Cameron D J
Jpn J Exp Med. 1987 Feb;57(1):31-9.
The role of enkephalins, endorphins and other neuropeptides produced by the nervous system in the alteration of immune responsiveness is generally unknown. The present studies were undertaken to investigate the role of these neuropeptides in the modulation of cytotoxicity induced by LPS activated macrophages obtained from normal donors as well as breast cancer and Hodgkins disease patients. When the macrophages from normal donors were pretreated with these neuropeptides for 1 hr prior to co-culturing with target cells, macrophage mediated cytotoxicity was enhanced with 10(-6) M and 10(-8) M of [met]-enkephalin, 10(-6) M of [leu]-enkephalin and 10(-6) M and 10(-12) M of alpha-endorphin. However, when the macrophages were co-cultured with target cells in the presence of the neuropeptides, it was observed that 10(-6) M and 10(-12) M of alpha-endorphin enhanced cytotoxicity whereas no enhancement in cytotoxicity was observed when [met]-enkephalin or [leu]-enkephalin were added to the cultures. In fact, it appears that 10(-10) M of [met]-enkephalin and 10(-12) M of [leu]-enkephalin actually suppressed macrophage mediated cytotoxicity. When the opioid antagonist Naloxone was incubated with the neuropeptides in the presence of the macrophages the enhancement of macrophage killing produced by [met]-enkephalin, [leu]-enkephalin or alpha-endorphin was suppressed. When the breast cancer patients' macrophages were pretreated with these neuropeptides, enhancement in cytotoxicity was observed at 10(-10) M of [met]-enkephalin, and [leu]-enkephalin and at 10(-8) M and 10(-12) M of alpha-endorphin.(ABSTRACT TRUNCATED AT 250 WORDS)
由神经系统产生的脑啡肽、内啡肽及其他神经肽在免疫反应性改变中的作用通常尚不清楚。本研究旨在探讨这些神经肽在调节由正常供体以及乳腺癌和霍奇金病患者的脂多糖激活巨噬细胞诱导的细胞毒性中的作用。当来自正常供体的巨噬细胞在与靶细胞共培养前用这些神经肽预处理1小时时,巨噬细胞介导的细胞毒性在10(-6)M和10(-8)M的[甲硫氨酸]-脑啡肽、10(-6)M的[亮氨酸]-脑啡肽以及10(-6)M和10(-12)M的α-内啡肽作用下增强。然而,当巨噬细胞在神经肽存在下与靶细胞共培养时,观察到10(-6)M和10(-12)M的α-内啡肽增强了细胞毒性,而当向培养物中添加[甲硫氨酸]-脑啡肽或[亮氨酸]-脑啡肽时未观察到细胞毒性增强。事实上,似乎10(-10)M的[甲硫氨酸]-脑啡肽和10(-12)M的[亮氨酸]-脑啡肽实际上抑制了巨噬细胞介导的细胞毒性。当阿片类拮抗剂纳洛酮在巨噬细胞存在下与神经肽一起孵育时,[甲硫氨酸]-脑啡肽、[亮氨酸]-脑啡肽或α-内啡肽产生的巨噬细胞杀伤增强被抑制。当用这些神经肽预处理乳腺癌患者的巨噬细胞时,在10(-10)M的[甲硫氨酸]-脑啡肽、[亮氨酸]-脑啡肽以及10(-8)M和10(-12)M的α-内啡肽作用下观察到细胞毒性增强。(摘要截短至250字)