The interactome era: Integrating RNA-seq, proteomics, and network biology to decode cellular senescence

IF 12.4 1区 医学 Q1 CELL BIOLOGY
Mohd Shahzaib , Domenico Aprile , Tiziana Squillaro , Nicola Alessio , Gianfranco Peluso , Giovanni Di Bernardo , Umberto Galderisi
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引用次数: 0

Abstract

Cellular senescence is a dynamic state in which cells permanently withdraw from the cell cycle while continuing to reshape their internal and external environment. It is characterized by persistent DNA damage responses, chromatin reorganization, and the secretion of a complex mixture of cytokines and proteases collectively known as the senescence-associated secretory phenotype (SASP). Transcriptomic and proteomic studies have defined key markers, including CDKN2A, CDKN1A, TP53, and SASP factors, but these approaches provide only static inventories. They do not explain how regulatory programs are executed through protein interactions that assemble, dissolve, and reorganize over time. Interactomics now fills this gap. Advances such as affinity purification mass spectrometry (AP-MS), proximity labeling (BioID/TurboID), and cross-linking mass spectrometry (XL-MS) reveal that senescence is driven not by single molecules but by the rewiring of protein–protein interactions (PPIs). These dynamic networks stabilize DNA damage response hubs, restructure chromatin and the nuclear lamina, regulate SASP secretion, and remodel metabolism. By integrating interactomic data with transcriptomic and proteomic profiles, it is now possible to uncover therapeutic vulnerabilities and guide the design of senolytics, senomorphics, and strategies that block senescence escape. Important challenges remain. Weak or transient interactions are often lost, background signals can obscure specificity, and membrane complexes are under-represented. Emerging single-cell and spatial technologies are beginning to overcome these limitations, revealing how senescence differs across tissues, contexts, and disease states. In essence, senescence is not just a change in gene expression but a reorganization of the cell’s communication networks. Interactomics offers the framework needed to decode this complexity and to design precision therapies for aging and age-related disease.
相互作用组时代:整合RNA-Seq,蛋白质组学和网络生物学解码细胞衰老。
细胞衰老是细胞永久退出细胞周期,同时继续重塑其内外环境的一种动态状态。它的特征是持续的DNA损伤反应,染色质重组,以及细胞因子和蛋白酶的复杂混合物的分泌,统称为衰老相关分泌表型(SASP)。转录组学和蛋白质组学研究已经定义了关键标记,包括CDKN2A、CDKN1A、TP53和SASP因子,但这些方法只能提供静态清单。它们没有解释调控程序是如何通过蛋白质相互作用,随着时间的推移组装、溶解和重组而执行的。互动性现在填补了这一空白。亲和纯化质谱(AP-MS)、接近标记(BioID/TurboID)和交联质谱(XL-MS)等技术的进步表明,衰老不是由单个分子驱动的,而是由蛋白质-蛋白质相互作用(PPIs)的重新连接驱动的。这些动态网络稳定DNA损伤反应中心,重组染色质和核层,调节SASP分泌,重塑代谢。通过将相互作用组学数据与转录组学和蛋白质组学数据相结合,现在有可能发现治疗脆弱性,并指导设计抗衰老药物、同形药物和阻止衰老逃逸的策略。重要的挑战依然存在。弱或瞬态相互作用经常丢失,背景信号可能模糊特异性,膜复合物代表性不足。新兴的单细胞和空间技术正在开始克服这些限制,揭示衰老在组织、环境和疾病状态之间的差异。从本质上讲,衰老不仅仅是基因表达的变化,而且是细胞通信网络的重组。相互作用组学提供了解码这种复杂性和设计针对衰老和年龄相关疾病的精确疗法所需的框架。
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来源期刊
Ageing Research Reviews
Ageing Research Reviews 医学-老年医学
CiteScore
19.80
自引率
2.30%
发文量
216
审稿时长
55 days
期刊介绍: With the rise in average human life expectancy, the impact of ageing and age-related diseases on our society has become increasingly significant. Ageing research is now a focal point for numerous laboratories, encompassing leaders in genetics, molecular and cellular biology, biochemistry, and behavior. Ageing Research Reviews (ARR) serves as a cornerstone in this field, addressing emerging trends. ARR aims to fill a substantial gap by providing critical reviews and viewpoints on evolving discoveries concerning the mechanisms of ageing and age-related diseases. The rapid progress in understanding the mechanisms controlling cellular proliferation, differentiation, and survival is unveiling new insights into the regulation of ageing. From telomerase to stem cells, and from energy to oxyradical metabolism, we are witnessing an exciting era in the multidisciplinary field of ageing research. The journal explores the cellular and molecular foundations of interventions that extend lifespan, such as caloric restriction. It identifies the underpinnings of manipulations that extend lifespan, shedding light on novel approaches for preventing age-related diseases. ARR publishes articles on focused topics selected from the expansive field of ageing research, with a particular emphasis on the cellular and molecular mechanisms of the aging process. This includes age-related diseases like cancer, cardiovascular disease, diabetes, and neurodegenerative disorders. The journal also covers applications of basic ageing research to lifespan extension and disease prevention, offering a comprehensive platform for advancing our understanding of this critical field.
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