“…Moreover, NO from other sources, such as macrophages, can regulate MC activities (12). Endogenous and exogenous NO can inhibit MC degranulation; protease release; adherence to fibronectin; and leukotriene, cytokine, and chemokine production (4,7). By contrast, NO can also upregulate MC properties, such as CD8 expression (13), cytotoxicity (14), and cyclooxygenase-2 expression (15).…”