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Representative images of immunohistochemical staining and histopathological assessment from study specimens. (a) At Week 4, Group II, increased neovascularization (asterisk) is observed between collagen fibre bundles (arrow) within the tendon tissue (H&E staining, ×100 magnification). (b) At Week 4, Group II, collagen fibres stained blue and vascular structures were clearly distinguishable (Masson's trichrome staining, ×100 magnification). (c) Strong cytoplasmic immunopositivity for BMP‐7 in multinucleated cell formations, Group III, staining observed in cell clusters at the tendon–bone interface at Week 8 (immunoperoxidase staining, ×400 magnification). (d) Positive immunopositivity for CD34 was observed in vascular endothelial cells within the tendon region at Week 4, Group II (immunoperoxidase staining, ×200 magnification). (e) Membranous TGF‐β1 staining in the tendon–muscle junction at Week 4, Group I, showing sparse immunopositivity (immunoperoxidase staining, ×400 magnification). (f) Cytoplasmic immunopositivity for BMP‐2 at the tendon–bone interface at Week 8, Group III (immunoperoxidase staining, ×400 magnification). BMP‐2, bone morphogenetic <t>protein‐2;</t> BMP‐7, bone morphogenetic protein‐7; TGF‐β1, transforming growth factor‐β1.
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Representative images of immunohistochemical staining and histopathological assessment from study specimens. (a) At Week 4, Group II, increased neovascularization (asterisk) is observed between collagen fibre bundles (arrow) within the tendon tissue (H&E staining, ×100 magnification). (b) At Week 4, Group II, collagen fibres stained blue and vascular structures were clearly distinguishable (Masson's trichrome staining, ×100 magnification). (c) Strong cytoplasmic immunopositivity for BMP‐7 in multinucleated cell formations, Group III, staining observed in cell clusters at the tendon–bone interface at Week 8 (immunoperoxidase staining, ×400 magnification). (d) Positive immunopositivity for CD34 was observed in vascular endothelial cells within the tendon region at Week 4, Group II (immunoperoxidase staining, ×200 magnification). (e) Membranous TGF‐β1 staining in the tendon–muscle junction at Week 4, Group I, showing sparse immunopositivity (immunoperoxidase staining, ×400 magnification). (f) Cytoplasmic immunopositivity for BMP‐2 at the tendon–bone interface at Week 8, Group III (immunoperoxidase staining, ×400 magnification). BMP‐2, bone morphogenetic <t>protein‐2;</t> BMP‐7, bone morphogenetic protein‐7; TGF‐β1, transforming growth factor‐β1.
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Representative images of immunohistochemical staining and histopathological assessment from study specimens. (a) At Week 4, Group II, increased neovascularization (asterisk) is observed between collagen fibre bundles (arrow) within the tendon tissue (H&E staining, ×100 magnification). (b) At Week 4, Group II, collagen fibres stained blue and vascular structures were clearly distinguishable (Masson's trichrome staining, ×100 magnification). (c) Strong cytoplasmic immunopositivity for BMP‐7 in multinucleated cell formations, Group III, staining observed in cell clusters at the tendon–bone interface at Week 8 (immunoperoxidase staining, ×400 magnification). (d) Positive immunopositivity for CD34 was observed in vascular endothelial cells within the tendon region at Week 4, Group II (immunoperoxidase staining, ×200 magnification). (e) Membranous TGF‐β1 staining in the tendon–muscle junction at Week 4, Group I, showing sparse immunopositivity (immunoperoxidase staining, ×400 magnification). (f) Cytoplasmic immunopositivity for BMP‐2 at the tendon–bone interface at Week 8, Group III (immunoperoxidase staining, ×400 magnification). BMP‐2, bone morphogenetic protein‐2; BMP‐7, bone morphogenetic protein‐7; TGF‐β1, transforming growth factor‐β1.

Journal: Journal of Experimental Orthopaedics

Article Title: Comparative effects of bone marrow stimulation and shockwave therapy on rotator cuff healing in chronic massive rotator cuff tears: A rat model study

doi: 10.1002/jeo2.70622

Figure Lengend Snippet: Representative images of immunohistochemical staining and histopathological assessment from study specimens. (a) At Week 4, Group II, increased neovascularization (asterisk) is observed between collagen fibre bundles (arrow) within the tendon tissue (H&E staining, ×100 magnification). (b) At Week 4, Group II, collagen fibres stained blue and vascular structures were clearly distinguishable (Masson's trichrome staining, ×100 magnification). (c) Strong cytoplasmic immunopositivity for BMP‐7 in multinucleated cell formations, Group III, staining observed in cell clusters at the tendon–bone interface at Week 8 (immunoperoxidase staining, ×400 magnification). (d) Positive immunopositivity for CD34 was observed in vascular endothelial cells within the tendon region at Week 4, Group II (immunoperoxidase staining, ×200 magnification). (e) Membranous TGF‐β1 staining in the tendon–muscle junction at Week 4, Group I, showing sparse immunopositivity (immunoperoxidase staining, ×400 magnification). (f) Cytoplasmic immunopositivity for BMP‐2 at the tendon–bone interface at Week 8, Group III (immunoperoxidase staining, ×400 magnification). BMP‐2, bone morphogenetic protein‐2; BMP‐7, bone morphogenetic protein‐7; TGF‐β1, transforming growth factor‐β1.

Article Snippet: For the purpose of histopathological evaluation, hematoxylin–eosin (H&E) staining and Masson's trichrome staining were performed in accordance with standard protocols, and for immunohistochemical analysis, antibodies against bone morphogenetic protein‐2 (BMP‐2), bone morphogenetic protein‐7 (BMP‐7) and transforming growth factor‐β1 (TGF‐β1) were obtained from Invitrogen (Thermo Fisher Scientific) and CD34 from Dako (Glostrup).

Techniques: Immunohistochemical staining, Staining, Immunoperoxidase Staining