TY - JOUR T1 - An aggrecan fragment drives osteoarthritis pain through Toll-like receptor 2 JF - bioRxiv DO - 10.1101/160432 SP - 160432 AU - Rachel E. Miller AU - Richard J. Miller AU - Shingo Ishihara AU - Phuong B. Tran AU - Suzanne B. Golub AU - Karena Last AU - Amanda J. Fosang AU - Anne-Marie Malfait Y1 - 2017/01/01 UR - http://biorxiv.org/content/early/2017/07/07/160432.abstract N2 - Pain is the predominant symptom of osteoarthritis, but the connection between joint damage and the genesis of pain is not well understood. Loss of articular cartilage is a hallmark of osteoarthritis, and it occurs through enzymatic degradation of aggrecan by ADAMTS-4/5-mediated cleavage in the interglobular domain (E373-374 A). Further cleavage by MMPs (N341-342 F) releases a 32-amino-acid aggrecan fragment (32-mer). We investigated the role of this 32-mer in driving joint pain. We demonstrated that the 32-mer excites dorsal root ganglion (DRG) nociceptive neurons, both in culture and in intact explants. Treatment of cultured sensory neurons with the 32-mer induced them to express the pro-algesic chemokine, MCP-1/CCL2. These effects were mediated through Toll-like receptor (TLR)2, which we demonstrated was expressed by nociceptive neurons. In addition, intra-articular injection of the 32-mer provoked knee hyperalgesia in wild-type but not Tlr2 null mice. Blocking the production or action of the 32-mer in transgenic mice prevented the development of knee hyperalgesia in a murine model of osteoarthritis. These findings suggest that the aggrecan 32-mer fragment directly activates TLR2 on joint nociceptors and is an important mediator of the development of osteoarthritis-associated joint pain. ER -