is increasing in the brain tissue. Pituitary receptors are not modified during the evolution of the disease. Stress and glucocorticoid treatment are strong inhibitors of immune functions by inhibiting IL-1 synthesis. Neither treatment modified brain receptors suggesting that IL-1 synthesis is not modulated by glucocorticoids in the CNS as in the immune system. However an increase in pituitary receptor level was observed in both cases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

免疫系统(IS)与中枢神经系统(CNS)之间的功能相互作用通过以下事实得到明确体现:这两个系统共享介质和受体。白细胞介素,尤其是白细胞介素-1(IL-1),已被证明是这两个系统活动的强大调节因子,这表明中枢神经系统中存在IL-1受体。与I型淋巴细胞受体相似的IL-1受体,已在小鼠神经结构(海马齿状回和额叶皮质)、血管结构(血管、脉络丛)和神经内分泌结构(垂体前叶)中得到表征。细菌产物(腹腔注射LPS)刺激免疫系统并诱导IL-1合成,导致中枢神经系统中IL-1受体水平显著降低。在相同条件下,垂体受体未受影响,表明脑功能具有自主性。这种降低与脑组织中IL-1 mRNA增加所表明的局部IL-1合成增加有关。在病毒感染(狂犬病病毒)期间,观察到非常相似的结果。感染后第4天,脑内的脑受体减少,而脑组织中的IL-1浓度增加。在疾病发展过程中,垂体受体未发生改变。应激和糖皮质激素治疗通过抑制IL-1合成,是免疫功能的强抑制剂。两种治疗均未改变脑受体,这表明中枢神经系统中的IL-1合成不像免疫系统那样受糖皮质激素调节。然而,在这两种情况下均观察到垂体受体水平增加。(摘要截短于250字)

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引用本文的文献

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Regulation of brain interleukin-1 beta (IL-1 beta) system mRNAs in response to pathophysiological concentrations of IL-1 beta in the cerebrospinal fluid.脑脊液中白细胞介素-1β(IL-1β)病理生理浓度对脑白细胞介素-1β系统mRNA的调节作用。
J Mol Neurosci. 1996 Fall;7(3):169-81. doi: 10.1007/BF02736838.