端粒酶缺陷斑马鱼衰老模型可通过MMP抑制恢复肌肉再生。

IF 7.1 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-09-25 DOI:10.1111/acel.70238
Yue Yuan, Carlene Dyer, Robert D Knight
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引用次数: 0

摘要

衰老会逐渐损害骨骼肌的再生,导致行动能力下降和生活质量下降。虽然肌肉老化背后的分子变化已经被很好地表征,但它们对再生过程中肌肉干细胞(muSC)行为的影响仍然知之甚少。在这里,我们利用端粒酶缺陷tert突变斑马鱼幼虫作为加速衰老的体内模型,对肌肉损伤后的muSC动态进行实时分析。我们证明,tert突变体中衰老样炎症环境破坏muSC迁移,损害激活和增殖,并损害再生能力。我们进一步表明,由持续巨噬细胞存在和基质金属蛋白酶(MMP)活性升高介导的持续炎症限制了muSC的募集和迁移效率。MMP9/13活性的药理抑制和巨噬细胞的基因消耗部分恢复了muSC的迁移行为和再生结果。值得注意的是,我们证明了muSC迁移动力学与再生成功相关,为治疗筛选提供了功能读数。我们的研究结果揭示斑马鱼突变体提供了一个易于处理的系统,用于解剖与年龄相关的细胞行为变化和识别返老还衰干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Muscle Regeneration Can Be Rescued in a Telomerase Deficient Zebrafish Model of Ageing by MMP Inhibition.

Ageing progressively impairs skeletal muscle regeneration, contributing to reduced mobility and quality of life. While the molecular changes underlying muscle ageing have been well characterised, their impact on muscle stem cell (muSC) behaviour during regeneration remains poorly understood. Here, we leverage telomerase-deficient tert mutant zebrafish larvae as an in vivo model of accelerated ageing to perform real-time analysis of muSC dynamics following muscle injury. We demonstrate that the ageing-like inflammatory environment in tert mutant disrupts muSC migration, impairs activation and proliferation, and compromises regenerative capacity. We further show that sustained inflammation, mediated by persistent macrophage presence and elevated matrix metalloproteinase (MMP) activity, limits muSC recruitment and migration efficiency. Pharmacological inhibition of MMP9/13 activity and genetic depletion of macrophages partially restore muSC migratory behaviour and regenerative outcomes. Notably, we demonstrate that muSC migration dynamics correlate with regenerative success, providing a functional readout for therapeutic screening. Our findings reveal zebrafish tert mutants offer a tractable system for dissecting age-associated changes to cell behaviour and for identifying rejuvenation interventions.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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