TY - JOUR
T1 - Emerging potential of exosomes in regenerative medicine for temporomandibular joint osteoarthritis
AU - Lee, Yeon Hee
AU - Park, Hee Kyung
AU - Auh, Q. Schick
AU - Nah, Haram
AU - Lee, Jae Seo
AU - Moon, Ho Jin
AU - Heo, Dong Nyoung
AU - Kim, In San
AU - Kwon, Il Keun
N1 - Funding Information:
This research was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) (No. 2017M3A9E4048170).
Funding Information:
Funding: This research was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) (No. 2017M3A9E4048170).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/2/2
Y1 - 2020/2/2
N2 - Exosomes are nanosized vesicles (30–140 nm) of endocytic origin that play important roles in regenerative medicine. They are derived from cell membranes during endocytic internalization and stabilize in biological fluids such as blood and synovia. Temporomandibular joint osteoarthritis (TMJ OA) is a degenerative disease, which, in addition to chronic pain, is characterized by progressive cartilage breakdown, condylar bone remodeling, and synovitis. However, traditional clinical treatments have limited symptom‐ and structure‐modifying effects to restore damaged cartilage and other TMJ tissues. This is due to the limited self‐healing capacity of condylar cartilage. Recently, stem‐cell‐derived exosomes have been studied as an alternative therapeutic approach to tissue repair and regeneration. It is known that trophic regulation of mesenchymal stem cells (MSCs) has anti‐inflammatory and immunomodulatory effects under pathological conditions, and research on MSC‐derived exosomes is rapidly accumulating. MSC‐derived exosomes mimic the major therapeutic effects of MSCs. They affect the activity of immune effector cells and possess multilineage differentiation potential, including chondrogenic and osteogenic differentiation. Furthermore, exosomes are capable of regenerating cartilage or osseous compartments and restoring injured tissues and can treat dysfunction and pain caused by TMJ OA. In this review, we looked at the uniqueness of TMJ, the pathogenesis of TMJ OA, and the potential role of MSC‐derived exosomes for TMJ cartilage and bone regeneration.
AB - Exosomes are nanosized vesicles (30–140 nm) of endocytic origin that play important roles in regenerative medicine. They are derived from cell membranes during endocytic internalization and stabilize in biological fluids such as blood and synovia. Temporomandibular joint osteoarthritis (TMJ OA) is a degenerative disease, which, in addition to chronic pain, is characterized by progressive cartilage breakdown, condylar bone remodeling, and synovitis. However, traditional clinical treatments have limited symptom‐ and structure‐modifying effects to restore damaged cartilage and other TMJ tissues. This is due to the limited self‐healing capacity of condylar cartilage. Recently, stem‐cell‐derived exosomes have been studied as an alternative therapeutic approach to tissue repair and regeneration. It is known that trophic regulation of mesenchymal stem cells (MSCs) has anti‐inflammatory and immunomodulatory effects under pathological conditions, and research on MSC‐derived exosomes is rapidly accumulating. MSC‐derived exosomes mimic the major therapeutic effects of MSCs. They affect the activity of immune effector cells and possess multilineage differentiation potential, including chondrogenic and osteogenic differentiation. Furthermore, exosomes are capable of regenerating cartilage or osseous compartments and restoring injured tissues and can treat dysfunction and pain caused by TMJ OA. In this review, we looked at the uniqueness of TMJ, the pathogenesis of TMJ OA, and the potential role of MSC‐derived exosomes for TMJ cartilage and bone regeneration.
KW - Exosome
KW - Mesenchymal stem cell
KW - Osteoarthritis
KW - Osteochondral regeneration
KW - Regenerative medicine
KW - Temporomandibular joint
UR - http://www.scopus.com/inward/record.url?scp=85079843905&partnerID=8YFLogxK
U2 - 10.3390/ijms21041541
DO - 10.3390/ijms21041541
M3 - Review article
C2 - 32102392
AN - SCOPUS:85079843905
SN - 1661-6596
VL - 21
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 4
M1 - 1541
ER -