2023
DOI: 10.1016/j.jot.2023.06.003
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MATN3 delivered by exosome from synovial mesenchymal stem cells relieves knee osteoarthritis: Evidence from in vitro and in vivo studies

Long Long,
Guoyou Zou,
Yi Cheng
et al.
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Cited by 10 publications
(4 citation statements)
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“…This point notwithstanding, there is great interest in harnessing the potential of stem cells [ 44 ]. This includes utilizing them as cell based therapies or as similarly derived exosomes with signaling factors to halt the progression of degeneration and even potentially reverse it [ 45 , 46 , 47 , 48 , 49 , 50 ].…”
Section: Non-surgical Managementmentioning
confidence: 99%
“…This point notwithstanding, there is great interest in harnessing the potential of stem cells [ 44 ]. This includes utilizing them as cell based therapies or as similarly derived exosomes with signaling factors to halt the progression of degeneration and even potentially reverse it [ 45 , 46 , 47 , 48 , 49 , 50 ].…”
Section: Non-surgical Managementmentioning
confidence: 99%
“…Synovial MSC-derived exosomes with MATN3 improved OA scores in mice. Long et al identified that MATN3 interacted with IL-17A to prevent the activation of its downstream signaling (PI3K pathway) [160].…”
Section: Mesenchymal Stem-cell-derived Extracellular Vesicles and Cho...mentioning
confidence: 99%
“…Osteoarthritis (OA) is a common degenerative disease that is caused by various factors leading to articular cartilage degeneration and damage, with joint pain as the main symptom. More than 250 million people worldwide suffer from OA, most of whom have decreased mobility and quality of life. , Conventional drug therapy is palliative, while it remains challenging to effectively promote cartilage regeneration and reverse the process of OA. By contrast, stem cell-derived exosome (Exo) therapy, emerged from the perspective of regenerative medicine, has achieved preliminary success in OA treatment. Moreover, previous studies have demonstrated that Exo can exert therapeutic effects in OA treatment by inhibiting inflammatory factors, preventing extracellular matrix extracellular matrix and promoting cartilage regeneration. However, the scarcity of Exo and their complex isolation procedures pose great limitations for their applications . In addition, half-life of Exo in vivo is short, since they can be easily recognized by the mononuclear phagocyte system and rapidly cleared. To address this problem, different Exo-delivered systems have been developed for OA treatment, such as nanoparticles, , liposomes, , and hydrogels. These strategies can extend the half-life of Exo and many successes have been achieved.…”
Section: Introductionmentioning
confidence: 99%