用计算多组学推进对细胞衰老的生物学理解

IF 29 1区 生物学 Q1 GENETICS & HEREDITY
Sheng Li, Paula A. Agudelo Garcia, Constantin Aliferis, Michael J. Becich, Jazmin Calyeca, Benjamin D. Cosgrove, Jennifer Elisseeff, Negin Farzad, Elana J. Fertig, Carolyn Glass, Liangcai Gu, Qianjiang Hu, Zhicheng Ji, Melanie Königshoff, Nathan K. LeBrasseur, Dongmei Li, Anjun Ma, Qin Ma, Vilas Menon, Jacob T. Mitchell, Ana L. Mora, Sushma Nagaraj, Andrew C. Nelson, Laura J. Niedernhofer, Mauricio Rojas, Hash Brown Taha, Jinhua Wang, Siyuan Wang, Pei-Hsun Wu, Jichun Xie, Ming Xu, Miao Yu, Xu Zhang, Yue Zhao, Peter D. Adams, Cristina Aguayo-Mazzucato, Darren J. Baker, Christopher Benz, David A. Bernlohr, Marta Bueno, Jin Chen, Bennett G. Childs, Jeffrey H. Chuang, Dongjun Chung, Mythili Dileepan, Li Ding, Mingze Dong, Francesca Duncan, Archibald Enninful, William F. Flynn, Ana Catarina Franco, David Furman, Vesna Garovic, Stephanie Halene, Allison B. Herman, Ann V. Hertzel, Kanako Iwasaki, Hyeongseon Jeon, Jeon Woong Kang, Shilpita Karmakar, James L. Kirkland, Ron Korstanje, Erich Kummerfeld, Jun Hee Lee, Yang Liu, Yao Lu, Jose Lugo-Martinez, Helene Martini, Simon Melov, Nicolas Musi, João F. Passos, Samuel T. Peters, Irfan Rahman, Ramalakshmi Ramasamy, Alexandra N. Rindone, Paul D. Robbins, Paul Robson, Jhonny Rodriguez-Lopez, Lorena Rosas, Nadia Rosenthal, Marissa J. Schafer, Birgit Schilling, Elizabeth L. Schmidt, Kevin Schneider, Kaustav Sengupta, Jian Shu, Peter T. C. So, Li Sun, Tamar Tchkonia, Marcos G. Teneche, Natalia Vanegas, Julia Wang, Juan Xie, Shanshan Yin, Ke Zhang, Quan Zhu, Rong Fan
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引用次数: 0

摘要

细胞衰老是一个复杂的生物学过程,在衰老和与年龄有关的疾病中起着病理生理作用。由于缺乏特定的生物标志物,以及衰老细胞的相对罕见性、表型异质性和动态特征,在细胞和组织水平上对衰老的生物学理解仍然不完整。这篇综述提供了一个全面的概述多组学方法表征和细胞衰老的生物学理解。讨论了每种方法的技术能力和挑战,并为选择识别,表征和空间映射衰老细胞的工具提供了实用指南。强调了计算分析在多组学研究中的重要性,包括衰老细胞鉴定、特征检测和衰老细胞与微环境的相互作用。此外,组织特异性的案例研究和实验设计的考虑,个别器官提出。最后,讨论了多组学方法对细胞衰老生物学理解的未来方向和潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advancing biological understanding of cellular senescence with computational multiomics

Advancing biological understanding of cellular senescence with computational multiomics

Cellular senescence is a complex biological process that plays a pathophysiological role in aging and age-related diseases. The biological understanding of senescence at the cellular and tissue levels remains incomplete due to the lack of specific biomarkers as well as the relative rarity of senescent cells, their phenotypic heterogeneity and dynamic features. This Review provides a comprehensive overview of multiomic approaches for the characterization and biological understanding of cellular senescence. The technical capability and challenges of each approach are discussed, and practical guidelines are provided for selecting tools for identifying, characterizing and spatially mapping senescent cells. The importance of computational analyses in multiomics research, including senescent cell identification, signature detection and interactions of senescent cells with microenvironments, is highlighted. Moreover, tissue-specific case studies and experimental design considerations for individual organs are presented. Finally, future directions and the potential impact of multiomic approaches on the biological understanding of cellular senescence are discussed.

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来源期刊
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
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