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衰老治疗递送的最新进展

Recent Advances in Senotherapeutics Delivery.

机构信息

Tissue Engineering and Biomaterials Laboratory, Fischell Department of Bioengineering, A. James Clark School of Engineering, University of Maryland, College Park, Maryland, USA.

NIBIB/NIH Center of Engineering Complex Tissues, University of Maryland, College Park, Maryland, USA.

出版信息

Tissue Eng Part B Rev. 2022 Dec;28(6):1223-1234. doi: 10.1089/ten.TEB.2021.0212. Epub 2022 Jul 12.

DOI:10.1089/ten.TEB.2021.0212
PMID:35451328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9805860/
Abstract

Accumulation of senescent cells (SnCs) in various tissue types has been connected to an occurrence of different age-related diseases that are indicated by its own tissue-specific hallmarks. Discovery of novel senolytic compounds that target major cellular mechanisms to inhibit the level of SnCs within the specific tissues or organs has been an emerging field in the age-related disease research. Although the positive effect of senolytics in global suppression of SnCs has been well studied in the past, effective tissue-specific delivery strategy of senotherapeutics before clinical application needs to be further investigated. In this review, we discuss the latest biological insights to currently available senotherapeutic options and explore the impactful tissue-engineered models possibly as a testbed for replicable testing of tissue-specific potency of senolytics. Impact statement Senotherapy, the inhibition of accumulated senescent cells, is recognized as a significantly impactful way to treat various human diseases. However, there is limited comprehensive reviews on this topic. This review provides in-depth discussion on diverse delivery strategies of senolytic agents and latest updates on a novel senotherapeutic research.

摘要

衰老细胞 (SnC) 在各种组织类型中的积累与不同的与年龄相关的疾病的发生有关,这些疾病具有其自身的组织特异性特征。发现针对主要细胞机制的新型衰老细胞选择性杀伤化合物,以抑制特定组织或器官中衰老细胞的水平,这是与年龄相关的疾病研究中的一个新兴领域。尽管过去已经很好地研究了衰老细胞选择性杀伤化合物在全球抑制衰老细胞方面的积极作用,但在临床应用之前,还需要进一步研究有效的组织特异性衰老治疗药物输送策略。在这篇综述中,我们讨论了当前可用的衰老治疗选择的最新生物学见解,并探讨了有影响力的组织工程模型,作为可复制测试衰老细胞选择性杀伤化合物的组织效力的试验台。 影响评估 衰老细胞抑制疗法,即抑制积累的衰老细胞,被认为是治疗各种人类疾病的一种非常有影响力的方法。然而,关于这个主题的综合评论非常有限。本综述深入讨论了衰老细胞选择性杀伤化合物的多种输送策略,以及衰老治疗研究的最新进展。

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Microfluidic Separation of Canine Adipose-Derived Mesenchymal Stromal Cells.微流控分离犬脂肪间充质基质细胞。
Tissue Eng Part C Methods. 2021 Aug;27(8):445-461. doi: 10.1089/ten.TEC.2021.0082.
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Extracellular vesicle mediated feto-maternal HMGB1 signaling induces preterm birth.细胞外囊泡介导的胎-母 HMGB1 信号诱导早产。
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Netrin-4 expression by human endothelial cells inhibits endothelial inflammation and senescence.人内皮细胞表达轴突导向因子 4 抑制内皮细胞炎症和衰老。
Int J Biochem Cell Biol. 2021 May;134:105960. doi: 10.1016/j.biocel.2021.105960. Epub 2021 Feb 23.
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Building Scaffolds for Tubular Tissue Engineering.用于管状组织工程的构建支架
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Cellular senescence contributes to radiation-induced hyposalivation by affecting the stem/progenitor cell niche.细胞衰老通过影响干细胞/祖细胞龛来导致辐射诱导的唾液分泌减少。
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A 3D-Bioprinted dual growth factor-releasing intervertebral disc scaffold induces nucleus pulposus and annulus fibrosus reconstruction.一种3D生物打印的双生长因子释放椎间盘支架可诱导髓核和纤维环重建。
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Aurora-A/SOX8/FOXK1 signaling axis promotes chemoresistance via suppression of cell senescence and induction of glucose metabolism in ovarian cancer organoids and cells.极光激酶 A/性别决定区 Y 框蛋白 8/叉头框转录因子 K1 信号轴通过抑制卵巢癌细胞球体和细胞衰老及诱导葡萄糖代谢促进化疗耐药性。
Theranostics. 2020 May 25;10(15):6928-6945. doi: 10.7150/thno.43811. eCollection 2020.
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Senescent Cells in Cancer Therapy: Friends or Foes?衰老细胞在癌症治疗中的作用:朋友还是敌人?
Trends Cancer. 2020 Oct;6(10):838-857. doi: 10.1016/j.trecan.2020.05.004. Epub 2020 May 29.
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Tissue engineering to better understand senescence: Organotypics come of age.组织工程学以更好地了解衰老:器官型培养技术日趋成熟。
Mech Ageing Dev. 2020 Sep;190:111261. doi: 10.1016/j.mad.2020.111261. Epub 2020 May 24.
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The CD153 vaccine is a senotherapeutic option for preventing the accumulation of senescent T cells in mice.CD153 疫苗是一种预防衰老 T 细胞在小鼠体内积累的衰老治疗选择。
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