Chambers D A, Cohen R L, Perlman R L
Department of Biochemistry, University of Illinois, Chicago 60612.
Neurochem Int. 1993 Feb;22(2):95-110. doi: 10.1016/0197-0186(93)90002-m.
In recent years, much interest has centered on the commonalities and bi-directional interactions between the nervous system and the immune system. This review focuses on mechanisms through which, catecholamines, a class of neuro-endocrine molecules, modulate immune functions. Catecholamines can be immune suppressive and inhibit lymphocyte activation of both T and B cells as well as the generation of immune-mediated anti-tumor responses. Some of these catecholamine-regulated activities appear to be modulated through the second messenger, cyclic AMP, whereas others appear to be catecholamine-dependent but cyclic AMP independent. Further delineation of the interacting ligand-receptor complexes, populations of responding cells and signal transduction mechanisms leading to the activation of specifically involved genes and gene products, will lead to enhanced understanding of the integratory functions of the nervous system in immune responses, the biology of stress, the role of stress-associated molecular mechanisms in perturbations of physiological homeostasis and the development of a new biological psychiatry with accompanying rational therapeutic modalities.
近年来,人们的诸多兴趣集中在神经系统与免疫系统之间的共性及双向相互作用上。本综述聚焦于一类神经内分泌分子——儿茶酚胺调节免疫功能的机制。儿茶酚胺具有免疫抑制作用,可抑制T细胞和B细胞的淋巴细胞活化以及免疫介导的抗肿瘤反应的产生。这些儿茶酚胺调节的活动中,有些似乎是通过第二信使环磷酸腺苷(cAMP)介导的,而另一些则似乎依赖于儿茶酚胺但不依赖于cAMP。进一步阐明相互作用的配体-受体复合物、反应细胞群体以及导致特定相关基因和基因产物激活的信号转导机制,将有助于增强对神经系统在免疫反应中的整合功能、应激生物学、应激相关分子机制在生理稳态扰动中的作用以及伴随合理治疗方式的新生物精神病学发展的理解。