Abstract

Bone morphogenetic proteins (BMPs) are multi-functional growth factors belonging to the Transforming Growth Factor-Beta (TGF-β) superfamily. These proteins are essential to many developmental processes, including cardiogenesis, neurogenesis, and osteogenesis. Specifically, within the BMP family, Bone Morphogenetic Protein-2 (BMP-2) was the first BMP to be characterized and has been well-studied. BMP-2 has important roles during embryonic development, as well as bone remodeling and homeostasis in adulthood. Some of its specific functions include digit formation and activating osteogenic genes, such as Runt-Related Transcription Factor 2 (RUNX2). Because of its diverse functions and osteogenic potential, the Food and Drug Administration (FDA) approved usage of recombinant human BMP-2 (rhBMP-2) during spinal fusion surgery, tibial shaft repair, and maxillary sinus reconstructive surgery. However, shortly after initial injections of rhBMP-2, several adverse complications were reported, and alternative therapeutics have been developed to limit these side-effects. As the clinical application of BMP-2 is largely implicated in bone, we focus primarily on its role in bone. However, we also describe briefly the role of BMP-2 in development. We then focus on the structure of BMP-2, its activation and regulation signaling pathways, BMP-2 clinical applications, and limitations of using BMP-2 as a therapeutic. Further, this review explores other potential treatments that may be useful in treating bone disorders.

Highlights

  • Bone Morphogenetic Proteins (BMPs) are multi-functional growth factors belonging to the Transforming Growth Factor-Beta (TGF-β) superfamily, which is shared by Growth Differentiation

  • mesenchymal stem cells (MSCs) are located in bone marrow and differentiate into pre-osteoblasts when exposed to RUNX2 and and Bone Morphogenetic Protein-2 (BMP-2)

  • BMP-2 is a powerful player in all organs

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Summary

Introduction

Bone Morphogenetic Proteins (BMPs) are multi-functional growth factors belonging to the Transforming Growth Factor-Beta (TGF-β) superfamily, which is shared by Growth Differentiation. When new bone needs to be formed, MSCs can differentiate into osteoblasts, and these osteoblasts can become embedded in the bone as osteocytes, which provide additional bone support and structure [41]. The main factor that differentiates MSCs into osteoblasts is BMP-2, which is released within the bone matrix or serum during osteoclast-driven bone resorption (Figure 2). MSCs are located in bone marrow and differentiate into pre-osteoblasts when exposed to RUNX2. MSCs are located in bone marrow and differentiate into pre-osteoblasts when exposed to RUNX2 and and BMP-2. MSCs located in bone marrow and differentiate into pre-osteoblasts when exposed to RUNX2 and rebuilding, and BMP-2 can assist in this process. The pre-osteoblasts differentiate into inactive osteoblasts in the presence of RUNX2, BMP-2, bone and function as osteocytes.

BMP-2 and Development
BMP-2 Receptors and Expression
BMP-2 Structure and Receptor Binding
BMP-2 Signaling Pathways
Intracellular and Extracellular Regulation of BMP-2
Endocytosis and Degradation of BMP-2 and BMPRs
Clinical Applications and Limitations of BMP-2
Findings
Conclusions
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