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P 物质对 NK92-MI 细胞细胞毒性的调节。

Regulation of NK92-MI cell cytotoxicity by substance P.

机构信息

Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, China.

出版信息

Scand J Immunol. 2011 Aug;74(2):107-13. doi: 10.1111/j.1365-3083.2011.02550.x.

Abstract

The neuropeptide substance P (SP) can regulate a number of immunological functions in vitro and in vivo and may regulate natural killer (NK) cell activity. Here, we investigated whether SP has a role in regulating NK92-MI cell function in vitro, and how it influences NK cell activity. We found that SP dose dependently increased the cytotoxicity of NK92-MI cells and had a maximal effect at a concentration of 10(-12) and 10(-10) m. Furthermore, the expression of cytotoxic-associated molecules (perforin, granzyme) and activating receptor NKp46 [a member of natural cytotoxicity receptors (NCRs)] was observed to be upregulated by SP at optimal concentration, at which SP enhanced the cytotoxicity of NK92-MI cells. Neurokinin-1 receptor (NK-1R), a functional receptor of SP, was found on NK92-MI cells, and the observed effects of SP on NK92-MI cells could be more partially blocked by an NK-1R antagonist. Our data suggest that SP induces NK92-MI cell cytotoxicity by directly increasing the expression of cytotoxic granules and upregulates NK92-MI cell receptor-mediated functions indirectly. Thus, SP may regulate NK cell function mainly through NK-1R.

摘要

神经肽 P 物质(SP)可在体外和体内调节多种免疫功能,可能调节自然杀伤(NK)细胞活性。在这里,我们研究了 SP 是否在体外调节 NK92-MI 细胞功能,以及它如何影响 NK 细胞活性。我们发现 SP 呈浓度依赖性地增加 NK92-MI 细胞的细胞毒性,在 10(-12) 和 10(-10) m 的浓度下具有最大作用。此外,在最佳浓度下,观察到 SP 上调了与细胞毒性相关的分子(穿孔素、颗粒酶)和激活受体 NKp46(自然细胞毒性受体(NCR)的成员)的表达,SP 增强了 NK92-MI 细胞的细胞毒性。NK92-MI 细胞上存在 SP 的功能性受体神经激肽-1 受体(NK-1R),并且 SP 对 NK92-MI 细胞的观察到的作用可以被 NK-1R 拮抗剂部分阻断。我们的数据表明,SP 通过直接增加细胞毒性颗粒的表达诱导 NK92-MI 细胞的细胞毒性,并间接上调 NK92-MI 细胞受体介导的功能。因此,SP 可能主要通过 NK-1R 调节 NK 细胞功能。

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