Effect of titanium surface characteristics on chondrocytes and osteoblasts in vitro

B. D. Boyan, T. W. Hummert, K. Kieswetter, D. Schraub, D. D. Dean, Z. Schwartz

Research output: Contribution to journalReview article

47 Scopus citations

Abstract

Material surfaces can directly influence cell response, ultimately affecting the rate and quality of new tissue formation. Initial events include oriented adsorption of molecules from the surrounding fluid, creating a conditioned interface to which the cell responds. Surface chemistry and energy determine the type and orientation of adsorbed molecules, which then directs cellular attachment. Focal attachments between the cells and substrate determine cell shape which, when transduced via the cytoskeleton to the nucleus, may result in expression of specific phenotypes. Osteoblasts and chondrocytes are sensitive to subtle differences in surface roughness and surface chemistry. Cellular response also depends on the local environment and state of maturation of responding cells. Titanium (Ti) is one of the most commonly used materials in bone. Morphologic and cell adhesion studies have provided information concerning the interface and initial interaction with Ti, while studies investigating the biochemical response of cells to Ti have lagged behind. The optimal surface characteristics necessary to predictably elicit good bone formation are still under investigation. In this paper, we review how surface characteristics affect cellular response to implant materials and discuss studies suggesting that cell maturation state plays a role in cellular response to Ti.

Original languageEnglish (US)
Pages (from-to)323-335
Number of pages13
JournalCells and Materials
Volume5
Issue number4
StatePublished - Dec 1 1995

Keywords

  • Chondrocytes
  • Implant
  • In vitro
  • Osteoblasts
  • Titanium

ASJC Scopus subject areas

  • Anatomy
  • Biophysics

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    Boyan, B. D., Hummert, T. W., Kieswetter, K., Schraub, D., Dean, D. D., & Schwartz, Z. (1995). Effect of titanium surface characteristics on chondrocytes and osteoblasts in vitro. Cells and Materials, 5(4), 323-335.