Premium
RADIATION EFFECTS ON MAST CELLS: SECRETORY ABILITY, HISTAMINE RELEASE AND RECOVERY, AND CELL NUMBER
Author(s) -
NORRBY K.,
ADAMSON P.,
FORSBERG B.
Publication year - 1984
Publication title -
acta pathologica microbiologica scandinavica series a :pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0108-0164
DOI - 10.1111/j.1699-0463.1984.tb04423.x
Subject(s) - histamine , mast cell , mast (botany) , microbiology and biotechnology , liberation , chemistry , immunology , biology , pharmacology , in vitro , biochemistry
We studied the effects of irradiation with a single fraction of high‐energy electrons, in the absorbed dose range used in radiotherapy, on features related to the rat mesenteric mast‐cell (MC) population. Such features were energy dispersive X‐ray microanalysis for zinc, light and transmission electron microscopic changes, histamine content, and secretory ability of MCs when exposed to the potent secretagogue 48/80. The observation period was 14 days. Also studied were the effects of radiation on the number and histamine content of free peritoneal MCs. Irradiation‐induced decrease in histamine content was delayed for at least two days and the rate of subsequent recovery of mesenteric histamine was approximately 70% below normal. This was corroborated by the findings of necrotic and fragmented mesenteric MCs during the entire experimental period. Fibroblasts and macrophages phagocytosed groups of MC granules as well as individual MC granules. A fraction of the extruded MC granules retained an almost normal appearance. This suggests that they were solubilized unduly slow presumably because the irradiation destroyed the mechanisms and enzymes which normally degrade the heparin‐protein granule matrix and its heparin. Moreover, the irradiation suppressed the secretory ability of mesenteric MCs and significantly reduced the number of free peritoneal MCs. The findings indicate that the MC is a remarkably radiosensitive connective‐tissue cell.