Spreading and proliferation of cultured rat bone marrow stromal cells on the surface of bioactive glass ceramics

Authors

  • V. V. Kiroshka Institute for Problems of Cryobiology and Cryomedicine, NAS of Ukraine 23, Pereyaslavskaya Str., Kharkiv, Ukraine, 61015 Author
  • O. V. Savvova National Technical University “Kharkiv Polytechnic Institute” 2, Kyrpychova str., Kharkiv, Ukraine, 61002 Author
  • Yu. O. Bozhkova Institute for Problems of Cryobiology and Cryomedicine, NAS of Ukraine 23, Pereyaslavskaya Str., Kharkiv, Ukraine, 61015 Author
  • I. V. Tamarina Institute for Problems of Cryobiology and Cryomedicine, NAS of Ukraine 23, Pereyaslavskaya Str., Kharkiv, Ukraine, 61015 Author
  • A. I. Fesenko National Technical University “Kharkiv Polytechnic Institute” 2, Kyrpychova str., Kharkiv, Ukraine, 61002 Author

DOI:

https://doi.org/10.7124/bc.00093F

Keywords:

glass-crystalline materials, bone marrow stromal cells

Abstract

Aim. To study spreading profile, cytoskeleton organization and proliferation of bone marrow stromal cells upon cultivation on the glass-crystalline material (GCM) surfaces with different chemical composition and solubility. Methods. GCMs with different CaO: P2O5 ratios were used. Actin cytoskeleton in cells was visualized using fluorescent TRITC-conjugated phalloidin. Cell proliferation was studied using MTT test. Results. Cell cultivation on highly soluble B-series GCM (Ca/P=5) led to appearance of fibroblast-like cells; their actin cytoskeleton filaments were uniformly distributed within the cytoplasm. In this case, proliferation dynamics was similar to that under cultivation on plastic. Cultivation on A and C series of GCM with a reduced Ca/P (1.4–2.58) resulted in a decrease of cell spreading and their proliferation index (up to 2–3 times) relative to the control. Conclusions. The material solubility and Ca/P superficial ratio are the main factors, determining cell interaction with GCMs.

References

Lanza RP, Langer R, Vacanti JP. Principles of tissue engineering. 4th ediition. Academic Press: Elsevier 2013, 1936 p.

Rezwan K, Chen QZ, Blaker JJ, Boccaccini AR. Biodegradable and bioactive porous polymer/inorganic composite scaffolds for bone tissue engineering. Biomaterials. 2006;27(18):3413-31.

Gerhardt L-C, Boccaccini AR. Bioactive glass and glass-ceramic scaffolds for bone tissue engineering. Materials. 2010; 3(7): 3867-910.

Hoppe A, Güldal NS, Boccaccini AR. A review of the biological response to ionic dissolution products from bioactive glasses and glass-ceramics. Biomaterials. 2011;32(11):2757-74.

Sarkisov PD. Controlled glass crystallization as the basis for synthesis of multifunctional glass-crystalline materials. Moscow: D. Mendeleev University of Chemical Technology of Russia. 1997. 218 p.

Jones JR, Tsigkou O, Coates EE, Stevens MM, Polak JM, Hench LL. Extracellular matrix formation and mineralization on a phosphate-free porous bioactive glass scaffold using primary human osteoblast (HOB) cells. Biomaterials. 2007;28(9):1653-63.

Gough JE, Notingher I, Hench LL. Osteoblast attachment and mineralized nodule formation on rough and smooth 45S5 bioactive glass monoliths. J Biomed Mater Res A. 2004;68(4):640-50.

Karageorgiou V, Kaplan D. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials. 2005;26(27):5474-91.

Hutmacher DW. Scaffolds in tissue engineering bone and cartilage. Biomaterials. 2000;21(24):2529-43.

Bianco P, Riminucci M, Gronthos S, Robey PG. Bone marrow stromal stem cells: nature, biology, and potential applications. Stem Cells. 2001;19(3):180-92. Review.

Ciapetti G, Ambrosio L, Marletta G, Baldini N, Giunti A. Human bone marrow stromal cells: In vitro expansion and differentiation for bone engineering. Biomaterials. 2006;27(36):6150-60.

Kim DH, Lee H, Lee YK, Nam JM, Levchenko A. Biomimetic nanopatterns as enabling tools for analysis and control of live cells. Adv Mater. 2010;22(41):4551-66.

International Organization for Standardization. Biological evaluation of medical devices: identification and quantification of degradation products from ceramics, ISO 10993-14:2001

Kim K, Dean D, Mikos AG, Fisher JP. Effect of initial cell seeding density on early osteogenic signal expression of rat bone marrow stromal cells cultured on cross-linked poly(propylene fumarate) disks. Biomacromolecules. 2009;10(7):1810-7.

Anokhina EB, Buravkova LB. [Heterogeneity of stromal precursor cells isolated from rat bone marrow]. Tsitologiia. 2007;49(1):40-7.

Huang Y, Siewe M, Madihally SV. Effect of spatial architecture on cellular colonization. Biotechnol Bioeng. 2006;93(1):64-75.

Lai JY, Lin PK, Hsiue GH, Cheng HY, Huang SJ, Li YT. Low Bloom strength gelatin as a carrier for potential use in retinal sheet encapsulation and transplantation. Biomacromolecules. 2009;10(2):310-9.

Huang Y, Siewe M, Madihally SV. Effect of spatial architecture on cellular colonization. Biotechnol Bioeng. 2006;93(1):64-75.

Davis JM. Ed. Basic Cell Culture. Oxford University Press, 2002. 408 p.

Gehrke P, Neugebauer J. Implant surface design: using biotechnology to enhance osseointegration. Interview. Dent Implantol Update. 2003;14(8):57-64.

Teixeira AI, Abrams GA, Bertics PJ, Murphy CJ, Nealey PF. Epithelial contact guidance on well-defined micro- and nanostructured substrates. J Cell Sci. 2003;116(Pt 10):1881-92.

Evans DJ, Britland S, Wigmore PM. Differential response of fetal and neonatal myoblasts to topographical guidance cues in vitro. Dev Genes Evol. 1999;209(7):438-42.

Karuri NW, Liliensiek S, Teixeira AI, Abrams G, Campbell S, Nealey PF, Murphy CJ. Biological length scale topography enhances cell-substratum adhesion of human corneal epithelial cells. J Cell Sci. 2004;117(Pt 15):3153-64.

Ducheyne P, Qiu Q. Bioactive ceramics: the effect of surface reactivity on bone formation and bone cell function. Biomaterials. 1999;20(23-24):2287-303.

Barinov SM, Shvorneva LI, Ferro D, Fadeeva IV, Tumanov SV. Solid solution formation at the sintering of hydroxyapatite–fluorapatite ceramics. Sci Tech Adv Mater. 2004; 5(5-6): 537-41.

Danilchenko SN. Structure and properties of calcium apatite’s regarding biomineralogy and biomaterial science (Review). Visnyk SSU, Ser Fiz-Mat Nauk. 2007; 2:33-59.

Sudarsanan K, Mackie PE, Young RA. Comparison of synthetic and mineral fluorapatite, Ca5(PO4)3F, in crystallographic detail. Math Res Bull. 1972; 7(11):1331-7.

Okazaki M, Tohda H, Yanagisawa T, Taira M, Takahashi J. Differences in solubility of two types of heterogeneous fluoridated hydroxyapatites. Biomaterials. 1998;19(7-9):611-6.

Driessens FCM. Formation and stability of calcium phosphates in relation to the phase composition of the mineral in calcified tissues. In: Bioceramics of calciumphosphate Eds de Groot K, CRC Press, Boxa Raton, Florida 1983: 1-32.

Gibson IR, Bonfield W. Novel synthesis and characterization of an AB-type carbonate-substituted hydroxyapatite. J Biomed Mater Res. 2002;59(4):697-708.

Lakhkar NJ, Lee IH, Kim HW, Salih V, Wall IB, Knowles JC. Bone formation controlled by biologically relevant inorganic ions: role and controlled delivery from phosphate-based glasses. Adv Drug Deliv Rev. 2013;65(4):405-20.

Thamilselvan V, Fomby M, Walsh M, Basson MD. Divalent cations modulate human colon cancer cell adhesion. J Surg Res. 2003;110(1):255-65.

Balaban NQ, Schwarz US, Riveline D, Goichberg P, Tzur G, Sabanay I, Mahalu D, Safran S, Bershadsky A, Addadi L, Geiger B. Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates. Nat Cell Biol. 2001;3(5):466-72.

Chrzanowska-Wodnicka M, Burridge K. Rho-stimulated contractility drives the formation of stress fibers and focal adhesions. J Cell Biol. 1996;133(6):1403-15.

Hu DD, Barbas CF, Smith JW. An allosteric Ca2+ binding site on the beta3-integrins that regulates the dissociation rate for RGD ligands. J Biol Chem. 1996;271(36):21745-51.

Downloads

Published

2017-02-28

Issue

Section

Molecular and Cell Biotechnologies