A new approach to demonstrate cellular activity in bone formation adjacent to implants

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A new approach to demonstrate cellular activity in bone formation adjacent to implants. / Röser, K; Johansson, C B; Donath, K; Albrektsson, T.

In: J Biomed Mater Res, Vol. 51, No. 2, 08.2000, p. 280-91.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Röser, K, Johansson, CB, Donath, K & Albrektsson, T 2000, 'A new approach to demonstrate cellular activity in bone formation adjacent to implants', J Biomed Mater Res, vol. 51, no. 2, pp. 280-91.

APA

Röser, K., Johansson, C. B., Donath, K., & Albrektsson, T. (2000). A new approach to demonstrate cellular activity in bone formation adjacent to implants. J Biomed Mater Res, 51(2), 280-91.

Vancouver

Röser K, Johansson CB, Donath K, Albrektsson T. A new approach to demonstrate cellular activity in bone formation adjacent to implants. J Biomed Mater Res. 2000 Aug;51(2):280-91.

Bibtex

@article{7beb29734f4c44489db4374ec1a85495,
title = "A new approach to demonstrate cellular activity in bone formation adjacent to implants",
abstract = "Bone tissue repeatedly formed in titanium 6-aluminum 4-vanadium rabbit bone harvest implants was collected in vivo at various times between 12 days and 5 weeks. Qualitative and quantitative examinations on undecalcified thin sections were performed in the light microscope. The amount of bone tissue was calculated on routinely stained sections. Alkaline (ALP) and acid phosphatase (ACP) enzyme activities were investigated. We also performed immunohistological detection of bone matrix proteins. Increasing bone density as well as an increasing mineralization of the tissue was observed in the biopsies with increasing time. The ALP and ACP activities were similar at short times (12 days and 2 weeks). With increasing time the ALP activity was stronger than that of ACP. The results from the immunohistochemical detection of osteonectin, osteopontin, bone sialoprotein, and collagen I and II demonstrated changes in the tissue differentiation with time. The tissue formation in the canal became more mature with time of ingrowth, as observed with the various techniques used in this study. Owing to these methodical developments, undecalcified ground sections may be used for detailed analysis of various phases of tissue formation in close proximity to implants.",
keywords = "Acid Phosphatase, Alkaline Phosphatase, Animals, Biocompatible Materials, Biomarkers, Bone Screws, Collagen, Integrin-Binding Sialoprotein, Internal Fixators, Osteogenesis, Osteopontin, Phosphoproteins, Rabbits, Sialoglycoproteins, Titanium, Journal Article, Research Support, Non-U.S. Gov't",
author = "K R{\"o}ser and Johansson, {C B} and K Donath and T Albrektsson",
note = "Copyright 2000 John Wiley & Sons, Inc.",
year = "2000",
month = aug,
language = "English",
volume = "51",
pages = "280--91",
number = "2",

}

RIS

TY - JOUR

T1 - A new approach to demonstrate cellular activity in bone formation adjacent to implants

AU - Röser, K

AU - Johansson, C B

AU - Donath, K

AU - Albrektsson, T

N1 - Copyright 2000 John Wiley & Sons, Inc.

PY - 2000/8

Y1 - 2000/8

N2 - Bone tissue repeatedly formed in titanium 6-aluminum 4-vanadium rabbit bone harvest implants was collected in vivo at various times between 12 days and 5 weeks. Qualitative and quantitative examinations on undecalcified thin sections were performed in the light microscope. The amount of bone tissue was calculated on routinely stained sections. Alkaline (ALP) and acid phosphatase (ACP) enzyme activities were investigated. We also performed immunohistological detection of bone matrix proteins. Increasing bone density as well as an increasing mineralization of the tissue was observed in the biopsies with increasing time. The ALP and ACP activities were similar at short times (12 days and 2 weeks). With increasing time the ALP activity was stronger than that of ACP. The results from the immunohistochemical detection of osteonectin, osteopontin, bone sialoprotein, and collagen I and II demonstrated changes in the tissue differentiation with time. The tissue formation in the canal became more mature with time of ingrowth, as observed with the various techniques used in this study. Owing to these methodical developments, undecalcified ground sections may be used for detailed analysis of various phases of tissue formation in close proximity to implants.

AB - Bone tissue repeatedly formed in titanium 6-aluminum 4-vanadium rabbit bone harvest implants was collected in vivo at various times between 12 days and 5 weeks. Qualitative and quantitative examinations on undecalcified thin sections were performed in the light microscope. The amount of bone tissue was calculated on routinely stained sections. Alkaline (ALP) and acid phosphatase (ACP) enzyme activities were investigated. We also performed immunohistological detection of bone matrix proteins. Increasing bone density as well as an increasing mineralization of the tissue was observed in the biopsies with increasing time. The ALP and ACP activities were similar at short times (12 days and 2 weeks). With increasing time the ALP activity was stronger than that of ACP. The results from the immunohistochemical detection of osteonectin, osteopontin, bone sialoprotein, and collagen I and II demonstrated changes in the tissue differentiation with time. The tissue formation in the canal became more mature with time of ingrowth, as observed with the various techniques used in this study. Owing to these methodical developments, undecalcified ground sections may be used for detailed analysis of various phases of tissue formation in close proximity to implants.

KW - Acid Phosphatase

KW - Alkaline Phosphatase

KW - Animals

KW - Biocompatible Materials

KW - Biomarkers

KW - Bone Screws

KW - Collagen

KW - Integrin-Binding Sialoprotein

KW - Internal Fixators

KW - Osteogenesis

KW - Osteopontin

KW - Phosphoproteins

KW - Rabbits

KW - Sialoglycoproteins

KW - Titanium

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

M3 - SCORING: Journal article

C2 - 10825228

VL - 51

SP - 280

EP - 291

IS - 2

ER -