TY - JOUR
T1 - Effect of vibration on osteoblastic and osteoclastic activities
T2 - Analysis of bone metabolism using goldfish scale as a model for bone
AU - Suzuki, N.
AU - Kitamura, K.
AU - Nemoto, T.
AU - Shimizu, N.
AU - Wada, S.
AU - Kondo, T.
AU - Tabata, M. J.
AU - Sodeyama, F.
AU - Ijiri, K.
AU - Hattori, A.
N1 - Funding Information:
This study was supported in part by grants to N.S. (Grant-in-Aid for Scientific Research (C) No. 18500375), to K.K. (Grant-in-Aid for Exploratory Research (C) No.18650197), to S.W. (Grant-in-Aid for Scientific Research (C) No. 18592214), and to A.H. (Grant-in-Aid for Scientific Research (C) No. 18570055) sponsored by the Japan Society for the Promotion of Science. This study was carried out as a part of “Ground-based Research Announcement for Space Utilization” promoted by the Japan Space Forum.
PY - 2007
Y1 - 2007
N2 - In osteoclastic activity during space flight as well as hind limb unloading by tail suspension, inconsistent results have been reported in an in vivo study. The bone matrix plays an important role in the response to physical stress. However, there is no suitable in vitro co-culture system of osteoblasts and osteoclasts including bone matrix. On the other hand, fish scale is a calcified tissue that contains osteoblasts, osteoclasts, and bone matrix, all of which are similar to those found in human bones. Recently, we developed a new in vitro model system using goldfish scale. This system can detect the activities of osteoclasts and osteoblasts with tartrate-resistant acid phosphatase and alkaline phosphatase as the respective markers and precisely analyze the co-relationship between osteoblasts and osteoclasts. Using this system, we analyzed the bone metabolism under various degrees of acceleration (0.5-, 1-, 2-, 4-, and 6-G) by vibration with a G-load apparatus. After loading for 5 and 10 min, the scales were incubated for 6 and 24 h. The osteoblastic and osteoclastic activities were then measured. The osteoblastic activities gradually increased corresponding to 1-G to 6-G acceleration. In addition, ER mRNA expression was the highest under 6-G acceleration. On the other hand, the osteoclastic activity decreased at 24 h of incubation under low acceleration (0.5- and 1-G). This change coincided with TRAP mRNA expression. Under 2-G acceleration, the strength of suppression in osteoclastic activity was the highest. The strength of the inhibitory action under 4- and 6-G acceleration was lower than that under 2-G acceleration. In our co-culture system, osteoblasts and osteoclasts in the scale sensitively responded to several degrees of acceleration. Therefore, we strongly believe that our in vitro co-culture system is useful for the analysis of bone metabolism under loading or unloading.
AB - In osteoclastic activity during space flight as well as hind limb unloading by tail suspension, inconsistent results have been reported in an in vivo study. The bone matrix plays an important role in the response to physical stress. However, there is no suitable in vitro co-culture system of osteoblasts and osteoclasts including bone matrix. On the other hand, fish scale is a calcified tissue that contains osteoblasts, osteoclasts, and bone matrix, all of which are similar to those found in human bones. Recently, we developed a new in vitro model system using goldfish scale. This system can detect the activities of osteoclasts and osteoblasts with tartrate-resistant acid phosphatase and alkaline phosphatase as the respective markers and precisely analyze the co-relationship between osteoblasts and osteoclasts. Using this system, we analyzed the bone metabolism under various degrees of acceleration (0.5-, 1-, 2-, 4-, and 6-G) by vibration with a G-load apparatus. After loading for 5 and 10 min, the scales were incubated for 6 and 24 h. The osteoblastic and osteoclastic activities were then measured. The osteoblastic activities gradually increased corresponding to 1-G to 6-G acceleration. In addition, ER mRNA expression was the highest under 6-G acceleration. On the other hand, the osteoclastic activity decreased at 24 h of incubation under low acceleration (0.5- and 1-G). This change coincided with TRAP mRNA expression. Under 2-G acceleration, the strength of suppression in osteoclastic activity was the highest. The strength of the inhibitory action under 4- and 6-G acceleration was lower than that under 2-G acceleration. In our co-culture system, osteoblasts and osteoclasts in the scale sensitively responded to several degrees of acceleration. Therefore, we strongly believe that our in vitro co-culture system is useful for the analysis of bone metabolism under loading or unloading.
KW - Estrogen receptor
KW - Osteoblasts
KW - Osteoclasts
KW - Scale
KW - Tartrate-resistant acid phosphatase
KW - Vibration
UR - http://www.scopus.com/inward/record.url?scp=35649000055&partnerID=8YFLogxK
U2 - 10.1016/j.asr.2007.04.104
DO - 10.1016/j.asr.2007.04.104
M3 - 学術論文
AN - SCOPUS:35649000055
SN - 0273-1177
VL - 40
SP - 1711
EP - 1721
JO - Advances in Space Research
JF - Advances in Space Research
IS - 11
ER -