Overview of bone morphogenetic proteins

被引:293
作者
Wozney, JM [1 ]
机构
[1] Wyeth Res, Cambridge, MA 02140 USA
关键词
bone graft; bone morphogenetic protein; osteoinduction;
D O I
10.1097/00007632-200208151-00002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. A literature review was conducted. Objectives. To review the discovery of the bone morphogenetic proteins and describe the bone morphogenetic protein products that will or may be available for clinical use. Summary of Background Data. Bone morphogenetic proteins comprise the osteoinductive component of several tissue engineering products in late-stage development as replacements for autogenous bone graft, and for bone augmentation and repair. Methods. The literature on bone morphogenetic proteins was reviewed. Results. Bone morphogenetic proteins were discovered origionally on the basis of their presence in osteoinductive extracts of bone matrix. Molecular cloning of bone morphogenetic proteins demonstrated that they are a family of related differentiation factors, ecah capable of inducting the formation of new bone tissue when implanted. Two of the molecules in clinical use, recombinant human bone morphogenetic protein-2 and recombinant human bone morphogenetic protein-7 (OP-1) are produced in a biotechnoligy process using recombinant deoxyribonucleic acid technology that offers unlimited supply and substantial control over purity and reproducible activity. A third material, bovine bone morphogenetic protein extract, is extracted from bone, and contains a mixture of bone morphogenetic protein molecules. Each of these molecules, although osteoinductive in vivo has different physiologic roles and biologic activities in vivio and in trivo. Successful development of a product for use in spinal fusion involves selecting the oesteoinductive molecule, and the method of delivery, as well as conducting subsequent preclinical studies to evaluate its efficacy and safety. Conclusions. On the basis of the data provided in this issue of spine, some of these bone morphogenetic protein-based products provide for revolutionary therapies in orthopedic practice.
引用
收藏
页码:S2 / S8
页数:7
相关论文
共 52 条
[1]  
Bahamonde ME, 2001, J BONE JOINT SURG AM, V83A, pS56
[2]   Characterization of receptors for osteogenic protein-1/bone morphogenetic protein-7 (OP-1/BMP-7) in rat kidneys [J].
Bosukonda, D ;
Shih, MS ;
Sampath, KT ;
Vukicevic, S .
KIDNEY INTERNATIONAL, 2000, 58 (05) :1902-1911
[3]   A BONE-DERIVED GROWTH-FACTOR ISOLATED FROM RAT CALVARIAE IS BETA-2 MICROGLOBULIN [J].
CANALIS, E ;
MCCARTHY, T ;
CENTRELLA, M .
ENDOCRINOLOGY, 1987, 121 (03) :1198-1200
[4]   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
[5]  
*COMM PROPR MED PR, 2000, EUR PUBL ASS REP
[6]  
D'Alessandro J. S., 1991, J BONE MINER RES, V6, pS153
[7]   Bone morphogenetic protein-3 is a negative regulator of bone density [J].
Daluiski, A ;
Engstrand, T ;
Bahamonde, ME ;
Gamer, LW ;
Agius, E ;
Stevenson, SL ;
Cox, K ;
Rosen, V ;
Lyons, KM .
NATURE GENETICS, 2001, 27 (01) :84-88
[8]   RECOMBINANT VGR-1 BMP-6 EXPRESSING TUMORS INDUCE FIBROSIS AND ENDOCHONDRAL BONE-FORMATION IN-VIVO [J].
GITELMAN, SE ;
KOBRIN, MS ;
YE, JQ ;
LOPEZ, AR ;
LEE, A ;
DERYNCK, R .
JOURNAL OF CELL BIOLOGY, 1994, 126 (06) :1595-1609
[9]  
HARRIS SE, 1994, J BONE MINER RES, V9, P855
[10]   Bone morphogenetic proteins: Multifunctional regulators of vertebrate development [J].
Hogan, BLM .
GENES & DEVELOPMENT, 1996, 10 (13) :1580-1594