Copper-incorporated bioactive glass-ceramics inducing anti-inflammatory phenotype and regeneration of cartilage/bone interface

被引:181
作者
Lin, Rongcai [1 ]
Deng, Cuijun [2 ,3 ]
Li, Xuxiang [1 ]
Liu, Yaqin [2 ]
Zhang, Meng [2 ]
Qin, Chen [2 ]
Yao, Qingqiang [1 ]
Wang, Liming [1 ]
Wu, Chengtie [2 ]
机构
[1] Nanjing Med Univ, Nanjing Hosp 1, Dept Orthopaed, Nanjing 210006, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[3] Tongji Univ, Sch Med, Inst Biomed Engn & Nano Sci, Shanghai East Hosp, 150 Jimo Rd, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
copper; bioactive glass ceramics; osteoarthritis; cartilage regeneration; immunomodulation; AUTOLOGOUS CHONDROCYTE IMPLANTATION; ANIMAL-MODELS; OSTEOARTHRITIS; ANGIOGENESIS; MACROPHAGES; REPAIR; BONE; CERULOPLASMIN; OSTEOGENESIS; PATHOGENESIS;
D O I
10.7150/thno.36120
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Osteoarthritis not only results in cartilage lesion, but also is accompanied with subchondral bone damage caused by the inflammatory response. It is of great significance to treat osteoarthritis by regulating the immune response. As copper (Cu) plays an essential role in immune response and anti-arthritis, a copper-incorporated bioactive glass-ceramics (Cu-BGC) may achieve the aim of healing cartilage lesion and reducing inflammatory response caused by osteoarthritis. We hypothesized that the Cu2+ released from Cu-BGC scaffolds may satisfy the requirements of cartilage regeneration and anti-arthritis. Methods: 3D-printing method was employed to prepare Cu-BGC scaffolds. The stimulating effect on the chondrocytes and macrophages cultured with Cu-BGC extracts was investigated. Furthermore, the in vivo regenerative effect of Cu-BGC scaffolds on osteochondral defects was studied. Results: The incorporation of Cu2+ into BGC considerably promoted the proliferation and maturation of chondrocytes, and induced macrophages shifting to anti-inflammatory phenotype. Histological analysis demonstrated that the Cu-BGC scaffolds meaningfully improved the regeneration of cartilage and elevated the recovery of the osteochondral interface as compared with the CTR and BGC groups. The potential mechanism is related to Cu2+ ions triggering the immune response of cartilage via activating HIF signaling pathway and inhibiting the inflammatory response in osteochondral tissue. Conclusion: These results demonstrated that Cu-BGC scaffolds significantly facilitated the regeneration of cartilage and osteochondral interface, as well as inhibited inflammatory response, which may prevent the development of osteoarthritis associated with osteochondral defects.
引用
收藏
页码:6300 / 6313
页数:14
相关论文
共 49 条
[1]   Inhibition of Hif1α prevents both trauma-induced and genetic heterotopic ossification [J].
Agarwal, Shailesh ;
Loder, Shawn ;
Brownley, Cameron ;
Cholok, David ;
Mangiavini, Laura ;
Li, John ;
Breuler, Christopher ;
Sunga, Hsiao H. ;
Li, Shuli ;
Ranganathan, Kavitha ;
Peterson, Joshua ;
Tompkins, Ronald ;
Herndon, David ;
Xiao, Wenzhong ;
Jumlongras, Dolrudee ;
Olsen, Bjorn R. ;
Davis, Thomas A. ;
Mishina, Yuji ;
Schipani, Ernestina ;
Levi, Benjamin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (03) :E338-E347
[2]   Anabolic role of lysyl oxidase like-2 in cartilage of knee and temporomandibular joints with osteoarthritis [J].
Alshenibr, Weam ;
Tashkandi, Mustafa M. ;
Alsaqer, Saqer F. ;
Alkheriji, Yazeed ;
Wise, Amelia ;
Fulzele, Sadanand ;
Mehra, Pushkar ;
Goldring, Mary B. ;
Gerstenfeld, Louis C. ;
Bais, Manish V. .
ARTHRITIS RESEARCH & THERAPY, 2017, 19
[3]   Osteoarthritis as an inflammatory disease (osteoarthritis is not osteoarthrosis!) [J].
Berenbaum, F. .
OSTEOARTHRITIS AND CARTILAGE, 2013, 21 (01) :16-21
[4]   Dietary copper and human health: Current evidence and unresolved issues [J].
Bost, Muriel ;
Houdart, Sabine ;
Oberli, Marion ;
Kalonji, Esther ;
Huneau, Jean-Francois ;
Margaritis, Irene .
JOURNAL OF TRACE ELEMENTS IN MEDICINE AND BIOLOGY, 2016, 35 :107-115
[5]   Interaction of HIF1α and β-catenin inhibits matrix metalloproteinase 13 expression and prevents cartilage damage in mice [J].
Bouaziz, Wafa ;
Sigaux, Johanna ;
Modrowski, Dominique ;
Devignes, Claire-Sophie ;
Funck-Brentano, Thomas ;
Richette, Pascal ;
Ea, Hang-Korng ;
Provot, Sylvain ;
Cohen-Solal, Martine ;
Hay, Eric .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (19) :5453-5458
[6]   Advancing biomaterials of human origin for tissue engineering [J].
Chen, Fa-Ming ;
Liu, Xiaohua .
PROGRESS IN POLYMER SCIENCE, 2016, 53 :86-168
[7]   Nanoporous microstructures mediate osteogenesis by modulating the osteo-immune response of macrophages [J].
Chen, Zetao ;
Ni, Siyu ;
Han, Shengwei ;
Crawford, Ross ;
Lu, Shifeier ;
Wei, Fei ;
Chang, Jiang ;
Wu, Chengtie ;
Xiao, Yin .
NANOSCALE, 2017, 9 (02) :706-718
[8]  
Chu CR, 2010, TISSUE ENG PART B-RE, V16, P105, DOI [10.1089/ten.teb.2009.0452, 10.1089/ten.TEB.2009.0452]
[9]   Animal models of cartilage repair [J].
Cook, J. L. ;
Hung, C. T. ;
Kuroki, K. ;
Stoker, A. M. ;
Cook, C. R. ;
Pfeiffer, F. M. ;
Sherman, S. L. ;
Stannard, J. P. .
BONE & JOINT RESEARCH, 2014, 3 (04) :89-94
[10]   Inflammatory biomarkers in osteoarthritis [J].
Daghestani, H. N. ;
Kraus, V. B. .
OSTEOARTHRITIS AND CARTILAGE, 2015, 23 (11) :1890-1896