TY - JOUR
T1 - BMP-12 gene transfer augmentation of lacerated tendon repair
AU - Lou, Jueren
AU - Tu, Yizheng
AU - Burns, Meghan
AU - Silva, Matthew J.
AU - Manske, Paul
N1 - Funding Information:
This research was supported by Shriners Hospitals for Children, grant #8510. The authors thank Genetic Institute for the generous gift of BMP-12 cDNA and monoclone antibody F2B12/15.4.15.
PY - 2001
Y1 - 2001
N2 - Bone morphogenetic protein (BMP) 12 is a recently discovered member of the human BMP family. It is the human homolog of mouse growth/differentiation factor (GDF)-7. Previously we reported that injection of mesenchymal progenitor cells transferred with the BMP-12 gene into the muscles of nude mice induced tendon-like tissue formation. In this study, we further investigated the effect of BMP-12 gene transfer on tendon cells. We observed that adenovirus mediated in vitro BMP-12 gene transfer into chicken tendon cells increased type I collagen synthesis. No change in alkaline phosphatase activity was observed following BMP-12 gene transfer. We also determined that BMP-12 gene transfer into a complete tendon laceration chicken model resulted in a two-fold increase of tensile strength and stiffness of repaired tendons, indicating improved tendon healing in vivo. We conclude that BMP-12 gene transfer is a promising procedure for improving the tendon repair process.
AB - Bone morphogenetic protein (BMP) 12 is a recently discovered member of the human BMP family. It is the human homolog of mouse growth/differentiation factor (GDF)-7. Previously we reported that injection of mesenchymal progenitor cells transferred with the BMP-12 gene into the muscles of nude mice induced tendon-like tissue formation. In this study, we further investigated the effect of BMP-12 gene transfer on tendon cells. We observed that adenovirus mediated in vitro BMP-12 gene transfer into chicken tendon cells increased type I collagen synthesis. No change in alkaline phosphatase activity was observed following BMP-12 gene transfer. We also determined that BMP-12 gene transfer into a complete tendon laceration chicken model resulted in a two-fold increase of tensile strength and stiffness of repaired tendons, indicating improved tendon healing in vivo. We conclude that BMP-12 gene transfer is a promising procedure for improving the tendon repair process.
UR - http://www.scopus.com/inward/record.url?scp=0035217756&partnerID=8YFLogxK
U2 - 10.1016/S0736-0266(01)00042-0
DO - 10.1016/S0736-0266(01)00042-0
M3 - Article
C2 - 11781024
AN - SCOPUS:0035217756
SN - 0736-0266
VL - 19
SP - 1199
EP - 1202
JO - Journal of Orthopaedic Research
JF - Journal of Orthopaedic Research
IS - 6
ER -