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bioRxiv · 10.1101/160432

An aggrecan fragment drives osteoarthritis pain through Toll-like receptor 2

Miller, R.·Miller, R. J.·Ishihara, S.·Tran, P. B.·Golub, S. B.·Last, K.·Fosang, A. J.·Malfait, A.-M.
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Abstract

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.

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Miller, R., Miller, R. J., Ishihara, S., Tran, P. B., Golub, S. B., Last, K., Fosang, A. J., Malfait, A.-M.. 2017-07-07. An aggrecan fragment drives osteoarthritis pain through Toll-like receptor 2. https://doi.org/10.1101/160432

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