Intra-articular injection of hUC-MSCs expressing miR-140-5p induces cartilage self-repairing in the rat osteoarthritis.
Animals
Cartilage, Articular
/ metabolism
Cell Differentiation
/ genetics
Chondrocytes
/ cytology
Chondrogenesis
Disease Models, Animal
Humans
Injections, Intra-Articular
Lentivirus
/ metabolism
Male
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells
/ cytology
MicroRNAs
/ metabolism
Osteoarthritis
/ genetics
Rats, Sprague-Dawley
Regeneration
Umbilical Cord
/ cytology
Cartilage
Human umbilical cord mesenchymal stem cells
Osteoarthritis
miR-140-5p
Journal
Journal of bone and mineral metabolism
ISSN: 1435-5604
Titre abrégé: J Bone Miner Metab
Pays: Japan
ID NLM: 9436705
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
05
06
2019
accepted:
10
10
2019
pubmed:
25
11
2019
medline:
26
6
2020
entrez:
25
11
2019
Statut:
ppublish
Résumé
Currently, osteoarthritis (OA) receives global increasing attention because it associates severe joint pain and serious disability. Stem cells intra-articular injection therapy showed a potential therapeutic superiority to reduce OA development and to improve treating outputs. However, the long-term effect of stem cells intra-articular injection on the cartilage regeneration remains unclear. Recently, miR-140-5p was confirmed as a critical positive regulator in chondrogenesis. We hypothesized that hUC-MSCs overexpressing miR-140-5p have better therapeutic effect on osteoarthritis. To enhance stem cell chondrogenic differentiation, we have transfected human umbilical cord mesenchymal stem cells (hUC-MSCs) with miR-140-5p mimics and miR-140-5p lentivirus to overexpress miR-140-5p in a short term or a long term accordingly. Thereafter, MSCs proliferation, chondrogenic genes expression and extracellular matrix were assessed. Destabilization of the medial meniscus (DMM) surgery was performed on the knee joints of SD rats as an OA model, and then intra-articular injection of hUC-MSCs or hUC-MSCs transfected with miR-140-5p lentivirus was carried to evaluate the cartilage healing effect with histological staining and OARSI scores. The localization of hUC-MSCs after intra-articular injection was further confirmed by immunohistochemical staining. Significant induction of chondrogenic differentiation in the miR-140-5p-hUC-MSCs (140-MSCs), while its proliferation was not influenced. Interestingly, intra-articular injection of 140-MSCs significantly enhanced articular cartilage self-repairing in comparison to normal hUC-MSCs. Moreover, we noticed that intra-articular injection of high 140-MSCs numbers reinforces cells assembling on the impaired cartilage surface and subsequently differentiated into chondrocytes. In conclusion, these results indicate therapeutic superiority of hUC-MSCs overexpressing miR-140-5p to treat OA using intra-articular injection.
Identifiants
pubmed: 31760502
doi: 10.1007/s00774-019-01055-3
pii: 10.1007/s00774-019-01055-3
doi:
Substances chimiques
MicroRNAs
0
Mirn140 microRNA, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
277-288Subventions
Organisme : National Natural Science Foundation of China
ID : 81572198
Organisme : National Natural Science Foundation of China
ID : 81772394
Organisme : Key Program of Natural Science Foundation of Guangdong Province
ID : 2018B0303110003
Organisme : Shenzhen Peacock Project
ID : KQTD20170331100838136
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20170817172023838
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20170306092215436
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20170412150609690
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20170413161649437
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20170413161800287
Organisme : Shenzhen Science and Technology Projects
ID : SGLH20161209105517753
Organisme : Shenzhen Science and Technology Projects
ID : JCYJ20160301111338144
Organisme : Fund for High Level Medical Discipline Construction of Shenzhen University
ID : 2016031638
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