Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells

被引:3
|
作者
Hoffmann, A
Pelled, G
Turgeman, G
Eberle, P
Zilberman, Y
Shinar, H
Keinan-Adamsky, K
Winkel, A
Shahab, S
Navon, G
Gross, G
Gazit, D
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Skeletal Biotechnol Lab, IL-91120 Jerusalem, Israel
[2] Gesell Biotechnol Forsch mbH, Signaling & Gene Regulat, D-3300 Braunschweig, Germany
[3] Tel Aviv Univ, Sch Chem, IL-69978 Tel Aviv, Israel
来源
JOURNAL OF CLINICAL INVESTIGATION | 2006年 / 116卷 / 04期
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tissue regeneration requires the recruitment of adult stem cells and their differentiation into mature committed cells. In this study we describe what we believe to be a novel approach for tendon regeneration based on a specific signalling molecule, Smad8, which mediates the differentiation of mesenchymal stem cells (MSCs) into tendon-like cells. A biologically active Smad8 variant was transfected into an MSC fine that coexpressed the osteogenic gene bone morphogenetic protein 2 (BMP2). The engineered cells demonstrated the morphological characteristics and gene expression profile of tendon cells both in vitro and in vivo. In addition, following implantation in an Achilles tendon partial defect, the engineered cells were capable of inducing tendon regeneration demonstrated by double quantum filtered MRI. The results indicate what we believe to be a novel mechanism in which Smad8 inhibits the osteogenic pathway in MSCs known to be induced by BMP2 while promoting tendon differentiation. These findings may have considerable importance for the therapeutic replacement of tendons or ligaments and for engineering other tissues in which BMP plays a pivotal developmental role.
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收藏
页码:940 / 952
页数:13
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