Diflunisal targets the HMGB1/CXCL12 heterocomplex and blocks immune cell recruitment

De Leo, F.; Quilici, G.; Tirone, M.; Mannella, V.; De Marchis, F.; Preti, A.; Gori, A.; Casalgrandi, M.; Mezzapelle, R.; Bianchi, M.; Musco, G.

doi:10.1101/563890

bioRxiv · 10.1101/563890

Diflunisal targets the HMGB1/CXCL12 heterocomplex and blocks immune cell recruitment

De Leo, F.·Quilici, G.·Tirone, M.·Mannella, V.·De Marchis, F.·Preti, A.·Gori, A.·Casalgrandi, M.·Mezzapelle, R.·Bianchi, M.·Musco, G.

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Abstract

Extracellular HMGB1 triggers inflammation following infection or injury, and supports tumorigenesis in inflammation-related malignancies. HMGB1 has several redox states: reduced HMGB1 recruits inflammatory cells to injured tissues forming a heterocomplex with CXCL12 and signaling via its receptor CXCR4; disulfide-containing HMGB1 binds to TLR4 and promotes inflammatory responses. Here we show that Diflunisal, an aspirin-like nonsteroidal anti-inflammatory drug (NSAID) that has been in clinical use for decades, specifically inhibits in vitro and in vivo the chemotactic activity of HMGB1 at nanomolar concentrations, at least in part by binding directly to both HMGB1 and CXCL12 and disrupting their heterocomplex. Importantly, Diflunisal does not inhibit TLR4-dependent responses. Our findings clarify the mode of action of Diflunisal, and open the way to the rational design of functionally specific anti-inflammatory drugs.

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De Leo, F., Quilici, G., Tirone, M., Mannella, V., De Marchis, F., Preti, A., Gori, A., Casalgrandi, M., Mezzapelle, R., Bianchi, M., Musco, G.. 2019-03-01. Diflunisal targets the HMGB1/CXCL12 heterocomplex and blocks immune cell recruitment. https://doi.org/10.1101/563890

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