Merrill J E
Department of Neurology, Reed Neurological Research Center, UCLA School of Medicine.
Dev Neurosci. 1991;13(3):130-7. doi: 10.1159/000112150.
Microglia and astrocytes undergo proliferative and differentiative changes in vivo after trauma or diseases such as multiple sclerosis (MS). Oligodendrocytes are destroyed in lesions in MS. Interleukin-1 (IL1) and tumor necrosis factor-alpha (TNF alpha) are involved in inflammation of the central nervous system and are elevated in MS. We have investigated the changes in cell morphology and cell number induced by IL1 and TNF alpha in purified and mixed populations of primary rat brain microglia, astrocytes, oligodendrocytes, and glial precursors. Depending on the target population, proliferation, differentiation, or inhibition of cultured cells was observed. The data also suggest that interactions among cell populations occur and support the hypothesis that IL1 and TNF alpha effects may be indirect, possibly through induction of other factors.
在遭受创伤或诸如多发性硬化症(MS)等疾病后,小胶质细胞和星形胶质细胞会在体内发生增殖和分化变化。少突胶质细胞在MS的病灶中会被破坏。白细胞介素-1(IL1)和肿瘤坏死因子-α(TNFα)参与中枢神经系统的炎症反应,且在MS中水平升高。我们研究了IL1和TNFα对原代大鼠脑小胶质细胞、星形胶质细胞、少突胶质细胞和神经胶质前体细胞的纯化及混合群体所诱导的细胞形态和细胞数量变化。根据目标细胞群体的不同,观察到了培养细胞的增殖、分化或抑制现象。数据还表明细胞群体之间存在相互作用,并支持这样的假说,即IL1和TNFα的作用可能是间接的,可能是通过诱导其他因子来实现的。