• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

生命周期中再生能力的变化。

Changes in Regenerative Capacity through Lifespan.

作者信息

Yun Maximina H

机构信息

Institute of Structural and Molecular Biology, Division of Biosciences, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

Int J Mol Sci. 2015 Oct 23;16(10):25392-432. doi: 10.3390/ijms161025392.

DOI:10.3390/ijms161025392
PMID:26512653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4632807/
Abstract

Most organisms experience changes in regenerative abilities through their lifespan. During aging, numerous tissues exhibit a progressive decline in homeostasis and regeneration that results in tissue degeneration, malfunction and pathology. The mechanisms responsible for this decay are both cell intrinsic, such as cellular senescence, as well as cell-extrinsic, such as changes in the regenerative environment. Understanding how these mechanisms impact on regenerative processes is essential to devise therapeutic approaches to improve tissue regeneration and extend healthspan. This review offers an overview of how regenerative abilities change through lifespan in various organisms, the factors that underlie such changes and the avenues for therapeutic intervention. It focuses on established models of mammalian regeneration as well as on models in which regenerative abilities do not decline with age, as these can deliver valuable insights for our understanding of the interplay between regeneration and aging.

摘要

大多数生物体在其生命周期中都会经历再生能力的变化。在衰老过程中,许多组织的稳态和再生能力逐渐下降,导致组织退化、功能失常和病理变化。造成这种衰退的机制既有细胞内在的,如细胞衰老,也有细胞外在的,如再生环境的变化。了解这些机制如何影响再生过程对于设计改善组织再生和延长健康寿命的治疗方法至关重要。本综述概述了各种生物体的再生能力如何随生命周期变化、导致这种变化的因素以及治疗干预的途径。它重点关注已确立的哺乳动物再生模型以及再生能力不会随年龄下降的模型,因为这些模型可以为我们理解再生与衰老之间的相互作用提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/3da0569c1f9a/ijms-16-25392-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/7a70e67849c8/ijms-16-25392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/d7af1b23fa4f/ijms-16-25392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/e1460ed51e8b/ijms-16-25392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/90303c48f8ab/ijms-16-25392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/3da0569c1f9a/ijms-16-25392-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/7a70e67849c8/ijms-16-25392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/d7af1b23fa4f/ijms-16-25392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/e1460ed51e8b/ijms-16-25392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/90303c48f8ab/ijms-16-25392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b25b/4632807/3da0569c1f9a/ijms-16-25392-g005.jpg

相似文献

1
Changes in Regenerative Capacity through Lifespan.生命周期中再生能力的变化。
Int J Mol Sci. 2015 Oct 23;16(10):25392-432. doi: 10.3390/ijms161025392.
2
Hallmarks of aging Drosophila intestinal stem cells.衰老的果蝇肠道干细胞的特征。
Mech Ageing Dev. 2020 Sep;190:111285. doi: 10.1016/j.mad.2020.111285. Epub 2020 Jun 13.
3
Metabolic regulation of stem cell function in tissue homeostasis and organismal ageing.组织稳态和机体衰老过程中干细胞功能的代谢调控。
Nat Cell Biol. 2016 Aug;18(8):823-32. doi: 10.1038/ncb3385. Epub 2016 Jul 18.
4
Rejuvenating aged stem cells: therapeutic strategies to extend health and lifespan.延缓衰老的干细胞:延长健康和寿命的治疗策略。
FEBS Lett. 2024 Nov;598(22):2776-2787. doi: 10.1002/1873-3468.14865. Epub 2024 Apr 11.
5
Aging, metabolism and stem cells: Spotlight on muscle stem cells.衰老、新陈代谢与干细胞:聚焦肌肉干细胞
Mol Cell Endocrinol. 2017 Apr 15;445:109-117. doi: 10.1016/j.mce.2016.08.021. Epub 2016 Aug 12.
6
Intestinal Stem Cell Aging: Origins and Interventions.肠道干细胞衰老:起源与干预。
Annu Rev Physiol. 2020 Feb 10;82:203-226. doi: 10.1146/annurev-physiol-021119-034359. Epub 2019 Oct 14.
7
Canonical Wnt Signaling Ameliorates Aging of Intestinal Stem Cells.经典Wnt信号通路可改善肠道干细胞衰老。
Cell Rep. 2017 Mar 14;18(11):2608-2621. doi: 10.1016/j.celrep.2017.02.056.
8
Interaction between epigenetic and metabolism in aging stem cells.衰老干细胞中表观遗传学与新陈代谢之间的相互作用。
Curr Opin Cell Biol. 2017 Apr;45:1-7. doi: 10.1016/j.ceb.2016.12.009. Epub 2017 Jan 24.
9
Muscle stem cell aging: identifying ways to induce tissue rejuvenation.肌肉干细胞衰老:寻找诱导组织再生的方法。
Mech Ageing Dev. 2020 Jun;188:111246. doi: 10.1016/j.mad.2020.111246. Epub 2020 Apr 18.
10
Highly regenerative species-specific genes improve age-associated features in the adult Drosophila midgut.高度再生的种特异性基因可改善成年果蝇肠道的与年龄相关的特征。
BMC Biol. 2024 Aug 2;22(1):157. doi: 10.1186/s12915-024-01956-4.

引用本文的文献

1
Endothelin B receptor inhibition rescues aging-dependent neuronal regenerative decline.内皮素B受体抑制可挽救衰老相关的神经元再生衰退。
Elife. 2025 Sep 9;13:RP100217. doi: 10.7554/eLife.100217.
2
Unlocking longevity through the comparative biology of aging.通过衰老的比较生物学解锁长寿之道。
Nat Aging. 2025 Aug 28. doi: 10.1038/s43587-025-00945-8.
3
The evolution of cancer and ageing: a history of constraint.癌症与衰老的演变:一部受限史。

本文引用的文献

1
Current advances in tissue repair and regeneration: the future is bright.组织修复与再生的当前进展:前景光明。
Regeneration (Oxf). 2015 Apr 23;2(2):84-91. doi: 10.1002/reg2.30. eCollection 2015 Apr.
2
Experimentally induced metamorphosis in axolotls reduces regenerative rate and fidelity.实验诱导蝾螈变态会降低其再生速度和保真度。
Regeneration (Oxf). 2014 Feb 20;1(1):2-14. doi: 10.1002/reg2.8. eCollection 2014 Feb.
3
Aging-Dependent Demethylation of Regulatory Elements Correlates with Chromatin State and Improved β Cell Function.
Nat Rev Cancer. 2025 Aug 26. doi: 10.1038/s41568-025-00861-4.
4
Regeneration and Musculature in Halved Ephyrae.半叶碟状幼体的再生与肌肉组织
Integr Org Biol. 2025 Jul 26;7(1):obaf030. doi: 10.1093/iob/obaf030. eCollection 2025.
5
Disrupted macrophage metabolic adaptation and function drive senescence-induced decline in vertebrate regeneration.巨噬细胞代谢适应和功能的破坏驱动衰老诱导的脊椎动物再生能力下降。
Theranostics. 2025 Jun 20;15(15):7308-7326. doi: 10.7150/thno.111352. eCollection 2025.
6
Analysis of cell turnover in the macula densa through the normal aging process.通过正常衰老过程分析致密斑中的细胞更新。
Biomed Rep. 2025 Jul 21;23(3):155. doi: 10.3892/br.2025.2033. eCollection 2025 Sep.
7
Mapping Small Extracellular Vesicle Secretion Potential in Healthy Human Gingiva Using Spatial Transcriptomics.利用空间转录组学绘制健康人牙龈中小细胞外囊泡的分泌潜能
Curr Issues Mol Biol. 2025 Apr 7;47(4):256. doi: 10.3390/cimb47040256.
8
Gene therapy strategies for aging intervention.衰老干预的基因治疗策略。
Cell Insight. 2025 May 23;4(4):100254. doi: 10.1016/j.cellin.2025.100254. eCollection 2025 Aug.
9
Cellular and Molecular Interactions in CNS Injury: The Role of Immune Cells and Inflammatory Responses in Damage and Repair.中枢神经系统损伤中的细胞与分子相互作用:免疫细胞及炎症反应在损伤与修复中的作用
Cells. 2025 Jun 18;14(12):918. doi: 10.3390/cells14120918.
10
Endothelin B receptor inhibition rescues aging-dependent neuronal regenerative decline.内皮素B受体抑制可挽救衰老依赖性神经元再生衰退。
bioRxiv. 2025 Jun 9:2024.06.08.597928. doi: 10.1101/2024.06.08.597928.
调控元件的衰老依赖性去甲基化与染色质状态及改善的β细胞功能相关。
Cell Metab. 2015 Oct 6;22(4):619-32. doi: 10.1016/j.cmet.2015.07.025. Epub 2015 Aug 27.
4
Increased Stiffness in Aged Skeletal Muscle Impairs Muscle Progenitor Cell Proliferative Activity.衰老骨骼肌中增加的僵硬会损害肌肉祖细胞的增殖活性。
PLoS One. 2015 Aug 21;10(8):e0136217. doi: 10.1371/journal.pone.0136217. eCollection 2015.
5
Nerves Regulate Cardiomyocyte Proliferation and Heart Regeneration.神经调节心肌细胞增殖和心脏再生。
Dev Cell. 2015 Aug 24;34(4):387-99. doi: 10.1016/j.devcel.2015.06.017. Epub 2015 Aug 6.
6
Leg regeneration is epigenetically regulated by histone H3K27 methylation in the cricket Gryllus bimaculatus.在双斑蟋中,腿部再生受组蛋白H3K27甲基化的表观遗传调控。
Development. 2015 Sep 1;142(17):2916-27. doi: 10.1242/dev.122598. Epub 2015 Aug 7.
7
Macrophages decide between regeneration and fibrosis in muscle.巨噬细胞在肌肉中决定是再生还是纤维化。
Trends Endocrinol Metab. 2015 Sep;26(9):449-50. doi: 10.1016/j.tem.2015.07.005. Epub 2015 Aug 4.
8
Stem Cells and Aging: What's Next?干细胞与衰老:接下来会怎样?
Cell Stem Cell. 2015 Jun 4;16(6):578-81. doi: 10.1016/j.stem.2015.05.005.
9
Reactive Oxygen Species in Planarian Regeneration: An Upstream Necessity for Correct Patterning and Brain Formation.涡虫再生中的活性氧:正确模式形成和脑形成的上游必要条件
Oxid Med Cell Longev. 2015;2015:392476. doi: 10.1155/2015/392476. Epub 2015 Jun 9.
10
MTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation.mTOR通过促进IL1A翻译来调节促肿瘤的衰老相关分泌表型。
Nat Cell Biol. 2015 Aug;17(8):1049-61. doi: 10.1038/ncb3195. Epub 2015 Jul 6.