Extracellular matrix formation and mineralization on a phosphate-free porous bioactive glass scaffold using primary human osteoblast (HOB) cells

被引:222
作者
Jones, Julian R.
Tsigkou, Olga
Coates, Emily E.
Stevens, Molly M.
Polak, Julia M.
Hench, Larry L.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Tissue Engn & Regenerat Med Ctr, London, England
[3] Univ London Imperial Coll Sci Technol & Med, Inst Biomed Engn, London SW7 2AZ, England
基金
英国医学研究理事会;
关键词
osteoblast; bioactive glass; porous scaffold; ion release; mineralization;
D O I
10.1016/j.biomaterials.2006.11.022
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Sol-get derived bioactive glasses of the 70S30C (70mol% SiO(2), 30mol% CaO) composition have been foamed to produce 3D bioactive scaffolds with hierarchical interconnected pore morphologies similar to trabecular bone. The aim of this study was to investigate primary human osteoblast response to porous bioactive glass scaffolds. The scaffolds supported osteoblast growth and induced differentiation, within the 3-week culture period, as depicted by enhanced ALPase enzymatic activity, without the addition of supplementary factors such as ascorbic acid, ss-glycerophosphate and dexamethasone. This is the first time this has been observed on a bioactive glass that does not contain phosphate. Deposition of extracellular matrix was also confirmed by enhanced production of the extracellular matrix protein collagen type I. SEM showed indications of mineralized bone nodule formation without the addition of growth factors. The 70S30C bioactive glass scaffolds therefore fulfil many of the criteria for an ideal scaffold for bone tissue engineering applications. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1653 / 1663
页数:11
相关论文
共 37 条
[1]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[2]   PRODUCTION OF OSTEOCALCIN BY HUMAN-BONE CELLS-INVITRO - EFFECTS OF 1,25(OH)2D3, 24,25(OH)2D3, PARATHYROID-HORMONE, AND GLUCOCORTICOIDS [J].
BERESFORD, JN ;
GALLAGHER, JA ;
POSER, JW ;
RUSSELL, RGG .
METABOLIC BONE DISEASE & RELATED RESEARCH, 1984, 5 (05) :229-234
[3]   On a theory of the van der Waals adsorption of gases [J].
Brunauer, S ;
Deming, LS ;
Deming, WE ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1940, 62 :1723-1732
[4]   Mechanisms of glucocorticoid action in bone: Implications to glucocorticoid-induced osteoporosis [J].
Canalis, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (10) :3441-3447
[5]   Mechanisms of glucocorticoid action in bone [J].
Canalis, E ;
Delany, AM .
NEUROENDOCRINE IMMUNE BASIS OF THE RHEUMATIC DISEASES II, PROCEEDINGS, 2002, 966 :73-81
[6]   Human bone cell cultures in biocompatibility testing.: Part II:: effect of ascorbic acid, β-glycerophosphate and dexamethasone on osteoblastic differentiation [J].
Coelho, MJ ;
Fernandes, MH .
BIOMATERIALS, 2000, 21 (11) :1095-1102
[7]  
FRANCESCHI RT, 1992, J BONE MINER RES, V7, P235
[8]  
FRANCESCHI RT, 1994, J BONE MINER RES, V9, P843
[9]   Cellular materials as porous scaffolds for tissue engineering [J].
Freyman, TM ;
Yannas, IV ;
Gibson, LJ .
PROGRESS IN MATERIALS SCIENCE, 2001, 46 (3-4) :273-282
[10]   Nodule formation and mineralisation of human primary osteoblasts cultured on a porous bioactive glass scaffold [J].
Gough, JE ;
Jones, JR ;
Hench, LL .
BIOMATERIALS, 2004, 25 (11) :2039-2046