Change in the viscoelastic properties of agarose gel by HAp precipitation by osteoblasts cultured in an agarose gel matrix
Tóm tắt
The viscoelastic properties of cell-seeded agarose gel were measured as a function of culture time. Because the seeded cells, MC3T3-E1, were osteoblast-like cells, the system can be regarded as a model osteogenesis system. For all specimens the characteristic stress relaxation curve of agarose gel was observed—a large relaxation up to 104 s followed by a gel plateau, where the former was attributed to molecular motion of polymer chains between two adjacent cross-links of the gel and the latter to the elasticity of the gel network. The viscoelasticity was quantified by fitting stress relaxation data to an empirical equation. The relaxation time and its distribution did not change with culture time. The initial and equilibrium moduli, E
0 and E
e, respectively, and relaxation strength, ΔE = E
0 − E
e, did not change up to day 15 of culture but changed significantly at day 18 of culture. The change in ΔE with culture period correlated well with that in E
0. The changes in the mechanical properties of the cell-seeded agarose gel system were explained in terms of the function of MC3T3-E1 in precipitating calcium phosphate mineral particles. The precipitation was detected by alizarin red S staining of the system at day 9 of culture. The precipitated calcium phosphate was confirmed to be hydroxyapatite (HAp) and the amount of HAp increased monotonically with culturing time, both of which were observed by X-ray diffraction studies. The dependence of the modulus of the composite on mineral fraction is discussed. A simple model of mixing of the components based on the continuum material concept was not applicable, but a model considering percolation of mineral particles in a network chain with culture time was suitable to explain the observed results. The results may be particularly important for predicting the stiffness of functionally engineered bony tissue implanted in a fractured bone.
Tài liệu tham khảo
Doll BA. Basic bone biology and tissue engineering. Bone tissue engineering. Florida: CRC Press; 2005. p. 3–43.
Gilmore RS, Katz JL. Elastic properties of apatites. J Mater Sci Mater. 1982;17(4):1131–41.
Zaheer A, Lenkinski RE, Mahmood A, Jones AG, Cantley LC, Frangioni JV. In vivo near-infrared fluorescence imaging of osteoblastic activity. Nat Biotech. 2001;19(12):1148–54.
Venugopal J, Low S, Choon AT, Sampath Kumar TS, Ramakrishna S. Mineralization of osteoblasts with electrospun collagen/hydroxyapatite nanofibers. J Mater Sci Mater Med. 2008;19:2039–46.
Benoit DSW, Durney AR, Anseth KS. Manipulations in hydrogel degradation behavior enhance osteoblast function and mineralized tissue formation. Tissue Eng. 2006;12(6):1663–73.
Arnott S, Fulmer A, Scott WE, Dea IC, Moorhouse R, Rees DA. The agarose double helix and its function in agarose gel structure. J Mol Biol. 1974;90(2):269–72.
Watase M, Nishinari K. Rheological properties of agarose gels with different molecular weights. Rheol Acta. 1983;22(6):580–7.
Anseth KS, Bowman CN, Brannon-Peppas L. Mechanical properties of hydrogels and their experimental determination. Biomaterials. 1996;17(17):1647–57.
Sasaki N, Imai T, Hashimoto A, Yasuda H. Effect of pericellular matrix formation by chondrocytes cultured in agarose gel on the viscoelastic properties of agarose gel matrix. J Biorheol. 2009;23:95–101.
Hayes WC, Keer LM, Herrmann G, Mockros LF. A mathematical analysis for indentation tests of articular cartilage. J Biomech. 1972;5(5):541–51.
Okazaki M, Taira M, Takahashi J. Rietveld analysis and Fourier maps of hydroxyapatite. Biomaterials. 1997;18(11):795–9.
Foord SA, Atkins EDT. New X-ray diffraction results from agarose: extended single helix structures and implications for gelation mechanism. Biopolymers. 1989;28(8):1345–65.
Kim HM, Himeno T, Kokubo T, Nakamura T. Process and kinetics of bonelike apatite formation on sintered hydroxyapatite in a simulated body fluid. Biomaterials. 2005;26(21):4366–73.
Eanes ED. Amorphous calcium phosphate. Monogr Oral Sci. 2001;18:4366–73.
Zhan JH, Tseng YH, Chan JCC, Mou CY. Biomimetic formation of hydroxyapatite nanorods by a single-crystal-to-single-crystal transformation. Adv Funct Mater. 2005;15(12):2005–10.
Suzuki O, Kamakura S, Katagiri T. Surface chemistry and biological responses to synthetic octacalcium phosphate. J Biomed Mater Res Part B Appl Biomater. 2006;77B(1):201–12.
Termine JD, Posner AS. Amorphous/crystalline interrelationships in bone mineral. Calcif Tissue Res. 1967;1(1):8–23.
Francis MD. Solubility behavior of dental enamel and other calcium phosphates. Ann N Y Acad Sci. 1965;131(2):694–712.
Levine RS. Remineralization of human carious dentine in vitro. Arch Oral Biol. 1972;17(6):1005–8.
Kakudo M, Kasai N. X-ray diffraction by polymers. Tokyo: Kodansha; 1972.
Nielsen LE. Mechanical properties and composites. New York: Marcel Dekker; 1975.
Buschmann MD, Gluzband YA, Grodzinsky AJ, Hunziker EB. Mechanical compression modulates matrix biosynthesis in chondrocyte/agarose culture. J Cell Sci. 1995;108:1497–508.
Kim HM, Kim Y, Park SJ, Rey C, Glimcher MJ. Thin film of low-crystalline calcium phosphate apatite formed at low temperature. Biomaterials. 2000;21(11):1129–34.
