Si and Ca individually and combinatorially target enhanced MC3T3-E1 subclone 4 early osteogenic marker expression.

This study tests the hypothesis that silicon and calcium ions combinatorially target gene expression during osteoblast differentiation. MC3T3-E1 subclone 4 osteoblast progenitors (transformed mouse calvarial osteoblasts) were exposed to Si(4+) (from Na(2)SiO(3)) and Ca(2+) (from CaCl(2):H(2)O) ion treatments both individually (0.4 mM each + control treatment) and combinatorially (0.4 mM Si(4+) + 0.4 mM Ca(2+) + control treatment) and compared to control treated (α-minimum essential medium, 10% fetal bovine serum, and 1% penicillin-streptomycin) cells. Cell proliferation studies showed no significant increase in cell density between treatments over 5 days of culture. Cellular differentiation studies involved addition of ascorbic acid (50 mg/L) for all treatments. Relative gene expression was determined for collagen type 1 (Col(I)α1/Col(I)α2), core-binding factor a (cbfa1/Runx2), and osteocalcin (OCN), which indicated osteoblast progenitor differentiation into a mineralizing phenotype. Increased Si(4+) or Ca(2+) ion treatments enhanced Col(I)α1, Col(I)α2, Runx2, and OCN expression, while increased Si(4+) + Ca(2+) ion treatments enhanced OCN expression. Moreover, it was found that a Si(4+)/Ca(2+) ratio of unity was optimal for maximal expression of OCN. Collagen fiber bundles were dense, elongated, and thick within extracellular matrices (ECM) exposed to Si(4+) and Si(4+) + Ca(2+) treatments, while collagen fiber bundles were sparse, short, and thin within Ca(2+) and control treated ECM. These results indicated that individual ions enhance multiple osteogenic gene expression, while combined ion treatments enhance individual gene expression. In addition, these results indicated that Si(4+) enhanced osteoblast gene expression and ECM formation at higher levels than Ca(2+). These results support the larger concept that ions (possibly released from bioactive glasses) could control bone formation by targeting osteoblast marker expression.

[1]  G. Marshall,et al.  The ionic products of bioactive glass particle dissolution enhance periodontal ligament fibroblast osteocalcin expression and enhance early mineralized tissue development. , 2011, Journal of biomedical materials research. Part A.

[2]  Aldo R Boccaccini,et al.  A review of the biological response to ionic dissolution products from bioactive glasses and glass-ceramics. , 2011, Biomaterials.

[3]  M. Lee,et al.  Transcriptional upregulation of DDR2 by ATF4 facilitates osteoblastic differentiation through p38 MAPK‐mediated Runx2 activation , 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[4]  G. Marshall,et al.  Enhanced osteocalcin expression by osteoblast-like cells (MC3T3-E1) exposed to bioactive coating glass (SiO2-CaO-P2O5-MgO-K2O-Na2O system) ions. , 2009, Acta biomaterialia.

[5]  Larry L. Hench,et al.  Genetic design of bioactive glass , 2009 .

[6]  R. St-Arnaud,et al.  FIAT inhibition increases osteoblast activity by modulating Atf4‐dependent functions , 2009, Journal of cellular biochemistry.

[7]  Shibing Yu,et al.  Parathyroid hormone increases activating transcription factor 4 expression and activity in osteoblasts: requirement for osteocalcin gene expression. , 2008, Endocrinology.

[8]  Eduardo Saiz,et al.  Bioactive glass coatings affect the behavior of osteoblast-like cells. , 2007, Acta biomaterialia.

[9]  F. Sturtz,et al.  Gene expression of HIF-1alpha and XRCC4 measured in human samples by real-time RT-PCR using the sigmoidal curve-fitting method. , 2007, BioTechniques.

[10]  G. Karsenty,et al.  Cooperative Interactions between Activating Transcription Factor 4 and Runx2/Cbfa1 Stimulate Osteoblast-specific Osteocalcin Gene Expression* , 2005, Journal of Biological Chemistry.

[11]  Junzo Tanaka,et al.  The effect of calcium ion concentration on osteoblast viability, proliferation and differentiation in monolayer and 3D culture. , 2005, Biomaterials.

[12]  P. Roughley,et al.  FIAT represses ATF4-mediated transcription to regulate bone mass in transgenic mice , 2005, The Journal of cell biology.

[13]  J. Polak,et al.  Enhanced derivation of osteogenic cells from murine embryonic stem cells after treatment with ionic dissolution products of 58S bioactive sol-gel glass. , 2005, Tissue engineering.

[14]  K. Chihara,et al.  Involvement of calcium-sensing receptor in osteoblastic differentiation of mouse MC3T3-E1 cells. , 2005, American journal of physiology. Endocrinology and metabolism.

[15]  R. P. Thompson,et al.  Orthosilicic acid stimulates collagen type 1 synthesis and osteoblastic differentiation in human osteoblast-like cells in vitro. , 2003, Bone.

[16]  D. Eide,et al.  Combinatorial Control of Yeast FET4 Gene Expression by Iron, Zinc, and Oxygen* , 2002, The Journal of Biological Chemistry.

[17]  Larry L Hench,et al.  Third-Generation Biomedical Materials , 2002, Science.

[18]  G. Xiao,et al.  Bone Morphogenetic Proteins, Extracellular Matrix, and Mitogen‐Activated Protein Kinase Signaling Pathways Are Required for Osteoblast‐Specific Gene Expression and Differentiation in MC3T3‐E1 Cells , 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[19]  S. Ivanovski,et al.  Expression of Bone Matrix Protein mRNAs by Primary and Cloned Cultures of the Regenerative Phenotype of Human Periodontal Fibroblasts , 2001, Journal of dental research.

[20]  L L Hench,et al.  Gene-expression profiling of human osteoblasts following treatment with the ionic products of Bioglass 45S5 dissolution. , 2001, Journal of biomedical materials research.

[21]  E. Moran,et al.  Phosphate is a specific signal for induction of osteopontin gene expression. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Hartle,et al.  A Distinct Cation‐Sensing Mechanism in MC3T3‐E1 Osteoblasts Functionally Related to the Calcium Receptor , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[23]  Takashi Nakamura,et al.  Bioactivity of Na2O‐CaO‐SiO2 Glasses , 1995 .

[24]  S. Dixon,et al.  Requirement for Na(+)-dependent ascorbic acid transport in osteoblast function. , 1995, The American journal of physiology.

[25]  T. Saito,et al.  Effect of glycemic control on calcium and phosphorus handling and parathyroid hormone level in patients with non-insulin-dependent diabetes mellitus. , 1995, Endocrine journal.

[26]  R. Franceschi,et al.  Effects of ascorbic acid on collagen matrix formation and osteoblast differentiation in murine MC3T3‐E1 cells , 1994, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[27]  P. Frayssinet,et al.  A study of structure and degradation of nonpolymeric biomaterials implanted in bone using reflected and transmitted light microscopy. , 1993, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

[28]  L. Quarles,et al.  Distinct proliferative and differentiated stages of murine MC3T3‐E1 cells in culture: An in vitro model of osteoblast development , 1992, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[29]  R. Franceschi,et al.  Relationship between collagen synthesis and expression of the osteoblast phenotype in MC3T3‐E1 cells , 1992, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.