Pettmann B, Labourdette G, Devilliers G, Sensenbrenner M
Dev Neurosci. 1981;4(1):37-45. doi: 10.1159/000112739.
Different soluble extracts were prepared from chick brains and tested for their effect on the development of glial cells prepared from the cerebral hemispheres of newborn rats and grown in primary culture. Every brain extract tested, from animals between 8 days embryonic and adult ages, stimulated astroblast proliferation and accelerated their maturation as shown by morphological changes, the appearance of gliofilament bundles and by the increase of the amount of the glial-specific protein S-100 between 10 and 40 days in culture. These effects were observed in cultures continuously treated with extracts beginning with the 5th day after seeding. In cultures in which treatment was stopped 25 days after seeding, S-100 level continued to increase like in continuously treated cells. An identical increase of S-100 protein level was induced by treatments started as early as 24 h or as late as 25 days after seeding. In contrast, when the extracts were added at time 0 a toxic effect was observed and no stimulation of the maturation occurred.
从鸡脑中制备了不同的可溶性提取物,并测试了它们对新生大鼠大脑半球制备的神经胶质细胞发育的影响,这些细胞在原代培养中生长。所测试的每种脑提取物,均来自胚胎8天至成年期的动物,刺激了成星形细胞的增殖,并加速了它们的成熟,这表现为形态变化、胶质丝束的出现以及培养10至40天期间神经胶质特异性蛋白S-100含量的增加。从接种后第5天开始用提取物持续处理的培养物中观察到了这些效应。在接种后25天停止处理的培养物中,S-100水平继续像在持续处理的细胞中一样增加。早在接种后24小时或晚至25天开始的处理诱导了S-100蛋白水平的相同增加。相反,当在时间0添加提取物时,观察到有毒作用,并且没有刺激成熟发生。