Figure 1
Figure 1. GP1a inhibits Mmp9 expression induced by CCP in myeloid immune cells. (A) BMMΦs, BMDCs, or primary microglia were treated with CCP with or without CB2R agonists GP1a (5μM) or O-1966 (5μM) for 24 hours. RNA was extracted and subjected to qRT-PCR for Mmp9. N.D. indicates not determined. (B) BMDCs were treated with CCP with or without GP1a (5μM), and RNA was extracted at different time points and subjected to qRT-PCR for Mmp9. (C) BMDCs were treated as described in panel B, and supernatants collected at various time points were subjected to MMP-9 ELISA. (D) BMDCs were treated with different concentrations of GP1a for 48 hours, and the resulting supernatants were subjected to MMP-9 ELISA. Data in panels A and B are normalized to housekeeping gene β-actin and presented as fold change compared with untreated samples. *P < .05, **P < .01, *** P < .001 compared with CCP. Data are representative of 2 (A-B) and 4 (C-D) independent experiments.

GP1a inhibits Mmp9 expression induced by CCP in myeloid immune cells. (A) BMMΦs, BMDCs, or primary microglia were treated with CCP with or without CB2R agonists GP1a (5μM) or O-1966 (5μM) for 24 hours. RNA was extracted and subjected to qRT-PCR for Mmp9. N.D. indicates not determined. (B) BMDCs were treated with CCP with or without GP1a (5μM), and RNA was extracted at different time points and subjected to qRT-PCR for Mmp9. (C) BMDCs were treated as described in panel B, and supernatants collected at various time points were subjected to MMP-9 ELISA. (D) BMDCs were treated with different concentrations of GP1a for 48 hours, and the resulting supernatants were subjected to MMP-9 ELISA. Data in panels A and B are normalized to housekeeping gene β-actin and presented as fold change compared with untreated samples. *P < .05, **P < .01, *** P < .001 compared with CCP. Data are representative of 2 (A-B) and 4 (C-D) independent experiments.

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