Hanisch Uwe-Karsten
Department of Cellular Neurosciences, Max Delbrück Center for Molecular Medicine, Berlin-Buch, Germany.
University of Applied Sciences Lausitz, Senftenberg, Germany.
Glia. 2002 Nov;40(2):140-155. doi: 10.1002/glia.10161.
Cytokines constitute a significant portion of the immuno- and neuromodulatory messengers that can be released by activated microglia. By virtue of potent effects on resident and invading cells, microglial cyto- and chemokines regulate innate defense mechanisms, help the initiation and influence the type of immune responses, participate in the recruitment of leukocytes to the CNS, and support attempts of tissue repair and recovery. Microglia can also receive cyto- and chemokine signals as part of auto- and paracrine communications with astrocytes, neurons, the endothelium, and leukocyte infiltrates. Strong responses and modulatory influences can be demonstrated, adding to the emerging view that microglial behavior is highly dependent on the (cytokine) environment and that reactions to a challenge may vary with the stimulation context. In principle, microglial activation aims at CNS protection. However, failed microglial engagement due to excessive or sustained activation could significantly contribute to acute and chronic neuropathologies. Dysregulation of microglial cytokine production could thereby promote harmful actions of the defense mechanisms, result in direct neurotoxicity, as well as disturb neural cell functions as they are sensitive to cytokine signaling.
细胞因子构成了免疫和神经调节信使的重要部分,这些信使可由活化的小胶质细胞释放。凭借对驻留细胞和侵入细胞的强大作用,小胶质细胞的细胞因子和趋化因子调节先天防御机制,帮助启动并影响免疫反应的类型,参与白细胞向中枢神经系统的募集,并支持组织修复和恢复的尝试。小胶质细胞还可以接收细胞因子和趋化因子信号,作为与星形胶质细胞、神经元、内皮细胞和白细胞浸润进行自分泌和旁分泌通讯的一部分。可以证明存在强烈的反应和调节影响,这进一步支持了一种新出现的观点,即小胶质细胞的行为高度依赖于(细胞因子)环境,并且对挑战的反应可能因刺激背景而异。原则上,小胶质细胞的激活旨在保护中枢神经系统。然而,由于过度或持续激活导致小胶质细胞参与失败,可能会显著促成急性和慢性神经病理学。小胶质细胞细胞因子产生的失调可能会因此促进防御机制的有害作用,导致直接神经毒性,并扰乱对细胞因子信号敏感的神经细胞功能。