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Ultrastructure of the coelomic lining in the podium of the starfish Stylasterias forreri

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Summary

Ultrastructural examination of the podium of the asteroid echinoderm Stylasterias forreri reveals that cells of the coelomic epithelium and cells of the retractor muscle are, in fact, components of a single epithelium. The basal lamina of this unified epithelium adjoins the connective tissue layer of the podium.

The principal epithelial cells in the coelomic lining are the flagellated adluminal cells and the myofilament-bearing retractor cells. Adluminal cells interdigitate extensively with each other and form zonular intermediate and septate junctions at their apicolateral surfaces. The adluminal cells emit processes which extend between the underlying retractor cells and terminate on the basal lamina of the epithelium. Retractor cells exhibit unregistered arrays of thick and thin myofilaments. The periphery of the retractor cell is characteristically thrown into keel-like folds which interdigitate with the processes of neighboring cells. Specialized intermediate junctions bind the retractor cells to each other and anchor the retractor cells to the basal lamina of the epithelium. The retractor cells are not surrounded by external laminae or connective tissue envelopes.

It is concluded that the coelomic lining in the podium of S. forreri is a bipartite epithelium and that the retractor cells of the podium are myoepithelial in nature. There are no detectable communicating (gap) junctions between the epithelial cells of the coelomic lining.

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Refrence

  • Atwood DG (1973) Ultrastructure of the gonadal wall of the sea cucumber, Leptosynapta clarki (Echinodermata: Holothuroidea). Z Zellforsch 141:319–330

    Google Scholar 

  • Baccetti B, Rosati F (1968) The fine structure of the Polian vesicles of holothurians. Z Zellforsch 90:148–160

    Google Scholar 

  • Bargmann W, Behrens B (1963) Über den Feinbau des Nervensystems des Seesterns (Asterias rubens L.). II. Mitteilung. Zur Frage des Baues und der Innervation der Ampullen. Z Zellforsch 59:746–770

    Google Scholar 

  • Bargmann W, Behrens B (1964) Über die Tiedemannschen Organe des Seesterns (Asterias rubens L.). Z Zellforsch 63:120–133

    Google Scholar 

  • Bargmann W, Harnack M, Jacob K (1962) Über den Feinbau des Nervensystems des Seesternes (Asterias rubens L.). I. Mitteilung. Ein Beitrag zur Vergleichenden Morphologie der Glia. Z Zellforsch 56:573–594

    Google Scholar 

  • Buchanan JB (1962) A re-examination of the glandular elements in the tube feet of some common British ophiuroids. Proc Zool Soc London 138:645–650

    Google Scholar 

  • Cavey MJ, Cloney RA (1972) Fine structure and differentiation of ascidian muscle. I. Differentiated caudal musculature of Distaplia occidentalis tadpoles. J Morphol 138:349–374

    Google Scholar 

  • Cavey MJ, Wood RL (1979) Sarcoplasmic reticulum and sarcolemmal couplings in the podial muscle cells of an asteroid echinoderm. Am Zoologist 19:903

    Google Scholar 

  • Cavey MJ, Wood RL (1981) Specializations for excitation-contraction coupling in the podial retractor cells of the starfish Stylasterias forreri. Cell Tissue Res 218:475–485

    Google Scholar 

  • Cloney RA, Florey E (1968) Ultrastructure of cephalopod chromatophore organs. Z Zellforsch 89:250–280

    Google Scholar 

  • Cobb JLS (1967) The innervation of the ampulla of the tube foot in the starfish Astropecten irregularis. Proc Roy Soc London Ser B 168:91–99

    Google Scholar 

  • Cobb JLS, Raymond AM (1979) The basiepithelial nerve plexus of the viscera and coelom of eleutherozoan Echinodermata. Cell Tissue Res 202:155–163

    Google Scholar 

  • Coleman R (1969a) Ultrastructure of the tube foot sucker of a regular echinoid, Diadema antillarum Philippi, with especial reference to secretory cells. Z Zellforsch 96:151–161

    Google Scholar 

  • Coleman R (1969b) Ultrastructure of the tube foot wall of a regular echinoid, Diadema antillarum Philippi. Z Zellforsch 96:162–172

    Google Scholar 

  • Dolder H (1972) Ultrastructural study of the smooth muscle in the tubefeet of the echinoderms, Asterina stellifera and Pentacta peterseni. J Submicr Cytol 4:221–232

    Google Scholar 

  • Engster MS, Brown SC (1972) Histology and ultrastructure of the tube foot epithelium in the phanerozonian starfish, Astropecten. Tissue & Cell 4:503–518

    Google Scholar 

  • Florey E, Cahill MA (1977) Ultrastructure of sea urchin tube feet. Evidence for connective tissue involvement in motor control. Cell Tissue Res 177:195–214

    Google Scholar 

  • Green CR, Bergquist PR, Bullivant S (1979) An anastomosing septate junction in endothelial cells of the phylum Echinodermata. J Ultrastruct Res 68:72–80

    Google Scholar 

  • Hamann O (1889) Anatomie und Histologie der Crinoiden. Jena Z Naturwiss 23:233–388

    Google Scholar 

  • Holland ND (1971) The fine structure of the ovary of the feather star Nemaster rubiginosa (Echinodermata: Crinoidea). Tissue &Cell 3:161–175

    Google Scholar 

  • Hyman LH (1955) The invertebrates, vol 4. McGraw-Hill Book Company, New York

    Google Scholar 

  • Jensen H (1975) Ultrastructure of the dorsal hemal vessel in the sea-cucumber Parastichopus tremulus (Echinodermata: Holothuroidea). Cell Tissue Res 160:355–369

    Google Scholar 

  • Kawaguti S (1964) Electron microscopic structures of the podial wall of an echinoid with special references to the nerve plexus and the muscle. Biol J Okayama Univ 10:1–12

    Google Scholar 

  • Kawaguti S (1965) Electron microscopy on the ampulla of the echinoid. Biol J Okayama Univ 11:75–86

    Google Scholar 

  • Kawaguti S, Kamishima Y (1964) Electron microscopic study on the integument of the echinoid, Diadema setosum. Annot Zool Japon 37:147–152

    Google Scholar 

  • Kelley RO, Dekker RAF, Bluemink JG (1973) Ligand-mediated osmium binding: Its application in coating biological specimens for scanning electron microscopy. J Ultrastruct Res 45:254–258

    Google Scholar 

  • Kelly DE, Shienvold FL (1976) The desmosome: Fine structural studies with freeze-fracture replication and tannic acid staining of sectioned epidermis. Cell Tissue Res 172:309–323

    Google Scholar 

  • Lazarides E, Revel JP (1979) The molecular basis of cell movement. Scientific American 240:100–113

    Google Scholar 

  • Luft JH (1961) Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol 9:409–414

    Article  CAS  PubMed  Google Scholar 

  • Maximow AA (1930) A textbook of histology. Bloom W (ed) WB Saunders Company, Philadelphia

  • McNutt NS (1975) Ultrastructure of the myocardial sarcolemma. Circ Res 37:1–13

    Google Scholar 

  • Menton DN, Eisen AZ (1970) The structure of the integument of the sea cucumber, Thyone briareus. J Morphol 131:17–36

    Google Scholar 

  • Nichols D (1959a) The histology of the tube-feet and clavulae of Echinocardium cordatum. Quart J Microsc Sci 100:73–87

    Google Scholar 

  • Nichols D (1959b) The histology and activities of the tube-feet of Echinocyamus pusillus. Quart J Microsc Sci 100:539–555

    Google Scholar 

  • Nichols D (1960) The histology and activities of the tube-feet of Antedon bifida. Quart J Microsc Sci 101:105–117

    Google Scholar 

  • Nichols D (1961) A comparative histological study of the tube-feet of two regular echinoids. Quart J Microsc Sci 102:157–180

    Google Scholar 

  • Nichols D (1966) Functional morphology of the water-vascular system. In: Boolootian RA (ed) Physiology of Echinodermata. Interscience Publishers, New York

    Google Scholar 

  • Nichols D (1967) Echinoderms. Hutchinson and Company, London

    Google Scholar 

  • Nørrevang A, Wingstrand KG (1970) On the occurrence and structure of choanocyte-like cells in some echinoderms. Acta Zoologica Stockholm 51:249–270

    Google Scholar 

  • Reynolds ES (1963) The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol 17:208–212

    Article  CAS  PubMed  Google Scholar 

  • Richardson KC, Jarett L, Finke EH (1960) Embedding in epoxy resins for ultrathin sectioning in electron microscopy. Stain Technol 35:313–323

    CAS  PubMed  Google Scholar 

  • Schantz A, Scheeter A (1965) Iron-hematoxylin and safranin O as a polychrome stain for Epon sections. Stain Technol 40:279–282

    Google Scholar 

  • Shienvold FL, Kelly DE (1976) The hemidesmosome: New fine structural features revealed by freezefracture techniques. Cell Tissue Res 172:289–307

    Google Scholar 

  • Smith JE (1937) The structure and function of the tube feet in certain echinoderms. J Mar Biol Ass U K 22:345–357

    Google Scholar 

  • Souza Santos H, Sasso WS (1968) Morphological and histochemical studies on the secretory glands of starfish tube feet. Acta Anat 69:41–51

    Google Scholar 

  • Souza Santos H, Sasso WS (1970) Ultrastructural and histochemical studies on the epithelium revestment layer in the tube feet of the starfish Asterina stellifera. J Morphol 130:287–296

    Google Scholar 

  • Walker CW (1979) Ultrastructure of the somatic portion of the gonads in asteroids, with emphasis on flagellated-collar cells and nutrient transport. J Morphol 162:127–162

    Google Scholar 

  • Wood RL (1977) The cell junctions of hydra as viewed by freeze-fracture replication. J Ultrastruct Res 58:299–315

    Google Scholar 

  • Wood RL, Cavey MJ (1980) Myoepithelial nature of podial retractor musculature in echinoderms. Am Zoologist 20:911

    Google Scholar 

  • Wood RL, Kuda AM (1980) Formation of junctions in regenerating hydra: Septate junctions. J Ultrastruct Res 70:104–117

    Google Scholar 

  • Wood RL, Luft JH (1965) The influence of buffer systems on fixation with osmium tetroxide. J Ultrastruct Res 12:22–45

    Google Scholar 

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Authors and Affiliations

  1. Department of Anatomy, School of Medicine, University of Southern California, Los Angeles, California, USA

    Richard L. Wood & Michael J. Cavey

  2. Department of Biology, Faculty of Science, University of Calgary, Calgary, Alberta, Canada

    Richard L. Wood & Michael J. Cavey

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  1. Richard L. Wood
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  2. Michael J. Cavey
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Additional information

This investigation was supported by general research funds from the Department of Anatomy of the University of Southern California (R.L.W.) and by Research Operating Grant A0484 from the Natural Sciences and Engineering Research Council of Canada (M.J.C.). Ms. Aileen Kuda and Mr. Steve Osborne provided technical assistance. A portion of this study was conducted at the Friday Harbor Laboratories of the University of Washington, and the authors gratefully acknowledge the cooperation and hospitality of the Director, Dr. A.O. Dennis Willows

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Wood, R.L., Cavey, M.J. Ultrastructure of the coelomic lining in the podium of the starfish Stylasterias forreri . Cell Tissue Res. 218, 449–473 (1981). https://doi.org/10.1007/BF00210107

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