TY - JOUR
T1 - Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells
AU - Hoffmann, Andrea
AU - Pelled, Gadi
AU - Turgeman, Gadi
AU - Eberle, Peter
AU - Zilberman, Yoram
AU - Shinar, Hadassah
AU - Keinan-Adamsky, Keren
AU - Winkel, Andreas
AU - Shahab, Sandra
AU - Navon, Gil
AU - Gross, Gerhard
AU - Gazit, Dan
PY - 2006/4/1
Y1 - 2006/4/1
N2 - 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 line 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.
AB - 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 line 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.
UR - http://www.scopus.com/inward/record.url?scp=33645529161&partnerID=8YFLogxK
U2 - 10.1172/JCI22689
DO - 10.1172/JCI22689
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C2 - 16585960
AN - SCOPUS:33645529161
SN - 0021-9738
VL - 116
SP - 940
EP - 952
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 4
ER -