TY - JOUR
T1 - In vitro effects of mechanical stimulation and photobiomodulation on osteoblastic cell function
T2 - A proof of concept study
AU - Chintavalakorn, Rochaya
AU - Khantachawana, Anak
AU - Viravaidya-Pasuwat, Kwanchanok
AU - Santiwong, Peerapong
AU - Surarit, Rudee
N1 - Publisher Copyright:
© 2016 Japanese Society of Pediatric Dentistry
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Background The effect of mechanical stimulation and photobiomodulation on tissue defect restoration has recently been investigated in various fields of tissue engineering such as acceleration of healing process and bone calcification. Mechanical stimulation generates shear stress on bone cells resulting in promotion of bone formation whereas photobiomodulation regulates inflammation, decreases pain, accelerates cell proliferation and enhances healing. Methods MC3T3-E1 cells were cultured in 3 dimensional collagen scaffolds. Cells were daily stimulated by either mechanical loading of 3 Hz sinusoidal with 3000 μstrain vibration, or photobiomodulation using LED with 3 J/cm2 fluency or combination of both. The calcifications of 3D tissue-engineered bones were examined by non-destructive monitoring device every day for 42 days. Results The 3D tissue-engineered bones that exposed to mechanical alone or combined stimulation exhibited early calcification, higher calcium content and bulk density comparing to control and light stimulation alone. Furthermore, the mRNA expression level of bone formation related genes such as RUNX2, ALP, osteopontin and osteocalcin were examined 7 days after stimulations. We showed the potential upregulation of ALP gene after mechanical stimulation alone or combined with light treatment. On day 28 Von Kossa stain revealed higher calcium deposition and increased cell migration to the deeper zone of 3D tissue-engineered bones. Conclusion We suggested that the mechanical treatment alone and combination with light treatment could accelerate the calcification of 3D tissue-engineered bone possibly through up-regulation of ALP gene during early stage of bone formation.
AB - Background The effect of mechanical stimulation and photobiomodulation on tissue defect restoration has recently been investigated in various fields of tissue engineering such as acceleration of healing process and bone calcification. Mechanical stimulation generates shear stress on bone cells resulting in promotion of bone formation whereas photobiomodulation regulates inflammation, decreases pain, accelerates cell proliferation and enhances healing. Methods MC3T3-E1 cells were cultured in 3 dimensional collagen scaffolds. Cells were daily stimulated by either mechanical loading of 3 Hz sinusoidal with 3000 μstrain vibration, or photobiomodulation using LED with 3 J/cm2 fluency or combination of both. The calcifications of 3D tissue-engineered bones were examined by non-destructive monitoring device every day for 42 days. Results The 3D tissue-engineered bones that exposed to mechanical alone or combined stimulation exhibited early calcification, higher calcium content and bulk density comparing to control and light stimulation alone. Furthermore, the mRNA expression level of bone formation related genes such as RUNX2, ALP, osteopontin and osteocalcin were examined 7 days after stimulations. We showed the potential upregulation of ALP gene after mechanical stimulation alone or combined with light treatment. On day 28 Von Kossa stain revealed higher calcium deposition and increased cell migration to the deeper zone of 3D tissue-engineered bones. Conclusion We suggested that the mechanical treatment alone and combination with light treatment could accelerate the calcification of 3D tissue-engineered bone possibly through up-regulation of ALP gene during early stage of bone formation.
KW - Bulk density
KW - Calcium content
KW - MC3T3-E1
KW - Mechanical stimulation
KW - Photobiomodulation
UR - http://www.scopus.com/inward/record.url?scp=85008474193&partnerID=8YFLogxK
U2 - 10.1016/j.pdj.2016.10.004
DO - 10.1016/j.pdj.2016.10.004
M3 - Article
AN - SCOPUS:85008474193
SN - 0917-2394
VL - 27
SP - 29
EP - 41
JO - Pediatric Dental Journal
JF - Pediatric Dental Journal
IS - 1
ER -