Stem Cell Res Ther. 2013;4(5):107. doi: 10.1186/scrt318.
Bones adapt to accommodate the physical forces they experience through changes in architecture and mass. Stem cells differentiate into bone-forming osteoblasts, and mechanical stimulation is involved in this process. Various studies have applied controlled mechanical stimulation to stem cells and investigated the effects on osteogenic lineage commitment. These studies demonstrate that physical stimuli can induce osteogenic lineage commitment. Tension, fluid shear stress, substrate material properties, and cell shape are all factors that influence osteogenic differentiation. In particular, the level of tension is important. Also, rigid substrates with stiffness similar to collagenous bone induce osteogenic differentiation, while softer substrates induce other lineages. Finally, cells allowed to adhere over a larger area are able to differentiate towards the osteogenic lineage while cells adhering to a smaller area are restricted to the adipogenic lineage. Stem cells are able to sense their mechanical environments through various mechanosensors, including the cytoskeleton, focal adhesions, and primary cilia. The cytoskeleton provides a structural frame for the cell, and myosin interacts with actin to generate cytoskeletal tension, which is important for mechanically induced osteogenesis of stem cells. Adapter proteins link the cytoskeleton to integrins, which attach the cell to the substrate, forming a focal adhesion. A variety of signaling proteins are also associated with focal adhesions. Forces are transmitted to the substrate at these sites, and an intact focal adhesion is important for mechanically induced osteogenesis. The primary cilium is a single, immotile, antenna-like structure that extends from the cell into the extracellular space. It has emerged as an important signaling center, acting as a microdomain to facilitate biochemical signaling. Mechanotransduction is the process by which physical stimuli are converted into biochemical responses. When potential mechanosensors are disrupted, the activities of components of mechanotransduction pathways are also inhibited, preventing mechanically induced osteogenesis. Calcium, mitogen-activated protein kinase/extracellular signal-regulated kinase, Wnt, Yes-associated protein/transcriptional coactivator with PDZ-binding motif and RhoA/Rho kinase signaling are some of the mechanotransduction pathways proposed to be important. In this review, types of mechanical stimuli, mechanosensors, and key pathways involved in mechanically induced osteogenesis of stem cells are discussed.
骨骼通过改变其结构和质量来适应所承受的物理力。干细胞分化为成骨细胞,机械刺激参与了这一过程。各种研究已经将受控的机械刺激应用于干细胞,并研究了其对成骨谱系定向的影响。这些研究表明,物理刺激可以诱导成骨谱系定向。张力、流体切应力、基底材料特性和细胞形状都是影响成骨分化的因素。特别是,张力水平很重要。此外,具有类似于胶原骨的刚度的刚性基底诱导成骨分化,而较软的基底则诱导其他谱系。最后,允许在更大面积上附着的细胞能够向成骨谱系分化,而附着在较小面积上的细胞则被限制在成脂谱系中。干细胞能够通过各种机械感受器感知其机械环境,包括细胞骨架、黏附斑和初级纤毛。细胞骨架为细胞提供了一个结构框架,肌球蛋白与肌动蛋白相互作用产生细胞骨架张力,这对于干细胞的机械诱导成骨非常重要。衔接蛋白将细胞骨架与整合素连接起来,整合素将细胞附着在基底上,形成黏附斑。各种信号转导蛋白也与黏附斑相关。力在这些部位传递到基底,完整的黏附斑对于机械诱导的成骨非常重要。初级纤毛是从细胞延伸到细胞外空间的单一、非运动、天线状结构。它已成为一个重要的信号中心,作为一个微域促进生化信号。机械转导是将物理刺激转化为生化反应的过程。当潜在的机械感受器被破坏时,机械转导途径的组成部分的活动也被抑制,从而阻止机械诱导的成骨。钙、丝裂原激活的蛋白激酶/细胞外信号调节激酶、Wnt、Yes 相关蛋白/转录共激活因子与 PDZ 结合基序和 RhoA/Rho 激酶信号转导是一些被认为重要的机械转导途径。在这篇综述中,讨论了机械刺激的类型、干细胞机械诱导成骨中的机械感受器和关键途径。