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Immunocytochemical localization of the neuropeptide S1 and serotonin in larvae of the starfish Pisaster ochraceus and Asterias rubens

Published online by Cambridge University Press:  11 May 2009

Claire Moss
Affiliation:
Department of Biology, Royal Holloway, University of London, Egham, Surrey, TW20 OEX
Robert D. Burke
Affiliation:
Department of Biology, University of Victoria, Victoria, British Columbia, V8W 2Y2, Canada
Michael C. Thorndyke
Affiliation:
Department of Biology, Royal Holloway, University of London, Egham, Surrey, TW20 OEX

Extract

Studies of the larval nervous system of two species of starfish were carried out using antisera to a recently isolated native echinoderm neuropeptide, GFNSALMFamide (S1), and to serotonin. S1-like immunoreactivity was found in the larvae of the asteroids Pisaster ochraceus and Asterias rubens (Echinodermata: Asteroidea), originating in the apical region and becoming concentrated as two groups of cells in the dorsal ciliary band, the preoral transverse and adoral ciliary bands in larvae up to the early brachiolarian stage (five weeks). The pattern of serotonin immunoreactivity, although appearing earlier in the apical nerve plexus, is very similar to that of the peptide, with paired groups of immuno- reactivity apparent in the dorsal ciliary band. This evidence, together with other recent studies, indicates that this neuropeptide is present in both the larval and adult nervous system, despite the complete reformation of the system at metamorphosis. The close localization of SI with serotonin may also suggest a possible function for the peptide in larval and adult nervous systems.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1994

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References

Bisgrove, B.W. & Burke, R.D., 1986. Development of serotonergic neurons in embryos of the sea urchin, Strongylocentrotus pupuratus. Development, Growth and Differentiation, 28, 569574.CrossRefGoogle Scholar
Bisgrove, B.W. & Burke, R.D., 1987. Development of the nervous system of the pluteus larva of Strongylocentrotus droebachiensis. Cell and Tissue Research, 248, 335343.CrossRefGoogle Scholar
Bisgrove, B.W. & Raff, R.A., 1989. Evolutionary conservation of the larval serotonergic nervous system in a direct developing sea urchin. Development, Growth and Differentiation, 31, 363370.CrossRefGoogle Scholar
Burke, R.D., 1978. The structure of the nervous system of the pluteus larva of Strongylocentrotus purpuratus. Cell and Tissue Research, 191, 233247.CrossRefGoogle ScholarPubMed
Burke, R.D., 1983 a. Neural control of metamorphosis in Dendraster excentricus. Biological Bulletin. Marine Biological Laboratory, Woods Hole, 164, 176188.CrossRefGoogle Scholar
Burke, R.D., 1983 b. The structure of the larval nervous system of Pisaster ochraceus (Echinodermata: Asteroidea). Journal of Morphology, 178, 2335.CrossRefGoogle ScholarPubMed
Buznikov, G.A., Chudakova, I.V., Berdysheva, L.V. & Vyazmina, N.M., 1968. The role of neurohumours in early embryogenesis. II. Acetylcholine and catecholamine content in developing embryos of sea urchin. Journal of Embryology and Experimental Morphology, 20, 119128.Google Scholar
Chia, F.-S. & Burke, R.D., 1978. Echinoderm metamorphosis: fate of larval structures. In Settlement and metamorphosis of marine invertebrate larvae (ed. F.-S., Chia and M.E., Rice), pp. 219234. New York: Elsevier.Google Scholar
Chia, F.-S., Burke, R.D., Koss, R., Mladenov, P.V. & Rumrill, S.S., 1986. Fine structure of the doliolaria larva of the feather star Florometra serratissima (Echinodermata: Crinoidea), with special emphasis on the nervous system. Journal of Morphology, 189, 99120.CrossRefGoogle ScholarPubMed
Cottrell, G.A. & Pentreath, V.W., 1970. Localization of catecholamines in the nervous system of a starfish, Asterias rubens, and of a brittlestar, Ophiothrix fragilis. Comparative and General Pharmacology, 1, 7381.CrossRefGoogle ScholarPubMed
Davidson, E.H., 1989. Lineage specific gene expression and the regulative capacities of the sea urchin embryo: a proposed mechanism. Development, 105, 421445.CrossRefGoogle ScholarPubMed
Díaz-Miranda, L., Price, D.A., Greenberg, M.J., Lee, T.D., Doble, K.E. & García-Arrarás, J.E., 1992. Characterization of two novel neuropeptides from the sea cucumber Holothuria glaberrima. Biological Bulletin. Marine Biological Laboratory, Woods Hole, 182, 241247.CrossRefGoogle ScholarPubMed
Elphick, M.R., Beeson, J.R., Moore, S.J. & Thorndyke, M.C., 1991 a. Purification of peptides from the sea urchin Echinus esculentus using a new antiserum to the starfish neuropeptide S2. Regulatory Peptides, 35, 235.CrossRefGoogle Scholar
Elphick, M.R., Price, D.A., Lee, T.D. & Thorndyke, M.C., 1991 b. The SALMFamides: a new family of neuropeptides isolated from an echinoderm. Proceedings of the Royal Society (B), 243, 121127.Google ScholarPubMed
Gemmill, J.F., 1914. The development and certain points in the adult structure of the starfish Asterias rubens. Philosophical Transactions of the Royal Society of London (B), 205, 213294.Google Scholar
Gilmour, T.H.J., 1988. Particle paths and streamlines in the feeding behaviour of echinoderm larvae. In Echinoderm biology (ed. Burke, R.D.et al.), pp. 253257. Rotterdam: A.A. Balkema.Google Scholar
Lacalli, T.C., 1981. Structure and development of the apical organ in trochophores of Spirobranchus polycerus, Phyllodoce maculata and Phyllodoce mucosa (Polychaeta). Proceedings of the Royal Society (B), 212, 381402.Google Scholar
Lacalli, T.C. & Gilmour, T.H.J., 1990. Ciliary reversal and locomotory control in the pluteus larva of Lytechinus pictus. Philosophical Transactions of the Royal Society (B), 330, 391396.Google Scholar
Lacalli, T.C., Gilmour, T.H.J. & West, J.E., 1990. Ciliary band innervation in the bipinnarian larva of Pisaster ochraceus. Philosophical Transactions of the Royal Society of London (B), 330, 371390.Google Scholar
Macbride, E.W., 1914. Text-book of embryology, vol. 1. pp 456567. London: MacMillan & Co. Ltd.Google Scholar
Moore, S.J. & Thorndyke, M.C., 1993. Immunocytochemical mapping of the novel echinoderm neuropeptide SALMFamide 1 (SI) in the starfish, Asterias rubens. Cell and Tissue Research, in press.CrossRefGoogle Scholar
Nakajima, Y., 1986. Development of the nervous system of sea urchin embryos: formation of ciliary bands and the appearance of two types of ectoneural cells in the pluteus. Development, Growth and Differentiation, 28, 531542.CrossRefGoogle ScholarPubMed
Nakajima, Y., 1988. Serotonergic nerve cells of starfish larvae. In Echinoderm biology (ed. R.D., Burkeet al.), pp. 235239. Rotterdam: A.A. Balkema.Google Scholar
Strathmann, M.F., 1987. Reproduction and development of marine invertebrates of the northern Pacific coast: data and methods for the study of eggs, embryos and larvae. Seattle: University of Washington Press.Google Scholar
Strathmann, R.R., 1971. The feeding behaviour of planktotrophic echinoderm larvae: mechanisms, regulation, and rates of suspension feeding. Journal of Experimental Marine Biology and Ecology, 6, 109160.CrossRefGoogle Scholar
Strathmann, R.R., 1975. Larval feeding in echinoderms. American Zoologist, 15, 717730.CrossRefGoogle Scholar
Thorndyke, M.C., Crawford, B.D. & Burke R.D., 1992. Localization of a SALMFamide neuropeptide in the larval nervous system of the sand dollar Dendraster excentricus. Acta Zoologica, 73, 207212.CrossRefGoogle Scholar