TY - JOUR
T1 - Current understanding of osteoarthritis pathogenesis and relevant new approaches
AU - Tong, Liping
AU - Yu, Huan
AU - Huang, Xingyun
AU - Shen, Jie
AU - Xiao, Guozhi
AU - Chen, Lin
AU - Wang, Huaiyu
AU - Xing, Lianping
AU - Chen, Di
N1 - Funding Information:
This work has been supported by the National Natural Science Foundation of China (NSFC) grants (82030067, 82161160342, and 82172397) to D.C. and L.T. and a grant from the Youth Innovation Promotion Association of the Chinese Academy of Sciences (2020353) to L.T. This work was also supported by the National Key Research and Development Program of China (2021YFB3800800 to L.T. and D.C). This work was also supported by the research grant NIH AG0599775. The data in Fig. 6 were generated by Dr. Xi Lin, a postdoctoral fellow at the University of Rochester Medical Center.
Funding Information:
This work has been supported by the National Natural Science Foundation of China (NSFC) grants (82030067, 82161160342, and 82172397) to D.C. and L.T. and a grant from the Youth Innovation Promotion Association of the Chinese Academy of Sciences (2020353) to L.T. This work was also supported by the National Key Research and Development Program of China (2021YFB3800800 to L.T. and D.C). This work was also supported by the research grant NIH AG0599775. The data in Fig. were generated by Dr. Xi Lin, a postdoctoral fellow at the University of Rochester Medical Center.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Osteoarthritis (OA) is the most common degenerative joint disease that causes painful swelling and permanent damage to the joints in the body. The molecular mechanisms of OA are currently unknown. OA is a heterogeneous disease that affects the entire joint, and multiple tissues are altered during OA development. To better understand the pathological mechanisms of OA, new approaches, methods, and techniques need to be used to understand OA pathogenesis. In this review, we first focus on the epigenetic regulation of OA, with a particular focus on DNA methylation, histone modification, and microRNA regulation, followed by a summary of several key mediators in OA-associated pain. We then introduce several innovative techniques that have been and will continue to be used in the fields of OA and OA-associated pain, such as CRISPR, scRNA sequencing, and lineage tracing. Next, we discuss the timely updates concerning cell death regulation in OA pathology, including pyroptosis, ferroptosis, and autophagy, as well as their individual roles in OA and potential molecular targets in treating OA. Finally, our review highlights new directions on the role of the synovial lymphatic system in OA. An improved understanding of OA pathogenesis will aid in the development of more specific and effective therapeutic interventions for OA.
AB - Osteoarthritis (OA) is the most common degenerative joint disease that causes painful swelling and permanent damage to the joints in the body. The molecular mechanisms of OA are currently unknown. OA is a heterogeneous disease that affects the entire joint, and multiple tissues are altered during OA development. To better understand the pathological mechanisms of OA, new approaches, methods, and techniques need to be used to understand OA pathogenesis. In this review, we first focus on the epigenetic regulation of OA, with a particular focus on DNA methylation, histone modification, and microRNA regulation, followed by a summary of several key mediators in OA-associated pain. We then introduce several innovative techniques that have been and will continue to be used in the fields of OA and OA-associated pain, such as CRISPR, scRNA sequencing, and lineage tracing. Next, we discuss the timely updates concerning cell death regulation in OA pathology, including pyroptosis, ferroptosis, and autophagy, as well as their individual roles in OA and potential molecular targets in treating OA. Finally, our review highlights new directions on the role of the synovial lymphatic system in OA. An improved understanding of OA pathogenesis will aid in the development of more specific and effective therapeutic interventions for OA.
UR - http://www.scopus.com/inward/record.url?scp=85138527215&partnerID=8YFLogxK
U2 - 10.1038/s41413-022-00226-9
DO - 10.1038/s41413-022-00226-9
M3 - Review article
C2 - 36127328
AN - SCOPUS:85138527215
SN - 2095-4700
VL - 10
JO - Bone Research
JF - Bone Research
IS - 1
M1 - 60
ER -