Dose-response Studies of Depletion and Repopulation of Rat Intestinal Mucosal Mast Cells after Irradiation

References

• Asekenase P.W. Immunopathology of parasitic diseases: involvement of basophils and mast cells. Springer Seminars Immunopathology 1980; 2: 417–442
   Google Scholar
• Baer A.R., Cheeseman C.I., Thomson A.B.R. The assessment of recovery of the intestine after acute radiation injury. Radiation Research 1987; 109: 319–329
   PubMed Web of Science ®Google Scholar
• Befus A.D., Bienenstock J., Denburg J.A. Mast Cell Differentiation and Heterogeneity. Raven, New York 1986
   Google Scholar
• Befus D., Pearce F., Bienenstock J. Intestinal mast cells in pathology and host resistance. Food Disorders and Allergy, J. Brostoff, S.J. Challacombe. Bailliere Tindall, London 1987; 88–102, In
   Google Scholar
• Bienenstock J. An update on mast cell heterogeneity. Journal of Allergy and Clinical Immunology 1988; 81: 763–769
   Google Scholar
• Capron M., Rousseaux J., Mazingue C., Bazin H., Capron A. Rat mast cell-eosinophil interaction in antibody-dependant eosinophil cytotoxicity to Schistosoma mansoni schistosomula. Journal of Immunology 1978; 121: 2518–2525
   PubMed Web of Science ®Google Scholar
• Carlsen R.A., Asboe-Hansen G. Changes in skin histamine induced by X-ray of differing quality. Journal of Investigative Dermatology 1971; 50: 69–71
   Google Scholar
• Carter B.G. Mast cell numbers and passive cutaneous anaphylaxis in irradiated mice. International Archives of Allergy and Applied Immunology 1977; 54: 378–381
   Google Scholar
• Crowder M.J., Hand D.J. Analysis of Repeated Measures. Chapman & Hall, London 1990
   Google Scholar
• Csaba G., Berlin I., Kapa E., Kovacs L. Effects of X-ray irradiation on mast cell production in the rat. Acta Morphologica Hungarica 1973; 21: 351–358
   Google Scholar
• Cummins A.G., Munro G.H., Huntley J.F., Miller H.R.P., Ferguson A. Separate effects of irradiation and of graft-versus-host reaction on rat mucosal mast cells. Gut 1989; 30: 355–360
   Google Scholar
• Dahlqvist A. Assay of intestinal disaccharidases. Analytical Biochemistry 1968; 22: 99–107
   PubMed Web of Science ®Google Scholar
• Donlon M.A. Role of mast cell mediators in radiation injury and protection. Pharmacology and Therapeutics 1988; 39: 373–377
   PubMed Web of Science ®Google Scholar
• Enerback L. Mast cells in rat gastrointestinal mucosa. I. Effects of fixation. Acta Pathologica Microbiologica Scandinavica 1966; 66: 289–302
   PubMedGoogle Scholar
• Ferguson A., Murray D. Quantitation of intra-epithelial lymphocytes in human jejunum. Gut 1971; 12: 988–994
   PubMed Web of Science ®Google Scholar
• Fukuzumi T., Waki N., Kanakura Y., Nagoshi J., Hirota S., Yochikawa K., Kitamura Y. Differences in irradiation susceptibility and turnover between mucosal and connective tissue-type mast cells of mice. Experimental Hematology 1990; 18: 843–847
   Google Scholar
• Gelfand M.D., Tepper M., Katz L.A., Binder H.J., Yesner R., Floch M.H. Acute irradiation proctitis in man: development of eosinophilic crypt abscesses. Gastroenterology 1968; 54: 401–411
   PubMed Web of Science ®Google Scholar
• Guy-Grand D., Dy M., Luffau G., Vassalli P. Gut mucosaal mast cells: origin, traffic and differentiation in mice and rats. Annals of the Institute Pasteur, Immunology 1984; 137: 215–222, D(2)
   Google Scholar
• Huntley J.F., Mackellar A., Newlands G.F.J., Irvine J., Miller H.R.P. Mapping of the rat mast cell granule proteinases RMCPI and II by enzyme-linked immunosorbent assay and paired immunofluorescent. Microbiologica Immunologica 1990
   Google Scholar
• Irani A.A., Schwartz L.B. Mast cell heterogencity. Clinical and Experimental Immunology 1989; 19: 143–155
   Google Scholar
• Kay A.B. The role of the eosinophil. Journal of Allergy and Clinical Immunology 1979; 64: 90–104
   Google Scholar
• Keelan M., Cheeseman C., Walker K., Thomson A.B.R. Effect of external abdominal irradiation on intestinal morphology and brush border membrane enzyme and lipid composition. Radiation Research 1986; 105: 84–96
   PubMed Web of Science ®Google Scholar
• Kerr J.F.R., Wyllie A.H., Currie A.R. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. British Journal of Cancer 1972; 26: 239–257
   PubMed Web of Science ®Google Scholar
• King D.P., Strober S. Immunoregulatory changes induced by total lymphoid irradiation. Journal of Experimental Medicine 1981; 154: 13–23
   Google Scholar
• King S.J., Miller H.R.P. Anaphylatic release of mucosal mast cell protease and its relationship to gut permeability in Nippostronglylus primed rats. Immunology 1984; 51: 653–660
   PubMed Web of Science ®Google Scholar
• King S.J., Miller H.R.P., Newlands G.F.J., Woodbury R.G. Depletion of mucosal mast cell protease by corticosteroids: effect on intestinal anaphylaxis in the rat. Proceedings of the National Academy of Sciences, USA 1985; 82: 1214–1218
   PubMed Web of Science ®Google Scholar
• King S.J., Miller H.R.P., Woodbury R.G. Gut mocosal mast cells in Nippostrongylus-primed rats are the major source of secreted rat mast cell protease II following systemic anaphylaxis. European Journal of Immunology 1986; 16: 151–155
   Google Scholar
• Kojima S., Ovary Z. Radioresistance of some biologic properties of mouse mast cells. Journal of Immunology 1974; 113: 673–676
   Google Scholar
• Levy D.A., Wefald A.F., Beschorner W.E. Intestinal mast mucosal cell proliferation in graft-versushost reaction in rats. International Archives of Allergy and Applied Immunology 1985; 77: 186–188
   Google Scholar
• MacDonald T.T., Ferguson A. Hypersensitivity reactions in the small intestine. 2. Effects of allograft rejection on mucosal architecture and lymphoid cell infiltrate. Gut 1976; 17: 81–91
   PubMed Web of Science ®Google Scholar
• MacQueen G., Marshall J., Perdue M., Siegel S., Bienenstock J. Pavlovian conditioning of rat mucosal mast cells to secrete rat mast cell protease II. Science 1989; 243: 83–85
   PubMed Web of Science ®Google Scholar
• Man W.K., Michalowski A., Li S.K., Barr J., Burgin J. Gastrointestinal histamine after gastric irradiation in the mouse. Agents and Actions 1986; 18: 210–213
   Google Scholar
• Miller H.R.P., Woodbury R.G., Huntley J.F., Newlands G. Systemic release of mucosal mast-cell protease in primed rats challenged with Nippostrongylus brasiliensis. Immunology 1985; 49: 471–479
   Google Scholar
• Miller H.R.P., King S.J., Gibson S., Huntley J.F., Newlands G.F.J., Woodbury R.G. Intestinal mucosal mast cells in normal and parasitised rats. Mast Cell Differentiation and Heterogeneity, A.D. Befus, J. Bienenstock, J.A. Denburg. Raven, New York 1986; 239–255, In
   Google Scholar
• Morson B.C. The large intestine. Systemic Pathology, Vol 3, Alimentary Pathology, B.C. Morson. Churchill Livingstone, London 1987, In
   Google Scholar
• Nawa Y., Miller H.R.P. Protection against Nippostrongylus brasiliensis by adoptive immunisation with immune thoracic duct lymphocytes. Cellular Immunology 1978; 37: 51–60
   Google Scholar
• Nawa Y., Miller H.R.P., Hall E., Jarrett E.E.E. Adoptive transfer of total and parasite-specific IgE responses in rats infected with Nippostrongylus brasiliensis. Immunology 1981; 44: 119–123
   Google Scholar
• Norrby K., Abok K., Adamson P., Forsberg B. Radiation effects on mast cells: secretory ability, histamine release and recovery and cell number. Acta Pathologica Microbiologica Immunologica Scandinavica A 1984; 92: 417–427
   Google Scholar
• Patrick M.K., Dunn I.J., Buret A., Miller H.R.P., Huntley J.F., Gibson S., Gall D.G. Mast cell protease release and mucosal ultrastructure during intestinal anaphylaxis in the rat. Gastroenterology 1988; 94: 1–9
   PubMedGoogle Scholar
• Raben M., Walach N., Galili U., Schlesinger M. The effect of radiation therapy on lymphocyte subpopulations in cancer patients. Cancer 1976; 37: 1417–1421
   PubMed Web of Science ®Google Scholar
• Robertson I., Greaves M.W. Responses of human skin blood vessels to synthetic histamine analogues. British Journal of Clinical Pharmacology 1978; 5: 319–322
   Google Scholar
• Schwartz L.B., Austen K.F. Structure and function of the chemical mediators of mast cells. Progress in Allergy 1984; 34: 271–321
   PubMedGoogle Scholar
• Sellins K.S., Cohen J.J. Gene induction by c-irradiation leads to DNA fragmentation in lymphocytes. Journal of Immunology 1987; 139: 3199–3206
   PubMed Web of Science ®Google Scholar
• Shanahan F., Denburg J.A., Fox J., Bienenstock J., Befus D. Mast cell heterogeneity: effects of neuroenteric peptides on histamine release. Journal of Immunology 1985; 135: 1331–1337
   PubMed Web of Science ®Google Scholar
• Smith D.E. The tissue mast cell. International Review of Cytology 1963; 14: 327–386
   Google Scholar
• Smith D.E., Lewis Y.S. Phagocytosis of granules from disrupted mast cells. Anatomical Record 1958; 132: 93–112
   PubMedGoogle Scholar
• Soda K., Kawabori S., Perdue M.H., Bienenstock J. Macrophage engulfment of mucosal mast cells in rats treated with dexamethasone. Gastroenterology 1991; 100: 929–937
   Google Scholar
• Stead R.H., Tomioka M., Quinonez G., Simon G.T., Felten S.Y., Bienenstock J. Intestinal mucosal mast cells in normal and nematode-infected rat intestines are in intimate contact with peptidergic nerves. Proceedings of the National Academy of Sciences, USA 1987; 84: 2975–2979
   PubMed Web of Science ®Google Scholar
• Strobel S., Miller H.R.P., Ferguson A. Human intestinal mucosal mast cells: Evaluatioon of fixation and staining techniques. Journal of Clinical Pathology 1981; 34: 851–858
   PubMed Web of Science ®Google Scholar
• Woodbury R.G., Everitt M., Sanada Y., Katunuma N., Lagunoff D., Neurath H. A major serine protease in rat skeletal muscle: evidence for its mast cell origin. Proceedings of the National Academy of Sciences, USA 1978b; 75: 5311–5313
   PubMedGoogle Scholar
• Woodbury R.G., Gruzenski G.M., Lagunoff D. Immunofluorescent localisation of a serine protease in rat small intestine. Proceedings of the National Academy of Sciences, USA 1978a; 75: 2785–2789
   PubMed Web of Science ®Google Scholar
• Woodbury R., Miller H.R.P. Quantitative analysis of mucosal mast cell protease in the intestines of Nippostrongylus-infected rats. Immunology 1982; 46: 487–495
   Google Scholar
• Woodbury R.G., Miller H.R.P., Huntley J.F., Newlands G.F.J., Palliser A.C., Wakelin D. Mucosal mast cells are functionally active during the spontaneous expulsion of primary intestinal nematode infections in the rat. Nature 1984; 312: 450–452
   PubMed Web of Science ®Google Scholar
• Wyllie A.H., Kerr J.F.R., Currie A.R. Cell death: the significance of apoptosis. International Review of Cytology 1980; 68: 251–305
   PubMedGoogle Scholar