Chondroprotective Effects of Combination Therapy of Acupotomy and Human Adipose Mesenchymal Stem Cells in Knee Osteoarthritis Rabbits via the GSK3β-Cyclin D1-CDK4/CDK6 Signaling Pathway

被引:23
作者
An, Xingyan [1 ]
Wang, Tong [1 ]
Zhang, Wei [1 ]
Yu, Hongliang [2 ]
Zhao, Robert Chunhua [2 ]
Guo, Yan [3 ]
Wang, Chunjiu [1 ]
Qin, Luxue [1 ]
Guo, Changqing [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Acupuncture Moxibust & Tuina, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Ctr Excellence Tissue Engn, Peking Union Med Coll Hosp,Beijing Key Lab, Inst Basic Med Sci,Sch Basic Med,Peking Union Med, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Tradit Chinese Med Hosp, Acupuncture & Moxibust Dept, Beijing, Peoples R China
来源
AGING AND DISEASE | 2020年 / 11卷 / 05期
基金
中国国家自然科学基金;
关键词
KOA; ASCs; acupotomy; chondrocytes; proliferation; CYCLIN D1; CHONDROCYTE PROLIFERATION; CARTILAGE REPAIR; KINASE-ACTIVITY; G1; ARREST; DISEASE; MODEL; INHIBITION; CANCER; ROLES;
D O I
10.14336/AD.2019.1104
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Adipose-derived stem cells (ASCs) are highly chondrogenic and can be used to treat knee osteoarthritis (KOA) by alleviating cartilage defects. Acupotomy, a biomechanical therapy guided by traditional Chinese medicine theory, alleviates cartilage degradation and is widely used in the clinic to treat KOA by correcting abnormal mechanics. However, whether combining acupotomy with ASCs will reverse cartilage degeneration by promoting chondrocyte proliferation in KOA rabbits is unknown. The present study aimed to investigate the effects of combination therapy of acupotomy and ASCs on chondrocyte proliferation and to determine the underlying mechanism in rabbits with KOA induced by knee joint immobilization for 6 weeks. After KOA modeling, five groups of rabbits (acupotomy, ASCs, acupotomy + ASCs, model and control groups) received the indicated intervention for 4 weeks. The combination therapy significantly restored the KOA-induced decrease in passive range of motion (PROM) in the knee joint and reduced the elevated serum level of cartilage oligomeric matrix protein (COMP), a marker for cartilage degeneration. Furthermore, magnetic resonance imaging (MRI) and scanning electron microscopy (SEM) images showed that the combination therapy inhibited cartilage injury. The combination therapy also significantly blocked increases in the mRNA and protein expression of glycogen synthase kinase-3 beta (GSK3 beta) and decreases in the mRNA and protein expression of cyclin D1/CDK4 and cyclin D1/CDK6 in cartilage. These findings indicated that the combination therapy mitigated knee joint immobility, promoted chondrocyte proliferation and alleviated cartilage degeneration in KOA rabbits, and these effects may be mediated by specifically regulating the GSK3 beta-cyclin D1-CDK4/CDK6 pathway.
引用
收藏
页码:1116 / 1132
页数:17
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