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Article Open Access

Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1

  • Authors:
    • Xiebo You
    • Yueqin Shen
    • Weihan Yu
    • Yaohua He
  • View Affiliations / Copyright

    Affiliations: Department of Orthopedics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, P.R. China, State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 200050, P.R. China
    Copyright: © You et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 4981-4988
    |
    Published online on: January 26, 2018
       https://doi.org/10.3892/mmr.2018.8499
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Abstract

The formation of fibrocartilage at the healing site following a rotator cuff tear repair is a major problem in the field of tendon‑bone healing. The present study aimed to enhance the healing of the tendon‑bone interface following rotator‑cuff tear repair by the interposition of hydroxyapatite (HA) encapsulated with transforming growth factor β1 (TGFβ1). Using an acute rotator cuff repair model, rats were divided into three groups: i) Repair only (control); ii) HA group; and iii) HA‑TGFβ1 group. Animals were sacrificed at 2, 4 and 8 weeks following surgery. Micro‑computed tomography (CT), histomorphometric analyses and biomechanical tests were used to evaluate the supraspinatus tendon‑bone complex. The micro‑CT images revealed notable novel bone formation in the groups treated with HA‑TGFβ1. The histomorphometric analyses demonstrated improved fibrocartilage formation and collagen organization at the tendon‑bone interface. The HA‑TGFβ1 combination significantly improved the area of fibrocartilage, particularly at early time points (2 and 4 weeks). There was a significantly greater load‑to‑failure force achieved in the HA and HA‑TGFβ1 groups compared with the control group at 4 and 8 weeks. Augmentation of the ceramic powder with HA‑TGFβ1 at the tendon‑bone interface was demonstrated to strengthen the healing entheses, increase bone and fibrocartilage formation and improve collagen organization compared with surgical repair alone. Local application of HA‑TGFβ1 demonstrates potential in improving tendon‑bone healing following rotator cuff repair.
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Copy and paste a formatted citation
Spandidos Publications style
You X, Shen Y, Yu W and He Y: Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1. Mol Med Rep 17: 4981-4988, 2018.
APA
You, X., Shen, Y., Yu, W., & He, Y. (2018). Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1. Molecular Medicine Reports, 17, 4981-4988. https://doi.org/10.3892/mmr.2018.8499
MLA
You, X., Shen, Y., Yu, W., He, Y."Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1". Molecular Medicine Reports 17.4 (2018): 4981-4988.
Chicago
You, X., Shen, Y., Yu, W., He, Y."Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1". Molecular Medicine Reports 17, no. 4 (2018): 4981-4988. https://doi.org/10.3892/mmr.2018.8499
Copy and paste a formatted citation
x
Spandidos Publications style
You X, Shen Y, Yu W and He Y: Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1. Mol Med Rep 17: 4981-4988, 2018.
APA
You, X., Shen, Y., Yu, W., & He, Y. (2018). Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1. Molecular Medicine Reports, 17, 4981-4988. https://doi.org/10.3892/mmr.2018.8499
MLA
You, X., Shen, Y., Yu, W., He, Y."Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1". Molecular Medicine Reports 17.4 (2018): 4981-4988.
Chicago
You, X., Shen, Y., Yu, W., He, Y."Enhancement of tendon‑bone healing following rotator cuff repair using hydroxyapatite with TGFβ1". Molecular Medicine Reports 17, no. 4 (2018): 4981-4988. https://doi.org/10.3892/mmr.2018.8499
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