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Article: A single-cell transcriptomic atlas characterizes ageing tissues in the mouse

TitleA single-cell transcriptomic atlas characterizes ageing tissues in the mouse
Authors
Issue Date2020
Citation
Nature, 2020, v. 583, n. 7817, p. 590-595 How to Cite?
AbstractAgeing is characterized by a progressive loss of physiological integrity, leading to impaired function and increased vulnerability to death. Despite rapid advances over recent years, many of the molecular and cellular processes that underlie the progressive loss of healthy physiology are poorly understood. To gain a better insight into these processes, here we generate a single-cell transcriptomic atlas across the lifespan of Mus musculus that includes data from 23 tissues and organs. We found cell-specific changes occurring across multiple cell types and organs, as well as age-related changes in the cellular composition of different organs. Using single-cell transcriptomic data, we assessed cell-type-specific manifestations of different hallmarks of ageing—such as senescence, genomic instability and changes in the immune system. This transcriptomic atlas—which we denote Tabula Muris Senis, or ‘Mouse Ageing Cell Atlas’—provides molecular information about how the most important hallmarks of ageing are reflected in a broad range of tissues and cell types.
Persistent Identifierhttp://hdl.handle.net/10722/298365
ISSN
2023 Impact Factor: 50.5
2023 SCImago Journal Rankings: 18.509
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAlmanzar, Nicole-
dc.contributor.authorAntony, Jane-
dc.contributor.authorBaghel, Ankit S.-
dc.contributor.authorBakerman, Isaac-
dc.contributor.authorBansal, Ishita-
dc.contributor.authorBarres, Ben A.-
dc.contributor.authorBeachy, Philip A.-
dc.contributor.authorBerdnik, Daniela-
dc.contributor.authorBilen, Biter-
dc.contributor.authorBrownfield, Douglas-
dc.contributor.authorCain, Corey-
dc.contributor.authorChan, Charles K.F.-
dc.contributor.authorChen, Michelle B.-
dc.contributor.authorClarke, Michael F.-
dc.contributor.authorConley, Stephanie D.-
dc.contributor.authorDarmanis, Spyros-
dc.contributor.authorDemers, Aaron-
dc.contributor.authorDemir, Kubilay-
dc.contributor.authorde Morree, Antoine-
dc.contributor.authorDivita, Tessa-
dc.contributor.authordu Bois, Haley-
dc.contributor.authorEbadi, Hamid-
dc.contributor.authorEspinoza, F. Hernán-
dc.contributor.authorFish, Matt-
dc.contributor.authorGan, Qiang-
dc.contributor.authorGeorge, Benson M.-
dc.contributor.authorGillich, Astrid-
dc.contributor.authorGòmez-Sjöberg, Rafael-
dc.contributor.authorGreen, Foad-
dc.contributor.authorGenetiano, Geraldine-
dc.contributor.authorGu, Xueying-
dc.contributor.authorGulati, Gunsagar S.-
dc.contributor.authorHahn, Oliver-
dc.contributor.authorHaney, Michael Seamus-
dc.contributor.authorHang, Yan-
dc.contributor.authorHarris, Lincoln-
dc.contributor.authorHe, Mu-
dc.contributor.authorHosseinzadeh, Shayan-
dc.contributor.authorHuang, Albin-
dc.contributor.authorHuang, Kerwyn Casey-
dc.contributor.authorIram, Tal-
dc.contributor.authorIsobe, Taichi-
dc.contributor.authorIves, Feather-
dc.contributor.authorJones, Robert C C.-
dc.contributor.authorKao, Kevin S.-
dc.contributor.authorKarkanias, Jim-
dc.contributor.authorKarnam, Guruswamy-
dc.contributor.authorKeller, Andreas-
dc.contributor.authorKershner, Aaron M.-
dc.contributor.authorKhoury, Nathalie-
dc.contributor.authorKim, Seung K.-
dc.contributor.authorKiss, Bernhard M.-
dc.contributor.authorKong, William-
dc.contributor.authorKrasnow, Mark A.-
dc.contributor.authorKumar, Maya E.-
dc.contributor.authorKuo, Christin S.-
dc.contributor.authorLam, Jonathan-
dc.contributor.authorLee, Davis P.-
dc.contributor.authorLee, Song E.-
dc.contributor.authorLehallier, Benoit-
dc.contributor.authorLeventhal, Olivia-
dc.contributor.authorLi, Guang-
dc.contributor.authorLi, Qingyun-
dc.contributor.authorLiu, Ling-
dc.contributor.authorLo, Annie-
dc.contributor.authorLu, Wan Jin-
dc.contributor.authorLugo-Fagundo, Maria F.-
dc.contributor.authorManjunath, Anoop-
dc.contributor.authorMay, Andrew P.-
dc.contributor.authorMaynard, Ashley-
dc.contributor.authorMcGeever, Aaron-
dc.contributor.authorMcKay, Marina-
dc.contributor.authorMcNerney, M. Windy-
dc.contributor.authorMerrill, Bryan-
dc.contributor.authorMetzger, Ross J.-
dc.contributor.authorMignardi, Marco-
dc.contributor.authorMin, Dullei-
dc.contributor.authorNabhan, Ahmad N.-
dc.contributor.authorNeff, Norma F.-
dc.contributor.authorNg, Katharine M.-
dc.contributor.authorNguyen, Patricia K.-
dc.contributor.authorNoh, Joseph-
dc.contributor.authorNusse, Roel-
dc.contributor.authorPálovics, Róbert-
dc.contributor.authorPatkar, Rasika-
dc.contributor.authorPeng, Weng Chuan-
dc.contributor.authorPenland, Lolita-
dc.contributor.authorPisco, Angela Oliveira-
dc.contributor.authorPollard, Katherine-
dc.contributor.authorPuccinelli, Robert-
dc.contributor.authorQi, Zhen-
dc.contributor.authorQuake, Stephen R.-
dc.contributor.authorRando, Thomas A.-
dc.contributor.authorRulifson, Eric J.-
dc.contributor.authorSchaum, Nicholas-
dc.contributor.authorSegal, Joe M.-
dc.contributor.authorSikandar, Shaheen S.-
dc.contributor.authorSinha, Rahul-
dc.contributor.authorSit, Rene V.-
dc.contributor.authorSonnenburg, Justin-
dc.date.accessioned2021-04-08T03:08:15Z-
dc.date.available2021-04-08T03:08:15Z-
dc.date.issued2020-
dc.identifier.citationNature, 2020, v. 583, n. 7817, p. 590-595-
dc.identifier.issn0028-0836-
dc.identifier.urihttp://hdl.handle.net/10722/298365-
dc.description.abstractAgeing is characterized by a progressive loss of physiological integrity, leading to impaired function and increased vulnerability to death. Despite rapid advances over recent years, many of the molecular and cellular processes that underlie the progressive loss of healthy physiology are poorly understood. To gain a better insight into these processes, here we generate a single-cell transcriptomic atlas across the lifespan of Mus musculus that includes data from 23 tissues and organs. We found cell-specific changes occurring across multiple cell types and organs, as well as age-related changes in the cellular composition of different organs. Using single-cell transcriptomic data, we assessed cell-type-specific manifestations of different hallmarks of ageing—such as senescence, genomic instability and changes in the immune system. This transcriptomic atlas—which we denote Tabula Muris Senis, or ‘Mouse Ageing Cell Atlas’—provides molecular information about how the most important hallmarks of ageing are reflected in a broad range of tissues and cell types.-
dc.languageeng-
dc.relation.ispartofNature-
dc.titleA single-cell transcriptomic atlas characterizes ageing tissues in the mouse-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41586-020-2496-1-
dc.identifier.pmid32669714-
dc.identifier.scopuseid_2-s2.0-85087975455-
dc.identifier.volume583-
dc.identifier.issue7817-
dc.identifier.spage590-
dc.identifier.epage595-
dc.identifier.eissn1476-4687-
dc.identifier.isiWOS:000623849200002-
dc.identifier.issnl0028-0836-

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