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Involvement of Indian hedgehog signaling in mesenchymal stem cell–augmented rotator cuff tendon repair in an athymic rat model

Background Bone marrow aspirate has been used in recent years to augment tendon-to-bone healing, including in rotator cuff repair. However, the healing mechanism in cell-based therapy has not been elucidated in detail. Methods Sixteen athymic nude rats were randomly allocated to 2 groups: experiment...

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Published in:Journal of shoulder and elbow surgery 2017-04, Vol.26 (4), p.580-588
Main Authors: Zong, Jian-Chun, MD, Mosca, Michael J., MS, Degen, Ryan M., MD, Lebaschi, Amir, MD, Carballo, Camila, PhD, Carbone, Andrew, MS, Cong, Guang-Ting, MS, Ying, Liang, Deng, Xiang-Hua, MD, Rodeo, Scott A., MD
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container_title Journal of shoulder and elbow surgery
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creator Zong, Jian-Chun, MD
Mosca, Michael J., MS
Degen, Ryan M., MD
Lebaschi, Amir, MD
Carballo, Camila, PhD
Carbone, Andrew, MS
Cong, Guang-Ting, MS
Ying, Liang
Deng, Xiang-Hua, MD
Rodeo, Scott A., MD
description Background Bone marrow aspirate has been used in recent years to augment tendon-to-bone healing, including in rotator cuff repair. However, the healing mechanism in cell-based therapy has not been elucidated in detail. Methods Sixteen athymic nude rats were randomly allocated to 2 groups: experimental (human mesenchymal stem cells in fibrin glue carrier) and control (fibrin glue only). Animals were sacrificed at 2 and 4 weeks. Immunohistochemical staining was performed to evaluate Indian hedgehog (Ihh) signaling and SOX9 signaling in the healing enthesis. Macrophages were identified using CD68 and CD163 staining, and proliferating cells were identified using proliferating cell nuclear antigen staining. Results More organized and stronger staining for collagen II and a higher abundance of SOX9+ cells were observed at the enthesis in the experimental group at 2 weeks. There was significantly higher Gli1 and Patched1 expression in the experimental group at the enthesis at 2 weeks and higher numbers of Ihh+ cells in the enthesis of the experimental group vs control at both 2 weeks and 4 weeks postoperatively. There were more CD68+ cells localized to the tendon midsubstance at 2 weeks compared with 4 weeks, and there was a higher level of CD163 staining in the tendon midsubstance in the experimental group than in the control group at 4 weeks. Conclusion Stem cell application had a positive effect on fibrocartilage formation at the healing rotator cuff repair site. Both SOX9 and Ihh signaling appear to play an important role in the healing process.
doi_str_mv 10.1016/j.jse.2016.09.036
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However, the healing mechanism in cell-based therapy has not been elucidated in detail. Methods Sixteen athymic nude rats were randomly allocated to 2 groups: experimental (human mesenchymal stem cells in fibrin glue carrier) and control (fibrin glue only). Animals were sacrificed at 2 and 4 weeks. Immunohistochemical staining was performed to evaluate Indian hedgehog (Ihh) signaling and SOX9 signaling in the healing enthesis. Macrophages were identified using CD68 and CD163 staining, and proliferating cells were identified using proliferating cell nuclear antigen staining. Results More organized and stronger staining for collagen II and a higher abundance of SOX9+ cells were observed at the enthesis in the experimental group at 2 weeks. There was significantly higher Gli1 and Patched1 expression in the experimental group at the enthesis at 2 weeks and higher numbers of Ihh+ cells in the enthesis of the experimental group vs control at both 2 weeks and 4 weeks postoperatively. There were more CD68+ cells localized to the tendon midsubstance at 2 weeks compared with 4 weeks, and there was a higher level of CD163 staining in the tendon midsubstance in the experimental group than in the control group at 4 weeks. Conclusion Stem cell application had a positive effect on fibrocartilage formation at the healing rotator cuff repair site. Both SOX9 and Ihh signaling appear to play an important role in the healing process.</description><identifier>ISSN: 1058-2746</identifier><identifier>EISSN: 1532-6500</identifier><identifier>DOI: 10.1016/j.jse.2016.09.036</identifier><identifier>PMID: 27887870</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antigens, CD - analysis ; Antigens, Differentiation, Myelomonocytic - analysis ; Cell Count ; Collagen Type II - metabolism ; enthesis ; Fibrocartilage ; Hedgehog Proteins - metabolism ; Humans ; Indian hedgehog ; Macrophages - chemistry ; Male ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stem Cells - metabolism ; Orthopedics ; Patched-1 Receptor - metabolism ; Rats ; Rats, Nude ; Rats, Sprague-Dawley ; Receptors, Cell Surface - analysis ; repair ; rotator cuff ; Rotator Cuff - metabolism ; Signal Transduction ; sox9 ; SOX9 Transcription Factor - metabolism ; stem cell ; Transplantation, Heterologous ; Wound Healing ; Zinc Finger Protein GLI1 - metabolism</subject><ispartof>Journal of shoulder and elbow surgery, 2017-04, Vol.26 (4), p.580-588</ispartof><rights>Journal of Shoulder and Elbow Surgery Board of Trustees</rights><rights>2017 Journal of Shoulder and Elbow Surgery Board of Trustees</rights><rights>Copyright © 2017 Journal of Shoulder and Elbow Surgery Board of Trustees. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-2e4f50f566a46e5a01e5efe85cb98fdfda8e2c8830abcf01ec13b96b2d64dda63</citedby><cites>FETCH-LOGICAL-c408t-2e4f50f566a46e5a01e5efe85cb98fdfda8e2c8830abcf01ec13b96b2d64dda63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27887870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zong, Jian-Chun, MD</creatorcontrib><creatorcontrib>Mosca, Michael J., MS</creatorcontrib><creatorcontrib>Degen, Ryan M., MD</creatorcontrib><creatorcontrib>Lebaschi, Amir, MD</creatorcontrib><creatorcontrib>Carballo, Camila, PhD</creatorcontrib><creatorcontrib>Carbone, Andrew, MS</creatorcontrib><creatorcontrib>Cong, Guang-Ting, MS</creatorcontrib><creatorcontrib>Ying, Liang</creatorcontrib><creatorcontrib>Deng, Xiang-Hua, MD</creatorcontrib><creatorcontrib>Rodeo, Scott A., MD</creatorcontrib><title>Involvement of Indian hedgehog signaling in mesenchymal stem cell–augmented rotator cuff tendon repair in an athymic rat model</title><title>Journal of shoulder and elbow surgery</title><addtitle>J Shoulder Elbow Surg</addtitle><description>Background Bone marrow aspirate has been used in recent years to augment tendon-to-bone healing, including in rotator cuff repair. However, the healing mechanism in cell-based therapy has not been elucidated in detail. Methods Sixteen athymic nude rats were randomly allocated to 2 groups: experimental (human mesenchymal stem cells in fibrin glue carrier) and control (fibrin glue only). Animals were sacrificed at 2 and 4 weeks. Immunohistochemical staining was performed to evaluate Indian hedgehog (Ihh) signaling and SOX9 signaling in the healing enthesis. Macrophages were identified using CD68 and CD163 staining, and proliferating cells were identified using proliferating cell nuclear antigen staining. Results More organized and stronger staining for collagen II and a higher abundance of SOX9+ cells were observed at the enthesis in the experimental group at 2 weeks. There was significantly higher Gli1 and Patched1 expression in the experimental group at the enthesis at 2 weeks and higher numbers of Ihh+ cells in the enthesis of the experimental group vs control at both 2 weeks and 4 weeks postoperatively. There were more CD68+ cells localized to the tendon midsubstance at 2 weeks compared with 4 weeks, and there was a higher level of CD163 staining in the tendon midsubstance in the experimental group than in the control group at 4 weeks. Conclusion Stem cell application had a positive effect on fibrocartilage formation at the healing rotator cuff repair site. 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However, the healing mechanism in cell-based therapy has not been elucidated in detail. Methods Sixteen athymic nude rats were randomly allocated to 2 groups: experimental (human mesenchymal stem cells in fibrin glue carrier) and control (fibrin glue only). Animals were sacrificed at 2 and 4 weeks. Immunohistochemical staining was performed to evaluate Indian hedgehog (Ihh) signaling and SOX9 signaling in the healing enthesis. Macrophages were identified using CD68 and CD163 staining, and proliferating cells were identified using proliferating cell nuclear antigen staining. Results More organized and stronger staining for collagen II and a higher abundance of SOX9+ cells were observed at the enthesis in the experimental group at 2 weeks. There was significantly higher Gli1 and Patched1 expression in the experimental group at the enthesis at 2 weeks and higher numbers of Ihh+ cells in the enthesis of the experimental group vs control at both 2 weeks and 4 weeks postoperatively. There were more CD68+ cells localized to the tendon midsubstance at 2 weeks compared with 4 weeks, and there was a higher level of CD163 staining in the tendon midsubstance in the experimental group than in the control group at 4 weeks. Conclusion Stem cell application had a positive effect on fibrocartilage formation at the healing rotator cuff repair site. Both SOX9 and Ihh signaling appear to play an important role in the healing process.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27887870</pmid><doi>10.1016/j.jse.2016.09.036</doi><tpages>9</tpages></addata></record>
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subjects Animals
Antigens, CD - analysis
Antigens, Differentiation, Myelomonocytic - analysis
Cell Count
Collagen Type II - metabolism
enthesis
Fibrocartilage
Hedgehog Proteins - metabolism
Humans
Indian hedgehog
Macrophages - chemistry
Male
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells - metabolism
Orthopedics
Patched-1 Receptor - metabolism
Rats
Rats, Nude
Rats, Sprague-Dawley
Receptors, Cell Surface - analysis
repair
rotator cuff
Rotator Cuff - metabolism
Signal Transduction
sox9
SOX9 Transcription Factor - metabolism
stem cell
Transplantation, Heterologous
Wound Healing
Zinc Finger Protein GLI1 - metabolism
title Involvement of Indian hedgehog signaling in mesenchymal stem cell–augmented rotator cuff tendon repair in an athymic rat model
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