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  • osteoblast  (2)
  • Wiley-Blackwell  (2)
  • American Geophysical Union
  • Springer Nature
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 39 (1998), S. 1-8 
    ISSN: 0021-9304
    Keywords: in situ hybridization ; collagen I ; osteoblast ; bioactive materials ; osteoconduction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Osteoblast activation after implantation of two kinds of surface-active material in bone was investigated chronologically using in situ hybridization with digoxygenin-labeled procollagen α1(I) complementary RNA probe. The bioactive materials used were hydroxyapatite (HA) and apatite- and wollastonite-containing glass-ceramic (A-W GC). A hole was drilled bilaterally in the distal epiphysis of rabbit femurs with subsequent implantation of HA or A-W GC cylinders in a press-fit manner. Specimens were collected at 3, 7, 14, and 28 days after operation and decalcified. Then the undecalcified implant cores were pushed out of the hole without causing damage to the bony side of the interface. In situ hybridization documented no qualitative differences in the expression of procollagen α1(I) RNA between HA and A-W GC. Few osteoblasts at the bone-material interface showed a specific signal at day 3, whereas many osteoblasts were positive around the materials at days 7 and 14, indicative of active new bone formation. The positive osteoblasts seemed to originate from preexisting trabeculae and lined the trabeculae, newly formed bone, and material surface. At day 28, many osteoblasts lining material-surrounding bone were negative, whereas those in remodeling canals were positive, suggesting that the bone was in the remodeling stage after bone formation. These findings were comparable to those with β-tricalcium phosphate in a previous study, thus suggesting osteoconductive bone formation on HA and A-W GC. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 39, 1-8, 1998.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 39 (1998), S. 71-76 
    ISSN: 0021-9304
    Keywords: in situ hybridization ; collagen I ; osteoblast ; β-tricalcium phosphate ; osteoconduction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Temporal and spatial patterns of osteoblast activation around β-TCP particles implanted into bone were analyzed by in situ hybridization with digoxygenin-labeled procollagen α1(I) RNA probes. β-TCP particles (150-300 μm in diameter) were implanted into rat tibiae, and specimens were collected 3, 5, 7, 14, and 28 days after operation. Activated osteoblasts displayed intense procollagen α1(I) RNA specific labeling. At day 3, osteoblasts lining pre-existing trabeculae in places showed a specific signal. Additionally, scattered activated cells compatible with preosteoblasts also were observed in the vicinity of the trabeculae among red blood cells that filled the space between β-TCP particles. Osteoblast activation on the surface of β-TCP rarely was observed. At days 5 and 7, osteoblast activation and bone formation advanced centripetally. At the forefront of bone formation positive cells were scattered in the blood cell clots, and some of the positive cells colonized forming new bone matrix. Formation of new bone did not always begin at the surface of β-TCP. At day 14, most of the β-TCP particles were tightly associated with newly formed bone, and the number of positive osteoblasts was reduced. At day 28, absorption of the newly formed bone and the β-TCP by multinuclear cells was sporadically demonstrated. Such cells often were accompanied by active osteoblasts, suggesting early bone remodeling. In conclusion, in situ hybridization with procollagen α1(I) was employed to demonstrate precisely the mode of recruitment of bone cell precursors. β-TCP does not positively guide collagen I expressing bone cells along its surface. It has no apparent effects on bone regeneration. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res, 39, 71-76, 1998.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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