TY - GEN
T1 - A better biomaterial for bone regeneration
T2 - Nanotechnology 2013: Bio Sensors, Instruments, Medical, Environment and Energy - 2013 NSTI Nanotechnology Conference and Expo, NSTI-Nanotech 2013
AU - Chiu, Li Hsuan
AU - Lai, Wen Fu T
AU - Tsai, Yu Hui
PY - 2013
Y1 - 2013
N2 - Type II collagen is crucial to the development of embryonic skeletal system. Its functional defect in transgenic animal model results in severe chondrodysplasia.12 The in vitro studies including ours showed that type II collagen promotes chondrogenesis of mesenchymal stem cells (MSCs). 3-6 Our recent studies have demonstrated that type II collagen also regulated MSC adipogenesis and the early stages of osteogenesis.7 Type II collagen-coated surface enhanced osteogenesis-induced MSC calcium deposition, and increased protein expression levels of RUNX2. This mineralization-enhancing effect of type II collagen was diminished by MEK inhibitors. On the other hand, integrin α2β1 presents as the predominant receptor that responses to type II collagen in the osteogenic-induced MSCs. While implanted in the fracture bone of rats, the type II collagen-HA/TCP (nano-particle) scaffold group showed higher SFI scoring of foot-stepping and better locomotion as comparing to that of control group or type I collagen-HA/TCP group did. Collectively, type II collagen serves as an important modulator during early osteogenic differentiation of BMSCs, and enhance bone defect repair through an endochondral ossification-like process. The information advances our understanding about the cartilaginous ECM-BMSC interaction and provides perspective strategies for faster bone regeneration.
AB - Type II collagen is crucial to the development of embryonic skeletal system. Its functional defect in transgenic animal model results in severe chondrodysplasia.12 The in vitro studies including ours showed that type II collagen promotes chondrogenesis of mesenchymal stem cells (MSCs). 3-6 Our recent studies have demonstrated that type II collagen also regulated MSC adipogenesis and the early stages of osteogenesis.7 Type II collagen-coated surface enhanced osteogenesis-induced MSC calcium deposition, and increased protein expression levels of RUNX2. This mineralization-enhancing effect of type II collagen was diminished by MEK inhibitors. On the other hand, integrin α2β1 presents as the predominant receptor that responses to type II collagen in the osteogenic-induced MSCs. While implanted in the fracture bone of rats, the type II collagen-HA/TCP (nano-particle) scaffold group showed higher SFI scoring of foot-stepping and better locomotion as comparing to that of control group or type I collagen-HA/TCP group did. Collectively, type II collagen serves as an important modulator during early osteogenic differentiation of BMSCs, and enhance bone defect repair through an endochondral ossification-like process. The information advances our understanding about the cartilaginous ECM-BMSC interaction and provides perspective strategies for faster bone regeneration.
UR - http://www.scopus.com/inward/record.url?scp=84881102199&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84881102199&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:84881102199
SN - 9781482205862
VL - 3
T3 - Technical Proceedings of the 2013 NSTI Nanotechnology Conference and Expo, NSTI-Nanotech 2013
SP - 343
EP - 346
BT - Technical Proceedings of the 2013 NSTI Nanotechnology Conference and Expo, NSTI-Nanotech 2013
Y2 - 12 May 2013 through 16 May 2013
ER -