Freshly isolated BMM and alveolar macrophage cell line (AMJ2-C8) were stimulated with MVs and with Pam3CSK4 in vitro (500,000 cells/500 μl of media). Supernatants and cell lysates were collected at time points ranging from 0 to 48 hours after stimulation (x axes of all graphs indicate time in hours). (A) The supernatants of cultures of WT (white bars) or TLR2-knockout (black bars) isolated BMMs were assayed for cytokines IL-1β, IL-10, IL-12p70, TNF-α, and chemokines CXCL1 by multiplex ELISA (MSD Systems). Cytokines IL-6 and MIP-1α were analyzed by standard ELISA. Data represent mean ± SEM. (B) The levels of Cox-2 and MMP-9 were analyzed by Western blot and zymography, respectively. For Cox-2 analysis (top), lysates were made from cells (AMJ2-C8 alveolar macrophage cell line (AM), WT BMM, or Tlr2–/– BMM collected at the indicated times, ranging from 0 to 48 hours after addition of PBS (unstimulated), Pam3CSK4, or BCG MVs. For measurement of MMP-9 activity, culture supernatants were collected at the indicated times following stimulation as shown. The graphs at the bottom show levels of MMP-9 activity relative to a recombinant MMP-9 protein standard. The data of the Cox-2 and MMP-9 analysis are representative of 3 independent experiments. Data represent mean ± SEM.