Complement receptor 3-like immunoreactivity in the light green cells and the canopy cells of the pond snail, Lymnaea stagnalis

Brain Research

Volumn 865, Issue 1, 2000, Pages 102-106

  Hatakeyama, Dai ^a   Ito, Iori ^a   Kojima, Satoshi ^a   Fujito, Yutaka ^b   Ito, Etsuro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b SAPPORO MEDICAL UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Canopy cell; Immunohistochemistry; Light green cell; Mollusc

Indexed keywords

COMPLEMENT RECEPTOR; PEPTIDE HORMONE; SEX HORMONE;

ARTICLE; CENTRAL NERVOUS SYSTEM; GENE EXPRESSION; HORMONE RELEASE; IMMUNOREACTIVITY; NEUROENDOCRINE SYSTEM; NEUROSECRETORY CELL; NONHUMAN; PRIORITY JOURNAL; SNAIL;

ANIMALS; CENTRAL NERVOUS SYSTEM; FLUORESCENT ANTIBODY TECHNIQUE; LYMNAEA; MACROPHAGE-1 ANTIGEN; NEURONS; NEUROSECRETION; NEUROSECRETORY SYSTEMS; PERIPHERAL NERVES;

EID: 0034685702     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(00)02203-4     Document Type: Article

References (20)

1. Brown G.E., Reed E.B., E M. Lanser, Neutrophil CR3 expression and specific granule exocytosis are controlled by different signal transduction pathways. J. Immunol. 147:1991;965-971.
2. Buma P., Roubos E.W., Buijs R.M. Ultrastructural demonstration of exocytosis of neural, neuroendocrine and endocrine secretions with an in vitro tannic acid (TARI-) method. Histochemistry. 80:1984;247-256.
3. Buma P., Roubos E.W. Ultrastructural demonstration of nonsynaptic release sites in the central nervous system of the snail Lymnaea stagnalis, the insect Periplaneta americana, and the rat. Neuroscience. 17:1986;867-879.
4. Geraert W.P.M. Control of growth by the neurosecretory hormone of the light green cells in the freshwater snail Lymnaea stagnalis. Gen. Comp. Endocrinol. 29:1976;61-71.
5. Geraert W.P.M., Buma P., Hogenes T.M. Isolation of neurosecretory granules from the neurohaemal areas of peptidergic systems of Lymnaea stagnalis, with special reference to the ovulation hormone-producing caudodorsal cells. Gen. Comp. Endocrinol. 53:1984;212-217.
6. Geraert W.P.M., Smit A.B., Li K.W., Hordijk P.L. The light green cells of Lymnaea: A neuroendocrine model system for stimulus-induced expression of multiple peptide genes in a single cell type. Experientia. 48:1992;464-473.
7. Hatakeyama D., Ito E. Three-dimensional reconstruction and mapping of serotonin-like immunoreactive neurons in the central nervous system of the pond snail, Lymnaea stagnalis, with the confocal laser scanning microscope. Bioimages. 7:1999;1-12.
8. Hatakeyama D., Ito E. Distribution and Developmental Changes in GABA-like Immunoreactive Neurons in the Central Nervous System of Pond Snail, Lymnaea stagnalis. J. Comp. Neurol. 418:2000;310-322.
9. Ito E., Kobayashi S., Kojima S., Sadamoto H., Hatakeyama D. Associative learning in the pond snail, Lymnaea stagnalis. Zool. Sci. 16:1999;711-723.
10. Luchtel D.L., Martin A.W., Olsen I.D., Boer H.H. Gastropoda: pulmonata. Harrison F.W., Kohn A.J. Microscopic Anatomy of Invertebrate. Mollusca II. 6B:1997;459-718 Wiley-Liss, New York.
11. Meester I., Ramkema M.D., Van Minnen J., Boer H.H. Differential expression of four genes encoding molluscan insulin-related peptides in the central nervous system of the pond snail Lymnaea stagnalis. Cell Tissue Res. 269:1992;183-188.
12. Nolte A. The mode of release of neurosecretory material in the freshwater pulmonate lymnaea stagnalis l. (gastropoda). Salanki J. Symposium on Neurobiology of Invertebrates. 1967;123-133 Plenum Press, New York.
13. O'Shea J.J., Brown E.J., Seligmann B.E., Matcalf J.A., Frank M.M., Gallin J.I. Evidence for distinct intracellular pools of receptors for C3b and C3bi in human neutrophils. J. Immunol. 134:1985;2580-2587.
14. Pryzwansky K.B., Wyatt T., Reed W., Ross G.D. Phorbol ester induces transient focal concentrations of functional, newly expressed CR3 in neutrophils at sites of specific granule exocytosis. Eur. J. Cell Biol. 54:1991;61-75.
15. Ross G.D., Lambris J.D. Identification of a C3bi-specific membrane complement receptor that is expressed on lymphocytes, monocytes, neurtophils, and erythrocytes. J. Exp. Med. 155:1982;96-110.
16. Smit A.B., Vreugdenhil E., Ebberink R.H.M., Geraerts W.P.M., Klootwijk J., Joosse J. Growth-controlling molluscan neurons produce the precursor of an insulin-related peptide. Nature. 331:1988;535-538.
17. Van Heumen W.R.A., Roubos E.W. Ultrastructural evidence for synthesis, storage and release of insulin-related peptides in the central nervous system of Lymnaea stagnalis. Neuroscience. 39:1990;493-500.
18. Van Minnen J., Reichelt D., Lodder J.C. An ultrastructural study of the neurosecretory canopy cell of the pond snail Lymnaea stagnalis (L.), with the use of the horseradish peroxidase tracer technique. Cell Tissue Res. 204:1979;453-462.
19. Van Minnen J., Reichelt D. Photoperiod-dependent neural control of the activity of the neurosecretory canopy cell in the lateral lobes of the cerebral ganglia of the freshwater pulmonate Lymnaea stagnalis (L.). Cell Tissue Res. 208:1980;457-465.
20. Wendelaar Bonga S.E. Ultrastructure and histochemistry of neurosecretory cells and neurohaemal areas in the pond snail Lymnaea stagnalis (L.). Z. Zellforsch. 108:1970;190-224.