Properties of Exocytotic Response in Vertebrate Photoreceptors

• Published in: Journal of neurophysiology 2003-07, Vol.90 (1), p.218-225
• Main Authors: Kreft, M, Krizaj, D, Grilc, S, Zorec, R
• Format: Article
• Language: English
• Subjects: Ambystoma tigrinum; Animals; Calcium - metabolism; Calcium-Binding Proteins; Caudata; Cell Culture Techniques; Egtazic Acid - analogs & derivatives; Exocytosis; Freshwater; Glutamic Acid - secretion; Immunohistochemistry; Membrane Glycoproteins - analysis; Microscopy, Confocal; Nerve Tissue Proteins - analysis; Patch-Clamp Techniques; Photolysis; Presynaptic Terminals - physiology; Retina - physiology; Retinal Cone Photoreceptor Cells - chemistry; Retinal Cone Photoreceptor Cells - metabolism; Retinal Cone Photoreceptor Cells - physiology; Retinal Rod Photoreceptor Cells - chemistry; Retinal Rod Photoreceptor Cells - metabolism; Retinal Rod Photoreceptor Cells - physiology; Synaptic Transmission; Synaptic Vesicles - physiology; Synaptotagmin I; Synaptotagmins; Urodela
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.01025.2002

1 Laboratory Neuroendocrinology-Molecular Cell Physiology, Institute of Pathophysiology, Medical Faculty, Zalo ka 4, and 2 Celica Biomedical Sciences Center, Stegne 21, 1000 Ljubljana, Slovenia; and 3 Departments of Ophthalmology and Physiology, University of California School of Medicine, San Francisco, California 94143-0730 Submitted 13 November 2002; accepted in final form 19 March 2003 Synaptic transmission at the photoreceptor synapse is characterized by continuous release of glutamate in darkness. Release is regulated by the intracellular calcium concentration ([Ca 2 + ] i ). We here examined the physiological properties of exocytosis in tiger salamander ( Ambystoma tigrinum ) retinal rods and cones. Patch-clamp capacitance measurements were used to monitor exocytosis elicited by a rapid and uniform increase in [Ca 2 + ] i by photolysis of the caged Ca 2 + compound NP-EGTA. The amplitude of flash-induced increases in membrane capacitance (C m ) varied monotonically with [Ca 2 + ] i beyond approximately 15 µM. The following two types of kinetic responses in C m were recorded in both rods and cones: 1 ) a single exponential rise (39% of cells) or 2 ) a double-exponential rise (61%). Average rate constants of rapid and slow exocytotic responses were 420 ± 168 and 7.85 ± 5.02 s – 1 , respectively. The rate constant for the single exponential exocytotic response was 17.5 ± 12.4 s – 1 , not significantly different from that of the slow exocytotic response. Beyond the threshold [Ca 2 + ] i of approximately 15 µM, the average amplitude of rapid, slow, and single C m response were 0.84 ± 0.35, 0.82 ± 0.20, and 0.70 ± 0.23 pF, respectively. Antibodies against synaptotagmin I, a vesicle protein associated with fast exocytosis, strongly stained the synaptic terminal of isolated photoreceptors, suggesting the presence of fusion-competent vesicles. Our results confirm that photoreceptors possess a large rapidly releasable pool activated by a low-affinity Ca 2 + sensor whose kinetic and calcium-dependent properties are similar to those reported in retinal bipolar cells and cochlear hair cells. Address for reprint requests: R. Zorec, Celica Biomedical Sciences Center, Stegne 21, 1000 Ljubljana, Slovenia (E-mail: Robert.Zorec{at}mf.uni-lj.si ).