Analysis of osteoblast activity around beta-TCP particles implanted into bone: Expression of bone matrix protein mRNAs

被引:2
|
作者
Ohsawa, K [1 ]
Neo, M [1 ]
Matsuoka, H [1 ]
Akiyama, H [1 ]
Ito, H [1 ]
Nakamura, T [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Orthopaed Surg, Sakyo Ku, Kyoto 6068507, Japan
来源
BIOCERAMICS | 2000年 / 192-1卷
关键词
biocompatibility; bone formation; in situ hybridization; macrophage; osteopontin; beta-tricalcium phosphate TCP;
D O I
10.4028/www.scientific.net/KEM.192-195.317
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Osteoblast activity around beta-tricalcium phosphate (beta -TCP) particles (150-300 mum in diameter) implanted into rat tibiae was analyzed by in situ hybridization with digoxygenin-labeled procollagen al(I) (COL), osteonectin (ON), osteocalcin (OC) and osteopontin (OPN) RNA probes. Holes without implantation were used as a control. Specimens were collected at 3, 5, 7 and 10 days after the operation. New bone was formed centripetally in both the beta -TCP implanted and control groups, and all four kinds of mRNA were expressed in activated osteoblasts. A COL signal was expressed most strongly and widely, and was detected at the peripheral region of the hole at day 3. The other three mRNAs were also expressed in bone forming osteoblasts by day 7. However, in the earlier cell reaction stage, OPN expression in the beta -TCP implanted group was different from that in the control group: OPN mRNA was seen exclusively in the cells on the particles, and an OPN signal was detected not only in COL-positive cells, but also in COL-negative cells. The former cells may be osteoblasts and reflect the early process of bone formation on biomaterials. The latter cells may be macrophages and reflect foreign body reactions. Expression of these OPN mRNAs induced by implantation of beta -TCP may play a role in bone formation on the materials and in determining the their biocompatibility.
引用
收藏
页码:317 / 320
页数:4
相关论文
共 27 条
  • [21] THE EFFECT OF LONG-TERM OVARIAN HORMONE DEFICIENCY ON TRANSFORMING GROWTH-FACTOR-BETA AND BONE-MATRIX PROTEIN MESSENGER-RNA EXPRESSION IN RAT FEMORA
    WESTERLIND, KC
    WRONSKI, TJ
    EVANS, GL
    TURNER, RT
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 200 (01) : 283 - 289
  • [22] Integrin-mediated expression of bone formation-related genes in osteoblast-like cells in response to fluid shear stress: Roles of extracellular matrix, Shc, and mitogen-activated protein kinase
    Lee, Ding-Yu
    Yeh, Chiuan-Ren
    Chang, Shun-Fu
    Lee, Pei-Ling
    Chien, Shu
    Cheng, Cheng-Kung
    Chiu, Jeng-Jiann
    JOURNAL OF BONE AND MINERAL RESEARCH, 2008, 23 (07) : 1140 - 1149
  • [23] Bone morphogenetic proteins, extracellular matrix, and mitogen-activated protein kinase signaling pathways are required for osteoblast-specific gene expression and differentiation in MC3T3-E1 cells
    Xiao, GZ
    Gopalakrishnan, R
    Jiang, D
    Reith, E
    Benson, MD
    Franceschi, RT
    JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (01) : 101 - 110
  • [24] RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2 ENHANCES MESSENGER-RNA EXPRESSION OF INTERLEUKIN-6 AND TRANSFORMING GROWTH-FACTOR-BETA-1 IN NORMAL HUMAN OSTEOBLAST-LIKE CELLS
    ZHENG, MH
    WOOD, DJ
    WYSOCKI, S
    PAPADIMITRIOU, JM
    WANG, EA
    JOURNAL OF BONE AND MINERAL RESEARCH, 1993, 8 : S377 - S377
  • [25] REGULATORY ROLE OF TRANSFORMING GROWTH-FACTOR-BETA, BONE MORPHOGENETIC PROTEIN-2, AND PROTEIN-4 ON GENE-EXPRESSION OF EXTRACELLULAR-MATRIX PROTEINS AND DIFFERENTIATION OF DENTAL-PULP CELLS
    NAKASHIMA, M
    NAGASAWA, H
    YAMADA, Y
    REDDI, AH
    DEVELOPMENTAL BIOLOGY, 1994, 162 (01) : 18 - 28
  • [26] The Expression of Bone Morphogenetic Protein 2 and Matrix Metalloproteinase 2 through Retinoic Acid Receptor Beta Induced by All-Trans Retinoic Acid in Cultured ARPE-19 Cells
    Gao, Zhenya
    Huo, Lijun
    Cui, Dongmei
    Yang, Xiao
    Zeng, Junwen
    PLOS ONE, 2016, 11 (03):
  • [27] BONE MORPHOGENETIC PROTEIN 4 (BMP-4), A MEMBER OF THE TGF-BETA FAMILY, IN EARLY EMBRYOS OF XENOPUS-LAEVIS - ANALYSIS OF MESODERM INDUCING ACTIVITY
    KOSTER, M
    PLESSOW, S
    CLEMENT, JH
    LORENZ, A
    TIEDEMANN, H
    KNOCHEL, W
    MECHANISMS OF DEVELOPMENT, 1991, 33 (03) : 191 - 200