静止区甲状旁腺激素相关蛋白的表达时间影响继发性骨化过程中生长板的维持:一项计算研究。

IF 3 3区 医学 Q2 BIOPHYSICS
Jorik Stoop, Yuka Yokoyama, Taiji Adachi
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引用次数: 0

摘要

二次骨化和生长板的维持是长骨形成的关键环节。甲状旁腺激素相关蛋白(PTHrP)被认为是维持生长板的关键因素,研究表明,静止区 PTHrP 的表达与二次骨化中心(SOC)的形成密切相关。然而,静止区 PTHrP 表达与生长板保存之间关系的细节仍不清楚。在本研究中,我们旨在利用计算方法研究静息区 PTHrP 表达对生长板维持的作用。我们扩展了现有的基于连续粒子的组织形态发生模型,将 PTHrP 和印度刺猬(Ihh)信号纳入其中,使该模型能够捕捉到单个细胞活动的生化和机械调控。我们的模型表明,静止区 PTHrP 的表达时间--特别是 SOC 形成之初的分泌增加率--可能是维持生长板的关键机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Timing of resting zone parathyroid hormone-related protein expression affects maintenance of the growth plate during secondary ossification: a computational study.

Secondary ossification and maintenance of the growth plate are crucial aspects of long bone formation. Parathyroid hormone-related protein (PTHrP) has been implicated as a key factor in maintaining the growth plate, and studies suggest that PTHrP expression in the resting zone is closely related with formation of the secondary ossification center (SOC). However, details of the relationship between resting zone PTHrP expression and preservation of the growth plate remain unclear. In this study, we aim to investigate the role of resting zone PTHrP expression on maintenance of the growth plate using a computational method. We extend an existing continuum-based particle model of tissue morphogenesis to include PTHrP and Indian hedgehog (Ihh) signaling, allowing the model to capture biochemical and mechanical regulation of individual cell activities. Our model indicates that the timing of resting zone PTHrP expression-specifically the rate of increase in production at the onset of SOC formation-is potentially a crucial mechanism for maintenance of the growth plate.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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