Cookson M R, Mead C, Austwick S M, Pentreath V W
Department of Biological Sciences, University of Salford, Salford M5 4WT, UK.
Toxicol In Vitro. 1995 Feb;9(1):39-48. doi: 10.1016/0887-2333(94)00193-x.
Primary cultures of rat cortical astrocytes were exposed to 25 neurotoxic and non-neurotoxic compounds for 24 hr over a concentration range of 0.001 to 1000 mug/ml and the effects were quantified using the MTT assay. EC(50) values were obtained for nine of the compounds in the tested range, while increases in MTT conversion were seen at sub-cytotoxic concentrations for 12 compounds. The concentrations causing activation of this system were found, with some exceptions (notably organotin compounds) to be similar to those previously reported to cause increases in expression of the astrocyte marker glial fibrillary acidic protein. MTT conversion was also measured in the C6 cell line and, with some exceptions, the response to toxicants was found to be the same as that in the primary cultures of astrocytes. However, this was only the case when the C6 cells were pretreated for 48 hr with 0.5 mM dibutyryl cyclic AMP. This study represents the first direct comparison between primary astrocytes and C6 cells using a broad range of chemical neurotoxicants.
将大鼠皮质星形胶质细胞的原代培养物暴露于25种神经毒性和非神经毒性化合物中24小时,浓度范围为0.001至1000微克/毫升,并使用MTT法对其效果进行定量分析。在测试范围内,9种化合物获得了半数有效浓度(EC50)值,而12种化合物在亚细胞毒性浓度下MTT转化率增加。发现激活该系统的浓度,除了一些例外情况(特别是有机锡化合物),与先前报道的导致星形胶质细胞标志物胶质纤维酸性蛋白表达增加的浓度相似。还在C6细胞系中测量了MTT转化率,除了一些例外情况,发现对毒物的反应与星形胶质细胞原代培养物中的反应相同。然而,只有当C6细胞用0.5 mM二丁酰环磷腺苷预处理48小时时才是这种情况。本研究是首次使用广泛的化学神经毒物对原代星形胶质细胞和C6细胞进行直接比较。