Autoradiographic identification of acetylcholine in the rabbit retina

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.

[1]  B. Collier,et al.  The metabolism of choline by a sympathetic ganglion. , 1969, Canadian journal of physiology and pharmacology.

[2]  R H Masland,et al.  Responses to acetylcholine of ganglion cells in an isolated mammalian retina. , 1976, Journal of neurophysiology.

[3]  D. R. Curtis,et al.  The excitation of lateral geniculate neurones by quaternary ammonium derivatives , 1963, The Journal of physiology.

[4]  S. Lindstro¨m,et al.  A potential screening technique for neurotransmitters in the CNS: Model studies in the cat spinal cord , 1977, Brain Research.

[5]  M. Neal,et al.  High-affinity choline transport in the isolated retina , 1975, Brain Research.

[6]  W. Dairman,et al.  AXOPLASMIC TRANSPORT OF AROMATIC l‐AMINO ACID DECARBOXYLASE (EC 4.1.1.26) AND DOPAMTNE β‐HYDROXYLASE (EC 1.14.2.I) IN RAT SCIATIC NERVE , 1973, Journal of neurochemistry.

[7]  F. C. Macintosh,et al.  ACETYLCHOLINE METABOLISM OF A SYMPATHETIC GANGLION , 1961 .

[8]  E. Kravitz,et al.  Screening for neurotransmitters: a rapid radiochemical procedure. , 1971, Journal of neurobiology.

[9]  A. Ames,et al.  FUNCTIONAL HOMOGENEITY OF LEUCINE POOL IN RETINA CELLS 1 , 1976, Journal of Neurochemistry.

[10]  R. Masland,et al.  Aspects of Choline Metabolism in Photoreceptor Cells , 1980 .

[11]  R. E. Anderson,et al.  Phospholipids of bovine outer segments. , 1970, Biochemistry.

[12]  C. Herb Choline acetylase in mammalian and avian sensory systems. , 1955, Quarterly journal of experimental physiology and cognate medical sciences.

[13]  G. Lunt,et al.  The turnover of phosphatidyl choline in rat cerebral cortex membranes in vivo. , 1969, Journal of Neurobiology.

[14]  E. Yavin Regulation of phospholipid metabolism in differentiating cells from rat brain cerebral hemispheres in culture. Patterns of acetylcholine phosphocholine, and choline phosphoglycerides labeling from (methyl-14C)choline. , 1976, Journal of Biological Chemistry.

[15]  G. Lunt,et al.  Incorporation of (Me-14C)choline into phosphatidyl choline of rat cerebral cortex membranes in vitro. , 1970, Brain research.

[16]  A. H. Bunt,et al.  Displaced ganglion cells in the retina of the monkey. , 1977, Investigative ophthalmology & visual science.

[17]  M. Spitznas,et al.  THE FINE STRUCTURAL LOCALIZATION OF ACETYLCHOLINESTERASE ACTIVITY IN THE RETINA AND OPTIC NERVE OF RABBITS , 1971, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[18]  R. Ledeen,et al.  AXONAL TRANSPORT OF LIPIDS IN THE RABBIT OPTIC SYSTEM , 1979, Journal of neurochemistry.

[19]  J. Freeman Possible regulatory function of acetylcholine receptor in maintenance of retinotectal synapses , 1977, Nature.

[20]  G. Koelle,et al.  Comparison of the localization of acetylcholinesterase and non‐specific cholinesterase activities in mammalian and avian retians , 1968, The Journal of comparative neurology.

[21]  C. Anfinsen,et al.  STUDIES ON MALARIAL PARASITES , 1946, The Journal of experimental medicine.

[22]  M. Kuhar Characteristics and Significance of Sodium-Dependent, High Affinity Choline Uptake , 1978 .

[23]  A. Ames,et al.  Intracellular and extracellular compartments of mammalian central nervous tissue * , 1966, The Journal of physiology.

[24]  Z. Vogel,et al.  Identification of synaptic acetylcholine receptor sites in retina with peroxidase-labeled alpha-bungarotoxin. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[25]  A. Silver Biology of cholinergic function Alan M. Goldberg & Israel Hanin (Eds). Raven Press, New York (1976). 716 pp., S42.00 , 1977, Neuroscience.

[26]  J. H. Schwartz,et al.  Cellular specificity of serotonin storage and axonal transport in identified neurones of Aplysia californica , 1974, The Journal of physiology.

[27]  J. Mills,et al.  Localization of Na+-pump sites in frog skin , 1977, The Journal of cell biology.

[28]  B. Y. Tang,et al.  Axoplasmic flow of phospholipids and cholesterol in the sciatic nerve of normal and dystrophic mice. , 1974, Experimental neurology.

[29]  C. Anfinsen,et al.  STUDIES ON MALARIAL PARASITES , 1946, The Journal of experimental medicine.

[30]  W. Stell,et al.  GABA‐ergic pathways in the goldfish retina , 1978, The Journal of comparative neurology.

[31]  R. Pourcho Localization of cholinergic synapses in mammalian retina with peroxidase-conjugated α-bungarotoxin , 1979, Vision Research.

[32]  D. McDougal,et al.  THE DISTRIBUTION OF CHOLINE ACETYLTRANSFERASE ACTIVITY IN VERTEBRATE RETINA 1 , 1976, Journal of neurochemistry.

[33]  A. Cohen,et al.  Choline acetyltransferase and acetylcholine esterase activities in normal and biologically fractionated mouse retinas. , 1975, Investigative Ophthalmology.

[34]  R. Anderson,et al.  Lipids of ocular tissues. IV. A comparison of the phospholipids from the retina of six mammalian species. , 1970, Experimental Eye Research.

[35]  D. V. Davies,et al.  Techniques of Autoradiography. , 1968 .

[36]  J. Phillis,et al.  A study of cholinoceptive cells in the lateral geniculate nucleus , 1967, The Journal of physiology.

[37]  R. W. Young,et al.  RENEWAL OF GLYCEROL IN THE VISUAL CELLS AND PIGMENT EPITHELIUM OF THE FROG RETINA , 1974, The Journal of cell biology.

[38]  O. Stein,et al.  Light and electron microscopic radioautography of lipids: techniques and biological applications. , 1971, Advances in lipid research.

[39]  A. Ames,et al.  Studies on water and electrolytes in nervous tissue. I. Rabbit retina: methods and interpretation of data. , 1956, Journal of neurophysiology.

[40]  C. Bader,et al.  Biochemical characterization and cellular localization of the cholinergic system in the chicken retina , 1977, Brain Research.

[41]  D. M. Lam,et al.  ENDOGENOUS LEVELS OF NEUROTRANSMITTER CANDIDATES IN PHOTORECEPTOR CELLS OF THE TURTLE RETINA , 1979, Journal of neurochemistry.

[42]  R. E. Anderson,et al.  Lipids of ocular tissues. II. The phospholipids of mature bovine and rabbit whole retina. , 1970, Biochimica et biophysica acta.

[43]  D. M. Lam Biosynthesis of acetylcholine in turtle photoreceptors. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[44]  R. E. Anderson,et al.  Lipids of ocular tissues. IX. The phospholipids of frog photoreceptor membranes. , 1974, Vision research.

[45]  A. Ames,et al.  REVERSIBLE AND IRREVERSIBLE CHANGES IN THE FINE STRUCTURE OF NERVOUS TISSUE DURING OXYGEN AND GLUCOSE DEPRIVATION , 1965, The Journal of cell biology.

[46]  S. Spanner,et al.  The metabolism of [Me-14C]choline in the brain of the rat in vivo. , 1968, The Biochemical journal.

[47]  A. Spurr A low-viscosity epoxy resin embedding medium for electron microscopy. , 1969, Journal of ultrastructure research.

[48]  R. Masland,et al.  Retinal-induced sensitization of light-adapted rabbit photoreceptors , 1978, Brain Research.

[49]  A. H. Bunt Fine structure and radioautography of rabbit photoreceptor cells. , 1978, Investigative ophthalmology & visual science.

[50]  M. Lavail KINETICS OF ROD OUTER SEGMENT RENEWAL IN THE DEVELOPING MOUSE RETINA , 1973, The Journal of cell biology.

[51]  S. Yazulla,et al.  Two types of receptors for α-bungarotoxin in the synaptic layers of the pigeon retina , 1977, Brain Research.

[52]  L. Potter Synthesis, storage and release of [14C]acetylcholine in isolated rat diaphragm muscles , 1970, The Journal of physiology.

[53]  J. H. Schwartz,et al.  Axonal transport of newly synthesized acetylcholine in an identified neuron of Aplysia. , 1972, Brain research.

[54]  J. Lund,et al.  Retrograde axonal transport of horseradish peroxidase by ganglion cells of the albino rat retina. , 1974, Brain research.

[55]  J. Mitchell,et al.  Biosynthesis of retinal phospholipids: incorporation of radioactivity from labeled phosphorylcholine and cytidine diphosphate choline. , 1970, Journal of lipid research.

[56]  S. Snyder,et al.  HIGH AFFINITY TRANSPORT OF CHOLINE INTO SYNAPTOSOMES OF RAT BRAIN 1 , 1973, Journal of neurochemistry.

[57]  A. Ames,et al.  TRANSPORT OF LEUCINE AND SODIUM IN CENTRAL NERVOUS TISSUE: STUDIES ON RETINA IN VITRO 1 , 1976, Journal of neurochemistry.

[58]  L. Potter,et al.  Electrophoresis of acetylcholinc, choline and related compounds , 1967 .

[59]  M. Kuhar Sodium-dependent high affinity choline uptake. , 1979, Progress in brain research.

[60]  L. Potter,et al.  Electrophoresis of acetylcholine, choline and related compounds. , 1967, Biochemical pharmacology.

[61]  H. Noda,et al.  Choline uptake systems of rat brain synaptosomes. , 1973, Biochimica et biophysica acta.

[62]  J. Folch,et al.  A simple method for the isolation and purification of total lipides from animal tissues. , 1957, The Journal of biological chemistry.

[63]  G. Pepeu,et al.  Acetylcholine and 5-hydroxytryptamine levels of the lateral geniculate bodies and superior colliculus of cats after visual deafferentation. , 1967, Experimental Neurology.

[64]  D. Bok,et al.  Electron microscopic localization of [125I]α-bungarotoxin binding sites in the outer plexiform layer of the goldfish retina , 1979, Journal of neurocytology.

[65]  G. Koelle,et al.  Acetylcholinesterase: Method for Demonstration in Amacrine Cells of Rabbit Retina , 1967, Science.

[66]  D. Jenden Cholinergic Mechanisms and Psychopharmacology , 1978, Advances in Behavioral Biology.

[67]  D. Tomlinson,et al.  Studies on the translocation of noradrenaline‐containing vesicles in post‐ganglionic sympathetic neurones in vitro. Inhibition of movement by colchicine and vinblastine and evidence for the involvement of axonal microtubules , 1971, The Journal of physiology.