Figures & data
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Table 1. Clinical features of OA and Control groups
Figure 2. Subcellular location of LINC00707 in chondrocytes and analysis of its interaction with miR-199-3p. To analyze the subcellular location of LINC00707, nuclear fractionation assay was performed on chondrocytes (a). The interaction between LINC00707 and miR-199-3p was predicted by IntaRNA 2.0 (b). The direct interaction between LINC00707 and miR-199-3p was analyzed by RNA pull-down assay (c). Dual-luciferase reporter assay was performed by transfecting LINC00707 and miRNA NC or LINC00707 and miR-199-3p into chondrocytes (d). *p < 0.05; ***p < 0.001.
![Figure 2. Subcellular location of LINC00707 in chondrocytes and analysis of its interaction with miR-199-3p. To analyze the subcellular location of LINC00707, nuclear fractionation assay was performed on chondrocytes (a). The interaction between LINC00707 and miR-199-3p was predicted by IntaRNA 2.0 (b). The direct interaction between LINC00707 and miR-199-3p was analyzed by RNA pull-down assay (c). Dual-luciferase reporter assay was performed by transfecting LINC00707 and miRNA NC or LINC00707 and miR-199-3p into chondrocytes (d). *p < 0.05; ***p < 0.001.](/cms/asset/1a23c013-b3f7-4f27-8b9d-214d352a40c8/kbie_a_2061287_f0002_oc.jpg)
Figure 3. Analysis of the regulator roles of LINC00707 and miR-199-3p in the expression of each other. The direct interaction may indicate the regulator roles of LINC00707 and miR-199-3p in the expression of each other. Pearson’s correlation coefficient analysis was done to analyze the correlations between LINC00707 and miR-199-3p across OA (a) and control (b) samples. Chondrocytes were overexpressed with LINC00707 or miR-199-3p, and the overexpression was confirmed by RT-qPCR every 24 h until 72 h (c). The role of LINC00707 in the expression of miR-199-3p (d), and the role of miR-199-3p in the expression of LINC00707 (e) were analyzed by RT-qPCR. *p < 0.05.
![Figure 3. Analysis of the regulator roles of LINC00707 and miR-199-3p in the expression of each other. The direct interaction may indicate the regulator roles of LINC00707 and miR-199-3p in the expression of each other. Pearson’s correlation coefficient analysis was done to analyze the correlations between LINC00707 and miR-199-3p across OA (a) and control (b) samples. Chondrocytes were overexpressed with LINC00707 or miR-199-3p, and the overexpression was confirmed by RT-qPCR every 24 h until 72 h (c). The role of LINC00707 in the expression of miR-199-3p (d), and the role of miR-199-3p in the expression of LINC00707 (e) were analyzed by RT-qPCR. *p < 0.05.](/cms/asset/5c4eecc0-186d-45c8-8b26-20f17e101b99/kbie_a_2061287_f0003_oc.jpg)
Figure 4. Analysis of the roles of LINC00707 and miR-199-3p in the proliferation and apoptosis of chondrocytes. The roles of LINC00707 and miR-199-3p in the proliferation and apoptosis (induced by 10 μg/ml LPS for 24 h) of chondrocytes were analyzed by BrdU assay (a) and cell apoptosis assay (b), respectively. *p < 0.05.
![Figure 4. Analysis of the roles of LINC00707 and miR-199-3p in the proliferation and apoptosis of chondrocytes. The roles of LINC00707 and miR-199-3p in the proliferation and apoptosis (induced by 10 μg/ml LPS for 24 h) of chondrocytes were analyzed by BrdU assay (a) and cell apoptosis assay (b), respectively. *p < 0.05.](/cms/asset/47af21b4-299d-4fdf-89bf-ad566a3f9727/kbie_a_2061287_f0004_oc.jpg)
Data availability statement
The datasets generated and/or analyzed during the current study are available in https://115.com/s/swnywtq3zyl?password=u576&#, the code is u576.