Abstract
There are a number of characteristics which should be considered in a definitive classification of hemocytes [40], but the initial criterion is most often morphology. Although no general agreement on the number of different cell types in oyster hemolymph has been reached, most investigators divide the hemocytes into at least two major classifications: the granular and the agranular [7,40]. There are apparent differences in the roles that granular and agranular cells play in any organism, and those roles are not necessarily the same for each species. The granular hemocytes are generally larger than the agranular cells and contain walled vesicles (granules) in the cytoplasm. Using light microscopy, investigators have also been able to distinguish acidophilic and basophilic granulocytes [7], stem cells [2], slightly granular cells [40], and differences based on nuclear size [28]. But even with ultrastructural investigation, these studies of oyster hemocytes have not led to a generally accepted scheme of nomenclature and classification. Rather, they have emphasized differences between oyster species and raised conflicting evidence within species. For example, there are major disagreements between invertigations examining the ultrastructure of Crassostrea virginica agranular hemocytes [27,34,48]. Also, the easily distinguishable C. virginia granulocytes was first beleived to be two cell types [30] due to its altered morphology upon degranulation [7].
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Acton RT, Evans EE (1968) Bacteriophage clearance in the oyster ( Crassostrea virginica ). J Bacteriol 95: 1260–1266
Auffret M (1984) Contribution of hematology to the knowledge of cellular immunity in bivalve molluscs (abstract). Invertebr Immunol Conf, Int Soc Dev Comp Immunol, Montpellier, France. Dev Comp Immunol (in press)
Bachere E, Comps M (1984) In: Pichot et al. 1980. Experimental infection of the flat oyster Ostrea edulis by the protistan Bonamia ostreae (abstract) 1st Int Colloq Pathol Marine Aquac, Montpellier, France, pp 37–38
Bang FB (1961) Reaction to injury in the oyster (Crassostrea virginica). Biol Bull (Woods Hole) 121: 57–68
Bayne CJ (1983) Molluscan immunobiology. In: Salleuddin ASM, Wilbur KM (eds) The Mollusca. Physiology, Part 2, Vol 4. Academic Press, New York, pp 407–486
Bretscher MS (1984) Endocytosis: relation to capping and cell locomotion. Science 224: 681–686
Cheng TC (1975) Functional morphology and biochemistry of molluscan phagocytes. Ann NY Acad Sci 266: 343–379
Cheng TC (1976) Aspects of substrate utilization and energy requirement during molluscan phagocytosis. J Invertebr Pathol 27: 263–268
Cheng TC (1977) Biochemical and ultrastructural evidence for the double role of phagocytosis in molluscs: defence and nutrition. In: Bulla LA Jr, Cheng TC (eds) Comparative Pathobiology, Vol 3. Invertebrate Immune Responses. Plenum, London, pp 21–30
Cheng TC (1983) The role of lysosomes in molluscan inflammation. Am Zool 23: 129–144
Cheng TC, Cali A (1974) An electron microscope study of the fate of bacteria phagocytized by granulocytes of Crassostrea virginica. Contemp Top Immunobiol 4: 25–35
Cheng TC, Howland KH (1979) Chemotactic attraction between hemocytes of the oyster Crassostrea virginica, and bacteria. J Invertebr Pathol 33: 204–210
Cheng TC, Howland KH (1982) Effects of colchicine and cytochalasin B on chemotaxis of oyster ( Crassostrea virginica) hemocytes. J Invertebr Pathol 40: 150–152
Cheng TC Huang JW, Karadogan H, Renwrantz LR, Yoshino TP (1980) Separation of oyster hemocytes by density gradient centrifugation and identification of their surface receptors. J Invertebr Pathol 36: 35–40
Cheng TC, Rifkin E (1970) Cellular reactions in marine molluscs in response to helminth parasitism. In: Snieszko SF (ed) A Symposium on Diseases of Fishes and Shellfishes. Am Fish Soc (Wash DC), pp 443–496
Cheng TC, Rodrick GE (1975) Lysosomal and other enzymes in the hemolymph of Crassostrea virginica and Mercenaria mercenaria. Comp Biochem Physiol 52B: 443–447
Cheng TC, Rodrick GE, Foley DA, Koehler SA (1975) Release of lysozyme from hemolymph cells of Mercenaria mercenaria during phagocytosis. J Invertebr Pathol 25: 261–265
Cheng TC, Rudo BM (1976) Distribution of glycogen resulting from degradation of 14C-la-belled bacteria in the American oyster, Crassostrea virginica. J Invertebr Pathol 27: 259–262
Dundee DS (1953) Formed elements of the blood of certain fresh-water mussels. Trans Am Microsc Soc 72: 254–264
Eble AF, Tripp MR (1969) Oyster leucocytes in tissue culture: a functional study. Proc Natl Shellfish Assoc 59: 5
Farley CA (1968) Minchinia nelsoni (Haplosporidia) disease syndrome in the American oy-ster Crassostrea virginica. J Protozool 15: 585–599
Feng JS (1966) The fate of a virus, Staphylococcus aureus Phage 80, injected into the oyster, Crassostrea virginica. J Invertebr Pathol 8: 496–504
Feng SY (1965a) Pinocytosis of proteins by oyster leucocytes. Biol Bull (Woods Hole) 129: 95–105
Feng SY (1965b) Heart rate and leucocyte circulation in Crassostrea virginica (Gmelin). Biol Bull (Woods Hole) 128: 198–210
Feng SY (1966) Experimental bacterial infections in the oyster Crassostrea virginica. J Invertebr Pathol 8: 505–511
Feng SY, Feng JS (1974) The effect of temperature on cellular reactions of Crassostrea virginica to the injection of avian erythrocytes. J Invertebr Pathol 23: 22–37
Feng SY, Feng JS, Burke CN, Khairallah LH (1971) Light and electron microscopy of the leucocytes of Crassostrea virginica ( Mollusca: Pelecypoda). Z Zellforsch Mikrosk Anat 120: 222–245
Feng SY, Feng JS, Yamasu T (1977) Roles of Mytilus coruscus and Crassostrea gigas blood cells in defense and nutrition. In: Bulla LA Jr, Cheng TC (eds) Comparative Pathobiology, Vol 3. Invertebrate Immune Responses. Plenum, London, pp 31 - 67
Fisher WS (1984) Osmotic and ionic effects on hemocyte function in the American oyster (abstract). Invertebr Immunol Conf, Int Soc Dev Comp Immunol, Montpellier, France, p. 70. Dev Comp Immunol (in press)
Foley DA, Cheng TC (1972) Interaction of molluscs and foreign substances: the morphology and behavior of hemolymph cells of the American oyster, Crassostrea virginica, in vitro. J Invertebr Pathol 19: 383–394
Foley DA, Cheng TC (1975) A quantitative study of phagocytosis by hemolymph cells of the Pelecypods Crassostrea virginica and Mercenaria mercenaria. J Invertebr Pathol 25: 189–197
Foley DA, Cheng TC (1977) Degranulation and other changes of molluscan granulocytes associated with phagocytosis. J Invertebr Pathol 29: 321–325
Fries CR, Tripp MR (1970) Uptake of viral particles by oyster leucocytes in vitro. J Invertebr Pathol 15: 136–137
Hawkins WE, Howse HD (1982) Ultrastructure of cardiac hemocytes and related cells in the oyster Crassostrea virginica. Trans Am Microsc Soc 101 (3): 241–252
Howland KH, Cheng TC (1982) Identification of bacterial chemoattractants for oyster ( Crassostrea virginica) hemocytes. J Invertebr Pathol 39: 123–132
Kanungo K (1982) In vitro studies on the effects of cell-free coelomic fluid, calcium, and/or magnesium on clumping of coelomocytes of the sea stei Asteria forbesi (Echinodermata: Asteroidea). Biol Bull (Woods Hole) 163: 438–452
Kenney DM, Belamarich FA, Shepro D (1972) Aggregation of horseshoe crab ( Limulus polyphemus) amebocytes and reversible inhibition of aggregation by EDTA. Biol Bull (Woods Hole) 143: 548–567
Mackin JG, Owen HM, Collier A (1950) Preliminary note on the occurence of a new protistan parasite, Dermocystidium marinum nasp. in Crassostrea virginica ( Gmelin ). Science 111: 328–329
McDade JE, Tripp MR (1967) Lysozyme in the hemolymph of the oyster, Crassostrea virginica. J Invertebr Pathol 9: 531–535
Narain AS (1973) The amoebocytes of lamellibranch molluscs, with special reference to the circulating amoebocytes. Malacol Rev 6: 1–12
Noble PB (1970) Coelomocyte aggregation in Cucumaria frondosa: Effect of ethylenediamin-etetraacetate, adenosine, and adenosine nucleotides. Biol Bull (Woods Hole) 139: 549–556
Pauley GB, Sparks AK (1965) Preliminary observations on the acute inflammatory reaction in the Pacific oyster, Crassostrea gigas ( Thunberg ). J Invertebr Pathol 7: 248–256
Perkins FO, Menzel RW (1967) Ultrastructure of sporulation in the oyster pathogen Dermo-cystidium marinum. J Invertebr Pathol 9: 205–229
Pichot Y, Comps M, Tige G, Grizel H, Rabouin MA (1979) Reserches sur Bonamia ostreae gen. n., sp. n., parasite nouveau de l’huitre plate Ostrea edulis ( L). Rev Trav Inst Peches Marit 43: 131–140
Pierce SK (1982) Invertebrate cell volume control mechanisms: A coordinated use of intracellular amino acids and inorganic ions as osmotic solute. Biol Bull (Woods Hole) 163: 405–419
Pierce SK, Amende LM (1981) Control mechanisms of amino acid-mediated cell volume regulation in salinity-stressed molluscs. J Exp Zool 215: 247–257
Renwrantz LR, Yoshino TP, Cheng TC, Auld KR (1979) Size determination of hemocytes from the American oyster, Crassostrea virginica, and the description of a phagocytosis me-chanism. Jahrb Zool Abt Physiol Zoomorph 83: 1–12
Rifkin E, Cheng TC, Hohl HR (1969) An electron microscope study of the constituents of encapsulating cysts in Crassostrea virginica formed in response to Tyolcephalum metacesto- des. J Invertebr Pathol 14: 211–226
Ruddell CL (1971a) The fine structure of oyster agranular amebocytes from regenerating mantle wounds in the Pacific oyster, Crassostrea gigas. J Invertebr Pathol 18: 260–268
Ruddell CL (1971b) The fine structure of the granular amebocytes of the Pacific oyster, Crassostrea gigas. J Invertebr Pathol 18: 269–275
Sparks AK, Pauley GB (1964) Studies of the normal post-mortem changes in the oyster, Crassostrea gigas ( Thunberg ). J Insect Pathol 6: 78–101
Stauber LA (1950) The fate of India ink injected intracardially into the oyster, Ostrea virginica (Gmelin). Biol Bull (Woods Hole) 98: 227–241
Stauber LA (1961) Immunity of invertebrates, with special reference to the oyster. Proc Natl Shellfish Assoc 50: 7–20
Takatsuki S (1934) On the nature and functions of the amoebocytes of Ostrea edulis. Q J Microsc Sci 76: 379–431
Tripp MR (1958) Disposal by the oyster of intracardially injected red blood cells of vertebrates. Proc Natl Shellfish Assoc 48: 143–147
Tripp MR (1960) Mechanisms of removal of infected microorganisms from the American oyster, Crassostrea virginica (Gmelin). Biol Bull (Woods Hole) 119: 210–223
Tripp MR (1966) Hemagglutinin in the blood of the oyster Crassostrea virginica. J Invertebr Pathol 8: 478–484
Tripp MR, Kent VE (1967) Studies on oyster cellular immunity. In Vitro 3: 129–135
Vasta GR, Sullivan JT, Cheng TC, Marchalonis JJ, Warr GW (1982) A cell membrane-associated lectin of the oyster hemocyte. J Invertebr Pathol 40: 367–377
Wagge LE (1951) The activity of amebocytes and of alkaline phosphatases during the regeneration of the shell in the snail Helix aspersa. Q J Microsc Sci 92: 3077–3210
Watanabe N (1983) Shell repair. In: Wilbur KM (ed) The Mollusca, Vol 4. Physiology, Part 1. Academic Press, New York, pp 289–316
Yonge CM (1946) Digestion of animals by lamellibranchs. Nature 157: 729
Yoshino TP, Cheng TC (1982) Experimentally induced elevation of aminopeptidase activity in hemolymph cells of the American oyster, Crassostrea virginica. J Invertebr Pathol 27: 267–270
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1986 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Fisher, W.S. (1986). Structure and Functions of Oyster Hemocytes. In: Brehélin, M. (eds) Immunity in Invertebrates. Proceedings in Life Sciences. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70768-1_3
Download citation
DOI: https://doi.org/10.1007/978-3-642-70768-1_3
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-70770-4
Online ISBN: 978-3-642-70768-1
eBook Packages: Springer Book Archive