Piezo2 expressing nociceptors mediate mechanical sensitization in experimental osteoarthritis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37120427.
- Also identified by DOI 10.1038/s41467-023-38241-x and PMC identifier 10148822.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Non-opioid targets are needed for addressing osteoarthritis pain, which is mechanical in nature and associated with daily activities such as walking and climbing stairs. Piezo2 has been implicated in the development of mechanical pain, but the mechanisms by which this occurs remain poorly understood, including the role of nociceptors. Here we show that nociceptor-specific Piezo2 conditional knock-out mice were protected from mechanical sensitization associated with inflammatory joint pain in female mice, joint pain associated with osteoarthritis in male mice, as well as both knee swelling and joint pain associated with repeated intra-articular injection of nerve growth factor in male mice. Single cell RNA sequencing of mouse lumbar dorsal root ganglia and in situ hybridization of mouse and human lumbar dorsal root ganglia revealed that a subset of nociceptors co-express Piezo2 and Ntrk1 (the gene that encodes the nerve growth factor receptor TrkA). These results suggest that nerve growth factor-mediated sensitization of joint nociceptors, which is critical for osteoarthritic pain, is also dependent on Piezo2, and targeting Piezo2 may represent a therapeutic option for osteoarthritis pain control.
Medical subject headings
- Animals
- Mice
- Male
- Female
- Humans
- Nociceptors
- Nociceptors/metabolism
- Pain
- Pain/metabolism
- Osteoarthritis
- Osteoarthritis/genetics
- Osteoarthritis/metabolism
- Mice, Knockout
- Arthralgia
- Nerve Growth Factors
- Nerve Growth Factors/metabolism
- Ganglia, Spinal
- Ganglia, Spinal/metabolism
- Ion Channels
- Ion Channels/genetics
- Ion Channels/metabolism