塔普斯加尔金
超声波
EGTA公司
钙
生物学中的钙
细胞内
蛋白多糖
化学
阿格里坎
刺激
巴普塔
细胞生物学
生物化学
内科学
医学
细胞外基质
生物
病理
骨关节炎
有机化学
替代医学
放射科
关节软骨
作者
Javad Parvizi,Vladimir Parpura,James F. Greenleaf,Mark E. Bolander
标识
DOI:10.1016/s0736-0266(01)00069-9
摘要
Abstract Low‐intensity ultrasound accelerates fracture healing in humans. In rat femur fracture models, ultrasound advanced healing is associated with increased proteoglycan expression. Here we report that ultrasound stimulation of primary rat chondrocytes elevated the intracellular concentration of calciums [Ca 2+ ] i . The [Ca 2+ ] i increase was rapid and transient at lower pressures (175–320 kPa), but rapid and sustained at higher ultrasound exposures (350–500 kPa). Chelating internal [Ca 2+ ] i with 1,2‐bis(2‐aminophenoxy) ethane‐ N ‐ N ‐ N ′‐ N ′‐tetraacetic acid (BAPTA‐AM), stopping the Ca 2+ /ATP‐ase induced mitochondrial release of [Ca 2+ ] i with Thapsigargin, or removing [Ca 2+ ] i from the medium with EGTA inhibited the stimulatory effects of ultrasound on proteoglycan synthesis. These results imply that ultrasound‐stimulated synthesis of cell matrix proteoglycan, associated with accelerated fracture healing, is mediated by intracellular calcium signaling. © 2002 Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.
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