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| DOI | 10.1016/J.JBIOMECH.2014.11.028 | ||||
| Año | 2015 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
In the United States, approximately eight million osseous fractures are reported annually, of which 5-10% fail to create a bony union. Osteoblast-specific deletion of the gene Pten in mice has been found to stimulate bone growth and accelerate fracture healing. Healing rates at four weeks increased in femurs from Pten osteoblast conditional knock-out mice (Pten-CKO) compared to wild-type mice (WT) of the same genetic strain as measured by an increase in mechanical stiffness and failure load in four-point bending tests. Preceding mechanical testing, each femur was imaged using a Skyscan 1172 micro-computed tomography (mu CT) scanner (Skyscan, Kontich, Belgium). The present study used mu CT image-based analysis to test the hypothesis that the increased femoral fracture force and stiffness in Pten-CKO were due to greater section properties with the same effective material properties as that of the WT. The second moment of area and section modulus were computed in ImageJ 1.46 (National Institutes of Health) and used to predict the effective flexural modulus and the stress at failure for fourteen pairs of intact and callus WT and twelve pairs of intact and callus Pten-CKO femurs. For callus and intact femurs, the failure stress and tissue mineral density of the Pten-CKO and WT were not different; however, the section properties of the Pten-CKO were more than twice as large 28 days post-fracture. It was therefore concluded, when the gene Pten was conditionally knocked-out in osteoblasts, the resulting increased bending stiffness and force to fracture were due to increased section properties. (C) 2014 Elsevier Ltd. All rights reserved.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Collins, Caitlyn J. | Mujer |
UNIV WISCONSIN - Estados Unidos
University of Wisconsin-Madison - Estados Unidos |
| 2 | VIVANCO-MORALES, JUAN FRANCISCO | Hombre |
UNIV WISCONSIN - Estados Unidos
Universidad Adolfo Ibáñez - Chile University of Wisconsin-Madison - Estados Unidos |
| 3 | Sokn, Scott A. | Hombre |
UNIV WISCONSIN - Estados Unidos
University of Wisconsin-Madison - Estados Unidos |
| 4 | Williams, Bart O. | Hombre |
Van Andel Res Inst - Estados Unidos
Van Andel Research Institute - Estados Unidos |
| 5 | Burgers, Travis A. | Hombre |
Van Andel Res Inst - Estados Unidos
Van Andel Research Institute - Estados Unidos |
| 6 | Ploeg, Heidi-Lynn | Mujer |
UNIV WISCONSIN - Estados Unidos
University of Wisconsin-Madison - Estados Unidos |
| Fuente |
|---|
| National Institutes of Health |
| United States National Institutes of Health |
| University of Wisconsin-Madison |
| National Institute of Arthritis and Musculoskeletal and Skin Diseases |
| Van Andel Research Institute |
| University of Wisconsin-Madison Graduate School |
| Agradecimiento |
|---|
| Funding was provided by the University of Wisconsin-Madison Graduate School, the Van Andel Research Institute, and was supported by United States National Institutes of Health grant AR053293 (BOW). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |
| Funding was provided by the University of Wisconsin-Madison Graduate School , the Van Andel Research Institute , and was supported by United States National Institutes of Health grant AR053293 (BOW). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |