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负责自然杀伤细胞活性条件增强的传出信号。

Efferent signal(s) responsible for the conditioned augmentation of natural killer cell activity.

作者信息

Hsueh C M, Tyring S K, Hiramoto R N, Ghanta V K

机构信息

Department of Microbiology, University of Alabama at Birmingham 35294, USA.

出版信息

Neuroimmunomodulation. 1994 Jan;1(1):74-81. doi: 10.1159/000097093.

Abstract

In in vivo studies, a conditioned increase in NK cell activity can be obtained by pairing odor of camphor (conditioned stimulus, CS) with poly I:C (unconditioned stimulus, US) in a single-association paradigm. We identified interferon (IFN) as the signal that reaches the central nervous system (CNS) to make an association with the camphor CS. We have also established that the CS/US association is an IFN-dependent step, and the expression stage is an opioid-dependent pathway which can be blocked with naltrexone and dexamethasone. Here we have focused on the signals responsible for the expression of conditioned augmentation of natural killer (NK) cell activity. The possible efferent signal molecules that were considered were IFN, beta-endorphin (beta-END), and adrenocorticotropic hormone (ACTH). Plasma levels of beta-END and ACTH of conditioned and control mice were quantitated by radioimmunoassay, and the changes in IFN message in the spleen cells were determined by Northern hybridization analysis. Results indicate that the ACTH levels and IFN-alpha gene expression were higher in the conditioned animals than in the controls. These studies support the view that ACTH released from the pituitary gland is involved in the up-regulation of IFN-alpha, which in turn stimulates the NK cells in the spleen.

摘要

在体内研究中,通过在单联想范式中将樟脑气味(条件刺激,CS)与聚肌胞苷酸(非条件刺激,US)配对,可以使自然杀伤(NK)细胞活性出现条件性增加。我们确定干扰素(IFN)是到达中枢神经系统(CNS)并与樟脑CS建立联想的信号。我们还证实,CS/US联想是一个依赖IFN的步骤,而表达阶段是一条依赖阿片类物质的途径,可被纳曲酮和地塞米松阻断。在此,我们聚焦于负责自然杀伤(NK)细胞活性条件性增强表达的信号。所考虑的可能传出信号分子为IFN、β-内啡肽(β-END)和促肾上腺皮质激素(ACTH)。通过放射免疫分析法对条件性小鼠和对照小鼠血浆中的β-END和ACTH水平进行定量,并通过Northern杂交分析确定脾细胞中IFN信息的变化。结果表明,条件性动物的ACTH水平和IFN-α基因表达高于对照动物。这些研究支持这样一种观点,即从垂体释放的ACTH参与了IFN-α的上调,而IFN-α反过来刺激脾脏中的NK细胞。

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