Morphology of two pairs of identified peptidergic neurons in the Buccal ganglia of the mollusc Tritonia diomedea
1985; Wiley; Volume: 16; Issue: 1 Linguagem: Inglês
10.1002/neu.480160104
ISSN1097-4695
AutoresBoris Masinovsky, Philip E. Lloyd, A. O. Dennis Willows,
Tópico(s)Neuropeptides and Animal Physiology
ResumoJournal of NeurobiologyVolume 16, Issue 1 p. 27-39 Article Morphology of two pairs of identified peptidergic neurons in the Buccal ganglia of the mollusc Tritonia diomedea Boris Masinovsky, Boris Masinovsky Department of Zoology, University of Washington, Seattle, Washington 98195Search for more papers by this authorPhilip E. Lloyd, Philip E. Lloyd Department of Zoology, University of Washington, Seattle, Washington 98195Search for more papers by this authorA. O. Dennis Willows, A. O. Dennis Willows Friday Harbor Laboratories, University of Washington, Friday Harbor, Washington 98250Search for more papers by this author Boris Masinovsky, Boris Masinovsky Department of Zoology, University of Washington, Seattle, Washington 98195Search for more papers by this authorPhilip E. Lloyd, Philip E. Lloyd Department of Zoology, University of Washington, Seattle, Washington 98195Search for more papers by this authorA. O. Dennis Willows, A. O. Dennis Willows Friday Harbor Laboratories, University of Washington, Friday Harbor, Washington 98250Search for more papers by this author First published: January 1985 https://doi.org/10.1002/neu.480160104Citations: 17AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract The morphology of two pairs of identified peptidergic neurons (B11 and B12) located in the buccal ganglia of Tritonia diomedea was described. Both pairs of neurons contained a large quantity of a small cardioactive peptide (SCP) in their somata. One of the pairs (B11), the large dorsal white cells, contained ACh in their somata along with SCP. Both pairs of cells appeared white in live preparations under epi-illumination. Each B11 and B12 was a unipolar neuron and sent its major axonal branch through the ipsilateral gastro-esophageal nerve to the gut. In addition, B12 sent a small branch to the contralateral buccal ganglion. A characteristic feature of both neuron pairs was their vesicular content. Three types of vesicles were observed in B11. Vesicles with electron-lucent core (LCV) and electron-dense core (DCV) were found in the somata. The axon hillock and the beginning of axon contained vesicles with variable electron dense core (VDCV) in addition to LCV and DCV. The ratio of DCV: LCV: VDCV changed from 5:95:0 for the perinuclear cytoplasm to 8:55:37 for the beginning of axon. The average maximum diameters were 97 ± 23 nm for DCV, 103 ± 32 nm for LCV and 106 ± 29 nm for VDCV. B12 somata contained DCV (average maximum diameter 100 ± 26 nm), LCV (109 ± 23 nm) and elliptical vesicles with eccentric electron-opaque core (115 ± 20 nm). References Audesirk, G., McCaman, R. E., and Willows, A. O. D. (1979). The role of serotonin in the control of pedal ciliary activity by identified neurons in Tritonia diomedea. Comp. Biochem. Physiol. 62C: 87–91. 10.1016/0306-4492(79)90104-7 CASPubMedWeb of Science®Google Scholar Birks, R., Huxley, H. E., and Katz, B. (1960). The fine structure of the neuromuscular junction of the frog. J. Physiol. 150: 134–144. 10.1113/jphysiol.1960.sp006378 CASPubMedWeb of Science®Google Scholar Christensen, B. N., and Quinn, J. (1979) The relationship between some measures of synaptic ultrastructure as a function of distance from the soma of lamprey reticulospinal neurons. J. Neurocytol. 8: 737–750. 10.1007/BF01206673 CASPubMedWeb of Science®Google Scholar Coggeshall, R. E. (1967). A light and electron microscope study of the abdominal ganglion of Aplysia californica. J. Neurophysiol. 30: 1263–1287. 10.1152/jn.1967.30.6.1263 CASPubMedGoogle Scholar Coggeshall, R. E., Kandel, E. R., Kupfermann, L., and Waziri, R. (1966). A morphological and functional study on a cluster of identifiable neurosecretory cells in the abdominal ganglion of Aplysia californica. J. Cell Biol. 31: 363–368. 10.1083/jcb.31.2.363 PubMedWeb of Science®Google Scholar Gainer, H., and Wollberg, Z. (1974). Specific protein metabolism in identifiable neurons of Aplysia califonica. J. Neurobiol. 5: 234–261. 10.1002/neu.480050306 Web of Science®Google Scholar Getting, P. A., Lennard, P. R., and Hume, R. I. (1980). Central pattern generator mediating swimming in Tritonia diomedea: 1. Identification and synaptic interactions. J. Neurophysiol. 44: 151–164. 10.1152/jn.1980.44.1.151 CASPubMedWeb of Science®Google Scholar Hokfelt, T., Johansson, O., Ljungdahl, A., Lundberg, J. M., and Schultzberg, M. (1980). Peptidergic neurones. Nature 284: 515–521. 10.1038/284515a0 CASPubMedWeb of Science®Google Scholar Kater, S. B., and Hadley, R. D. (1982). Intracellular staining combined with video fluorescence microscopy for viewing living identified neurons. In: Cytochemical methods in neuroanatomy. Alan R. Liss, Inc., New York, NY, pp. 441–459. Google Scholar Lloyd, P. E., Masinovsky, B. P., McCaman, R. E., and Willows, A. O. D. (1981). Coexistence of neuropeptide and acetylcholin in identified molluscan neuron. Soc. Neurosci. Abst. 7: 209.6. Google Scholar Lundberg, J. M., Fried, G., Fahrenkrug, J., Holmstedt, B., Hokfelt, T., Lagercrantz, H., Lundgren, G., and Anggard, A. (1981). Subcellular fractionation of cat submandibular gland: comparative studies on the distribution of acetylcholine and vasoactive intestinal polypeptide (VIP). Neuroscience 6: 1001–1010. 10.1016/0306-4522(81)90066-X CASPubMedWeb of Science®Google Scholar Pentreath, V. W., Osborne, N. N., and Cottrell, G. A. (1973). Anatomy of giant serotonin-containing neurons in the cerebral ganglia of Helix pomatia and Limax maximus Z. Zellforsch. mikroskop. Anat. 143: 1–20. 10.1007/BF00307447 CASPubMedWeb of Science®Google Scholar Price, C. H., and McAdoo, D. J. (1979). Anatomy and ultrastructure of the axons and terminals of neurons R3-R14 in Aplysia. J. Comp. Neurol. 188: 647–678. 10.1002/cne.901880409 PubMedWeb of Science®Google Scholar Potter, D. D., Furshpan, E. J., and Landis, S. C. (1981). Multiple-transmitter status and "Dale's principle". Neuroscience Commentaries 1: 1–9. Google Scholar Sakharov, D. A., Borovyagin, V. L., and Zs-Nagy, I. (1965). Light, fluorescence and electron microscopic studies on "neurosecretion" in Tritonia diomedea Bergh (Mollusca, Nudibranchia) Z. Zellforsch. mikroskop. Anat. 68: 660–673. 10.1007/BF00340092 CASPubMedWeb of Science®Google Scholar Simpson, L. (1969). Morphological studies of possible neuroendocrine structure in Helisoma tenue (Gastropoda: Pulmonata) Z. Zellforsch. mikroskop. Anat. 102: 570–593. 10.1007/BF00335494 CASPubMedWeb of Science®Google Scholar Stewart, W. W. (1978). Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphtalimide tracer. Cell 14: 741–749. 10.1016/0092-8674(78)90256-8 CASPubMedWeb of Science®Google Scholar Wagner, J. S., Carlson, S. S., and Kelly, R. B. (1978). Chemical and physical characterisation of cholinergic synaptic vesicles. Biochem. 17: 1199–1206. 10.1021/bi00600a010 CASPubMedWeb of Science®Google Scholar Weinreich, D., McCaman, M. W., McCaman, R. E., and Vaughn, J. E. (1973). Chemical, enzymatic and ultrastructural characterization of 5-hydroxyltryptamine-containing neurons from the ganglia of Aplysia californica and Tritonia diomedea. J. Neurochem. 20: 969–976. 10.1111/j.1471-4159.1973.tb00067.x CASPubMedWeb of Science®Google Scholar Willows, A. O. D. (1980). Physiological basis of feeding behavior in Tritonia diomedea. II. Neuronal mechanisms. J. Neurophysiol. 44: 849–861. CASPubMedWeb of Science®Google Scholar Willows, A. O. D., Dorsett, D. A., and Hoyle, G. (1967). Neuronal basis of behavior in Tritonia. I. Functional organization of the central nervous system. J. Neurobiol. 4: 207–237. 10.1002/neu.480040306 Web of Science®Google Scholar Citing Literature Volume16, Issue1January 1985Pages 27-39 ReferencesRelatedInformation
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