Enhanced matrix synthesis and in vitro formation of cartilage-like tissue by genetically modified chondrocytes expressing BMP-7

被引:63
作者
Hidaka, C [1 ]
Quitoriano, M
Warren, RF
Crystal, RG
机构
[1] Cornell Univ, Weill Med Coll, Div Pulm & Crit Care Med, New York, NY 10021 USA
[2] Hosp Special Surg, Lab Soft Tissue Res, New York, NY 10021 USA
[3] Cornell Univ, Weill Med Coll, Belfer Gene Therapy Core Facil, New York, NY USA
[4] Cornell Univ, Weill Med Coll, Inst Med Genet, New York, NY USA
关键词
D O I
10.1016/S0736-0266(01)00019-5
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Bone morphogenic protem-7 (BMP-7) supports ectopic cartilage and bone formation, is expressed in normal articular cartilage, and increases matrix synthesis in chondrocytes. Based on this knowledge, we hypothesized that an adenovirus (Ad) vector encoding human BMP-7 could be used to modify chondrocytes genetically to improve their capacity for cartilage repair. An adenovirus vector encoding BMP-7 (AdBMP-7) was constructed and its bioactivity confirmed by ectopic bone formation assay. AdBMP-7 modification of bovine chondrocytes induced expression of BMP-7 mRNA and bioactive protein. resulting in an increase in incorporation of (SO4-)-S-35 into proteoglycan. H-3-proline uptake into protein, and the expression of the cartilage-specific matrix genes, aggrecan and type II collagen. An in vitro model of chondrocyte transplantation was used to demonstrate the feasibility of using genetically modified chondrocytes to enhance formation of cartilage-like tissue. When transplanted onto cartilage explants and maintained in vitro for 3 weeks, chondrocytes modified with AdBMP-7 formed 1.9-fold thicker tissue than chondrocytes modified with a control vector (P<0.001). This tissue was positive for type II collagen and proteoglycan but negative for type X collagen and demonstrated a cartilage-like morphology. These observations suggest that Ad-mediated transfer of BMP-7 gene to chondrocytes enhances the chondrocyte-specific matrix synthesis and their capacity to form cartilage-like tissue, thus representing a strategy that may improve cell-based cartilage repair, (C) 2001 Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 44 条
[1]   Human osteogenic protein-1 induces chondroblastic, osteoblastic, and/or adipocytic differentiation of clonal murine target cells [J].
Asahina, I ;
Sampath, TK ;
Hauschka, PV .
EXPERIMENTAL CELL RESEARCH, 1996, 222 (01) :38-47
[2]   Expression of a stable articular cartilage phenotype without evidence of hypertrophy by adult human articular chondrocytes in vitro [J].
Binette, F ;
McQuaid, DP ;
Haudenschild, DR ;
Yaeger, PC ;
McPherson, JM ;
Tubo, R .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (02) :207-216
[3]  
Boskey AL, 1997, J CELL BIOCHEM, V64, P632, DOI 10.1002/(SICI)1097-4644(19970315)64:4<632::AID-JCB11>3.0.CO
[4]  
2-E
[5]   TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION [J].
BRITTBERG, M ;
LINDAHL, A ;
NILSSON, A ;
OHLSSON, C ;
ISAKSSON, O ;
PETERSON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :889-895
[6]   Adenovirus infection stimulates the Raf/MAPK signaling pathway and induces interleukin-8 expression [J].
Bruder, JT ;
Kovesdi, I .
JOURNAL OF VIROLOGY, 1997, 71 (01) :398-404
[7]   Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton [J].
Brunet, LJ ;
McMahon, JA ;
McMahon, AP ;
Harland, RM .
SCIENCE, 1998, 280 (5368) :1455-1457
[8]  
Buckwalter JA, 1998, AAOS INSTR COURS LEC, V47, P487
[9]   IDENTIFICATION OF TRANSFORMING GROWTH-FACTOR-BETA FAMILY MEMBERS PRESENT IN BONE-INDUCTIVE PROTEIN PURIFIED FROM BOVINE BONE [J].
CELESTE, AJ ;
IANNAZZI, JA ;
TAYLOR, RC ;
HEWICK, RM ;
ROSEN, V ;
WANG, EA ;
WOZNEY, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) :9843-9847
[10]  
CHANG SC, 1994, J BIOL CHEM, V269, P28227