Overview of bone morphogenetic proteins

被引:295
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
[11]   Osteogenic protein-1 prevents renal fibrogenesis associated with ureteral obstruction [J].
Hruska, KA ;
Guo, GJ ;
Wozniak, M ;
Martin, D ;
Miller, S ;
Liapis, H ;
Loveday, K ;
Klahr, S ;
Sampath, TK ;
Morrissey, J .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 279 (01) :F130-F143
[12]   The formation of bone under the influence of epithelium of the urinary tract [J].
Huggins, CB .
ARCHIVES OF SURGERY, 1931, 22 (03) :377-408
[13]   Expression and Characterization of Bone Morphogenetic Protein-2 in Chinese Hamster Ovary Cells [J].
Israel, David I. ;
Nove, John ;
Kerns, Kelvin M. ;
Moutsatsos, Ioannis K. ;
Kaufman, Randal J. .
GROWTH FACTORS, 1992, 7 (02) :139-150
[14]   Heterodimeric bone morphogenetic proteins show enhanced activity in vitro and in vivo [J].
Israel, DI ;
Nove, J ;
Kerns, KM ;
Kaufman, RJ ;
Rosen, V ;
Cox, KA ;
Wozney, JM .
GROWTH FACTORS, 1996, 13 (3-4) :291-300
[15]   BMP7 null mutation in mice: Developmental defects in skeleton, kidney, and eye [J].
Jena, N ;
MartinSeisdedos, C ;
McCue, P ;
Croce, CM .
EXPERIMENTAL CELL RESEARCH, 1997, 230 (01) :28-37
[16]   THE MOUSE SHORT-EAR SKELETAL MORPHOGENESIS LOCUS IS ASSOCIATED WITH DEFECTS IN A BONE MORPHOGENETIC MEMBER OF THE TGF-BETA SUPERFAMILY [J].
KINGSLEY, DM ;
BLAND, AE ;
GRUBBER, JM ;
MARKER, PC ;
RUSSELL, LB ;
COPELAND, NG ;
JENKINS, NA .
CELL, 1992, 71 (03) :399-410
[17]   BMP-7 IS AN INDUCER OF NEPHROGENESIS, AND IS ALSO REQUIRED FOR EYE DEVELOPMENT AND SKELETAL PATTERNING [J].
LUO, G ;
HOFMANN, C ;
BRONCKERS, ALJJ ;
SOHOCKI, M ;
BRADLEY, A ;
KARSENTY, G .
GENES & DEVELOPMENT, 1995, 9 (22) :2808-2820
[18]   THE DVR GENE FAMILY IN EMBRYONIC-DEVELOPMENT [J].
LYONS, KM ;
JONES, CM ;
HOGAN, BLM .
TRENDS IN GENETICS, 1991, 7 (11-12) :408-412
[19]   PLATELET-DERIVED GROWTH-FACTOR INHIBITS BONE REGENERATION INDUCED BY OSTEOGENIN, A BONE MORPHOGENETIC PROTEIN, IN RAT CRANIOTOMY DEFECTS [J].
MARDEN, LJ ;
FAN, RSP ;
PIERCE, GF ;
REDDI, AH ;
HOLLINGER, JO .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2897-2905
[20]   PRIMARY STRUCTURE OF HUMAN SKELETAL GROWTH-FACTOR - HOMOLOGY WITH HUMAN INSULIN-LIKE GROWTH FACTOR-II [J].
MOHAN, S ;
JENNINGS, JC ;
LINKHART, TA ;
BAYLINK, DJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 966 (01) :44-55