Effects of long intergenic non-protein coding RNA 00707 on chondrocyte injury and inflammatory factor secretion in osteoarthritis
- VernacularTitle:长基因间非蛋白编码RNA 00707对骨关节炎软骨细胞损伤及炎症因子分泌的影响
- Author:
Kai CHU
1
;
Jianhua SUN
Author Information
- Keywords: osteoarthritis; LINC00707; miR-423-5p; interleukin-1β; chondrocyte; apoptosis; inflammatory factor
- From: Chinese Journal of Tissue Engineering Research 2024;28(28):4565-4571
- CountryChina
- Language:Chinese
- Abstract: BACKGROUND:Long intergenic non-protein coding RNA 00707(LINC00707)and microRNA-423-5p(miR-423-5p)are both involved in the occurrence and development of osteoarthritis.Starbase predicts that LINC00707 and miR-423-5p have complementary sequences,but whether LINC00707 and miR-423-5p interact to regulate the progress of osteoarthritis still needs further research. OBJECTIVE:To investigate whether LINC00707 targets miR-423-5p to affect chondrocyte injury and inflammatory factor secretion in osteoarthritis. METHODS:Articular chondrocytes were divided into eight groups:(1)blank control group was given no treatment;(2)interleukin(IL)-1β group was cultured with 10 ng/mL IL-1β for 48 hours;(3)IL-1β+si-NC group was transfected with si-NC and then treated with 10 ng/mL IL-1β for 48 hours;(4)IL-1β+si-LINC00707 group was transfected with si-LINC00707 and then treated with 10 ng/mL IL-1β for 48 hours;(5)IL-1β+miR-NC group was transfected with miR-NC and then treated with 10 ng/mL IL-1β for 48 hours;(6)IL-1β+miR-423-5p group was transfected with miR-423-5p mimic and then treated with 10 ng/mL IL-1β for 48 hours;(7)IL-1β+si-LINC00707+anti-miR-NC group was co-transfected with si-LINC00707 and anti-miR-NC and then treated with 10 ng/mL IL-1β for 48 hours;(8)IL-1β+si-LINC00707+anti-miR-423-5p group was co-transfected with si-LINC00707 and anti-miR-423-5p and then treated with 10 ng/mL IL-1β for 48 hours.Relevant tests were performed at the end of the intervention. RESULTS AND CONCLUSION:Compared with the blank control group,the mRNA expression of LINC00707,apoptosis rate,protein expression of C-caspase3 and C-caspase9,and levels of tumor necrosis factor-α and IL-6 in articular chondrocytes were increased in the IL-1β group,while there was a decrease in miR-423-5p expression and IL-10 level(P<0.05).Compared with the IL-1β group,the mRNA expression of LINC00707,apoptosis rate,protein expression of C-caspase3 and C-caspase9,and levels of tumor necrosis factor-α and IL-6 in articular chondrocytes were decreased in the IL-1β+si-LINC00707 group,while miR-423-5p expression and IL-10 level increased(P<0.05).Compared with the IL-1β+miR-NC group,the protein expression of C-caspase3 and C-caspase9 and levels of tumor necrosis factor-α and IL-6 in articular chondrocytes were decreased in the IL-1β+miR-423-5p group,while miR-423-5p expression and IL-10 level increased(P<0.05).Compared with the IL-1β+si-LINC00707+anti-miR-NC group,apoptosis rate,protein expression of C-caspase3 and C-caspase9,and levels of tumor necrosis factor-α and IL-6 in articular chondrocytes were increased in the IL-1β+si-LINC00707+anti-miR-423-5p group,while miR-423-5p expression and IL-10 level decreased(P<0.05).To conclude,inhibiting LINC00707 by targeting miR-423-5p can reduce IL-1β-induced apoptosis and inflammation in articular chondrocytes.
