Raman spectroscopic evidence for octacalcium phosphate and other transient mineral species deposited during intramembranous mineralization.

UNLABELLED To understand early mineralization events, we studied living murine calvarial tissue by Raman spectroscopy using fibroblast growth factor 2 (FGF2)-soaked porous beads. We detected increased levels of a transient phase resembling octacalcium phosphate in sutures undergoing premature suture closure. INTRODUCTION Several calcium phosphates have been postulated as the earliest inorganic precursors to bone mineral. They are unstable and have not been previously detected in tissue specimens. Whether the same intermediates are formed in sutures undergoing premature closure is also unknown. METHODS Six coronal suture tissue specimens from fetal day 18.5 B6CBA F1/J wild-type mice were studied. Three sutures specimens were treated with FGF2-soaked heparin acrylic beads to induce accelerated mineralization and premature suture closure. Three control specimens were treated with empty heparin acrylic beads. All sutures were maintained as organ cultures to permit repeated spectral analyses at 12-24 h intervals over a 72-h period. RESULTS During the first 24 h, the spectra contained bands of octacalcium phosphate (OCP) or an OCP-like mineral. The main phosphorus-oxygen stretch was at 955 cm(-1), instead of the 957-959 cm(-1) seen in bone mineral, and there was an additional band at 1010-1014 cm(-1), as expected for OCP. A broad band was found at 945 cm(-1), characteristic of a highly disordered or amorphous calcium phosphate. An increased amount of mineral was observed in FGF2-treated sutures, but no qualitative differences in Raman spectra were observed between experimental and control specimens. CONCLUSIONS Inorganic mineral deposition proceeds through transient intermediates, including an OCP-like phase. Although this transient phase has been observed in purely inorganic model systems, this study is the first to report OCP or an OCP-like intermediate in living tissue. Raman microspectroscopy allows observation of this transient mineral and may allow observation of other precursors as well.

[1]  Milenko Markovic,et al.  Octacalcium phosphate. 3. Infrared and Raman vibrational spectra , 1993 .

[2]  G Penel,et al.  Composition of bone and apatitic biomaterials as revealed by intravital Raman microspectroscopy. , 2005, Bone.

[3]  Wee Chew,et al.  Band-target entropy minimization. A robust algorithm for pure component spectral recovery. Application to complex randomized mixtures of six components. , 2003, Analytical chemistry.

[4]  S A Goldstein,et al.  Spatial distribution of phosphate species in mature and newly generated Mammalian bone by hyperspectral Raman imaging. , 1999, Journal of biomedical optics.

[5]  H. Ryoo,et al.  Erk pathway and activator protein 1 play crucial roles in FGF2‐stimulated premature cranial suture closure , 2003, Developmental dynamics : an official publication of the American Association of Anatomists.

[6]  Michael D. Morris,et al.  Band-Target Entropy Minimization (BTEM) Applied to Hyperspectral Raman Image Data , 2003, Applied spectroscopy.

[7]  Michael D. Morris,et al.  Early mineralization of normal and pathologic calvaria as revealed by Raman spectroscopy , 2002, SPIE BiOS.

[8]  A. Wilkie,et al.  Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault. , 1999, Development.

[9]  Marc Garland,et al.  Fourier transform Raman spectral reconstruction of inorganic lead mixtures using a novel band‐target entropy minimization (BTEM) method , 2003 .

[10]  H. M. Kim,et al.  Phosphate Ions in Bone: Identification of a Calcium–Organic Phosphate Complex by 31P Solid-State NMR Spectroscopy at Early Stages of Mineralization , 2003, Calcified Tissue International.

[11]  Nicole J. Crane,et al.  Raman imaging demonstrates FGF2-induced craniosynostosis in mouse calvaria. , 2005, Journal of biomedical optics.

[12]  Wee Chew,et al.  Band-target entropy minimization (BTEM): An advanced method for recovering unknown pure component spectra. Application to the FTIR spectra of unstable organometallic mixtures , 2002 .

[13]  Eugenia Valsami-Jones,et al.  Lack of OH in nanocrystalline apatite as a function of degree of atomic order: implications for bone and biomaterials. , 2004, Biomaterials.

[14]  Nicole J. Crane,et al.  Compatibility of Staining Protocols for Bone Tissue with Raman Imaging , 2003, Calcified Tissue International.

[15]  W. E. Brown,et al.  Octacalcium Phosphate as a Precursor in Biomineral Formation , 1987, Advances in dental research.

[16]  M. Morris The contribution of electrostatic coupling to electrical migration in chronopotentiometry , 1964 .

[17]  S. Weiner,et al.  Transformation of Amorphous Calcium Phosphate to Crystalline Dahillite in the Radular Teeth of Chitons , 1985, Science.

[18]  Michael D. Morris,et al.  Study of localization of response to fibroblast growth factor-2 in murine calvaria using Raman spectroscopic imaging , 2004, SPIE BiOS.

[19]  Charles K. Mann,et al.  The Quest for Accuracy in Raman Spectra , 2001 .

[20]  L. Chaudhary,et al.  Differential growth factor control of bone formation through osteoprogenitor differentiation. , 2004, Bone.

[21]  C. Giachelli,et al.  Elevated extracellular calcium levels induce smooth muscle cell matrix mineralization in vitro. , 2004, Kidney international.

[22]  Marc Garland,et al.  Application of FT‐Raman and FTIR measurements using a novel spectral reconstruction algorithm , 2003 .

[23]  J L Ackerman,et al.  Structure, Composition, and Maturation of Newly Deposited Calcium‐Phosphate Crystals in Chicken Osteoblast Cell Cultures , 2000, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[24]  Michael D Morris,et al.  Mineralization of Developing Mouse Calvaria as Revealed by Raman Microspectroscopy , 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[25]  G. H. Nancollas,et al.  The role of brushite and octacalcium phosphate in apatite formation. , 1992, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[26]  D. A. Shea,et al.  Trends in early mineralization of murine calvarial osteoblastic cultures: a Raman microscopic study , 2002 .

[27]  S. Weiner,et al.  Choosing the Crystallization Path Less Traveled , 2005, Science.

[28]  A. Hassankhani,et al.  FT-IR microscopy of endochondral ossification at 20μ spatial resolution , 2007, Calcified Tissue International.

[29]  G. R. Sauer,et al.  Fourier transform infrared characterization of mineral phases formed during induction of mineralization by collagenase-released matrix vesicles in vitro. , 1988, The Journal of biological chemistry.

[30]  D H Kohn,et al.  Raman spectroscopic imaging markers for fatigue-related microdamage in bovine bone. , 2000, Analytical chemistry.

[31]  Brian G. Cox,et al.  Modern Liquid Phase Kinetics , 1994 .

[32]  A. Hassankhani,et al.  FT-IR microscopy of endochondral ossification at 20μ spatial resolution , 2007, Calcified Tissue International.

[33]  Wei Wang,et al.  Fibroblast Growth Factors Lead to Increased Msx2 Expression and Fusion in Calvarial Sutures , 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[34]  W. E. Brown,et al.  Octacalcium Phosphate and Hydroxyapatite: Crystal Structure of Octacalcium Phosphate , 1962, Nature.

[35]  C. Rey,et al.  MicroRaman Spectral Study of the PO4 and CO3 Vibrational Modes in Synthetic and Biological Apatites , 1998, Calcified Tissue International.

[36]  Michael D. Morris,et al.  Spectral imaging of mouse calvaria undergoing craniosynstosis , 2003, SPIE BiOS.

[37]  M. Morris,et al.  Application of vibrational spectroscopy to the study of mineralized tissues (review). , 2000, Journal of biomedical optics.

[38]  H. M. Kim,et al.  Structural and chemical characteristics and maturation of the calcium‐phosphate crystals formed during the calcification of the organic matrix synthesized by chicken osteoblasts in cell culture , 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[39]  L. Brečević,et al.  Precipitation of calcium phosphates from electrolyte solutions , 2005, Calcified Tissue Research.

[40]  J. Heath,et al.  Fgfr2 and osteopontin domains in the developing skull vault are mutually exclusive and can be altered by locally applied FGF2. , 1997, Development.

[41]  J. Durig,et al.  Fourier transform raman spectroscopy of synthetic and biological calcium phosphates , 1994, Calcified Tissue International.

[42]  H. M. Kim,et al.  Characterization of the apatite crystals of bone and their maturation in osteoblast cell culture: comparison with native bone crystals. , 1996, Connective tissue research.

[43]  A. Sasaki [On octacalcium phosphate]. , 1965, Kokubyo Gakkai zasshi. The Journal of the Stomatological Society, Japan.

[44]  J. Heath,et al.  Fgfr 2 and osteopontin domains in the developing skull vault are mutually exclusive and can be altered by locally applied FGF 2 , 1997 .

[45]  J. Moradian-Oldak,et al.  Control of octacalcium phosphate and apatite crystal growth by amelogenin matrices , 2004 .