Dayal Anuhya, Gray Mark, Vallejo Julian A, Lara-Castillo Nuria, Johnson Mark L, Wacker Michael J
Department of Biomedical Sciences, School of Medicine, University of Missouri-Kansas City, Kansas City, Missouri, United States.
Department of Oral & Craniofacial Sciences, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri, United States.
Am J Physiol Regul Integr Comp Physiol. 2025 May 1;328(5):R591-R600. doi: 10.1152/ajpregu.00287.2024. Epub 2025 Mar 26.
The skeleton is in complex interplay with the other systems of the body and is highly responsive to input from the external environment. Bone mechanical loading results in interstitial fluid flow via the lacunar-canalicular system, generating fluid flow sheer stress (FFSS). FFSS variably stresses osteocytes, subsequently causing the release of metabolites and protein factors that function locally to increase bone formation and may play a role in cross talk between various organ systems, for instance between bone and skeletal muscle. Therefore, we hypothesized that this cross talk includes altering cardiac function. To test this hypothesis, media conditioned by MLO-Y4 osteocyte-like cell culture line under FFSS was used to model the endocrine effects of bone during mechanical loading on contraction of ex vivo Langendorf-perfused isolated hearts. When hearts were externally paced at a fixed rate, FFSS osteocyte conditioned media (CM) induced significant premature contractions compared with vehicle (control). FFSS osteocyte CM administration to self-paced hearts increased total contraction force by 31%. To determine whether the mechanism involved intracellular Ca, vehicle and FFSS bone CM were perfused over cultured H9C2 cardiomyocytes while undergoing Ca imaging using Fluo-8. We observed an increase in intracellular Ca with FFSS CM perfusion of cardiomyocytes compared with vehicle. These increases were only present with exogenous electrical pacing. Our findings demonstrate that FFSS bone CM enhances cardiac contractility by increasing intracellular cardiomyocyte Ca. The results obtained in this study suggest that the skeleton, responding to mechanical strain, has the potential to augment cardiac output and provide evidence for bone-heart cross talk. The skeletal system operates as an endocrine organ, releasing factors that impact multi-tissue physiology. The results obtained in this study demonstrate that conditioned media collected from MLO-Y4 osteocytes exposed to fluid flow shear stress increases cardiomyocyte intracellular calcium and enhances cardiac contractility in vitro. These results support the concept of bone-heart cross talk that may have implications in exercise training, reduced-function settings such as bedrest, and the interplay between bone and heart health.
骨骼与身体的其他系统存在复杂的相互作用,并且对来自外部环境的输入具有高度响应性。骨骼机械负荷通过腔隙-小管系统导致组织液流动,产生流体流动切应力(FFSS)。FFSS以可变方式使骨细胞受力,随后导致代谢物和蛋白质因子的释放,这些物质在局部发挥作用以增加骨形成,并且可能在各种器官系统之间的相互作用中发挥作用,例如在骨骼和骨骼肌之间。因此,我们推测这种相互作用包括改变心脏功能。为了验证这一假设,我们使用在FFSS条件下由MLO-Y4骨细胞样细胞系培养的培养基来模拟机械负荷期间骨骼对离体Langendorf灌注的分离心脏收缩的内分泌作用。当心脏以固定速率进行外部起搏时,与载体(对照)相比,FFSS骨细胞条件培养基(CM)诱导了显著的早搏。将FFSS骨细胞CM给予自主起搏的心脏可使总收缩力增加31%。为了确定该机制是否涉及细胞内钙,在使用Fluo-8进行钙成像时,将载体和FFSS骨CM灌注到培养的H9C2心肌细胞上。与载体相比,我们观察到在心肌细胞灌注FFSS CM时细胞内钙增加。这些增加仅在外源性电起搏时出现。我们的研究结果表明,FFSS骨CM通过增加心肌细胞内钙来增强心脏收缩力。本研究获得的结果表明,对机械应变作出反应的骨骼有可能增加心输出量,并为骨-心相互作用提供证据。骨骼系统作为一个内分泌器官发挥作用,释放影响多组织生理学的因子。本研究获得的结果表明,从暴露于流体流动切应力的MLO-Y4骨细胞收集的条件培养基在体外增加心肌细胞内钙并增强心脏收缩力。这些结果支持了骨-心相互作用的概念,这可能对运动训练、诸如卧床休息等高功能减退情况以及骨骼与心脏健康之间的相互作用具有重要意义。