NIH SenNet Consortium to map senescent cells throughout the human lifespan to understand physiological health

Cells respond to many stressors by senescing, acquiring stable growth arrest, morphologic and metabolic changes, and a proinflammatory senescence-associated secretory phenotype. The heterogeneity of senescent cells (SnCs) and senescence-associated secretory phenotype are vast, yet ill characterized....

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Veröffentlicht in:Nature aging 2022-12, Vol.2 (12), p.1090-1100
Hauptverfasser: Lee, Patty J., Benz, Christopher C., Blood, Philip, Börner, Katy, Campisi, Judith, Chen, Feng, Daldrup-Link, Heike, De Jager, Phil, Ding, Li, Duncan, Francesca E., Eickelberg, Oliver, Fan, Rong, Finkel, Toren, Furman, David, Garovic, Vesna, Gehlenborg, Nils, Glass, Carolyn, Heckenbach, Indra, Joseph, Ziv-Bar, Katiyar, Pragati, Kim, So-Jin, Königshoff, Melanie, Kuchel, George A., Lee, Haesung, Lee, Jun Hee, Ma, Jian, Ma, Qin, Melov, Simon, Metis, Kay, Mora, Ana L., Musi, Nicolas, Neretti, Nicola, Passos, João F., Rahman, Irfan, Rivera-Mulia, Juan Carlos, Robson, Paul, Rojas, Mauricio, Roy, Ananda L., Scheibye-Knudsen, Morten, Schilling, Birgit, Shi, Pixu, Silverstein, Jonathan C., Suryadevara, Vidyani, Xie, Jichun, Wang, Jinhua, Wong, A. Ian, Niedernhofer, Laura J., Wang, Siyuan, Anvari, Hannah, Balough, Julia, Benz, Christopher, Bons, Joanna, Brenerman, Boris, Evans, William, Gerencser, Akos, Gregory, Heather, Hansen, Malene, Justice, Jamie, Kapahi, Pankaj, Murad, Natalia, O’Broin, Amy, Pavone, Mary Ellen, Powell, Mark, Scott, Gary, Shanes, Elisheva, Shankaran, Mahalakshmi, Verdin, Eric, Winer, Daniel, Wu, Fei, Adams, Andrew, Blood, Philip D., Bueckle, Andreas, Cao-Berg, Ivan, Chen, Hao, Davis, Michael, Filus, Shane, Hao, Yuhan, Hartman, Austin, Hasanaj, Euxhen, Helfer, Jesse, Herr, Bruce, Joseph, Ziv Bar, Molla, Gesmira, Mou, Gloria, Puerto, Juan, Quardokus, Ellen M., Ropelewski, Alexander J., Ruffalo, Matt, Satija, Rahul, Schwenk, Melissa, Scibek, Robin, Shirey, William, Sibilla, Max, Welling, Joel, Yuan, Zhou, Bonneau, Richard, Christiano, Angela, Izar, Benjamin, Menon, Vilas, Owens, David M.
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Sprache:eng
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Zusammenfassung:Cells respond to many stressors by senescing, acquiring stable growth arrest, morphologic and metabolic changes, and a proinflammatory senescence-associated secretory phenotype. The heterogeneity of senescent cells (SnCs) and senescence-associated secretory phenotype are vast, yet ill characterized. SnCs have diverse roles in health and disease and are therapeutically targetable, making characterization of SnCs and their detection a priority. The Cellular Senescence Network (SenNet), a National Institutes of Health Common Fund initiative, was established to address this need. The goal of SenNet is to map SnCs across the human lifespan to advance diagnostic and therapeutic approaches to improve human health. State-of-the-art methods will be applied to identify, define and map SnCs in 18 human tissues. A common coordinate framework will integrate data to create four-dimensional SnC atlases. Other key SenNet deliverables include innovative tools and technologies to detect SnCs, new SnC biomarkers and extensive public multi-omics datasets. This Perspective lays out the impetus, goals, approaches and products of SenNet. This Perspective lays out the impetus and goals of the Cellular Senescence Network established to comprehensively identify and characterize senescent cells (SnCs) across tissues and lifespan, providing a publicly available SnC atlas.
ISSN:2662-8465
2662-8465
DOI:10.1038/s43587-022-00326-5