Loss of Vhl in cartilage accelerated the progression of age-associated and surgically induced murine osteoarthritis  T. Weng, Y. Xie, L. Yi, J. Huang,

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Loss of Vhl in cartilage accelerated the progression of age-associated and surgically induced murine osteoarthritis  T. Weng, Y. Xie, L. Yi, J. Huang, F. Luo, X. Du, L. Chen, C. Liu, D. Chen, L. Chen  Osteoarthritis and Cartilage  Volume 22, Issue 8, Pages 1197-1205 (August 2014) DOI: 10.1016/j.joca.2014.06.031 Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 1 Basal cartilage characteristics in the knee joints of Cre-negative and Vhl cKO mice. (A) No gross differences were observed in the articular cartilage of knee joints between Vhl cKO and Cre-negative (Cre(−)) mice at 4-month-old (n = 5 mice each genotype, Scale bar, 200 μm). Lower panel shows the higher magnification of knee joint in Vhl cKO or Cre-negative mice, respectively (Scale bar, 100 μm). (B) The knee joints were analyzed by micro-CT in 4-month-old Vhl cKO and Cre-negative mice (n = 5 in each genotype). Asterisk showed increased trabecular bone mass in the Vhl cKO mice. (C) The subchondral bone density in the ROI described in (B) was comparable between Vhl cKO and Cre-negative mice. (D) Histomorphometric analyses showed that increased BV/TV in subchondral bone from Vhl cKO mice (n = 6 in each group). Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 2 Appearance of OA changes in Vhl cKO mice in the age-associated spontaneous OA model. (A) Representative histological feature of knee joints of 12-month-old Vhl cKO and Cre-negative mice (n = 3–5 mice each genotype, Scale bar in top panel, 200 μm). The lower panel showed higher magnification views of the boxed area (Scale bar, 100 μm). The arrow points to severe cartilage damage in Vhl cKO mice. Arrowhead points to the loss of proteoglycan in aged articular cartilage. (B) Summed score for cartilage structure damage and proteoglycan loss in femoral condyle and tibia plateau from 12-month-old Vhl cKO and Cre-negative mice. MFC = medial femoral condyle; MTP = medial tibial plateau. Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 3 Appearance of severe OA changes in Vhl cKO mice in the surgically induced OA model. (A) Representative Safranin O/fast green-stained histological sections of knee joints from Vhl cKO and Cre-negative mice 12 weeks after DMM surgery or Sham operation (N = 8–10 mice each genotype). GP = growth plate. Scale bar, 200 μm. (B) Higher magnification of articular cartilage in both Vhl cKO and WT mice subjected to DMM surgery. Scale bar, 100 μm. The arrow indicates structural damage in the knee joints. (C) Summed and maximal histologic structure score of knee cartilage 12 weeks after DMM surgery in Vhl cKO and Cre-negative mice. MFC = medial femoral condyle; MTP = medial tibial plateau. Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 4 Vhl deficiency increased articular chondrocyte apoptosis in DMM-induced and age-associated OA models. (A) Articular chondrocyte apoptosis was analyzed by TUNEL staining in the knee joints from Vhl cKO and Cre-negative mice 3 weeks after DMM surgery or Sham operation (n = 3 mice each genotype). Top panel scale bar, 100 μm. The bottom panel was TUNEL-positive apoptotic cells determined by DAB staining (Scale bar, 100 μm). (B) Increased apoptotic articular chondrocytes in the knee joints from aged Vhl cKO mice relative to Cre-negative mice (n = 3 mice each genotype, two replicates each group). Scale bar, 100 μm. (C) Immunohistochemical staining for Fas in aged knee joints from Vhl cKO and Cre-negative mice (n = 3 mice each genotype, two replicates each sample). Sale bar, 100 μm. (D) Quantification analysis of pro-apoptotic protein Bax and anti-apoptotic protein Bcl-2 in the knee joints from Vhl cKO and Cre-negative mice 3 weeks after DMM surgery determined by real-time PCR. Each PCR reaction was run in triplicates and performed twice. Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 5 Disruption of Vhl decreased autophagy-related gene expression of LC-3 and Beclin1 in articular chondrocytes. (A) Immunohistochemical staining showed that reduced LC-3 expression in articular cartilage 3 weeks after DMM surgery compared to Sham-operated mice in both genotypes (n = 3 mice each genotype, two replicates each group). Vhl deficiency decreases LC-3 expression in both DMM surgery and Sham-operated mice. Scale bar, 40 μm. (B) Reduction in LC-3 expression in the knee joints of 12-month-old Vhl cKO mice (n = 3 mice each genotype, two replicates each group). Scale bar, 20 μm. Right graph is the quantification of LC-3 positive chondrocytes in 12-month-old Vhl cKO and Cre-negative mice. Percentage of LC-3 positive cells was significantly decreased in Vhl deficient mice. Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). (C) Western blot analysis of LC3I, LC3II and Beclin1 in cultured chondrocytes from newborn Vhl cKO mice articular cartilage treated with or without 4-OH TM for 48 h. (D) Higher expression of p-mTOR was observed in the knee joints of 12-month-old Vhl cKO mice compared to that of Cre-negative mice (n = 3). Scale bar, 100 μm. Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 6 Deletion of Vhl in chondrocytes enhanced expression of HIF-2α and its downstream MMP-13, IL-6 and MMP-9. (A) Immunohistochemical staining for Vhl, HIF-1α and HIF-2α in the knee joints from Vhl cKO and WT mice at 10 months of age (n = 3 each group). Tamoxifen induced deletion of Vhl in adult joints leads to higher expression of HIF-2α. Scale bar, 40 μm. (B) Western blot analysis of HIF-2α, HIF-1α and Vhl in cultured chondrocytes from articular cartilage of Vhl cKO mice treated with or without 4-OH TM for 48 h. Decreased expression of Vhl and increased HIF-2α expression were observed. (C) Higher expression of MMP-13 were observed in the knee joints from Vhl cKO mice compared with that of Cre-negative mice (n = 3). Scale bar, 40 μm. (D) Quantification analysis of IL-6 and MMP-9 mRNA level in the knee joints from Vhl cKO and Cre-negative mice determined by real-time PCR. Each PCR reaction was run in triplicates and performed twice. Data are expressed as the mean (symbols) ± 95% confidence intervals (error bar). Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. S1 Expression of HIF-2α, MMP-13 and Fas in articular cartilage of DMM model. (A) Immunohistochemical staining for HIF-2α in the knee joints of Cre-negative and Vhl cKO mice 3 weeks after DMM surgery (n = 3 mice each genotype). Scale bar, 40 μm. (B) Increased expression of MMP-13 in articular cartilage was observed in DMM model in both genotypes (n = 3). Scale bar, 20 μm. (C) Increased expression of Fas in articular cartilage was found in DMM model in both genotypes (n = 3). Scale bar, 40 μm. Osteoarthritis and Cartilage 2014 22, 1197-1205DOI: (10.1016/j.joca.2014.06.031) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions