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利用肌腱负荷动物模型为组织工程方法提供信息。

Leveraging animal models of tendon loading to inform tissue engineering approaches.

作者信息

Muscat Samantha, Nichols Anne E C

机构信息

Department of Pathology and Laboratory Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, United States.

Department of Orthopedics and Physical Performance, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, United States.

出版信息

Front Bioeng Biotechnol. 2024 Oct 7;12:1449372. doi: 10.3389/fbioe.2024.1449372. eCollection 2024.

DOI:10.3389/fbioe.2024.1449372
PMID:39434716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11491380/
Abstract

Tendon injuries disrupt successful transmission of force between muscle and bone, resulting in reduced mobility, increased pain, and significantly reduced quality of life for affected patients. There are currently no targeted treatments to improve tendon healing beyond conservative methods such as rest and physical therapy. Tissue engineering approaches hold great promise for designing instructive biomaterials that could improve tendon healing or for generating replacement graft tissue. More recently, engineered microphysiological systems to model tendon injuries have been used to identify therapeutic targets. Despite these advances, current tissue engineering efforts that aim to regenerate, replace, or model injured tendons have largely failed due in large part to a lack of understanding of how the mechanical environment of the tendon influences tissue homeostasis and how altered mechanical loading can promote or prevent disease progression. This review article draws inspiration from what is known about tendon loading from animal models and identifies key metrics that can be used to benchmark success in tissue engineering applications. Finally, we highlight important challenges and opportunities for the field of tendon tissue engineering that should be taken into consideration in designing engineered platforms to understand or improve tendon healing.

摘要

肌腱损伤会破坏肌肉与骨骼之间力的成功传递,导致活动能力下降、疼痛加剧,严重影响患者的生活质量。目前,除了休息和物理治疗等保守方法外,尚无针对性的治疗方法来促进肌腱愈合。组织工程方法有望设计出具有指导作用的生物材料,以改善肌腱愈合或生成替代移植组织。最近,用于模拟肌腱损伤的工程化微生理系统已被用于确定治疗靶点。尽管取得了这些进展,但目前旨在再生、替换或模拟损伤肌腱的组织工程努力在很大程度上仍未成功,这主要是因为对肌腱的力学环境如何影响组织稳态以及改变的机械负荷如何促进或阻止疾病进展缺乏了解。这篇综述文章从动物模型中已知的肌腱负荷知识中汲取灵感,确定了可用于衡量组织工程应用成功与否的关键指标。最后,我们强调了肌腱组织工程领域的重要挑战和机遇,在设计工程平台以了解或改善肌腱愈合时应予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/933d5dc537cc/fbioe-12-1449372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/0934dfe1a074/fbioe-12-1449372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/5c65b1e199cc/fbioe-12-1449372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/933d5dc537cc/fbioe-12-1449372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/0934dfe1a074/fbioe-12-1449372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/5c65b1e199cc/fbioe-12-1449372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f90/11491380/933d5dc537cc/fbioe-12-1449372-g003.jpg

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本文引用的文献

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Single nucleus and spatial transcriptomic profiling of healthy human hamstring tendon.健康人体腘绳肌腱的单细胞和空间转录组分析。
FASEB J. 2024 May 31;38(10):e23629. doi: 10.1096/fj.202300601RRR.
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Guidelines for ex vivo mechanical testing of tendon.肌腱的体外力学测试指南。
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CD206+ tendon resident macrophages and their potential crosstalk with fibroblasts and the ECM during tendon growth and maturation.CD206+肌腱驻留巨噬细胞及其在肌腱生长和成熟过程中与成纤维细胞和细胞外基质的潜在相互作用。
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Recent advances in tendon tissue engineering strategy.肌腱组织工程策略的最新进展。
Front Bioeng Biotechnol. 2023 Feb 20;11:1115312. doi: 10.3389/fbioe.2023.1115312. eCollection 2023.
5
Scleraxis-lineage cells are required for tendon homeostasis and their depletion induces an accelerated extracellular matrix aging phenotype.腱细胞系细胞对于维持腱组织的稳态是必需的,其耗竭会导致细胞外基质加速老化表型。
Elife. 2023 Jan 19;12:e84194. doi: 10.7554/eLife.84194.
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Defining the spatial-molecular map of fibrotic tendon healing and the drivers of Scleraxis-lineage cell fate and function.定义纤维化肌腱愈合的空间-分子图谱,以及 Scleraxis 谱系细胞命运和功能的驱动因素。
Cell Rep. 2022 Nov 22;41(8):111706. doi: 10.1016/j.celrep.2022.111706.
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Achilles Tendons Display Region-Specific Transcriptomic Signatures Associated With Distinct Mechanical Properties.跟腱表现出与不同力学特性相关的区域特异性转录组特征。
Am J Sports Med. 2022 Dec;50(14):3866-3874. doi: 10.1177/03635465221128589. Epub 2022 Oct 28.
8
CCR2 is expressed by tendon resident macrophage and T cells, while CCR2 deficiency impairs tendon healing via blunted involvement of tendon-resident and circulating monocytes/macrophages.CCR2 由肌腱驻留巨噬细胞和 T 细胞表达,而 CCR2 缺陷通过削弱肌腱驻留和循环单核细胞/巨噬细胞的参与来损害肌腱愈合。
FASEB J. 2022 Nov;36(11):e22607. doi: 10.1096/fj.202201162R.
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A Survey of Musculoskeletal Disorders in the Orthopaedic Surgeon: Identifying Injuries, Exacerbating Workplace Factors, and Treatment Patterns in the Orthopaedic Community.骨科医生肌肉骨骼疾病调查:识别损伤、加剧工作场所因素和骨科社区的治疗模式。
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Structure-function specialisation of the interfascicular matrix in the human achilles tendon.人跟腱腱束间基质的结构-功能特化。
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