FT-IR imaging spectroscopy of genetically modified bovine chondrocytes

被引:7
作者
Camacho, NP [1 ]
West, P [1 ]
Griffith, MH [1 ]
Warren, RF [1 ]
Hidaka, C [1 ]
机构
[1] Hosp Special Surg, Lab Soft Tissue Res, Div Res, New York, NY 10021 USA
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2001年 / 17卷 / 1-2期
基金
美国国家卫生研究院;
关键词
FT-IR imaging spectroscopy; chondrocyte; regeneration;
D O I
10.1016/S0928-4931(01)00326-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Repair of articular cartilage defects remains a challenging problem in orthopaedic surgery. Although novel tissue engineering technologies have facilitated the synthesis of cartilage-like tissue for implantation into defect sites, questions persist as to how to best evaluate the integration of these matrices into cartilage and to assess their capability for regeneration and repair of the tissue. In the current study, Fourier transform infrared imaging spectroscopy (FT-IRI) was utilized to study compositional changes in genetically modified bovine chondrocytes. With this technique, it was possible to evaluate the integration of the newly formed matrix into the articular cartilage substrate, and the content and distribution of the collagen and proteoglycan components in the repair tissue compared to native articular cartilage. Bovine chondrocytes were treated with an adenovirus (Ad) vector encoding bone morphogenetic protein-7 (AdBMP-7), transplanted onto bovine cartilage explants in vitro and the matrix evaluated by FT-IRI after 3 weeks of growth. Data were acquired from a 400 X 400-mum region of a histological specimen at 7-mum spatial resolution. FT-IR images were created based on collagen and proteoglycan content. It was apparent from these images that the AdBMP-7-treated chondrocyte matrix produced significantly more proteoglycan compared to both naive chondrocyte matrix, and to native bovine articular cartilage. However, the distribution of proteoglycan was very heterogeneous. In contrast, there was significantly less type II collagen in both AdBMP-7 and in naive chondrocyte matrix compared to the articular cartilage substrate. Overall, the new information obtained by FT-IR imaging spectroscopy will facilitate in design of new materials for cartilage regeneration and repair. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 9
页数:7
相关论文
共 26 条
[1]   Structure and dynamics of membrane proteins as studied by infrared spectroscopy [J].
Arrondo, JLR ;
Goñi, FM .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1999, 72 (04) :367-405
[2]   Effect of cultured autologous chondrocytes on repair of chondral defects in a canine model [J].
Breinan, HA ;
Minas, T ;
Hsu, HP ;
Nehrer, S ;
Sledge, CB ;
Spector, M .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1997, 79A (10) :1439-1451
[3]  
Buckwalter JA, 1998, AAOS INSTR COURS LEC, V47, P487
[4]  
Camacho NP, 2001, BIOPOLYMERS, V62, P1, DOI 10.1002/1097-0282(2001)62:1<1::AID-BIP10>3.0.CO
[5]  
2-O
[6]   BOVINE ARTICULAR CHONDROCYTES DO NOT UNDERGO HYPERTROPHY WHEN CULTURED IN THE PRESENCE OF SERUM AND OSTEOGENIC PROTEIN-1 [J].
CHEN, P ;
VUKICEVIC, S ;
SAMPATH, TK ;
LUYTEN, FP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (03) :1253-1259
[7]   Human articular chondrocytes express osteogenic protein-1 [J].
Chubinskaya, S ;
Merrihew, C ;
Cs-Szabo, G ;
Mollenhauer, J ;
McCartney, J ;
Rueger, DC ;
Kuettner, KE .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (02) :239-250
[8]   Recombinant human osteogenic protein 1 is a potent stimulator of the synthesis of cartilage proteoglycans and collagens by human articular chondrocytes [J].
Flechtenmacher, J ;
Huch, K ;
Thonar, EJMA ;
Mollenhauer, JA ;
Davies, SR ;
Schmid, TM ;
Puhl, W ;
Sampath, TK ;
Aydelotte, MB ;
Kuettner, KE .
ARTHRITIS AND RHEUMATISM, 1996, 39 (11) :1896-1904
[9]  
Fraser ROB, 1973, CONFORMATION FIBROUS, P344
[10]   Attenuated total reflection infrared spectroscopy of proteins and lipids in biological membranes [J].
Goormaghtigh, E ;
Raussens, V ;
Ruysschaert, JM .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON BIOMEMBRANES, 1999, 1422 (02) :105-185