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深度行为表型分析追踪小鼠胫骨骨折后的功能恢复情况。

Deep behavioral phenotyping tracks functional recovery following tibia fracture in mice.

作者信息

Layne Jonathan E, Snapper Dustin M, Czachor Molly E, Lam Charles, Matityahu Jacob D, Lind Dane R G, Huard Matthieu, Huard Johnny, Morioka Kazuhito, Motzkin Julian C, Basbaum Allan I, Weinrich Jarret A P, Bahney Chelsea S

机构信息

Department of Orthopaedic Surgery, UCSF Orthopaedic Trauma Institute, San Francisco, CA, United States.

Center for Regenerative Medicine, Steadman Philippon Research Institute, Vail, CO, United States.

出版信息

Front Physiol. 2025 Aug 26;16:1630155. doi: 10.3389/fphys.2025.1630155. eCollection 2025.

DOI:10.3389/fphys.2025.1630155
PMID:40933304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12417503/
Abstract

INTRODUCTION

An estimated 178 million fractures occur worldwide annually, with lower limb fractures showing high rates of poor healing, often resulting in reduced mobility and chronic pain. Bone healing and the ability to bear weight are closely tied to the mechanical stability of the fracture site. Although fracture stabilization is a well-established factor modulating bone repair, there remains a notable gap in sophisticated non-destructive technologies that can rapidly and objectively quantify functional recovery in preclinical settings. We introduce a novel behavioral phenotyping approach enabling rapid quantification of post-fracture weightbearing and kinematic metrics in freely behaving mice. Our goals were to identify and characterize metrics most indicative of fracture-induced behavioral impairment and to use these metrics to quantify how functional recovery is altered in mice with pin stabilized non-stabilized fractures. We also explore sex-specific contributions to recovery.

METHODS

Male and female C57BL6/J mice received mid-shaft tibial fractures that were either unstabilized or fixed with intramedullary pins; non-fractured mice served as controls. Behavioral recordings were acquired pre-fracture and throughout healing (5-35 days post-fracture). To track mice and analyze changes in paw pressure and kinematics, we performed machine learning-enabled behavioral phenotyping.

RESULTS

Overall, mice with pin-stabilized fractures exhibited less behavioral impairment than mice with unstabilized fractures. Pin stabilization allowed increased weightbearing and produced smaller changes in kinematic metrics. By contrast, we observed only minor sex-specific differences in impairment and recovery following fracture. Our analysis revealed that functional recovery is more complex than individual parameters viewed in isolation, with different parameters identifying distinct recovery timeframes. Therefore, we developed a comprehensive, unified graph theoretic metric encompassing all behavioral parameters. This unified approach confirmed increased severity in unstabilized fractures and identified clear functional recovery windows for both fracture groups.

DISCUSSION

This methodology forms a foundation for future mechanistic experiments focused on biological and mechanical variables influencing functional healing and enables more rapid testing of strategies to accelerate bone healing.

摘要

引言

全球每年估计发生1.78亿例骨折,下肢骨折愈合不良率很高,常导致活动能力下降和慢性疼痛。骨愈合和负重能力与骨折部位的机械稳定性密切相关。尽管骨折固定是调节骨修复的一个既定因素,但在能够快速、客观地量化临床前环境中功能恢复的先进无损技术方面仍存在显著差距。我们引入了一种新的行为表型分析方法,能够快速量化自由活动小鼠骨折后的负重和运动学指标。我们的目标是识别和表征最能指示骨折引起的行为损伤的指标,并使用这些指标来量化髓内针固定或未固定骨折小鼠的功能恢复如何改变。我们还探讨了性别对恢复的影响。

方法

雄性和雌性C57BL6/J小鼠接受胫骨中段骨折,骨折要么不固定,要么用髓内针固定;未骨折的小鼠作为对照。在骨折前和整个愈合过程(骨折后5 - 35天)进行行为记录。为了跟踪小鼠并分析爪压力和运动学的变化,我们进行了基于机器学习的行为表型分析。

结果

总体而言,髓内针固定骨折的小鼠比未固定骨折的小鼠表现出的行为损伤更少。髓内针固定使负重增加,运动学指标变化更小。相比之下,我们观察到骨折后损伤和恢复方面只有轻微的性别差异。我们的分析表明,功能恢复比单独查看的单个参数更复杂,不同参数识别出不同的恢复时间框架。因此,我们开发了一种包含所有行为参数的综合统一的图论指标。这种统一方法证实了未固定骨折的严重程度增加,并确定了两个骨折组明确的功能恢复窗口。

讨论

这种方法为未来关注影响功能愈合的生物学和力学变量的机制实验奠定了基础,并能够更快地测试加速骨愈合的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/dc3a36d93208/fphys-16-1630155-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/d66c0446f615/fphys-16-1630155-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/dc3a36d93208/fphys-16-1630155-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/d66c0446f615/fphys-16-1630155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/647eec28553f/fphys-16-1630155-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/d12c4dcfca6f/fphys-16-1630155-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/8405ad7be266/fphys-16-1630155-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e6/12417503/dc3a36d93208/fphys-16-1630155-g005.jpg

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