Effects of growth factors on heparin-carrying polystyrene-coated atelocollagen scaffold for articular cartilage tissue engineering

被引:29
作者
Sato, Masato
Ishihara, Masayuki
Ishihara, Miya
Kaneshiro, Nagatoshi
Mitani, Genya
Nagai, Toshihiro
Kutsuna, Toshiharu
Asazuma, Takashi
Kikuchi, Makoto
Mochidal, Joji
机构
[1] Tokai Univ, Sch Med, Dept Orthopaed Surg Surg Sci, Isehara, Kanagawa 2591193, Japan
[2] Natl Def Med Coll, Inst Res, Div Biomed Engn, Tokorozawa, Saitama 3598513, Japan
[3] Natl Def Med Coll, Dept Med Engn, Tokorozawa, Saitama 3598513, Japan
[4] Tokai Univ, Sch Med, Dept Orthopaed Surg, Oiso, Kanagawa 2590193, Japan
[5] Natl Def Med Coll, Dept Orthopaed Surg, Tokorozawa, Saitama 3598513, Japan
关键词
heparin-binding protein; heparin-carrying-polystyrene; scaffold; tissue engineering; growth factor; FGF-2; TGF-beta; 1; collagen; extracellular matrix; chondrocyte; articular cartilage;
D O I
10.1002/jbm.b.30782
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
The specific aim of our investigation is to study the potential use of a collagen/heparin-carrying polystyrene (HCPS) composite extracellular matrix for articular cartilage tissue engineering. Here, we created a high-performance extracellular matrix (HpECM) scaffold to build an optimal extracellular environment using an HCPS we originally developed, and an atelocollagen honeycomb-shaped-scaffold (ACHMS-scaffold) with a membrane seal. This scaffold was coated with HCPS to enable aggregation of heparin-binding growth factors such as FGF-2 and TGF-beta 1 within the scaffold. Three-dimensional culture of rabbit articular chondrocytes within the HpECM-scaffold and subsequent preparation of a tissue-engineered cartilage were investigated. The results showed remarkably higher cell proliferative activity within the HpECM-pretreated-FGF-2 scaffold and the sustenance of phenotype within the HpECM-pretreated-TGF-beta 1 scaffold. It was thought that both FGF-2 and TGF-beta 1 were stably immobilized in the HpEMC-scaffold since HCPS generated an extracellular environment similar to that of heparan sulfate proteoglycan within the scaffold. These results suggest that an ACHMS-scaffold immobilized with HCPS can be a HpECM for cartilage regeneration to retain the heparin-binding growth factors within the scaffolds. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 29 条
[1]
Delivery of basic fibroblast growth factor (bFGF) from photoresponsive hydrogel scaffolds [J].
Andreopoulos, FM ;
Persaud, I .
BIOMATERIALS, 2006, 27 (11) :2468-2476
[2]
COLLAGEN HETEROGENEITY IN HUMAN CARTILAGE - IDENTIFICATION OF SEVERAL NEW COLLAGEN CHAINS [J].
BURGESON, RE ;
HOLLISTER, DW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 87 (04) :1124-1131
[3]
Activation of valvular interstitial cells is mediated by transforming growth factor-β1 interactions with matrix molecules [J].
Cushing, MC ;
Liao, JT ;
Anseth, KS .
MATRIX BIOLOGY, 2005, 24 (06) :428-437
[4]
Stimulation of gene expression and loss of anular architecture caused by experimental disc degeneration -: An in vivo animal study [J].
Guehring, T ;
Omlor, GW ;
Lorenz, H ;
Bertram, H ;
Steck, E ;
Richter, W ;
Carstens, C ;
Kroeber, M .
SPINE, 2005, 30 (22) :2510-2515
[5]
Osteogenic potential of human adipose tissue-derived stromal cells as an alternative stem cell source [J].
Hattori, H ;
Sato, M ;
Masuoka, K ;
Ishihara, M ;
Kikuchi, T ;
Matsui, T ;
Takase, B ;
Ishizuka, T ;
Kikuchi, M ;
Fujikawa, K ;
Ishihara, M .
CELLS TISSUES ORGANS, 2004, 178 (01) :2-12
[6]
Bone formation using human adipose tissue-derived stromal cells and a biodegradable scaffold [J].
Hattori, H ;
Masuoka, K ;
Sato, M ;
Ishihara, M ;
Asazuma, T ;
Takase, B ;
Kikuchi, M ;
Nemoto, K ;
Ishihara, M .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2006, 76B (01) :230-239
[7]
Usefulness of photoacoustic measurements for evaluation of biomechanical properties of tissue-engineered cartilage [J].
Ishihara, M ;
Sato, M ;
Sato, S ;
Kikuchi, T ;
Mochida, J ;
Kikuchi, M .
TISSUE ENGINEERING, 2005, 11 (7-8) :1234-1243
[8]
Controlled release of fibroblast growth factors and heparin from photocrosslinked chitosan hydrogels and subsequent effect on in vivo vascularization [J].
Ishihara, M ;
Obara, K ;
Ishizuka, T ;
Fujita, M ;
Sato, M ;
Masuoka, K ;
Saito, Y ;
Yura, H ;
Matsui, T ;
Hattori, H ;
Kikuchi, M ;
Kurita, A .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 64A (03) :551-559
[9]
STRUCTURAL FEATURES IN HEPARIN WHICH MODULATE SPECIFIC BIOLOGICAL-ACTIVITIES MEDIATED BY BASIC FIBROBLAST GROWTH-FACTOR [J].
ISHIHARA, M ;
SHAKLEE, PN ;
YANG, ZC ;
LIANG, WS ;
WEI, Z ;
STACK, RJ ;
HOLME, K .
GLYCOBIOLOGY, 1994, 4 (04) :451-458
[10]
STRUCTURAL REQUIREMENTS IN HEPARIN FOR BINDING AND ACTIVATION OF FGF-1 AND FGF-4 ARE DIFFERENT FROM THAT FOR FGF-2 [J].
ISHIHARA, M .
GLYCOBIOLOGY, 1994, 4 (06) :817-824