机械代谢轴通过BMP/Smad对亲环蛋白D的调控作用参与线粒体反应。

IF 20.1 1区 医学 Q1 CELL & TISSUE ENGINEERING
Rubens Sautchuk, Josaranie Nieves Santana, Chen Yu, Hani Awad, Roman A Eliseev
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引用次数: 0

摘要

机械刺激是包括骨在内的各种组织合成代谢的基础。重要的是,机械刺激已被证明可以诱导细胞代谢的重编程,可能调整它以增加合成代谢。机械代谢轴内的信号转导尚不完全清楚。为了描述这种信号转导,我们将骨祖细胞暴露在流体剪切应力(FSS)下,并评估细胞信号传导和生物能量学。BMP/Smad通路被机械应力激活,我们确实通过FSS检测到了它的激活。我们之前报道过BMP下调亲环蛋白D (CypD),这是线粒体通透性过渡孔(MPTP)的开启器。下调CypD/MPTP可改善线粒体内膜完整性,从而改善氧化功能。我们发现,在fss刺激的细胞中,CypD确实下调,线粒体以bmp依赖的方式被激活。同时,FSS的成骨作用依赖于CypD下调和线粒体反应。为了在体内验证我们的体外结果,我们优化了一种新的小鼠拔牙介导的颅面骨卸载模型。这种卸载导致骨丢失和受影响骨中CypD的上调。CypD的成骨细胞特异性缺失可防止卸载介导的骨质流失,而CypD在这些小鼠中的重新表达可恢复骨质流失。总之,我们在这里提出了新的证据,表明成骨细胞的机械代谢轴涉及BMP/ smad介导的CypD和CypD依赖性线粒体反应的下调。这种调节对于机械刺激的骨合成代谢作用是重要的。我们的数据还表明,靶向CypD可以有效预防由于不动、太空飞行或拔牙引起的骨质流失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechano-metabolic axis involves mitochondrial responses via BMP/Smad regulatory effect on cyclophilin D.

Mechanical stimulation is fundamental for anabolism in various tissues, including bone. Importantly, mechanical stimulation has been shown to induce reprogramming of cell metabolism, likely to adjust it to increased anabolism. The signal transduction within this mechano-metabolic axis is incompletely understood. Aiming to delineate such signal transduction, we exposed osteoprogenitors to fluid shear stress (FSS) and assessed cell signaling and bioenergetics. The BMP/Smad pathway is known to be activated by mechanical stress, and we indeed detected its activation by FSS. We previously reported that BMP downregulates cyclophilin D (CypD), an opener of the mitochondrial permeability transition pore (MPTP). Downregulation of CypD/MPTP improves mitochondrial inner membrane integrity and therefore oxidative function. We found that in FSS-stimulated cells, CypD was indeed downregulated and mitochondria were activated in a BMP-dependent manner. Meanwhile, the osteogenic effect of FSS was dependent on CypD downregulation and mitochondrial responses. To confirm our in vitro results in vivo, we optimized a novel model of tooth extraction-mediated unloading of craniofacial bones in mice. Such unloading led to bone loss and upregulation of CypD in the affected bone. Osteoblast-specific deletion of CypD protected against unloading-mediated bone loss, while CypD re-expression in these mice restored bone loss. In sum, we here present new evidence that the mechano-metabolic axis in osteogenic cells involves BMP/Smad-mediated downregulation of CypD and CypD-dependent mitochondrial responses. Such regulation is important for the osteoanabolic effect of mechanical stimulation. Our data also suggest that targeting CypD can be an effective strategy to prevent bone loss caused by unloading due to immobility, space flight, or tooth extraction.

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来源期刊
Bone Research
Bone Research CELL & TISSUE ENGINEERING-
CiteScore
20.00
自引率
4.70%
发文量
289
审稿时长
20 weeks
期刊介绍: Established in 2013, Bone Research is a newly-founded English-language periodical that centers on the basic and clinical facets of bone biology, pathophysiology, and regeneration. It is dedicated to championing key findings emerging from both basic investigations and clinical research concerning bone-related topics. The journal's objective is to globally disseminate research in bone-related physiology, pathology, diseases, and treatment, contributing to the advancement of knowledge in this field.
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