Insulin-induced NADPH oxidase activation promotes proliferation and matrix metalloproteinase activation in monocytes/macrophages

Insulin stimulates superoxide (O2−) production in monocytes and macrophages. However, the mechanisms through which insulin induces O2− production are not completely understood. In this study, we (a) characterized the enzyme and the pathways involved in insulin-stimulated O2− production in human monocytes and murine macrophages, and (b) analyzed the consequences of insulin-stimulated O2− production on the cellular phenotype in these cells. We showed that insulin stimulated O2− production, and promoted p47phox translocation to the plasma membrane. Insulin-induced O2− production and p47phox translocation were prevented in the presence of specific inhibitors of PI3K and PKC. Insulin-mediated NADPH oxidase activation stimulated MMP-9 activation in monocytes and cell proliferation in macrophages. The effect of insulin on these phenotypic responses was mediated through NFκB, p38MAPK, and ERK 1/2 activation. Small-interfering RNA-specific gene silencing targeted specifically against Nox2 reduced the cognate protein expression, decreased insulin-induced O2− production, inhibited the turn on of NFκB, p38MAPK, and ERK 1/2, and reduced cell proliferation in macrophages. These findings suggest a pivotal role for NADPH oxidase in insulin-induced proliferation and proteolytic activation in monocytes and macrophages, respectively, and identify a pathway that may play a pathological role in hyperinsulinemic states.