Review



col2a1 antibodies  (Bioss)


Bioz Verified Symbol Bioss is a verified supplier
Bioz Manufacturer Symbol Bioss manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94

    Structured Review

    Bioss col2a1 antibodies
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Col2a1 Antibodies, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/col2a1 antibodies/product/Bioss
    Average 94 stars, based on 7 article reviews
    col2a1 antibodies - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models"

    Article Title: Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models

    Journal: Inflammation

    doi: 10.1007/s10753-025-02411-4

    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and COL2A1 in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Figure Legend Snippet: Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and COL2A1 in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test

    Techniques Used: Expressing, Staining, Biomarker Discovery, In Vitro

    Exacerbation of OA progression in miR-221/222 cluster KO mice. ( A ) X-ray images of mouse joints 8 weeks post-DMM showing increased osteophytes, irregular joints, and pronounced joint stenosis in the KO + DMM group compared with the WT + DMM group. ( B-F ) Histological staining of joint sections at 8 weeks post-DMM confirms more severe degradation of cartilage and synovial fibrosis in the KO + DMM group ( n = 5 independent biological samples). ( G-K ) Western blot analysis indicates elevated type I collagen expression ( G ), while immunofluorescence analysis shows reduced COL2A1 levels ( H , I ) and increased MMP-13 expression ( J , K ) in KO + DMM joints at 8 weeks post-surgery ( n = 3 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test
    Figure Legend Snippet: Exacerbation of OA progression in miR-221/222 cluster KO mice. ( A ) X-ray images of mouse joints 8 weeks post-DMM showing increased osteophytes, irregular joints, and pronounced joint stenosis in the KO + DMM group compared with the WT + DMM group. ( B-F ) Histological staining of joint sections at 8 weeks post-DMM confirms more severe degradation of cartilage and synovial fibrosis in the KO + DMM group ( n = 5 independent biological samples). ( G-K ) Western blot analysis indicates elevated type I collagen expression ( G ), while immunofluorescence analysis shows reduced COL2A1 levels ( H , I ) and increased MMP-13 expression ( J , K ) in KO + DMM joints at 8 weeks post-surgery ( n = 3 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Techniques Used: Staining, Western Blot, Expressing, Immunofluorescence

    Increased inflammatory mediator levels and the expression of chondrocyte OA-related factors in miR-221/222 cluster KO mice. ( A-C ) Levels of IL-6 ( A ), TNF-α ( B ), and NO ( C ) production in IL-1β (10 ng/ml) treated chondrocyte-free supernatant from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). ( D-E ) Expression of inflammation-related proteins (COX2 and iNOS), OA-associated proteins (MMP-13), and COL2A1 in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 3 independent biological samples). ( F-I ) Immunofluorescence confirming COL2A1 ( F and G ) and MMP-13 ( H and I ) expression in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test
    Figure Legend Snippet: Increased inflammatory mediator levels and the expression of chondrocyte OA-related factors in miR-221/222 cluster KO mice. ( A-C ) Levels of IL-6 ( A ), TNF-α ( B ), and NO ( C ) production in IL-1β (10 ng/ml) treated chondrocyte-free supernatant from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). ( D-E ) Expression of inflammation-related proteins (COX2 and iNOS), OA-associated proteins (MMP-13), and COL2A1 in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 3 independent biological samples). ( F-I ) Immunofluorescence confirming COL2A1 ( F and G ) and MMP-13 ( H and I ) expression in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Techniques Used: Expressing, Immunofluorescence

    Alleviation of OA progression by the administration of agomir miR-221/222. ( A ) Schematic of the experimental design. ( B–D ) Intra-articular injection of the miR-221/222 agomir for 8 weeks attenuated OA progression in DMM-induced WT mice, as evidenced by improved histological staining ( B ) and decreased MMP-13 expression in joint tissues ( C , D ). E–F) Treatment also enhanced COL2A1 expression levels in the joints. ( n = 9 biologically independent samples). Data are presented as mean ± SEM. p values were determined using one-way ANOVA followed by Tukey’s post hoc test
    Figure Legend Snippet: Alleviation of OA progression by the administration of agomir miR-221/222. ( A ) Schematic of the experimental design. ( B–D ) Intra-articular injection of the miR-221/222 agomir for 8 weeks attenuated OA progression in DMM-induced WT mice, as evidenced by improved histological staining ( B ) and decreased MMP-13 expression in joint tissues ( C , D ). E–F) Treatment also enhanced COL2A1 expression levels in the joints. ( n = 9 biologically independent samples). Data are presented as mean ± SEM. p values were determined using one-way ANOVA followed by Tukey’s post hoc test

    Techniques Used: Injection, Staining, Expressing



    Similar Products

    94
    Bioss col2a1 antibodies
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Col2a1 Antibodies, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/col2a1 antibodies/product/Bioss
    Average 94 stars, based on 1 article reviews
    col2a1 antibodies - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    99
    Thermo Fisher streptavidin pe cy5
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Streptavidin Pe Cy5, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/streptavidin pe cy5/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    streptavidin pe cy5 - by Bioz Stars, 2026-02
    99/100 stars
      Buy from Supplier

    94
    Croda International Plc cy5 pe
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Cy5 Pe, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cy5 pe/product/Croda International Plc
    Average 94 stars, based on 1 article reviews
    cy5 pe - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    95
    Croda International Plc dioleoyl sn glycero 3 phosphoethanolamine n
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Dioleoyl Sn Glycero 3 Phosphoethanolamine N, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dioleoyl sn glycero 3 phosphoethanolamine n/product/Croda International Plc
    Average 95 stars, based on 1 article reviews
    dioleoyl sn glycero 3 phosphoethanolamine n - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    94
    Croda International Plc distearoyl sn glycero 3phosphoethanolamine n
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Distearoyl Sn Glycero 3phosphoethanolamine N, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/distearoyl sn glycero 3phosphoethanolamine n/product/Croda International Plc
    Average 94 stars, based on 1 article reviews
    distearoyl sn glycero 3phosphoethanolamine n - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    94
    Croda International Plc 1 2 dioleoyl sn glycero 3 phosphoethanolamine n cyanine 5 5
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    1 2 Dioleoyl Sn Glycero 3 Phosphoethanolamine N Cyanine 5 5, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/1 2 dioleoyl sn glycero 3 phosphoethanolamine n cyanine 5 5/product/Croda International Plc
    Average 94 stars, based on 1 article reviews
    1 2 dioleoyl sn glycero 3 phosphoethanolamine n cyanine 5 5 - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    94
    Croda International Plc cyanine 5 pe
    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and <t>COL2A1</t> in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test
    Cyanine 5 Pe, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cyanine 5 pe/product/Croda International Plc
    Average 94 stars, based on 1 article reviews
    cyanine 5 pe - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    Image Search Results


    Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and COL2A1 in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test

    Journal: Inflammation

    Article Title: Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models

    doi: 10.1007/s10753-025-02411-4

    Figure Lengend Snippet: Downregulation of miR-221 and miR-222 expression in OA tissue and IL-1β-stimulated chondrocytes. ( A-B ) Safranin O staining of the knee joints of OA model mice post-DMM surgery at the indicated time point showed progressive deterioration of articular cartilage. ( C ) Decreased expression of miR-221 and miR-222 in cartilage tissues from mouse joints ( n = 5 biologically independent samples). ( D ) Validation of in vitro OA model induction: NO levels were measured in the supernatant of IL-1β (10 ng/ml)-stimulated chondrocytes, along with mRNA expression levels of MMP-13 and COL2A1 in the same cells ( n = 5 biologically independent samples). ( E-F ) Time- and dose-dependent reduction in miR-221 and miR-222 expression in chondrocytes treated with IL-1β ( n = 5 independent biological samples). Data are presented as mean ± SEM. p values were calculated using one-way ANOVA followed by Tukey’s post hoc test

    Article Snippet: After that, cells were incubated with anti-MMP-13 or COL2A1 antibodies (Both 1:500, Bioss), followed by FITC-conjugated goat anti-rabbit IgG (1:500, Proteintech).

    Techniques: Expressing, Staining, Biomarker Discovery, In Vitro

    Exacerbation of OA progression in miR-221/222 cluster KO mice. ( A ) X-ray images of mouse joints 8 weeks post-DMM showing increased osteophytes, irregular joints, and pronounced joint stenosis in the KO + DMM group compared with the WT + DMM group. ( B-F ) Histological staining of joint sections at 8 weeks post-DMM confirms more severe degradation of cartilage and synovial fibrosis in the KO + DMM group ( n = 5 independent biological samples). ( G-K ) Western blot analysis indicates elevated type I collagen expression ( G ), while immunofluorescence analysis shows reduced COL2A1 levels ( H , I ) and increased MMP-13 expression ( J , K ) in KO + DMM joints at 8 weeks post-surgery ( n = 3 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Journal: Inflammation

    Article Title: Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models

    doi: 10.1007/s10753-025-02411-4

    Figure Lengend Snippet: Exacerbation of OA progression in miR-221/222 cluster KO mice. ( A ) X-ray images of mouse joints 8 weeks post-DMM showing increased osteophytes, irregular joints, and pronounced joint stenosis in the KO + DMM group compared with the WT + DMM group. ( B-F ) Histological staining of joint sections at 8 weeks post-DMM confirms more severe degradation of cartilage and synovial fibrosis in the KO + DMM group ( n = 5 independent biological samples). ( G-K ) Western blot analysis indicates elevated type I collagen expression ( G ), while immunofluorescence analysis shows reduced COL2A1 levels ( H , I ) and increased MMP-13 expression ( J , K ) in KO + DMM joints at 8 weeks post-surgery ( n = 3 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Article Snippet: After that, cells were incubated with anti-MMP-13 or COL2A1 antibodies (Both 1:500, Bioss), followed by FITC-conjugated goat anti-rabbit IgG (1:500, Proteintech).

    Techniques: Staining, Western Blot, Expressing, Immunofluorescence

    Increased inflammatory mediator levels and the expression of chondrocyte OA-related factors in miR-221/222 cluster KO mice. ( A-C ) Levels of IL-6 ( A ), TNF-α ( B ), and NO ( C ) production in IL-1β (10 ng/ml) treated chondrocyte-free supernatant from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). ( D-E ) Expression of inflammation-related proteins (COX2 and iNOS), OA-associated proteins (MMP-13), and COL2A1 in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 3 independent biological samples). ( F-I ) Immunofluorescence confirming COL2A1 ( F and G ) and MMP-13 ( H and I ) expression in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Journal: Inflammation

    Article Title: Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models

    doi: 10.1007/s10753-025-02411-4

    Figure Lengend Snippet: Increased inflammatory mediator levels and the expression of chondrocyte OA-related factors in miR-221/222 cluster KO mice. ( A-C ) Levels of IL-6 ( A ), TNF-α ( B ), and NO ( C ) production in IL-1β (10 ng/ml) treated chondrocyte-free supernatant from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). ( D-E ) Expression of inflammation-related proteins (COX2 and iNOS), OA-associated proteins (MMP-13), and COL2A1 in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 3 independent biological samples). ( F-I ) Immunofluorescence confirming COL2A1 ( F and G ) and MMP-13 ( H and I ) expression in IL-1β (10 ng/ml) treated chondrocytes from WT and miR-221/222 cluster KO mice ( n = 5 independent biological samples). For all the graphs, the values represent the mean ± SEM. p values were calculated via one-way ANOVA, followed by Tukey’s post hoc test

    Article Snippet: After that, cells were incubated with anti-MMP-13 or COL2A1 antibodies (Both 1:500, Bioss), followed by FITC-conjugated goat anti-rabbit IgG (1:500, Proteintech).

    Techniques: Expressing, Immunofluorescence

    Alleviation of OA progression by the administration of agomir miR-221/222. ( A ) Schematic of the experimental design. ( B–D ) Intra-articular injection of the miR-221/222 agomir for 8 weeks attenuated OA progression in DMM-induced WT mice, as evidenced by improved histological staining ( B ) and decreased MMP-13 expression in joint tissues ( C , D ). E–F) Treatment also enhanced COL2A1 expression levels in the joints. ( n = 9 biologically independent samples). Data are presented as mean ± SEM. p values were determined using one-way ANOVA followed by Tukey’s post hoc test

    Journal: Inflammation

    Article Title: Loss of the miR-221/222 Cluster Promotes the Pathogenesis of Osteoarthritis in Inflamed Mouse Chondrocytes and Osteoarthritis Models

    doi: 10.1007/s10753-025-02411-4

    Figure Lengend Snippet: Alleviation of OA progression by the administration of agomir miR-221/222. ( A ) Schematic of the experimental design. ( B–D ) Intra-articular injection of the miR-221/222 agomir for 8 weeks attenuated OA progression in DMM-induced WT mice, as evidenced by improved histological staining ( B ) and decreased MMP-13 expression in joint tissues ( C , D ). E–F) Treatment also enhanced COL2A1 expression levels in the joints. ( n = 9 biologically independent samples). Data are presented as mean ± SEM. p values were determined using one-way ANOVA followed by Tukey’s post hoc test

    Article Snippet: After that, cells were incubated with anti-MMP-13 or COL2A1 antibodies (Both 1:500, Bioss), followed by FITC-conjugated goat anti-rabbit IgG (1:500, Proteintech).

    Techniques: Injection, Staining, Expressing