Gehrmann J, Mies G, Bonnekoh P, Banati R, Iijima T, Kreutzberg G W, Hossmann K A
Max-Planck-Institute of Psychiatry, Department of Neuromorphology, Martinsried/Munich, Germany.
Brain Pathol. 1993 Jan;3(1):11-7. doi: 10.1111/j.1750-3639.1993.tb00720.x.
The response of microglial cells to cortical spreading depression (CSD) was studied in rat brain by immunocytochemistry. CSD was elicited for one hour by the topical application of 4M potassium chloride solution and the microglial reaction examined immunocytochemically after 4, 16, 24 and 72 hours. CSD was sufficient to induce a microglial reaction throughout the cortex at 24 hours. Activated microglial cells furthermore showed a striking de-novo expression of major histocompatibility complex class II antigens. In contrast, no microglial reaction was observed in the cortex of sham-operated animals. This microglial reaction in response to CSD was not associated with histologically detectable neuronal damage. These results support the view that microglial cells are extremely sensitive to changes of the brain microenvironment. Their activation may be related to changes of ion homeostasis in the brain which are not sufficient to trigger neuronal injury.
通过免疫细胞化学方法,在大鼠脑内研究了小胶质细胞对皮质扩散性抑制(CSD)的反应。通过局部应用4M氯化钾溶液引发CSD持续1小时,并在4、16、24和72小时后通过免疫细胞化学检查小胶质细胞反应。CSD足以在24小时时诱导整个皮质的小胶质细胞反应。此外,活化的小胶质细胞显示出主要组织相容性复合体II类抗原的显著重新表达。相比之下,假手术动物的皮质中未观察到小胶质细胞反应。这种对CSD的小胶质细胞反应与组织学上可检测到的神经元损伤无关。这些结果支持这样的观点,即小胶质细胞对脑微环境的变化极其敏感。它们的激活可能与脑中离子稳态的变化有关,而这些变化不足以引发神经元损伤。