Osteopontin and bone metabolism: a histology and scintigraphy study in rats

被引:11
作者
Gordjestani, M
Dermaut, L
De Ridder, L
Thierens, H
De Waele, P
Willy, WD
Bosman, F
机构
[1] Univ Ghent, Dept Orthodont, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Histol, B-9000 Ghent, Belgium
关键词
D O I
10.1016/j.ijom.2005.04.013
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Osteopontin (OPN) is one of the major non-collagen proteins in extracellular bone matrix. To elucidate the function of OPN in bone metabolism, a cellular defect was created in parietal bone and tibia of 12 rats. In Group 1, the left defects were filled with OPN-coated hydroxyapatite (OPN-H). In Group 2, the right defects were filled with non-coated hydroxyapatite (N-H). In both groups, the contra lateral defects were used as control defects. In Group 3, OPN-H was inserted in the left defects and N-H in the right defects. Bone metabolism was measured by Ca-45 and technetium-99m methylene diphosphonate scintigraphy for 4 weeks. Scintigraphy did not show any significant differences in bone metabolism between the defects filled with OPN-H and N-H. A higher bone metabolism was measured between the parietal defects filled with OPN-H or N-H in comparison with the parietal control defects. This difference, however, was not significant and was less for tibia defects. Histological observation (7th week) shows less inflammatory cells at the tibia defects filled with OPN-H compared to the tibia defects filled with N-H. This study did not show any acceleration or inhibition of bone metabolism in parietal or tibia bone in rats, but there is some evidence that OPN might influence inflammatory cells in bone matrix.
引用
收藏
页码:794 / 799
页数:6
相关论文
共 23 条
[1]
CHEN JK, 1992, J BONE MINER RES, V7, P987
[2]
DEVELOPMENTAL EXPRESSION OF OSTEOPONTIN (OPN) MESSENGER-RNA IN RAT-TISSUES - EVIDENCE FOR A ROLE FOR OPN IN BONE-FORMATION AND RESORPTION [J].
CHEN, JK ;
SINGH, K ;
MUKHERJEE, BB ;
SODEK, J .
MATRIX, 1993, 13 (02) :113-123
[3]
De Bie A C, 1991, J Biol Buccale, V19, P211
[4]
Binding of bone sialoprotein, osteopontin and synthetic polypeptides to hydroxyapatite [J].
Goldberg, HA ;
Warner, KJ ;
Li, MC ;
Hunter, GK .
CONNECTIVE TISSUE RESEARCH, 2001, 42 (01) :25-37
[5]
INFRARED-LASER AND BONE METABOLISM - A PILOT-STUDY [J].
GORDJESTANI, M ;
DERMAUT, L ;
THIERENS, H .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1994, 23 (01) :54-56
[6]
HOLINGER JO, 1990, J CRANIOFAC SURG, V1, P1
[7]
EXPRESSION OF BONE-MATRIX PROTEINS ASSOCIATED WITH MINERALIZED TISSUE FORMATION BY ADULT-RAT BONE-MARROW CELLS-INVITRO - INDUCTIVE EFFECTS OF DEXAMETHASONE ON THE OSTEOBLASTIC PHENOTYPE [J].
KASUGAI, S ;
TODESCAN, R ;
NAGATA, T ;
YAO, KL ;
BUTLER, WT ;
SODEK, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 147 (01) :111-120
[8]
Establishment of an osteoid preosteocyte-like cell MLO-A5 that spontaneously mineralizes in culture [J].
Kato, Y ;
Boskey, K ;
Spevak, L ;
Dallas, M ;
Hori, M ;
Bonewald, LF .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (09) :1622-1633
[9]
Acidic fibroblast growth factor signaling inhibits peroxynitrite-induced death of osteoblasts and osteoblast precursors [J].
Kelpke, SS ;
Reiff, D ;
Prince, CW ;
Thompson, JA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (10) :1917-1925
[10]
Kuyl MH, 1999, CLEFT PALATE-CRAN J, V36, P207, DOI 10.1597/1545-1569(1999)036<0207:AMATTH>2.3.CO