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Central regulation of photosensitive membrane turnover in the lateral eye of Limulus. II. Octopamine acts via adenylate cyclase/cAMP-dependent protein kinase to prime the retina for transient rhabdom shedding

Published online by Cambridge University Press:  01 September 2004

SCOTT L. RUNYON
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
KEVIN J. WASHICOSKY
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
RANDALL J. BRENNEMAN*
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
JEREMY R. KELLY
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
RASHMI V. KHADILKAR
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
KEVIN F. HEACOCK
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
SHAELAN M. MCCORMICK
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
KELLY E. WILLIAMS
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania
ROBERT N. JINKS
Affiliation:
Department of Biology, Biological Foundations of Behavior Program, and Biochemistry and Molecular Biology Program, Franklin & Marshall College, Lancaster, Pennsylvania

Abstract

Why photoreceptors turn over a portion of their photoreceptive membrane daily is not clear; however, failure to do so properly leads to retinal degeneration in vertebrates and invertebrates. Little is known about the molecular mechanisms that regulate shedding and renewal of photoreceptive membrane. Photoreceptor cells in the lateral eye of the horseshoe crab Limulus turn over their photoreceptive membrane (rhabdom) in a brief, synchronous burst in response to dawn each morning. Transient rhabdom shedding (TRS), the first phase of rhabdom turnover in Limulus, is triggered by dawn, but requires a minimum of 3–5 h of overnight priming from the central circadian clock (Chamberlain & Barlow, 1984). We determined previously that the clock primes the lateral eye for TRS using the neurotransmitter octopamine (OA) (Khadilkar et al., 2002), and report here that OA primes the eye for TRS through a Gs-coupled, adenylate cyclase (AC)/cyclic adenosine 3′,5′-monophosphate (cAMP)/cAMP-dependent protein kinase (PKA) signaling cascade. Long-term intraretinal injections (6–7 h @ 1.4 μl/min) of the AC activator forskolin, or the cAMP analogs Sp-cAMP[S] and 8-Br-cAMP primed the retina for TRS in eyes disconnected from the circadian clock, and/or in intact eyes during the day when the clock is quiescent. This suggests that OA primes the eye for TRS by stimulating an AC-mediated rise in intracellular cAMP concentration ([cAMP]i). Co-injection of SQ 22,536, an AC inhibitor, or the PKA inhibitors H-89 and PKI (14-22) with OA effectively antagonized octopaminergic priming by reducing the number of photoreceptors primed for TRS and the amount of rhabdom shed by those photoreceptors compared with eyes treated with OA alone. Our data suggest that OA primes the lateral eye for TRS in part through long-term phosphorylation of a PKA substrate.

Type
Research Article
Copyright
2004 Cambridge University Press

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References

REFERENCES

Abel, T. & Kandel, E. (1998). Positive and negative regulatory mechanisms that mediate long-term memory storage. Brain Research. Brain Research Reviews 26, 360378.Google Scholar
Aréchiga, H. & Rodríguez-Sosa, L. (1998). Circadian clock function in isolated eyestalk tissue of crayfish. Proceedings of the Royal Society B. (London) 265, 18191823.Google Scholar
Barlow, Jr., R.B. (1983). Circadian rhythms in the Limulus visual system. Journal of Neuroscience 3, 856870.Google Scholar
Barlow, R. (2001). Circadian and efferent modulation of visual sensitivity. Progress in Brain Research 131, 487503.Google Scholar
Basinger, S., Hoffman, R., & Matthes, M. (1976). Photoreceptor shedding is initiated by light in the frog retina. Science 194, 10741076.Google Scholar
Battelle, B.-A. (2002). Circadian efferent input to Limulus eyes: Anatomy, circuitry, and impact. Microscopy Research and Technique 58, 345355.Google Scholar
Battelle, B.-A. & Wishart, A.C. (1990). Cyclic AMP-linked octopamine receptors in Limulus eyes: Pharmacological characteristics. Investigative Ophthalmology and Visual Science (Suppl.) 31, 331.Google Scholar
Battelle, B.-A., Andrews, A.W., Calman, B.G., Sellers, J.R., Greenberg, R.M., & Smith, W.C. (1998). A myosin III from Limulus eyes is a clock-regulated phosphoprotein. Journal of Neuroscience 18, 45484559.Google Scholar
Battelle, B.-A., Williams, C.D., Schremser-Berlin, J.-L., & Cacciatore, C. (2000). Regulation of arrestin mRNA levels in Limulus lateral eye: Separate and combined influences of circadian efferent input and light. Visual Neuroscience 17, 217227.Google Scholar
Battelle, B.-A., Dabdoub, A., Malone, M.A., Andrews, A.W., Cacciatore, C., Calman, B.G., Smith, W.C., & Payne, R. (2001). Immunocytochemical localization of opsin, visual arrestin, myosin III, and calmodulin in Limulus lateral eye retinular cells and ventral photoreceptors. Journal of Comparative Neurology 435, 211225.Google Scholar
Besharse, J.C., Iuvone, P.M., & Pierce, M.E. (1988). Regulation of rhythmic photoreceptor metabolism: A role for post-receptoral neurons. In Progress in Retinal Research, Vol. 7, ed. Osborne, N.N. & Chader, G.J., pp. 2161. Oxford: Pergamon.
Birch, D.G., Berson, E.L., & Sandberg, M.A. (1984). Diurnal rhythm in the human rod ERG. Investigative Ophthalmology and Visual Science 25, 236238.Google Scholar
Birch, D.G., Sandberg, M.A., & Berson, E.L. (1986). Diurnal rhythm in the human rod ERG: Relationship to cyclic lighting. Investigative Ophthalmology and Visual Science 27, 268270.Google Scholar
Blest, A.D. (1988). The turnover of phototransductive membrane in compound eyes and ocelli. Advances in Insect Physiology 20, 153.Google Scholar
Cahill, G.M. & Hasegawa, M. (1997). Circadian oscillators in vertebrate retinal photoreceptor cells. Biological Signals 6, 191200.Google Scholar
Chamberlain, S.C. & Barlow, Jr., R.B. (1979). Light and efferent activity control rhabdom turnover in Limulus photoreceptors. Science 206, 361363.Google Scholar
Chamberlain, S.C. & Barlow, Jr., R.B. (1984). Transient membrane shedding in Limulus photoreceptors: Control mechanisms under natural lighting. Journal of Neuroscience 4, 27922810.Google Scholar
Chyb, S., Hevers, W., Forte, M., Wolfgang, W.J., Selinger, Z., & Hardie, R.C. (1999). Modulation of the light response by cAMP in Drosophila photoreceptors. Journal of Neuroscience 19, 87998807.Google Scholar
Dabdoub, A., Payne, R., & Jinks, R.N. (2002). Protein kinase C-induced disorganization and endocytosis of photosensitive membrane in Limulus photoreceptors. Journal of Comparative Neurology 442, 217225.Google Scholar
Delmas, P., Wanaverbecq, N., Abogadie, F.C., Mistry, M., & Brown, D.A. (2002). Signaling microdomains define the specificity of receptor-mediated InsP3 pathways in neurons. Neuron 14, 209220.Google Scholar
Dolph, P.J., Ranganathan, R., Colley, N.J., Hardy, R.W., Socolich, M., & Zuker, C.S. (1993). Arrestin function in inactivation of G protein-coupled receptor rhodopsin in vivo. Science 260, 19101916.Google Scholar
Edwards, S.C. & Battelle, B.-A. (1987). Octopamine- and cyclic AMP-stimulated phosphorylation of protein in Limulus ventral and lateral eyes. Journal of Neuroscience 7, 28112820.Google Scholar
Fahrenbach, W.H. (1975). The visual system of the horseshoe crab Limulus polyphemus. International Review of Cytology 41, 285349.Google Scholar
Fahrenbach, W.H. (1981). The morphology of the horseshoe crab (Limulus polyphemus) visual system. VII. Innervation of photoreceptor neurons by neurosecretory efferents. Cell and Tissue Research 216, 655659.Google Scholar
Glass, D.B., Cheng, H.-C., Mende-Mueller, L., Reed, J., & Walsh, D.A. (1989). Primary structural determinants essential for potent inhibition of cAMP-dependent protein kinase by inhibitory peptides corresponding to the active portion of the heat-stable inhibitor protein. Journal of Biological Chemistry 264, 88028810.Google Scholar
Goldsmith, B.A. & Abrams, T.W. (1991). Reversal of synaptic depression by serotonin at Aplysia sensory neuron synapses involves activation of adenylyl cyclase. Proceedings of the National Academy of Sciences of the U.S.A. 88, 90219025.Google Scholar
Grace, M.S., Chiba, A., & Menaker, M. (1999). Circadian control of photoreceptor outer segment membrane turnover in mice genetically incapable of melatonin synthesis. Visual Neuroscience 16, 909918.Google Scholar
Greengard, P., Jen, J., Nairn, A.C., & Stevens, C.F. (1991). Enhancement of the glutamate response by cAMP-dependent protein kinase in hippocampal neurons. Science 253, 11351138.Google Scholar
Herberg, F.W., Taylor, S.S., & Dostmann, W.R.G. (1996). Active site mutations define the pathway for the cooperative activation of cAMP-dependent protein kinase. Biochemistry 35, 29342942.Google Scholar
Hünenberger, P.H., Helms, V., Narayana, N., Taylor, S.S., & McCammon, J.A. (1999). Determinants of ligand binding to cAMP-dependent protein kinase. Biochemistry 38, 23582366.Google Scholar
Jinks, R.N., Asrican, B.W., & Khadilkar, R.V. (1999). Does octopamine, via a protein phosphatase inhibitor, mediate circadian efferent regulation of photosensitive membrane shedding in the lateral eye of the horseshoe crab Limulus? Investigative Ophthalmology and Visual Science 40, s612.Google Scholar
Jinks, R.N., White, R.H., & Chamberlain, S.C. (1996). Dawn, diacylglycerol, calcium, and protein kinase C—the retinal wrecking crew. A signal transduction cascade for rhabdom shedding in the Limulus eye. Journal of Photochemistry and Photobiology B: Biology 34, 4552.Google Scholar
Johnson, D.A., Akamine, P., Radzio-Andzelm, E., Madhusudan, & Taylor, S.S. (2001). Dynamics of cAMP-dependent protein kinase. Chemical Reviews 101, 22432270.Google Scholar
Kass, L. & Barlow, Jr., R.B. (1984). Efferent neurotransmission of circadian rhythms in Limulus lateral eye. I. Octopamine-induced increases in retinal sensitivity. Journal of Neuroscience 4, 908.Google Scholar
Kass, L. & Zhang, H.-J. (1992). Clock controls gain in Limulus photoreceptors by changing voltage-dependent conductances. Investigative Ophthalmology and Visual Science (Suppl.) 33, 1327.Google Scholar
Kass, L., Pelletier, J.L., Renninger, G.H., & Barlow, Jr., R.B. (1988). Efferent neurotransmission of circadian rhythms in Limulus lateral eye. II. Intracellular recordings in vitro. Journal of Comparative Physiology A 164, 95105.Google Scholar
Kaupp, U.B. & Seifert, R. (2002). Cyclic nucleotide-gated ion channels. Physiological Reviews 82, 769824.Google Scholar
Khadilkar, R.V., Mytinger, J.R., Thomason, L.E., Runyon, S.L., Washicosky, K.J., & Jinks, R.N. (2002). Central regulation of photosensitive membrane turnover in the lateral eye of Limulus. I. Octopamine primes the retina for daily transient rhabdom shedding. Visual Neuroscience 19, 283297.Google Scholar
LaVail, M.M. (1976). Rod outer segment disc shedding in rat retina: Relationship to cyclic lighting. Science 194, 10711074.Google Scholar
Lonze, B.E. & Ginty, D.D. (2002). Function and regulation of CREB family transcription factors in the nervous system. Neuron 35, 605623.Google Scholar
Mahoney, D.F., Sacunas, R.B., & Chamberlain, S.C. (2001). Rhabdom shedding in the Limulus lateral eye: Seasons and weather. Society for Neuroscience Abstracts 27, 1903.Google Scholar
Meyer, Jr., R.B. & Miller, J.P. (1974). Analogs of cyclic AMP and cyclic GMP: General methods of synthesis and the relationship of structure to enzymatic activity. Life Sciences 14, 10191040.Google Scholar
Montell, C. (1999). Visual transduction in Drosophila. Annual Review of Cell and Developmental Biology 15, 231268.Google Scholar
Nguyen-Legros, J. & Hicks, D. (2000). Renewal of photoreceptor outer segments and their phagocytosis by the retinal pigment epithelium. International Review of Cytology 196, 245313.Google Scholar
Pieprzyk, A.R., Weiner, W.W., & Chamberlain, S.C. (2003). Mechanisms controlling the sensitivity of the Limulus lateral eye in natural lighting. Journal of Comparative Physiology A 189, 643653.Google Scholar
Roeder, T. (1999). Octopamine in invertebrates. Progress in Neurobiology 59, 533561.Google Scholar
Rothermel, J.D. & Parker Botelho, L.H. (1988). A mechanistic and kinetic analysis of the interactions of the diastereoisomers of adenosine 3′,5′-(cyclic)phosphorothioate with purified cyclic AMP-dependent protein kinase. Biochemical Journal 251, 757762.Google Scholar
Rufiange, M., Dumont, M., & Lachapelle, P. (2002). Correlating retinal function with melatonin secretion in subjects with an early or late circadian phase. Investigative Ophthalmology and Visual Science 43, 24912499.Google Scholar
Runyon, S.L., Kelly, J.R., & Jinks, R.N. (2002). Cyclic adenosine 3′,5′-monophosphate (cAMP) analogs mimic circadian efferent priming of the Limulus lateral eye for transient rhabdom shedding. Society for Neuroscience Abstracts 28, 843.2.Google Scholar
Russ, J.C. (1986). Practical Stereology. pp. 3553. New York: Plenum Press.
Sacunas, R.B., Papuga, M.O., Malone, M.A., Pearson, Jr., A.C., Marjanovic, M., Stroope, D.G., Weiner, W.W., Chamberlain, S.C., & Battelle, B.-A. (2002). Multiple mechanisms of rhabdom shedding in the lateral eye of Limulus polyphemus. Journal of Comparative Neurology 449, 2642.Google Scholar
Scholubbers, H.G., van Knippenberg, P.H., Baraniak, J., Stec, W.J., Morr, M., & Jastorff, B. (1984). Investigations on stimulation of lac transcription in vivo in Escherichia coli by cAMP analogues. Biological activities and structure–activity correlations. European Journal of Biochemistry 138, 101109.Google Scholar
Seamon, K.B., Padgett, W., & Daly, J.W. (1981). Forskolin: Unique diterpene activator of adenylate cyclase in membranes and in intact cells. Proceedings of the National Academy of Sciences of the U.S.A. 78, 33633367.Google Scholar
Shabb, J.B. (2001). Physiological substrates of cAMP-dependent protein kinase. Chemical Reviews 101, 23812411.Google Scholar
Silva, A.J., Kogan, J.H., Frankland, P.W., & Kida, S. (1998). CREB and Memory. Annual Review of Neuroscience 21, 127148.Google Scholar
Smith, W.C., Greenberg, R.M., Calman, B.G., Hendrix, M.M., Hutchinson, L., Donoso, L.A., & Battelle, B.-A. (1995). Isolation and expression of an arrestin cDNA from the horseshoe crab lateral eye. Journal of Neurochemistry 64, 113.Google Scholar
Tsunoda, S., Sierralta, J., Sun, Y., Bodner, R., Suzuki, E., Becker, A., Socolich, M., & Zuker, C.S. (1997). A multivalent PDZ-domain protein assembles signaling complexes in a G-protein-coupled cascade. Nature 388, 243249.Google Scholar
Wang, L.-Y., Salter, M.W., & MacDonald, J.F. (1991). Regulation of kainate receptors by cAMP-dependent protein kinase and phosphatases. Science 253, 11321135.Google Scholar
White, M.P. & Hock, P.A. (1992). Effects of continuous darkness on ERG correlates of disc shedding in rabbit retina. Experimental Eye Research 54, 173180.Google Scholar
Wiebe, E.M., Wishart, A.C., Edwards, S.C., & Battelle, B.-A. (1989). Calcium/ calmodulin-stimulated phosphorylation of photoreceptor proteins in Limulus. Visual Neuroscience 3, 107118.Google Scholar
Wilden, U., Hall, S.W., & Kühn, H. (1986). Phosphodiesterase activation by photoexcited rhodopsin is quenched when rhodopsin is phosphorylated and binds the intrinsic 48-kDa protein of rod outer segments. Proceedings of the National Academy of Sciences of the U.S.A. 83, 11741178.Google Scholar
Young, R.W. (1976). Visual cells and the concept of renewal. Investigative Ophthalmology and Visual Science 15, 700725.Google Scholar
Yusta, B., Ortiz-Caro, J., Pascaul, A., & Aranda, A. (1988). Comparison of the effects of forskolin and dibutyryl cyclic AMP in neuroblastoma cells: Evidence that some of the actions of dibutyryl cyclic AMP are mediated by butyrate. Journal of Neurochemistry 51, 18081818.Google Scholar
Zhang, H.-J., Jinks, R.N., Wishart, A.C., Battelle, B.-A., Chamberlain, S.C., Fahrenbach, W.H., & Kass, L. (1994). An enzymatically enhanced recording technique for Limulus ventral photoreceptors: Physiology, biochemistry, and morphology. Visual Neuroscience 11, 4152.Google Scholar