collagen iii  (Proteintech)

Journal: PLOS One

Article Title: A bioactive hydrogel integrating bFGF/VEGFA gene-loaded nanoparticles and platelet-rich plasma for accelerated full-thickness skin wound healing

doi: 10.1371/journal.pone.0350087

Figure Lengend Snippet: (A) Representative Hematoxylin & eosin (H&E) staining images of wound sections; The red arrow refers to the skin appendage. (B) Representative Masson’s trichrome staining images of wound sections; blue color indicates collagen. (C) Representative immunohistochemical images of wound sections showing type-I collagen (COLI) expression. (D) Representative immunohistochemical images of wound sections showing type-III collagen (COLIII) expression. (E) Quantification of total collagen deposition (Masson-stained area %). (F) Quantification of COLI deposition (% positively stained area). (G) Quantification of COLIII deposition (% positively stained area). In E–G, data are mean ± SD from three independent animals (n = 3 mice per group). Statistical significance was evaluated by one-way ANOVA and LSD comparison test. Ns, no significant difference (P > 0.05); *P < 0.05, **P < 0.01, ***P < 0.001.

Article Snippet: Anti-bFGF antibody (bsm-34016R, Bioss, China, dilution 1:250), anti-VEGFA antibody (ab46154, Abcam, UK, dilution 1:250), anti-CD 31 antibody (28083–1-AP, Proteintech, USA, dilution 1:250), anti-Ki 67 antibody (ab209897, Abcam, UK, dilution 1:250), anti-Bcl 2 antibody (26593–1-AP, Proteintech, USA, dilution 1:250), anti-Collagen Type I antibody(HY- P81227 , MCE, USA, dilution 1:250), anti- Collagen Type III antibodies (HY- P81101 , MCE, USA, dilution 1:250) were added to the slices and incubated overnight.

Techniques: Staining, Immunohistochemical staining, Expressing, Comparison

Journal: Journal of Orthopaedic Translation

Article Title: ADSC-derived mitochondrial nanovesicles transplantation alleviates capsular fibrosis and inflammation and improves joint mobility in a rat model of adhesive capsulitis

doi: 10.1016/j.jot.2026.101195

Figure Lengend Snippet: Single-cell transcriptomic analysis and immunohistochemical analysis of joint capsule tissues from normal individuals and patients with adhesive capsulitis. (A) UMAP visualization of all cells. (B) Oxidative phosphorylation scores of subpopulations. (C) GSEA of differentially expressed genes in fibroblasts. (D) UMAP visualization of fibroblasts. (E) Oxidative phosphorylation scores of fibroblast subpopulations. (F) Representative images of IHC staining and the semi-quantitative statistical analysis for Col I, Col III, Cox4, Opa1, IL1 and TNF a. Statistical significance was determined by two-tailed two sample t test. *P < 0.05 , **P < 0.01 , ***P < 0.001, **** P < 0.0001; n = 4–5.

Article Snippet: Primary antibodies against Collagen type I (Col1, Cat. No.: A24112), Collagen type III (Col3, Cat. No.: A3795), matrix metalloproteinase 9 (MMP9, Cat. No.: A25299), matrix metalloproteinase 13 (MMP13, Cat. No.: A11755), IL-6 (Cat. No.: A0286), IL-10 (Cat. No.: A2171) and tumor necrosis factor-alpha (TNF-α, Cat. No.: A21265) (all Abclonal, 1:300 dilution) were applied at 4 °C overnight.

Techniques: Single Cell, Immunohistochemical staining, Adhesive, Phospho-proteomics, Immunohistochemistry, Two Tailed Test

Journal: Journal of Orthopaedic Translation

Article Title: ADSC-derived mitochondrial nanovesicles transplantation alleviates capsular fibrosis and inflammation and improves joint mobility in a rat model of adhesive capsulitis

doi: 10.1016/j.jot.2026.101195

Figure Lengend Snippet: Effects of AD-Mito-NPs on migration and ECM-related protein expression in joint capsule fibroblasts. (A) Representative images and quantification of cell migration assessed by wound healing assay. Scale bar, 100 μm. n = 4. (B–F) Representative immunofluorescence images (left) and quantification of fluorescence intensity (right) for collagen I (Col1, B), collagen III (Col3, C), fibronectin 1 (FN1, D), matrix metalloproteinase 9 (MMP9, E), and matrix metalloproteinase 13 (MMP13, F). Red: target protein; Green: Phalloidin (F-actin); Blue: DAPI (nuclei). n = 3. Scale bar, 50 μm. (G) Schematic diagram illustrating phenotypic changes in fibroblasts following inflammatory stimulation and AD-Mito-NPs delivery. Data are presented as mean ± SD. Statistical significance was determined by one-way ANOVA (B–F) or two-way ANOVA (A) with Tukey's multiple comparisons test. *P < 0.05 , **P < 0.01 , ***P < 0.001, **** P< 0.0001.

Article Snippet: Primary antibodies against Collagen type I (Col1, Cat. No.: A24112), Collagen type III (Col3, Cat. No.: A3795), matrix metalloproteinase 9 (MMP9, Cat. No.: A25299), matrix metalloproteinase 13 (MMP13, Cat. No.: A11755), IL-6 (Cat. No.: A0286), IL-10 (Cat. No.: A2171) and tumor necrosis factor-alpha (TNF-α, Cat. No.: A21265) (all Abclonal, 1:300 dilution) were applied at 4 °C overnight.

Techniques: Migration, Expressing, Wound Healing Assay, Immunofluorescence, Fluorescence

Journal: Journal of Orthopaedic Translation

Article Title: ADSC-derived mitochondrial nanovesicles transplantation alleviates capsular fibrosis and inflammation and improves joint mobility in a rat model of adhesive capsulitis

doi: 10.1016/j.jot.2026.101195

Figure Lengend Snippet: IHC analysis of adhesive capsulitis tissues in rats treated with AD-Mito-NPs or Dex and serum biochemical indicators analysis. (A-B) Histological evaluation of collagen deposition and organization in the joint capsule. (A) Representative images of Masson's trichrome staining, picrosirius red staining, and IHC staining for Col I and Col III. Scale bar, 100 μm. (B) Semi-quantitative statistical analysis of collagen content and the Col1/Col3 ratio based on IHC and histological stains. (C-D) Assessment of inflammatory infiltration. (C) Representative IHC images of pro-inflammatory cytokines IL-6 and TNF-α. Scale bar, 100 μm. (D) Semi-quantitative statistical analysis of positive area based on IHC staining. (E-F) Analysis of matrix metalloproteinases (MMPs) expression. (E) Representative IHC images of MMP9 and MMP13. Scale bar, 100 μm. (F) Semi-quantitative statistical analysis of positive area based on IHC staining. (G) Quantitative analysis of key serum biochemical indicators. n = 6. Data are presented as mean ± SD. Statistical significance was determined by one-way ANOVA (B, D, F and G) with Tukey's multiple comparisons test. *P < 0.05 , **P < 0.01 , ***P < 0.001, **** P < 0.0001.

Article Snippet: Primary antibodies against Collagen type I (Col1, Cat. No.: A24112), Collagen type III (Col3, Cat. No.: A3795), matrix metalloproteinase 9 (MMP9, Cat. No.: A25299), matrix metalloproteinase 13 (MMP13, Cat. No.: A11755), IL-6 (Cat. No.: A0286), IL-10 (Cat. No.: A2171) and tumor necrosis factor-alpha (TNF-α, Cat. No.: A21265) (all Abclonal, 1:300 dilution) were applied at 4 °C overnight.

Techniques: Adhesive, Staining, Immunohistochemistry, Expressing

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: NAD metabolism is disrupted in tendinopathic tendons in vivo . a . A schematic diagram of the harvested region of human Achilles tendons. (The mid-portion of Achilles tendon) and the gross image of healthy and AT tendons. b. NAD + /NADH ratio and quantification of NAD metabolism (including, NAD + , NADH, total NAD pool) in human Achilles tendons. c. Quantification of ATP production. d. GSEA revealing top NAD metabolism-related GO terms enriched in human Achilles tendons. e. GSEA revealing top degeneration-related GO terms enriched in human Achilles tendon. f. Images of H&E staining, AB (Alcian blue) staining and Masson staining of human normal tendons and tendinopathic tendons. Bonar scores. g. Immunohistochemical staining of COL1 and COL3. h. Immunohistochemical staining of PARP and NOX4. i. Quantitative analysis of COL1, COL3, PARP, NOX4, and ratio of COL3/COL1. j. Immunohistochemical staining and quantification of TUNEL. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: In Vivo, Staining, Immunohistochemical staining, TUNEL Assay

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: MB corrects NAD dysmetabolism and matrix degeneration in the rat tendinopathy model. a . A schematic illustration of the rat tendinopathy model. b. Gross image of the Rat AT model. c. Gait analysis results for the different groups. The blue dotted line represents stride length; the red dotted line represents step length. Blue print: forepaw; red print: hind paw. d. Quantification of stride length, step length, and the length of the front/rear paw prints. e. Hot plate test. f. Paw contraction thresholds were assessed utilizing von Frey fibers to gauge mechanical sensitivity (n = 6). g. Quantification of ATP in the rat AT model. h. NAD + /NADH ratio i. Quantification of NAD metabolism (including, NAD + , NADH, total NAD pool). j. H&E staining, AB staining and Masson staining. Bonar scores of rats AT model. k. Immunohistochemical staining of Col1 and Col3. l. Immunohistochemical staining of Parp and Nox4. m. Quantitative analysis of Col1, Col3, Parp, Nox4. n. TUNEL staining and quantitative analysis of apoptotic cells. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: Hot Plate Test, Staining, Immunohistochemical staining, TUNEL Assay

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: MB reduces TBHP-induced NAD metabolism disorder in vitro and in vivo. a . The cell viability. b. Quantitation of NAD metabolism (including NAD + /NADH ratio, NAD + , NADH, total NAD pool) in rat tenocytes. c. Quantitation of ATP in rat tenocytes. d. Representative Western blot results for Col3, Col1, MMP3, and MMP13 in rat tenocytes. e. Ratio of Col3/Col1 by d. f. Representative Western blot results for Parp, c-Parp, Nox4, Bcl2, and Bax. g, h. Immunofluorescence and quantification analysis of Col1, Col3, Parp, and Nox4 expression in rat tenocytes. The ratio of Col1/Col3. DAPI, 4′,6-diamidino-2-phenylindole. i. Fluorescence images of the DCFH-DA probe for hydrogen peroxide in rat tenocytes. j. JC-1 staining in rat tenocytes. k. Quantitative analysis of ROS. l. Quantitative analysis of JC-1. m. Annexin V and activated caspase-3 staining and quantitative analysis of apoptotic cells in rat tenocytes. The results are presented as medians with 95% CIs. n = 3, 5, ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: In Vitro, In Vivo, Quantitation Assay, Western Blot, Immunofluorescence, Expressing, Fluorescence, Staining

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: MB alleviates TBHP-induced tendinopathy in human Achilles tendon explant. a . A schematic illustration of the human extra explant. b. Quantification of NAD metabolism in human extra explants under TBHP treatment combined with or without MB. (n = 3) c. H&E staining, AB staining, and Masson staining of human tendon explants. The Bonar scores. d. Quantification of ATP in human tendon explants. e. NFR. f. Immunohistochemical staining of COL1 and COL3. g. Immunohistochemical staining of PARP and NOX4. h. Immunohistochemical staining of AIF and NDUFB8. i. Quantification of the immunohistochemical staining data. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: Staining, Immunohistochemical staining

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: MB alleviates oxidative stress in a MC1-dependent manner in rat tenocytes. a. Quantification of ATP in rat tenocytes after TBHP treatment combined with/without MB or rotenone (Rot, a complex I inhibitor). b. NFR. c. Quantification of NAD metabolism. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Parp, Nox4, Aif expression by immunofluorescence microscopy (n = 3). f. Col3, Col1, Ndufb8 expression by immunofluorescence microscopy. g. Quantification of the immunofluorescence data from e and f . h. JC-1 staining. i. Quantitative analysis of JC-1. j, k. Fluorescence images and quantitative analysis of ROS. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: Western Blot, Expressing, Immunofluorescence, Microscopy, Staining, Fluorescence

Journal: Journal of Orthopaedic Translation

Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

doi: 10.1016/j.jot.2026.101085

Figure Lengend Snippet: MB increases the expression of Aif under Aif knockdown in tenocytes. a. The NAD metabolism after Aif was knocked down in rat tenocytes. b. Quantification of ATP after Aif knockdown. c. NFR. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Quantification of the Western blot data from d. f. Quantification of the immunofluorescence staining data . g. Col3, Col1, Parp, Nox4, Ndufb8, and Aif expression by immunofluorescence microscopy; h. Fluorescence images of ROS. i. JC-1 staining. j. Quantification of DCFH-DA staining data. k. Quantification of JC-1 staining data. l. Schematic illustration of the mechanism of MB in tendinopathy. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

Techniques: Expressing, Knockdown, Western Blot, Immunofluorescence, Staining, Microscopy, Fluorescence