Masland R H, Mills J W
J Cell Biol. 1979 Oct;83(1):159-78. doi: 10.1083/jcb.83.1.159.
Rabbit retinas were studied in vitro under conditions known to maintain their physiological function. Retinas incubated in the presence of [3H]choline synthesized substantial amounts of both [3H]phosphorylcholine and [3H]acetylcholine. With time, [3H]phosphorylcholine proceeded into phospholipids, primarily phosphatidylcholine. Retinas pulse-labeled by a 15-min exposure to 0.3 microM [3H]choline were incubated for a subsequent hour under chase conditions designed either to retain newly synthesized acetylcholine within synapses or to promote its release. At the end of this time the two groups of retinas were found to contain equal amounts of radioactivity in the phospholipid pathway, but only the retinas incubated under the acetylcholine-protecting conditions contained [3H]acetylcholine. Freeze-dried, vacuum-embedded tissue from each retina was autoradiographed on dry emulsion. All retinas showed silver grains over the photoreceptor cells and faint labeling of all ganglion cells. In the retinas that contained [3H]acetylcholine, silver grains also accumulated densely over a few cells with the position of amacrine cells, over a subset of the cells of the ganglion cell layer, and in two bands over the inner plexiform layer. Fixation of the retina with aqueous osmium tetroxide retained only the radioactive compounds located in the photoreceptor and ganglion cells. Sections from freeze-dried tissue lost their water-soluble choline metabolites when exposed to water, and autoradiography of such sections again revealed radioactivity primarily in the photoreceptor and ganglion cells. Radioactive compounds extracted from the sections were found to faithfully reflect those present in the tissue before processing; analysis of the compounds eluted from sections microdissected along the outer plexiform layer showed [3H]acetylcholine to have been synthesized only by cells of the inner retina. Taken together, these results indicate that the photoreceptor and ganglion cells are distinguished by a rapid synthesis of choline-containing phospholipids, while acetylcholine synthesis is restricted to a few cells at both margins of the inner plexiform layer. They imply that the only neurons to release acetylcholine within the rabbit retina are a small group of probable amacrine cells.
在已知能维持其生理功能的条件下,对兔视网膜进行了体外研究。在含有[3H]胆碱的情况下孵育的视网膜合成了大量的[3H]磷酸胆碱和[3H]乙酰胆碱。随着时间的推移,[3H]磷酸胆碱进入磷脂,主要是磷脂酰胆碱。用0.3微摩尔[3H]胆碱进行15分钟脉冲标记的视网膜,随后在旨在将新合成的乙酰胆碱保留在突触内或促进其释放的追踪条件下孵育1小时。在这段时间结束时,发现两组视网膜在磷脂途径中含有等量的放射性,但只有在乙酰胆碱保护条件下孵育的视网膜含有[3H]乙酰胆碱。将每个视网膜的冻干、真空包埋组织在干乳剂上进行放射自显影。所有视网膜在光感受器细胞上均显示出银颗粒,并且所有神经节细胞均有微弱标记。在含有[3H]乙酰胆碱的视网膜中,银颗粒也密集地聚集在一些具有无长突细胞位置的细胞上、神经节细胞层的一部分细胞上以及内网状层的两条带中。用水溶性四氧化锇固定视网膜仅保留了位于光感受器和神经节细胞中的放射性化合物。冻干组织的切片在接触水时失去了其水溶性胆碱代谢物,并且此类切片的放射自显影再次显示放射性主要存在于光感受器和神经节细胞中。从切片中提取的放射性化合物被发现如实地反映了处理前组织中存在的化合物;对沿外网状层显微切割的切片洗脱的化合物进行分析表明,[3H]乙酰胆碱仅由内视网膜的细胞合成。综上所述,这些结果表明,光感受器和神经节细胞的特征是快速合成含胆碱的磷脂,而乙酰胆碱的合成仅限于内网状层两侧的少数细胞。它们意味着在兔视网膜内释放乙酰胆碱的唯一神经元是一小群可能的无长突细胞。