MODULATION OF CHEMILUMINESCENCE IN A MURINE MACROPHAGE CELL-LINE BY NEUROENDOCRINE HORMONES

被引:35
作者
TOSK, JM
GRIM, JR
KINBACK, KM
SALE, EJ
BOZZETTI, LP
WILL, AD
机构
[1] JERRY L PETTIS MEM VET AFFAIRS MED CTR, NEUROL SERV, LOMA LINDA, CA USA
[2] LOMA LINDA UNIV, SCH MED, DEPT PSYCHIAT, LOMA LINDA, CA 92354 USA
[3] LOMA LINDA UNIV, SCH MED, DEPT NEUROL, LOMA LINDA, CA 92354 USA
[4] LOMA LINDA UNIV, SCH MED, DEPT BIOL, LOMA LINDA, CA 92354 USA
[5] LOMA LINDA UNIV, SCH MED, DEPT PHYSIOL, LOMA LINDA, CA 92354 USA
来源
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY | 1993年 / 15卷 / 05期
基金
美国国家科学基金会;
关键词
D O I
10.1016/0192-0561(93)90079-E
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:615 / 620
页数:6
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