Tosk J M, Grim J R, Kinback K M, Sale E J, Bozzetti L P, Will A D
Psychiatry and Service, Jerry L. Pettis Memorial Veterans' Affairs Medical Center, Loma Linda, California 92357.
Int J Immunopharmacol. 1993 Jul;15(5):615-20. doi: 10.1016/0192-0561(93)90079-e.
This study determined the effects of neuropeptides and neuroendocrine hormones at the cellular level of the immune response using a murine macrophage cell line, J774, which exhibits a chemiluminescent oxidative burst upon acute stimulation with zymosan. We report that the zymosan-triggered oxidative burst of J774 cells can be modulated by the opioid peptides beta-endorphin (beta-END) and dynorphin A (DYN) in a naloxone-reversible fashion. Norepinephrine (NE) also modulated chemiluminescence (CL) emission of J774 cells, with dose-dependent suppression of CL dependent upon co-incubation with gamma-interferon (gamma-INF). Without gamma-INF co-incubation, NE shared with the opioid peptides beta-END and DYN the ability to modulate oxidative burst, producing an inverted-U dose response. These data indicate that J774 cells may be useful for explaining some mechanisms through which the neuroendocrine system interacts with the immune system.
本研究利用小鼠巨噬细胞系J774,在免疫反应的细胞水平上确定了神经肽和神经内分泌激素的作用。J774细胞在用酵母聚糖急性刺激时会产生化学发光氧化爆发。我们报告称,J774细胞由酵母聚糖引发的氧化爆发可被阿片肽β-内啡肽(β-END)和强啡肽A(DYN)以纳洛酮可逆的方式调节。去甲肾上腺素(NE)也可调节J774细胞的化学发光(CL)发射,CL的剂量依赖性抑制取决于与γ-干扰素(γ-INF)的共同孵育。在没有γ-INF共同孵育的情况下,NE与阿片肽β-END和DYN一样具有调节氧化爆发的能力,产生倒U型剂量反应。这些数据表明,J774细胞可能有助于解释神经内分泌系统与免疫系统相互作用的一些机制。