Homocysteine enhances MMP-9 production in murine macrophages via ERK and Akt signaling pathways

Homocysteine (Hcy) at elevated levels is an independent risk factor of cardiovascular diseases, including atherosclerosis. In the present study, we investigated the effect of Hcy on the production of matrix metalloproteinases (MMP) in murine macrophages. Among the MMP known to regulate the activities of collagenase and gelatinase, Hcy exclusively increased the gelatinolytic activity of MMP-9 in J774A.1 cells as well as in mouse peritoneal macrophages. Furthermore, this activity was found to be correlated with Western blot findings in J774A.1 cells, which showed that MMP-9 expression was concentration- and time-dependently increased by Hcy. Inhibition of the ERK and Akt pathways led to a significant decrease in Hcy-induced MMP-9 expression, and combined treatment with inhibitors of the ERK and Akt pathways showed an additive effects. Activity assays for ERK and Akt showed that Hcy increased the phosphorylation of both, but these phosphorylation were not affected by inhibitors of the Akt and ERK pathways. In line with these findings, the molecular inhibition of ERK and Akt using siRNA did not affect the Hcy-induced phosphorylation of Akt and ERK, respectively. Taken together, these findings suggest that Hcy enhances MMP-9 production in murine macrophages by separately activating the ERK and Akt signaling pathways.

► Homocysteine (Hcy) induced MMP-9 production in murine macrophages.
► Hcy induced MMP-9 production through ERK and Akt signaling pathways.
► ERK and Akt signaling pathways were activated by Hcy in murine macrophages.
► ERK and Akt pathways were additively act on Hcy-induced MMP-9 production.
► Hcy enhances MMP-9 production in macrophages via activation of ERK and Akt signaling pathways in an independent manner.