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IGFBP5 由衰老细胞释放,并被健康细胞内化,通过与维甲酸受体相互作用促进其衰老。

IGFBP5 is released by senescent cells and is internalized by healthy cells, promoting their senescence through interaction with retinoic receptors.

机构信息

Department of Experimental Medicine, Luigi Vanvitelli Campania University, via Luigi De Crecchio 7, Naples, 80138, Italy.

International Medical University UNICAMILLUS, Rome, Italy.

出版信息

Cell Commun Signal. 2024 Feb 13;22(1):122. doi: 10.1186/s12964-024-01469-1.

Abstract

Cells that are exposed to harmful genetic damage, either from internal or external sources, may undergo senescence if they are unable to repair their DNA. Senescence, characterized by a state of irreversible growth arrest, can spread to neighboring cells through a process known as the senescence-associated secretory phenotype (SASP). This phenomenon contributes to both aging and the development of cancer. The SASP comprises a variety of factors that regulate numerous functions, including the induction of secondary senescence, modulation of immune system activity, remodeling of the extracellular matrix, alteration of tissue structure, and promotion of cancer progression. Identifying key factors within the SASP is crucial for understanding the underlying mechanisms of senescence and developing effective strategies to counteract cellular senescence. Our research has specifically focused on investigating the role of IGFBP5, a component of the SASP observed in various experimental models and conditions.Through our studies, we have demonstrated that IGFBP5 actively contributes to promoting senescence and can induce senescence in neighboring cells. We have gained valuable insights into the mechanisms through which IGFBP5 exerts its pro-senescence effects. These mechanisms include its release following genotoxic stress, involvement in signaling pathways mediated by reactive oxygen species and prostaglandins, internalization via specialized structures called caveolae, and interaction with a specific protein known as RARα. By uncovering these mechanisms, we have advanced our understanding of the intricate role of IGFBP5 in the senescence process. The significance of IGFBP5 as a pro-aging factor stems from an in vivo study we conducted on patients undergoing Computer Tomography analysis. In these patients, we observed an elevation in circulating IGFBP5 levels in response to radiation-induced organismal stress.Globally, our findings highlight the potential of IGFBP5 as a promising therapeutic target for age-related diseases and cancer.

摘要

细胞如果无法修复 DNA,就会因为暴露在有害的遗传损伤下(这种损伤可能来自内部或外部)而衰老。衰老的特征是不可逆的生长停滞,可以通过一种称为衰老相关分泌表型(SASP)的过程传播到邻近细胞。这种现象既导致了衰老,也促进了癌症的发展。SASP 由多种调节多种功能的因子组成,包括诱导二次衰老、调节免疫系统活性、重塑细胞外基质、改变组织结构以及促进癌症进展。鉴定 SASP 中的关键因素对于理解衰老的潜在机制和开发对抗细胞衰老的有效策略至关重要。我们的研究特别关注研究 IGFBP5 的作用,IGFBP5 是各种实验模型和条件下观察到的 SASP 的一个组成部分。通过我们的研究,我们已经证明 IGFBP5 积极促进衰老,并可以诱导邻近细胞衰老。我们深入了解了 IGFBP5 发挥其促衰老作用的机制。这些机制包括在遗传毒性应激后释放、参与由活性氧和前列腺素介导的信号通路、通过称为 caveolae 的专门结构内化以及与特定蛋白质 RARα 相互作用。通过揭示这些机制,我们深入了解了 IGFBP5 在衰老过程中的复杂作用。IGFBP5 作为促衰老因子的重要性源于我们对接受计算机断层扫描分析的患者进行的一项体内研究。在这些患者中,我们观察到循环 IGFBP5 水平在辐射引起的机体应激下升高。从全球范围来看,我们的发现强调了 IGFBP5 作为与年龄相关的疾病和癌症的有前途的治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cde/10863175/8137c10dbcb6/12964_2024_1469_Fig1_HTML.jpg

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