Visual histological grading system for the evaluation of in vitro-generated neocartilage

被引:181
作者
Grogan, Shawn Patrick
Barbero, Andrea
Winkelmann, Verena
Rieser, Franz
Fitzsimmons, James S.
O'Driscoll, Shawn
Martin, Ivan
Mainil-Varlet, Pierre
机构
[1] Univ Bern, Inst Pathol, Osteoarticular Res Grp, CH-3010 Bern, Switzerland
[2] Univ Basel, Div Res, Dept Surg, Basel, Switzerland
[3] Zimmer Orthoped, Winterthur, Switzerland
[4] Mayo Clin, Coll Med, Cartilage & Connect Tissue Res, Rochester, MN USA
来源
TISSUE ENGINEERING | 2006年 / 12卷 / 08期
关键词
D O I
10.1089/ten.2006.12.2141
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Here we present the development of a visual evaluation system for routine assessment of in vitro-engineered cartilaginous tissue. Neocartilage was produced by culturing human articular chondrocytes in pellet culture systems or in a scaffold-free bioreactor system. All engineered tissues were embedded in paraffin and were sectioned and stained with Safranin O-fast green. The evaluation of each sample was broken into 3 categories (uniformity and intensity of Safranin O stain, distance between cells/amount of matrix produced, and cell morphology), and each category had 4 components with a score ranging from 0 to 3. Three observers evaluated each sample, and the new system was independently tested against an objective computer-based histomorphometry system. Pellets were also assessed biochemically for glycosaminoglycan (GAG) content. Pellet histology scores correlated significantly with GAG contents and were in agreement with the computer-based histomorphometry system. This system allows a valid and rapid assessment of in vitro-generated cartilaginous tissue that has a relevant association with objective parameters indicative of cartilage quality.
引用
收藏
页码:2141 / 2149
页数:9
相关论文
共 44 条
[1]   Molecular pathology and pathobiology of osteoarthritic cartilage [J].
Aigner, T ;
McKenna, L .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (01) :5-18
[2]   Age related changes in human articular chondrocyte yield, proliferation and post-expansion chondrogenic capacity [J].
Barbero, A ;
Grogan, S ;
Schäfer, D ;
Heberer, M ;
Mainil-Varlet, P ;
Martin, I .
OSTEOARTHRITIS AND CARTILAGE, 2004, 12 (06) :476-484
[3]   Science, medicine, and the future - Treating joint damage in young people [J].
Bentley, G ;
Minas, T .
BRITISH MEDICAL JOURNAL, 2000, 320 (7249) :1585-1588
[4]   Tissue engineering and cell therapy of cartilage and bone [J].
Cancedda, R ;
Dozin, B ;
Giannoni, P ;
Quarto, R .
MATRIX BIOLOGY, 2003, 22 (01) :81-91
[5]   IMPROVED QUANTITATION AND DISCRIMINATION OF SULFATED GLYCOSAMINOGLYCANS BY USE OF DIMETHYLMETHYLENE BLUE [J].
FARNDALE, RW ;
BUTTLE, DJ ;
BARRETT, AJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 883 (02) :173-177
[6]   Chondrocytes in culture produce a mechanically functional tissue [J].
Fedewa, MM ;
Oegema, TR ;
Schwartz, MH ;
MacLeod, A ;
Lewis, JL .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (02) :227-236
[7]   A static, closed and scaffold-free bioreactor system that permits chondrogenesis in vitro [J].
Grogan, SP ;
Rieser, F ;
Winkelmann, V ;
Berardi, S ;
Mainil-Varlet, P .
OSTEOARTHRITIS AND CARTILAGE, 2003, 11 (06) :403-411
[8]   Reoperation after autologous chondrocyte implantation - Indications and findings [J].
Henderson, I ;
Tuy, B ;
Oakes, B .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2004, 86B (02) :205-211
[9]   INCREASED DAMAGE TO TYPE-II COLLAGEN IN OSTEOARTHRITIC ARTICULAR-CARTILAGE DETECTED BY A NEW IMMUNOASSAY [J].
HOLLANDER, AP ;
HEATHFIELD, TF ;
WEBBER, C ;
IWATA, Y ;
BOURNE, R ;
RORABECK, C ;
POOLE, AR .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1722-1732
[10]  
HOWARD RD, 1994, AM J VET RES, V55, P1158