Weiler R, Schultz K
Department of Neurobiology, University of Oldenburg, Germany.
Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6533-7. doi: 10.1073/pnas.90.14.6533.
Horizontal cells invaginate the photoreceptors in the retina and form reciprocal synaptic connections in the cone pedicles. In fish retina the pattern of synaptic connections is plastic and modulated by the ambient light conditions. Numerous dendritic spinules protrude from the terminal horizontal-cell dendrites into the cone pedicle when the retina is light-adapted and are retracted during dark adaptation. The retraction of spinules can be induced during maintained illumination by an injection of the putative cone transmitter L-glutamate or its analogue kainic acid into the vitreous humor. The formation and the retraction of spinules have a time course of minutes. Activation of protein kinase C through phorbol esters initiates the formation of spinules, but the retraction has not yet been linked to a specific second messenger. Herein we report that physiological concentrations of the glutamate analogs quisqualic acid and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid induce retraction of spinules during maintained illumination. (+/-)-trans-1-Amino-1,3-cyclopentanedicarboxylic acid, an agonist for the metabotropic quisqualic acid receptor, was without effect on spinule retraction. N-Methyl-D-aspartate and L-2-amino-4-phosphonobutyric acid, agonists at other types of glutamate receptors, were also without any effect. The effects of the active agonists persisted when synaptic transmission was blocked. In the presence of the ionotropic quisqualate receptor antagonist 6-cyclo-7-nitro-quinoxaline-2,3-dione the effects of all active agonists were blocked. These results demonstrate that activation of ionotropic quisqualate receptors on the horizontal-cell membrane can induce dendritic spinule retraction, a process associated with dark adaptation.
水平细胞内陷视网膜中的光感受器,并在视锥细胞终足处形成相互的突触连接。在鱼类视网膜中,突触连接模式具有可塑性,并受环境光条件调节。当视网膜适应光照时,许多树突棘从水平细胞终末树突突出到视锥细胞终足内,而在暗适应过程中这些树突棘会缩回。在持续光照期间,向玻璃体内注射假定的视锥细胞递质L-谷氨酸或其类似物 kainic 酸可诱导树突棘缩回。树突棘的形成和缩回过程持续数分钟。通过佛波酯激活蛋白激酶C可引发树突棘的形成,但缩回过程尚未与特定的第二信使联系起来。在此我们报告,谷氨酸类似物quisqualic酸和α-氨基- 3-羟基-5-甲基-4-异恶唑丙酸的生理浓度在持续光照期间可诱导树突棘缩回。(±)-反式-1-氨基-1,3-环戊烷二羧酸,一种促代谢型 quisqualic 酸受体激动剂,对树突棘缩回没有影响。N-甲基-D-天冬氨酸和L-2-氨基-4-膦酰丁酸,其他类型谷氨酸受体的激动剂,也没有任何作用。当突触传递被阻断时,活性激动剂的作用仍然存在。在离子型 quisqualate 受体拮抗剂6-环-7-硝基喹喔啉-2,3-二酮存在的情况下,所有活性激动剂的作用都被阻断。这些结果表明,水平细胞膜上离子型 quisqualate 受体的激活可诱导树突棘缩回,这一过程与暗适应相关。