The effect of different titanium and hydroxyapatite-coated dental implant surfaces on phenotypic expression of human bone-derived cells

被引:56
作者
Knabe, C
Howlett, CR
Klar, F
Zreiqat, H
机构
[1] Free Univ Berlin, Hosp Benjamin Franklin, Dept Expt Dent, D-14197 Berlin, Germany
[2] Friadent Dentsply Inc, D-68229 Mannheim, Germany
[3] Univ New S Wales, Fac Med, Sch Med Sci, Dept Pathol, Sydney, NSW 2052, Australia
关键词
dental implants; human bone-derived cells; cell-biomaterial interactions; in situ hybridization; immunocyto-chemistry;
D O I
10.1002/jbm.a.30130
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Roughened titanium (Ti) surfaces have been widely used for dental implants. In recent years, there has been the tendency to replace Ti plasma-sprayed surfaces by sandblasted and acid-etched surfaces in order to enhance osseous apposition. Another approach has been the utilization of hydroxyapatite (HA)-coated implants. This study examines the effect of two roughened Ti dental implant surfaces on the osteoblastic phenotype of human bone-derived cells (HBDC) and compares this behavior to that for cells on an HA-coated surface. Test materials were an acidetched and sandblasted Ti surface (Ti-DPS), a porous Ti plasma-sprayed coating (Ti-TPS), and a plasma-sprayed porous HA coating (HA). Smooth Ti machined surfaces served as control (Ti-ma). HBDC were grown on the substrata for 3, 7, 14, and 21 days, counted and probed for various bone-related mRNAs and proteins (type I collagen, osteocalcin, osteopontin, osteonectin, alkaline phosphatase, and bone sialoprotein). All dental implant surfaces significantly affected cellular growth and the temporal expression of an array of bone-related genes and proteins. HA-coated Ti had the most effect on osteoblastic differentiation inducing a greater expression of an array of osteogenic markers than recorded for cells grown on Ti-DPS and Ti-TPS, thus suggesting that the HA-coated surface may possess a higher potency to enhance osteogenesis. Furthermore, Ti-DPS surfaces induced greater osteoblast proliferation and differentiation than Ti-TPS. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:98 / 107
页数:10
相关论文
共 91 条
  • [1] [Anonymous], 2000, BONE ENG
  • [2] [Anonymous], 2000, BONE ENG
  • [3] Anselme K, 1997, J BIOMED MATER RES, V34, P247, DOI 10.1002/(SICI)1097-4636(199702)34:2<247::AID-JBM14>3.0.CO
  • [4] 2-F
  • [5] Advances in the osteoblast lineage
    Aubin, JE
    [J]. BIOCHEMISTRY AND CELL BIOLOGY, 1998, 76 (06) : 899 - 910
  • [6] Aubin JE., 2000, BONE ENG, P19
  • [7] Bahat O, 2000, Int J Oral Maxillofac Implants, V15, P646
  • [8] MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS
    BELLOWS, CG
    AUBIN, JE
    HEERSCHE, JNM
    ANTOSZ, ME
    [J]. CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) : 143 - 154
  • [9] Bornstein MM, 2003, INT J ORAL MAX IMPL, V18, P659
  • [10] BRANEMARK P I, 1969, Scandinavian Journal of Plastic and Reconstructive Surgery, V3, P81