Abrams L, Politi L E, Adler R
Retinal Degenerations Research Center, Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Invest Ophthalmol Vis Sci. 1989 Nov;30(11):2300-8.
Dissociated cultures of mouse retinal neurons and photoreceptors in chemically defined medium were used to investigate the susceptibility of these cells to the neurotoxin kainic acid (KA). Cells isolated from the newborn mouse retina were initially insensitive to this toxin, and the cells that differentiated as rod photoreceptors retained this resistance throughout the culture period. However, amacrine neurons became increasingly sensitive to KA toxicity as they differentiated in culture; after the fifth day in vitro approximately 90% of these cells were killed by KA in a concentration- and time-dependent fashion. The neurons showed pronounced swelling within 10 min of treatment onset, and cell lysis and nuclear fragmentation were evident during the next few hours. KA-induced degeneration of these neurons was corroborated using the amacrine cell-specific monoclonal antibody HPC-1, as well as autoradiographic and biochemical determinations of the high affinity uptake for GABA. This inhibitory neurotransmitter was taken up by amacrine neurons but not by photoreceptor cells, and this uptake was completely abolished in KA-treated cultures. Similar results were obtained with the neuronal enzyme choline acetyltransferase. However, both photoreceptor survival and the expression of photoreceptor markers such as opsin and the retinoid-binding protein interphotoreceptor (IRBP) were similar in KA-treated and control cultures. Similarly, the high affinity uptake of glutamate, an excitatory amino acid which is predominantly taken up by photoreceptors, showed only modest changes in KA-treated cultures.(ABSTRACT TRUNCATED AT 250 WORDS)
在化学成分明确的培养基中培养的小鼠视网膜神经元和光感受器的解离培养物,被用于研究这些细胞对神经毒素海人藻酸(KA)的敏感性。从新生小鼠视网膜分离的细胞最初对这种毒素不敏感,分化为视杆光感受器的细胞在整个培养期间都保持这种抗性。然而,无长突神经元在培养中分化时对KA毒性变得越来越敏感;在体外培养的第五天后,约90%的这些细胞以浓度和时间依赖性方式被KA杀死。神经元在处理开始后10分钟内出现明显肿胀,在接下来的几个小时内细胞裂解和核碎裂明显。使用无长突细胞特异性单克隆抗体HPC-1以及对GABA高亲和力摄取的放射自显影和生化测定,证实了KA诱导的这些神经元的变性。这种抑制性神经递质被无长突神经元摄取,但不被光感受器细胞摄取,并且在KA处理的培养物中这种摄取完全被消除。神经元酶胆碱乙酰转移酶也得到了类似的结果。然而,在KA处理的培养物和对照培养物中,光感受器的存活以及视蛋白和视网膜色素结合蛋白等光感受器标志物的表达相似。同样,主要被光感受器摄取的兴奋性氨基酸谷氨酸的高亲和力摄取,在KA处理的培养物中仅显示出适度变化。(摘要截短至250字)