This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Letters to the Editor: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Letters to the Editor are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowReprints and Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Reddi, A. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Reddi, A. H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Technorati  
What's this?
The Journal of Bone and Joint Surgery (American) 83:S1-S6 (2001)
© 2001 The Journal of Bone and Joint Surgery, Inc.


Scientific Article

Bone Morphogenetic Proteins: From Basic Science to Clinical Applications

A. H. Reddi, PhD

A.H. Reddi, PhD Research Building 1, Room 2000, Center for Tissue Regeneration and Repair, Department of Orthopaedic Surgery, University of California-Davis School of Medicine, 4635 Second Avenue, Sacramento, CA 95817. E-mail address: ahreddi@ucdavis.edu
In support of the research or preparation of this manuscript, the author received grants or outside funding from Lawrence Ellison Endowed Chair. The author did not receive payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, educational institution, or other charitable or nonprofit organization with which the author is affiliated or associated.
The role of bone morphogenetic proteins (BMPs) in bone formation during development and in fracture-healing is now well established. In experimental animals, BMPs elicit bone formation in ectopic sites and healing of critical-sized segmental bone defects. Many of the studies on the capacity of BMPs to elicit the healing of segmental bone defects have been carried out in orthopaedic research laboratories and are familiar to orthopaedic surgeons.

The first 150 words of the full text of this article appear below.


    Introduction
 

However, until recently little was known about the cellular and molecular mechanisms by which BMPs elicit bone formation. In a series of stunning studies over the last several years, molecular cell biologists working intensively in several laboratories have elucidated some of these mechanisms. When BMPs bind to their cell surface receptors on mesenchymal cell, a BMP signaling cascade is activated. Signals are sent via specific proteins to the cell nucleus. This results in the expression of genes that lead to the synthesis of macromolecules involved in cartilage and bone formation, and the mesenchymal cell becomes a chondrocyte or an osteoblast.

The development of knowledge in this area of BMP signal transduction during the last several years has been phenomenal and has provided a substantial amount of new information that is clear-cut, specific, and useful. Some of this new information may be of clinical relevance because it suggests potential therapeutic approaches . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Dent. Res.Home page
Z.S. AI-Aql, A.S. Alagl, D.T. Graves, L.C. Gerstenfeld, and T.A. Einhorn
Molecular Mechanisms Controlling Bone Formation during Fracture Healing and Distraction Osteogenesis
J. Dent. Res., February 1, 2008; 87(2): 107 - 118.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
K. R. Blish, W. Wang, M. C. Willingham, W. Du, C. E. Birse, S. R. Krishnan, J. C. Brown, G. A. Hawkins, A. J. Garvin, R. B. D'Agostino Jr., et al.
A Human Bone Morphogenetic Protein Antagonist Is Down-Regulated in Renal Cancer
Mol. Biol. Cell, February 1, 2008; 19(2): 457 - 464.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
Z. Wang, C. C. Clark, and C. T. Brighton
Up-Regulation of Bone Morphogenetic Proteins in Cultured Murine Bone Cells with Use of Specific Electric Fields
J. Bone Joint Surg. Am., May 1, 2006; 88(5): 1053 - 1065.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
O. B. Betz, V. M. Betz, A. Nazarian, C. G. Pilapil, M. S. Vrahas, M. L. Bouxsein, L. C. Gerstenfeld, T. A. Einhorn, and C. H. Evans
Direct Percutaneous Gene Delivery to Enhance Healing of Segmental Bone Defects
J. Bone Joint Surg. Am., February 1, 2006; 88(2): 355 - 365.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. T. Fritz, D. Liu, J. Xu, S. Jiang, and M. B. Rogers
Conservation of Bmp2 Post-transcriptional Regulatory Mechanisms
J. Biol. Chem., November 19, 2004; 279(47): 48950 - 48958.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
K. Lehmann, P. Seemann, S. Stricker, M. Sammar, B. Meyer, K. Suring, F. Majewski, S. Tinschert, K.-H. Grzeschik, D. Muller, et al.
From the Cover: Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
PNAS, October 14, 2003; 100(21): 12277 - 12282.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
M.-J. Lee, C. W. Yang, D. C. Jin, Y. S. Chang, B. K. Bang, and Y.-S. Kim
Bone Morphogenetic Protein-7 Inhibits Constitutive and Interleukin-1{beta}-Induced Monocyte Chemoattractant Protein-1 Expression in Human Mesangial Cells: Role for JNK/AP-1 Pathway
J. Immunol., March 1, 2003; 170(5): 2557 - 2563.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
Y. C. Tian and A. O. Phillips
Interaction between the Transforming Growth Factor-{beta} Type II Receptor/Smad Pathway and {beta}-Catenin during Transforming Growth Factor-{beta}1-Mediated Adherens Junction Disassembly
Am. J. Pathol., May 1, 2002; 160(5): 1619 - 1628.
[Abstract] [Full Text] [PDF]