Effects of SIRT1 gene knock-out via activation of SREBP2 protein-mediated PI3K/AKT signaling on osteoarthritis in mice.
- Author:
Fei YU
1
;
Hui ZENG
2
;
Ming LEI
1
;
De-Ming XIAO
1
;
Wei LI
1
;
Hao YUAN
1
;
Jian-Jing LIN
1
Author Information
1. Department of Orthopedics, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
2. Department of Orthopedics, Peking University Shenzhen Hospital, Shenzhen, 518036, China. zenghui_36@163.com.
- Publication Type:Journal Article
- Keywords:
PI3K/AKT;
SIRT1;
SREBP2;
gene knock-out;
osteoarthritis
- MeSH:
Animals;
Cartilage;
pathology;
Chondrocytes;
metabolism;
Collagen Type II;
metabolism;
Disease Models, Animal;
Humans;
Knee Joint;
metabolism;
pathology;
Mice;
Mice, Knockout;
Oncogene Protein v-akt;
genetics;
Osteoarthritis;
genetics;
pathology;
Phosphatidylinositol 3-Kinases;
genetics;
Signal Transduction;
genetics;
Sirtuin 1;
genetics;
Sterol Regulatory Element Binding Protein 2;
biosynthesis;
genetics;
Vascular Endothelial Growth Factor A;
biosynthesis
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2016;36(5):683-690
- CountryChina
- Language:English
-
Abstract:
This study investigated the effects of SIRT1 gene knock-out on osteoarthritis in mice, and the possible roles of SREBP2 protein and the PI3K/AKT signaling pathway in the effects. Mice were randomly divided into a normal group and a SIRT1 gene knock-out group (6 mice in each group). In these groups, one side of the knee anterior cruciate ligament was traversed, and the ipsilateral medial meniscus was cut to establish an osteoarthritis model of knee joint. The countralateral synovial bursa was cut out, serving as controls. The knee joint specimens were then divided into four groups: SIRT1control group (group A, n=6); SIRT1osteoarthritis group (group B, n=6); SIRT1control group (group C, n=6); SIRT1osteoarthritis group (group D, n=6). HE staining, Masson staining, Safranin O-Fast Green staining and Van Gieson staining were used to observe the morphological changes in the articular cartilage of the knee. Immunohistochemical staining was employed to detect the expression of SIRT1, SREBP2, VEGF, AKT, HMGCR and type II collagen proteins. SA-β-gal staining was utilized to evaluate chondrocyte aging. The results showed clear knee joint cartilage destruction and degeneration in the SIRT1osteoarthritis group. The tidal line was twisted and displaced anteriorly. Type II collagen was destroyed and distributed unevenly. Compared with the SIRT1osteoarthritis group and SIRT1control group, SIRT1 protein expression was not obviously changed in the SIRT1osteoarthritis group (P>0.05), while the expression levels of the SREBP2, VEGF and HMGCR proteins were significantly increased (P<0.05) and the levels of AKT and type II collagen proteins were significantly decreased (P<0.05). SIRT1 gene knock-out may aggravate cartilage degeneration in osteoarthritis by activating the SREBP2 protein-mediated PI3K/AKT signalling pathway, suggesting that SIRT1 gene may play a protective role against osteoarthritis.
