Ganesh Thiagarajan, Laughrey Loretta E, Niroobakhsh Mohammadmehdi, Lara-Castillo Nuria
Department of Civil and Mechanical Engineering, University of Missouri-Kansas City, 350L Flarsheim Hall, 5100 Rockhill Road, Kansas City, MO 64110, United States of America.
Department of Civil and Mechanical Engineering, University of Missouri-Kansas City, 350L Flarsheim Hall, 5100 Rockhill Road, Kansas City, MO 64110, United States of America.
Bone. 2020 Aug;137:115328. doi: 10.1016/j.bone.2020.115328. Epub 2020 Mar 20.
Osteocytes form over 90% of the bone cells and are postulated to be mechanosensors responsible for regulating the function of osteoclasts and osteoblasts in bone modeling and remodeling. Physical activity results in mechanical loading on the bones. Osteocytes are thought to be the main mechanosensory cells in bone. Upon load osteocytes secrete key factors initiating downstream signaling pathways that regulate skeletal metabolism including the Wnt/β-catenin signaling pathway. Osteocytes have dendritic structures and are housed in the lacunae and canaliculi within the bone matrix. Mechanical loading is known to have two primary effects, namely a mechanical strain (membrane disruption by stretching) on the lacunae/cells, and fluid flow, in the form of fluid flow shear stress (FFSS), in the space between the cell membranes and the lacuna-canalicular walls. In response, osteocytes get activated via a process called mechanotransduction in which mechanical signals are transduced to biological responses. The study of mechanotransduction is a complex subject involving principles of engineering mechanics as well as biological signaling pathway studies. Several length scales are involved as the mechanical loading on macro sized bones are converted to strain and FFSS responses at the micro-cellular level. Experimental measurements of strain and FFSS at the cellular level are very difficult and correlating them to specific biological activity makes this a very challenging task. One of the methods commonly adopted is a multi-scale approach that combines biological and mechanical experimentation with in silico numerical modeling of the engineering aspects of the problem. Finite element analysis along with fluid-structure interaction methodologies are used to compute the mechanical strain and FFSS. These types of analyses often involve a multi-length scale approach where models of both the macro bone structure and micro structure at the cellular length scale are used. Imaging modalities play a crucial role in the development of the models and present their own challenges. This paper reviews the efforts of various research groups in addressing this problem and presents the work in our research group. A clear understanding of how mechanical stimuli affect the lacunae and perilacunar tissue strains and shear stresses on the cellular membranes may ultimately lead to a better understanding of the process of osteocyte activation.
骨细胞构成了超过90%的骨细胞,据推测它们是机械传感器,负责在骨建模和重塑过程中调节破骨细胞和成骨细胞的功能。身体活动会导致骨骼受到机械负荷。骨细胞被认为是骨骼中的主要机械感觉细胞。在负荷作用下,骨细胞分泌关键因子,启动下游信号通路,调节包括Wnt/β-连环蛋白信号通路在内的骨骼代谢。骨细胞具有树突状结构,位于骨基质内的腔隙和小管中。已知机械负荷有两个主要作用,即在腔隙/细胞上产生机械应变(通过拉伸破坏膜),以及在细胞膜与腔隙-小管壁之间的空间中以流体流动剪切应力(FFSS)的形式产生流体流动。作为响应,骨细胞通过一种称为机械转导的过程被激活,在这个过程中,机械信号被转化为生物学反应。机械转导的研究是一个复杂的课题,涉及工程力学原理以及生物学信号通路研究。由于宏观尺寸骨骼上的机械负荷在微观细胞水平上转化为应变和FFSS响应,涉及多个长度尺度。在细胞水平上对应变和FFSS进行实验测量非常困难,将它们与特定的生物学活性相关联是一项极具挑战性的任务。常用的方法之一是多尺度方法,该方法将生物学和机械实验与问题工程方面的计算机数值建模相结合。有限元分析以及流固相互作用方法用于计算机械应变和FFSS。这些类型的分析通常涉及多长度尺度方法,其中使用宏观骨结构和细胞长度尺度的微观结构模型。成像方式在模型开发中起着至关重要的作用,并且也带来了自身的挑战。本文回顾了各个研究小组在解决这个问题上所做的努力,并介绍了我们研究小组的工作。清楚地了解机械刺激如何影响腔隙和腔隙周围组织的应变以及细胞膜上的剪切应力,最终可能会更好地理解骨细胞激活过程。