Journal of Regenerative Medicine & Tissue Engineering

Journal of Regenerative Medicine & Tissue Engineering

ISSN 2050-1218
Original Research

In vitro BMP2 stimulation of osteoblast citrate production in concert with mineralized bone nodule formation

Leslie C. Costello1*, Meenakshi A. Chellaiah1, Jing Zou1, Mark A. Reynolds2 and Renty B. Franklin1

*Correspondence: Leslie C. Costello lcostello@umaryland.edu

1. Department of Oncology and Diagnostic Sciences, Dental School, University of Maryland, Baltimore, USA.

Author Affiliations

2. Department of Periodontics, Dental School, University of Maryland, Baltimore, USA.

Abstract

Background: That citrate is a major indispensible component of bone in humans and in all osteovertebrates has been known for about seventy-five years. Yet, its role and importance in the structure and function of bone and bone formation have remained unknown. However, recent studies have identified that citrate is a major and essential component of the apatite/collagen structure of bone; and that the biomechanical properties of bone (e.g., stability, strength, resistance to fracture) depend on the appropriate incorporation of citrate in the structure of bone. The osteoblasts have recently been identified as citrate-producing cells that provide the citrate that is incorporated in the apatite/collagen structure during osteogenesis. Little is known regarding the factors and mechanisms involved in the regulation of citrate that is incorporated along with mineralization during the process of bone formation. Because of the importance of BMP2 in the initiation of osteogenesis and the development of the osteoblasts, it is essential to determine its possible implication in the development of the citrate-producing capability of the osteoblasts (i.e., "citration") during the formation of mineralized bone nodules.

Methods: The goal of this study was to determine if BMP2 promotes the development of citrateproducing osteoblasts for increased citrate incorporation in the formation of mineralized bone nodules. The study employed MC3T3 mesenchyme stem cell osteogenic differentiation in the presence and absence of BMP2.

Results: The results showed that BMP2 treatment increased the osteogenic development of mineralized bone nodules. In addition, BMP2 increased osteoblast citrate production and incorporation in the mineralized bone nodule. This was accompanied by increased ZIP1 transporter, which is an essential genetic/metabolic event for citrate-producing cells.

Conclusions: The results demonstrate, for the first time, that BMP2 facilitates the osteoblast "citration" process in concert with mineralization during bone formation; and provide confirmation of the important role of osteoblasts as specialized citrate-producing cells in the process of bone formation. However, it is essential to determine if these in vitro effects will occur in vivo in BMP2-implant induction of bone formation. "Citration" is essential for osteoinductive bone to represent the chemical, structural, and biomechanical properties of "normal" bone.

Keywords: BMP2, citrate production, ZIP1 transporter, mineralized bone formation, osteoblasts, apatite/collagen complex, osteogenesis, citration and mineralization, mesenchyme stem cells

ISSN 2050-1218
Volume 4
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