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Osteoblasts respond to hydroxyapatite surfaces with immediate changes in gene expression
Author(s) -
Xie Jianwei,
Baumann Melissa J.,
McCabe Laura R.
Publication year - 2004
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.30140
Subject(s) - osteoblast , materials science , gene expression , extracellular , microbiology and biotechnology , gene , implant , biophysics , biology , in vitro , biochemistry , medicine , surgery
Bone mineral contains hydroxyapatite (HA). This is the surface that mature osteoblasts and osteocytes interact with. Synthetic HA is widely used in orthopedic surgeries as an implant or implant coating. The bone‐like HA surfaces increase implant union and bone formation; however, the mechanisms accounting for this effect on osteoblasts are not known. In this study, we compared gene expression profiles of osteoblasts responding to HA or plastic surfaces for 24 h. Expression profiles were also compared between HA discs processed with gravity‐sieved compared with combined gravity and air‐jet‐sieved HA powders. The latter, composed of smaller HA particles, exhibits an increase in grain boundary surface area. Discs made with either HA powder similarly up‐regulated osteoblast expression of 10 genes (including proliferin 3, Glvr‐1, DMP‐1, and tenascin C) and down‐regulated 15 genes (such as osteoglycin) by more than 2‐fold compared with plastic surfaces. The overall changes are indicative of an immediate (24‐h) response to the HA surface and a trend toward osteoblast differentiation. In addition, subsets of modulated genes exist that are unique to each HA subtype. Taken together, we identified HA responsive genes evident within 24 h of surface contact, indicating a critical role for extracellular mineral surfaces in the regulation of osteoblast gene expression and phenotype. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res 71A: 108–117, 2004