Abstract
Light microscopic observations of normal rat peritoneal mast cells and ultrastructural observations of human mast cells from lesions of nodular mastocytosis indicated that structural damage results in a pronounced increase in percentage of cells with a positive dopa reaction. Recent studies have indicated that the dopa reaction in mast cells is peroxidase-dependent. Enhancement of the dopa reaction by structural damage (latency) is probably related to increased substrate-enzyme interaction. Ultrastructural localization of dopa melanin to mast cell granules and the high percentage of mast cells showing a positive dopa reaction after structural damage is evidence against the possibility that dopa melanin is formed in mast cells by phagocytized enzyme.
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