Hughes J M, Petit M A
University of Minnesota, School of Kinesiology, Minneapolis, MN 55455, USA.
J Musculoskelet Neuronal Interact. 2010 Jun;10(2):128-35.
Harold Frost first proposed the existence of several mechanical thresholds in bone, two of which determine whether bone is added to, or lost from, the skeleton. Recent evidence from bone biology helps elucidate the role of osteocytes in determining these mechanical thresholds. Specifically, when mechanical stimuli fall below the resorption threshold, osteocyte apoptosis occurs, followed by bone resorption. Conversely, mechanical loading maintains osteocytes viability, and consequently, no bone is lost. With a greater than customary mechanical stimulus, osteocytes perturbation from pulsatile fluid flow results in release of anabolic factors and subsequent bone formation. Osteocytes also play a pivotal role in bone remodeling in response to alterations in the mechanical environment. In particular, osteocyte apoptosis results in bone turnover in disuse as well as in response to greater than customary mechanical stimuli due to microdamage accumulation. Given the important role of osteocytes in bone modeling and remodeling, these cells provide an ideal target for both drug therapies and exercise to prevent bone fragility.
哈罗德·弗罗斯特首先提出骨骼中存在多个力学阈值,其中两个阈值决定了骨骼是增加还是减少骨质。近期来自骨生物学的证据有助于阐明骨细胞在确定这些力学阈值中的作用。具体而言,当机械刺激低于吸收阈值时,骨细胞会发生凋亡,随后出现骨吸收。相反,机械负荷可维持骨细胞的活力,因此不会出现骨质流失。当机械刺激大于常规刺激时,搏动性流体流动引起的骨细胞扰动会导致合成代谢因子的释放及随后的骨形成。骨细胞在响应机械环境变化时对骨重塑也起着关键作用。特别是,由于微损伤积累,骨细胞凋亡会导致废用性骨转换以及对大于常规机械刺激的反应。鉴于骨细胞在骨建模和重塑中的重要作用,这些细胞为预防骨脆性的药物治疗和运动提供了理想靶点。