Reduced bactericidal activity and nitric oxide production in metallothionein-deficient macrophages in response to lipopolysaccharide stimulation

This study was designed to investigate bactericidal activity of and nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated peritoneal exudate macrophages (Mφ) from metallothionein (MT)-null mice. Control Mφ had a bactericidal effect on Staphylococcus aureus, but MT-null Mφ had significantly lower activity. NO is an important factor in the bactericidal function of Mφ. LPS-stimulated MT-null Mφ produced less NO than those of control mice. LPS-stimulated Mφ produce cytokines such as tumor necrosis factor (TNF)-alpha. TNF-alpha activate Mφ and stimulates NO production. We evaluated NO production by TNF-alpha-stimulated Mφ. MT-null Mφ produced less NO in response to TNF-alpha stimulation. Levels of expression of inducible NO synthase (iNOS) mRNA and production of iNOS protein in response to LPS stimulation were similar in MT-null and control cells, as were levels of expression of arginase, which competes in arginine metabolism with iNOS. No notable changes were found in arginine uptake or in expression of cationic amino acid transporter 2 (a major arginine transporter in Mφ) between control and MT-null Mφ. The rate of conversion of [14C]-L-arginine to citrulline, which is formed with NO by the action of iNOS, was much lower in MT-null Mφ than in control cells. These results indicate that the reduced production of NO in MT-deficient Mφ is due mainly to reduced activity of iNOS. Thus, MT plays important roles in bactericidal activity, NO production, and arginine metabolism in activated Mφ