Leibovic K N
J Neurosci Methods. 1986 Feb;15(4):301-6. doi: 10.1016/0165-0270(86)90143-3.
We have formulated a medium in which an electroretinogram (ERG) can be elicited from eyecup pieces of Bufo marinus up to 2 weeks after dissection. At the same time the retina can be dissociated into healthy, intact photoreceptors and other cells after soaking in the same medium from 4 to 24 h. Thus, no enzymes need be used which have deleterious effects on the cells; on the contrary the medium extends cell viability. Clearly, this method should be attractive in electrophysiological and biochemical studies.
我们已经配制出一种培养基,在这种培养基中,从海蟾蜍的眼杯切片上,在解剖后长达2周的时间里都能引出视网膜电图(ERG)。同时,将视网膜在同一培养基中浸泡4至24小时后,可解离成健康、完整的光感受器和其他细胞。因此,无需使用对细胞有有害影响的酶;相反,这种培养基能延长细胞活力。显然,这种方法在电生理学和生物化学研究中应该很有吸引力。