TY - JOUR
T1 - Influence of substrate curvature on osteoblast orientation and extracellular matrix deposition
AU - Pilia, Marcello
AU - Guda, Teja
AU - Shiels, Stefanie M.
AU - Appleford, Mark R.
N1 - Funding Information:
Thanks to Dr. Daniel Oh for his help and expertise in the casting of HAp materials, Beth Pollot for her assistance with scanning electron microscopy, and Cameron Taylor for his support analyzing cell orientation. Also a special thanks to the dental research staff at the United States Army Institute of Surgical research at Fort Sam Houston, San Antonio TX for allowing us to use their laser profilometer. This study was supported in part by the UT System South Texas Technology Management (STTM) POC Sparc grant program.
PY - 2013/10/3
Y1 - 2013/10/3
N2 - Background: The effects of microchannel diameter in hydroxyapatite (HAp) substrates on osteoblast behavior were investigated in this study. Microchannels of 100, 250 and 500 μm diameter were created on hydroxyapatite disks. The changes in osteoblast precursor growth, differentiation, extra cellular matrix (ECM) secretion and cell attachment/orientation were investigated as a function of microchannel diameter. Results: Curvature did not impact cellular differentiation, however organized cellular orientation was achieved within the 100 and 250 μm microchannels (mc) after 6 days compared to the 12 days it took for the 500mc group, while the flat substrate remained disorganized. Moreover, the 100, 250 and 500mc groups expressed a specific shift in orientation of 17.45°, 9.05°, and 22.86° respectively in 24 days. The secreted/mineralized ECM showed the 100 and 250mc groups to have higher modulus (E) and hardness (h) (E = 42.6GPa; h = 1.6GPa) than human bone (E = 13.4-25.7GPa; h = 0.47-0.74GPa), which was significantly greater than the 500mc and control groups (p < 0.05). It was determined that substrate curvature affects the cell orientation, the time required for initial response, and the shift in orientation with time. Conclusions: These findings demonstrate the ability of osteoblasts to organize and mineralize differentially in microchannels similar to those found in the osteons of compact bone. These investigations could lead to the development of osteon-like scaffolds to support the regeneration of organized bone.
AB - Background: The effects of microchannel diameter in hydroxyapatite (HAp) substrates on osteoblast behavior were investigated in this study. Microchannels of 100, 250 and 500 μm diameter were created on hydroxyapatite disks. The changes in osteoblast precursor growth, differentiation, extra cellular matrix (ECM) secretion and cell attachment/orientation were investigated as a function of microchannel diameter. Results: Curvature did not impact cellular differentiation, however organized cellular orientation was achieved within the 100 and 250 μm microchannels (mc) after 6 days compared to the 12 days it took for the 500mc group, while the flat substrate remained disorganized. Moreover, the 100, 250 and 500mc groups expressed a specific shift in orientation of 17.45°, 9.05°, and 22.86° respectively in 24 days. The secreted/mineralized ECM showed the 100 and 250mc groups to have higher modulus (E) and hardness (h) (E = 42.6GPa; h = 1.6GPa) than human bone (E = 13.4-25.7GPa; h = 0.47-0.74GPa), which was significantly greater than the 500mc and control groups (p < 0.05). It was determined that substrate curvature affects the cell orientation, the time required for initial response, and the shift in orientation with time. Conclusions: These findings demonstrate the ability of osteoblasts to organize and mineralize differentially in microchannels similar to those found in the osteons of compact bone. These investigations could lead to the development of osteon-like scaffolds to support the regeneration of organized bone.
KW - Curvature
KW - Extracellular Matrix
KW - Hydroxyapatite
KW - Microchannels
KW - Nano-indentation
KW - Osteon architecture
UR - http://www.scopus.com/inward/record.url?scp=84884845017&partnerID=8YFLogxK
U2 - 10.1186/1754-1611-7-23
DO - 10.1186/1754-1611-7-23
M3 - Article
AN - SCOPUS:84884845017
SN - 1754-1611
VL - 7
JO - Journal of Biological Engineering
JF - Journal of Biological Engineering
IS - 1
M1 - 23
ER -