In vitro evaluation of a bone morphogenetic protein-2 nanometer hydroxyapatite collagen scaffold for bone regeneration

被引:27
|
作者
Cai, Yue [1 ]
Tong, Shuang [2 ]
Zhang, Ran [1 ]
Zhu, Tong [1 ]
Wang, Xukai [1 ]
机构
[1] China Med Univ, Liaoning Inst Dent Res, Sch Stomatol, Dept Oral & Maxillofacial Surg, 117 Nan Jing North St, Shenyang 110002, Liaoning, Peoples R China
[2] China Med Univ, Dept Plast Surg, Affiliated Hosp 1, Shenyang 110002, Liaoning, Peoples R China
关键词
bone tissue engineering; bone marrow-derived mesenchymal stem cells; nanometer hydroxyapatite; collagen; biocompatibility; bone morphogenetic protein 2; MESENCHYMAL STEM-CELLS; TISSUE; VIVO; DIFFERENTIATION; OSTEOGENESIS; CARTILAGE; DELIVERY; RELEASE; REPAIR; SIZE;
D O I
10.3892/mmr.2018.8579
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Scaffold fabrication and biocompatibility are crucial for successful bone tissue engineering. Nanometer hydroxyapatite (nHAP) combined with collagen (COL) is frequently utilized as a suitable osseous scaffold material. Furthermore, growth factors, including bone morphogenetic protein-2 (BMP-2), are used to enhance the scaffold properties. The present study used blending and freeze-drying methods to develop a BMP-2-nHAP-COL scaffold. An ELISA was performed to determine the BMP-2 release rate from the scaffold. Flow cytometry was used to identify rat bone marrow-derived mesenchymal stem cells (BMSCs) prior to their combination with the scaffold. Scanning electron microscopy was used to observe the scaffold structure and BMSC morphology following seeding onto the scaffold. BMSCs were also used to assess the biological compatibility of the scaffold in vitro. BMP-2-nHAP-COL and nHAP-COL scaffolds were assessed alongside the appropriate control groups. Cells were counted to determine early cell adhesion. Cell Counting kit-8 and alkaline phosphatase assays were used to detect cell proliferation and differentiation, respectively. Gross morphology confirmed that the BMP-2-nHAP-COL scaffold microstructure conformed to the optimal characteristics of a bone tissue engineering scaffold. Furthermore, the BMP-2-nHAP-COL scaffold exhibited no biological toxicity and was demonstrated to promote BMSC adhesion, proliferation and differentiation. The BMP-2-nHAP-COL scaffold had good biocompatibility in vitro, and may therefore be modified further to construct an optimized scaffold for future bone tissue engineering.
引用
收藏
页码:5830 / 5836
页数:7
相关论文
共 50 条
  • [21] Bone Morphogenetic Protein-2 Derived Peptide Loaded Calcium Sulfate Hemihydrate Scaffold for Enhanced Bone Tissue Regeneration
    Liu, Jianheng
    Zhou, Liang
    Zhang, Licheng
    Mao, Kezheng
    Xu, Jiao
    Shi, Teng
    Su, Xiangzheng
    Wang, Xiumei
    Cui, Fuzhai
    Liu, Zhengsheng
    Zhang, Lihai
    Mao, Keya
    Tang, Peifu
    JOURNAL OF BIOMATERIALS AND TISSUE ENGINEERING, 2015, 5 (11) : 864 - 871
  • [22] Effects of Self-Assembling Peptide Hydrogel Scaffold on Bone Regeneration with Recombinant Human Bone Morphogenetic Protein-2
    Ikeno, Masayuki
    Hibi, Hideharu
    Kinoshita, Kazuhiko
    Hattori, Hisashi
    Ueda, Minoru
    INTERNATIONAL JOURNAL OF ORAL & MAXILLOFACIAL IMPLANTS, 2013, 28 (05) : E283 - E289
  • [23] Bone Morphogenetic Protein-2 Plasmid DNA as a Substitute for Bone Morphogenetic Protein-2 Protein in Bone Tissue Engineering
    Wegman, Fiona
    van der Helm, Yvonne
    Oner, F. Cumhur
    Dhert, Wouter J. A.
    Alblas, Jacqueline
    TISSUE ENGINEERING PART A, 2013, 19 (23-24) : 2686 - 2692
  • [24] PERIODONTAL REGENERATION AND RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2
    KING, GN
    CRUCHLEY, AC
    HUGHES, FJ
    JOURNAL OF DENTAL RESEARCH, 1995, 74 : 592 - 592
  • [25] Sustained delivery of a heterodimer bone morphogenetic protein-2/7 via a collagen hydroxyapatite scaffold accelerates and improves critical femoral defect
    Liu, Yang
    Puthia, Manoj
    Sheehy, Eamon J.
    Ambite, Ines
    Petrlova, Jitka
    Prithviraj, Sujeethkumar
    Oxborg, Maria Wimer
    Sebastian, Sujeesh
    Vater, Corina
    Zwingenberger, Stefan
    Struglics, Andre
    Bourgine, Paul E.
    O'Brien, Fergal J.
    Raina, Deepak Bushan
    ACTA BIOMATERIALIA, 2023, 162 : 164 - 181
  • [26] Periodontal Regeneration Using Recombinant Human Bone Morphogenetic Protein-2 and a Bilayer Collagen Matrix
    Lee, Jungwon
    Yun, Junseob
    Kim, Kyoung-Hwa
    Koo, Ki-Tae
    Seol, Yang-Jo
    Lee, Yong-Moo
    JOURNAL OF CRANIOFACIAL SURGERY, 2020, 31 (06) : 1602 - 1607
  • [27] In Vitro Evaluation of Recombinant Bone Morphogenetic Protein-2 Bioactivity for Regenerative Medicine
    Fung, Stephanie L.
    Wu, Xiaohuan
    Maceren, Julian P.
    Mao, Yong
    Kohn, Joachim
    TISSUE ENGINEERING PART C-METHODS, 2019, 25 (09) : 553 - 559
  • [28] Comparison between heparin-conjugated fibrin and collagen sponge as bone morphogenetic protein-2 carriers for bone regeneration
    Hee Seok Yang
    Wan-Geun La
    Yong-Min Cho
    Wangsoo Shin
    Guw-Dong Yeo
    Byung-Soo Kim
    Experimental & Molecular Medicine, 2012, 44 : 350 - 355
  • [29] Comparison between heparin-conjugated fibrin and collagen sponge as bone morphogenetic protein-2 carriers for bone regeneration
    Yang, Hee Seok
    La, Wan-Geun
    Cho, Yong-Min
    Shin, Wangsoo
    Yeo, Guw-Dong
    Kim, Byung-Soo
    EXPERIMENTAL AND MOLECULAR MEDICINE, 2012, 44 (05): : 350 - 355
  • [30] Efficient Bone Regeneration Induced by Bone Morphogenetic Protein-2 Released from Apatite-Coated Collagen Scaffolds
    Yang, Hee Seok
    La, Wan-Geun
    Park, Jooyeon
    Kim, Chang-Sung
    Im, Gun-Il
    Kim, Byung-Soo
    JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2012, 23 (13) : 1659 - 1671