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Ultrastructural characteristics of rat peritoneal mast cells undergoing differential release of serotonin without histamine and without degranulation

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Summary

Rat mast cells pretreated with the tricyclic antidepressant drug amitriptyline and stimulated with compound 48/80 secreted 60% of the total serotonin present in the cells, but only 15% of histamine, another amine stored in the same granules. Ultrastructural studies demonstrated that mast cells undergoing such differential release do not exhibit classical degranulation by compound sequential exocytosis. However, there were changes in granule shape and size, as well as alterations in many morphometric parameters consistent with secretion. Storage granules lost their homogeneity, exhibited greatly reorganized matrix and were surrounded by clear spaces which were often associated with small (0.1–0.01 μm) cytoplasmic vesicles, some of which contained electron-dense material. Secretory granules often had bud-like protrusions or were fused together in series. Quantitative autoradiography localized 3H-serotonin outside the storage granules, close to small vesicles, while staining with ruthenium red demonstrated that vesicular structures associated with differential release were not endocytotic. These results suggest that amitriptyline may inhibit regular exocytosis and permit at least serotonin to be moved selectively from storage granules to the cytosol or small vesicles from which it is eventually released.

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References

  • Benyon R, Robinson C, Church MK (1989) Differential release of histamine and eicosanoids from human skin mast cells activated by IgE-dependent and non-immunological stimuli. Br J Pharmacol 97:892–904

    Google Scholar 

  • Berlin G, Enerbäck L (1986) Non-differential inhibition of histamine and serotonin release from mast cells by amitriptyline. Agents Actions 18:89–91

    Google Scholar 

  • Carlsson SA, Ritzen M (1969) Mast cells and 5-HT. Intracellular release of 5-hydroxytryptamine (5-HT) from storage granules during anaphylaxis or treatment with compound 48/80. Acta Physiol Scand 77:449–464

    Google Scholar 

  • Carraway RE, Cochrane DE, Granier C, Kitabgi P, Leemman E, Singer EA (1984) Parallel secretion of endogenous 5-hydroxytryptamine and histamine from mast cells stimulated by vasoactive peptides and compound 48/80. Br J Pharmacol 81:227–229

    Google Scholar 

  • Cochrane DE, Douglas WW (1974) Calcium-induced extrusion of secretory granules (exocytosis) in mast cells exposed to 48/80 or the ionophores A23187 and X537A. Proc Nat Acad Sci USA 71:408–412

    Google Scholar 

  • Csaba G (1971) Mechanism and function of mast cell granules. Acad Sci Hung 22:155–168

    Google Scholar 

  • Dvorak AM, Hammond ME, Morgan E, Orenstein NS, Galli SJ, Dvorak HF (1980) Evidence for a vesicular transport mechanism in guinea pig basophilic leukocytes. Lab Invest 42:263–276

    Google Scholar 

  • Gustaffson B, Enerbäck L (1980) A cytofluorometric analysis of polymer-induced mast cell secretion. Exp Cell Biol 48:15–30

    Google Scholar 

  • Hammel I, Lagunoff D, Bauza M, Chi E (1983) Periodic, multimodal distribution of granule volumes in mast cells. Cell Tissue Res 228:51–59

    Google Scholar 

  • Ichikawa A, Kanedo H, Mon V, Tomita K (1975) Release of serotonin from mast cells induced by N-(2)-ethylhexyl-3-hydroxybutramide and catecholamine. Biochem Pharmacol 26:197–202

    Google Scholar 

  • Karnovsky MJ (1965) A formaldehyde-glutaraldehyde fixative of high osmolarity for use in electron microscopy. J Cell Biol 27:137A

  • Kashgarian M, Taylor CR, Binder HJ, Hayslett JP (1980) Amplification of cell membrane surface in potassium adaptation. Lab Invest 42:581–588

    Google Scholar 

  • Kraeuter Kops SK, Van Loveren H, Rosenstein RW, Ptak W, Askenase PW (1984) Mast cell activation and vascular alterations in immediate hypersensitivity-like reactions induced by a T cell derived antigen binding factor. Lab Invest 50:421–434

    Google Scholar 

  • Lagunoff D (1972) Vital staining of mast cells with ruthenium red. J Histochem Cytochem 20:938–944

    Google Scholar 

  • Lagunoff D (1973) Membrane fusion during mast cell secretion. J Cell Biol 57:252–259

    Google Scholar 

  • Lawson D, Raff MC, Gomperts B, Fewtrell C, Gilula NB (1977) Molecular events during membrane fusion: A study of exocytosis in rat peritoneal mast cells. J Cell Biol 72:242–259

    Google Scholar 

  • Lichentstein LM, Gillespie E (1975) The effects of the H1 and H2 antihistamines on “allergic” histamine release and its inhibition by histamine. J Pharmacol Exp Ther 192:441–450

    Google Scholar 

  • Moore HH, Kelly RB (1985) Secretory protein targeting in a pituitary cell line: differential transport of foreign secretory proteins to distinct secretory pathways. J Cell Biol 101:1773–1781

    Google Scholar 

  • Morrissey JJ, Cohn DV (1979) Regulation of secretion of parathyroid hormone and secretory protein I from separate intracellular pools by calcium, dibutyryl cyclic-AMP and isoproterenol. J Cell Biol 82:93–102

    Google Scholar 

  • Padawer J (1970) The reaction of rat mast cells to polylysine. J Cell Biol 47:352–372

    Google Scholar 

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

    Google Scholar 

  • Röhlich P, Anderson P, Uvnäs B (1971) Electron microscope observations on compound 48/80-induced degranulation in rat mast cells. J Cell Biol 51:465–483

    Google Scholar 

  • Rothman SS (1985) Nonvesicular transport. In: Ho JJL (ed) Protein Secretion: A critical analysis of the vesicular model. John Wiley and Sons, New York, pp 205–223

    Google Scholar 

  • Rudnick G (1987) Platelet responses and metabolism. In: Holmsen H (ed) Receptors and metabolism, vol. 2. CRC Press, Boca Raton, FL, pp 119–133

    Google Scholar 

  • Tamir H, Theoharides TC, Gershon MD, Askenase PW (1982) Serotonin storage pools in basophil leukemia and mast cells: Characterization of two types of serotonin binding protein and radio-autographic analysis of the intracellular distribution of 3H-serotonin. J Cell Biol 93:638–647

    Google Scholar 

  • Theoharides TC, Douglas WW (1978) Somatostatin induces histamine secretion from rat peritoneal mast cells. Endocrinology 102:1637–1640

    Google Scholar 

  • Theoharides TC, Kotkow KJ (1986) Calcium ion levels during differential mast cell secretion. FASEB 45:387

    Google Scholar 

  • Theoharides TC, Bondy PK, Tsakalos ND, Askenase PW (1980) Differential release of serotonin and histamine from mast cells. Nature 297:229–231

    Google Scholar 

  • Theoharides TC, Kraeuter-Kops S, Bondy PK, Askenase PW (1985) Differential release of serotonin without comparable histamine under diverse conditions in the rat mast cell. Biochem Pharmacol 34:1289–1398

    Google Scholar 

  • Van Loveren H, Kraeuter-Kops SK, Askenase PW (1984) Different mechanisms of release of vasoactive amines by mast cells occur in T-cell dependent compared to IgE-dependent cutaneous hypersensitivity response. Eur J Immunol 14:40–47

    Google Scholar 

  • Vindrola O, Ase A, Finkeilman S, Nahmod VE (1988) Differential release of enkephalin and enkephalin-containing peptides from perfused cat adrenal glands. J Neurochem 50:424–430

    Google Scholar 

  • Viveros OH, Diliberto EJ, Daniels AJ (1983) Biochemical and functional evidence for the cosecretion of multiple messengers from single and multiple compartments. Fed Proc 42:2923–2928

    Google Scholar 

  • Vliagoftis H, Dimitriadou V, Theoharides TC (1990) Progesterone triggers selective mast cell secretion of 5-hydroxytryptamine, Int Arch Allergy Appl Immunol (in press)

  • Weibel ER (1973) Stereological techniques for electron microscopy morphometry. In: Hayat MA (ed) Principles and techniques of electron microscopy: Biological applications, vol 3, pp 237–296

  • Woodbury RG, Miller HRP, Huntely JF, Newlands GFJ, Palliser AC, Wakelin D (1984) Mucosal mast cells are functionally active during spontaneous expulsion of intestinal nematode infections in rat. Nature 312:450–452

    Google Scholar 

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Kops, S.K., Theoharides, T.C., Cronin, C.T. et al. Ultrastructural characteristics of rat peritoneal mast cells undergoing differential release of serotonin without histamine and without degranulation. Cell Tissue Res 262, 415–424 (1990). https://doi.org/10.1007/BF00305238

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