An integrated cell atlas of the lung in health and disease.
Sikkema, L
Ramírez-Suástegui, C
Strobl, DC
Gillett, TE
Zappia, L
Madissoon, E
Markov, NS
Zaragosi, L-E
Ji, Y
Ansari, M
Arguel, M-J
Apperloo, L
Banchero, M
Bécavin, C
Berg, M
Chichelnitskiy, E
Chung, M-I
Collin, A
Gay, ACA
Gote-Schniering, J
Hooshiar Kashani, B
Inecik, K
Jain, M
Kapellos, TS
Kole, TM
Leroy, S
Mayr, CH
Oliver, AJ
von Papen, M
Peter, L
Taylor, CJ
Walzthoeni, T
Xu, C
Bui, LT
De Donno, C
Dony, L
Faiz, A
Guo, M
Gutierrez, AJ
Heumos, L
Huang, N
Ibarra, IL
Jackson, ND
Kadur Lakshminarasimha Murthy, P
Lotfollahi, M
Tabib, T
Talavera-López, C
Travaglini, KJ
Wilbrey-Clark, A
Worlock, KB
Yoshida, M
Lung Biological Network Consortium,
van den Berge, M
Bossé, Y
Desai, TJ
Eickelberg, O
Kaminski, N
Krasnow, MA
Lafyatis, R
Nikolic, MZ
Powell, JE
Rajagopal, J
Rojas, M
Rozenblatt-Rosen, O
Seibold, MA
Sheppard, D
Shepherd, DP
Sin, DD
Timens, W
Tsankov, AM
Whitsett, J
Xu, Y
Banovich, NE
Barbry, P
Duong, TE
Falk, CS
Meyer, KB
Kropski, JA
Pe'er, D
Schiller, HB
Tata, PR
Schultze, JL
Teichmann, SA
Misharin, AV
Nawijn, MC
Luecken, MD
Theis, FJ
- Publisher:
- Springer Nature
- Publication Type:
- Journal Article
- Citation:
- Nat Med, 2023, 29, (6), pp. 1563-1577
- Issue Date:
- 2023-06
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Sikkema, L | |
dc.contributor.author | Ramírez-Suástegui, C | |
dc.contributor.author | Strobl, DC | |
dc.contributor.author | Gillett, TE | |
dc.contributor.author | Zappia, L | |
dc.contributor.author | Madissoon, E | |
dc.contributor.author | Markov, NS | |
dc.contributor.author | Zaragosi, L-E | |
dc.contributor.author | Ji, Y | |
dc.contributor.author | Ansari, M | |
dc.contributor.author | Arguel, M-J | |
dc.contributor.author | Apperloo, L | |
dc.contributor.author | Banchero, M | |
dc.contributor.author | Bécavin, C | |
dc.contributor.author | Berg, M | |
dc.contributor.author | Chichelnitskiy, E | |
dc.contributor.author | Chung, M-I | |
dc.contributor.author | Collin, A | |
dc.contributor.author | Gay, ACA | |
dc.contributor.author | Gote-Schniering, J | |
dc.contributor.author | Hooshiar Kashani, B | |
dc.contributor.author | Inecik, K | |
dc.contributor.author | Jain, M | |
dc.contributor.author | Kapellos, TS | |
dc.contributor.author | Kole, TM | |
dc.contributor.author | Leroy, S | |
dc.contributor.author | Mayr, CH | |
dc.contributor.author | Oliver, AJ | |
dc.contributor.author | von Papen, M | |
dc.contributor.author | Peter, L | |
dc.contributor.author | Taylor, CJ | |
dc.contributor.author | Walzthoeni, T | |
dc.contributor.author | Xu, C | |
dc.contributor.author | Bui, LT | |
dc.contributor.author | De Donno, C | |
dc.contributor.author | Dony, L | |
dc.contributor.author |
Faiz, A https://orcid.org/0000-0003-1740-3538 |
|
dc.contributor.author | Guo, M | |
dc.contributor.author | Gutierrez, AJ | |
dc.contributor.author | Heumos, L | |
dc.contributor.author | Huang, N | |
dc.contributor.author | Ibarra, IL | |
dc.contributor.author | Jackson, ND | |
dc.contributor.author | Kadur Lakshminarasimha Murthy, P | |
dc.contributor.author | Lotfollahi, M | |
dc.contributor.author | Tabib, T | |
dc.contributor.author | Talavera-López, C | |
dc.contributor.author | Travaglini, KJ | |
dc.contributor.author | Wilbrey-Clark, A | |
dc.contributor.author | Worlock, KB | |
dc.contributor.author | Yoshida, M | |
dc.contributor.author | Lung Biological Network Consortium, | |
dc.contributor.author | van den Berge, M | |
dc.contributor.author | Bossé, Y | |
dc.contributor.author | Desai, TJ | |
dc.contributor.author | Eickelberg, O | |
dc.contributor.author | Kaminski, N | |
dc.contributor.author | Krasnow, MA | |
dc.contributor.author | Lafyatis, R | |
dc.contributor.author | Nikolic, MZ | |
dc.contributor.author | Powell, JE | |
dc.contributor.author | Rajagopal, J | |
dc.contributor.author | Rojas, M | |
dc.contributor.author | Rozenblatt-Rosen, O | |
dc.contributor.author | Seibold, MA | |
dc.contributor.author | Sheppard, D | |
dc.contributor.author | Shepherd, DP | |
dc.contributor.author | Sin, DD | |
dc.contributor.author | Timens, W | |
dc.contributor.author | Tsankov, AM | |
dc.contributor.author | Whitsett, J | |
dc.contributor.author | Xu, Y | |
dc.contributor.author | Banovich, NE | |
dc.contributor.author | Barbry, P | |
dc.contributor.author | Duong, TE | |
dc.contributor.author | Falk, CS | |
dc.contributor.author | Meyer, KB | |
dc.contributor.author | Kropski, JA | |
dc.contributor.author | Pe'er, D | |
dc.contributor.author | Schiller, HB | |
dc.contributor.author | Tata, PR | |
dc.contributor.author | Schultze, JL | |
dc.contributor.author | Teichmann, SA | |
dc.contributor.author | Misharin, AV | |
dc.contributor.author | Nawijn, MC | |
dc.contributor.author | Luecken, MD | |
dc.contributor.author | Theis, FJ | |
dc.date.accessioned | 2023-09-27T22:52:23Z | |
dc.date.available | 2023-03-30 | |
dc.date.available | 2023-09-27T22:52:23Z | |
dc.date.issued | 2023-06 | |
dc.identifier.citation | Nat Med, 2023, 29, (6), pp. 1563-1577 | |
dc.identifier.issn | 1078-8956 | |
dc.identifier.issn | 1546-170X | |
dc.identifier.uri | http://hdl.handle.net/10453/172342 | |
dc.description.abstract | Single-cell technologies have transformed our understanding of human tissues. Yet, studies typically capture only a limited number of donors and disagree on cell type definitions. Integrating many single-cell datasets can address these limitations of individual studies and capture the variability present in the population. Here we present the integrated Human Lung Cell Atlas (HLCA), combining 49 datasets of the human respiratory system into a single atlas spanning over 2.4 million cells from 486 individuals. The HLCA presents a consensus cell type re-annotation with matching marker genes, including annotations of rare and previously undescribed cell types. Leveraging the number and diversity of individuals in the HLCA, we identify gene modules that are associated with demographic covariates such as age, sex and body mass index, as well as gene modules changing expression along the proximal-to-distal axis of the bronchial tree. Mapping new data to the HLCA enables rapid data annotation and interpretation. Using the HLCA as a reference for the study of disease, we identify shared cell states across multiple lung diseases, including SPP1+ profibrotic monocyte-derived macrophages in COVID-19, pulmonary fibrosis and lung carcinoma. Overall, the HLCA serves as an example for the development and use of large-scale, cross-dataset organ atlases within the Human Cell Atlas. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer Nature | |
dc.relation.ispartof | Nat Med | |
dc.relation.isbasedon | 10.1038/s41591-023-02327-2 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 11 Medical and Health Sciences | |
dc.subject.classification | Immunology | |
dc.subject.classification | 32 Biomedical and clinical sciences | |
dc.subject.classification | 42 Health sciences | |
dc.subject.mesh | Humans | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Pulmonary Fibrosis | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Macrophages | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Macrophages | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Pulmonary Fibrosis | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Humans | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Pulmonary Fibrosis | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Macrophages | |
dc.title | An integrated cell atlas of the lung in health and disease. | |
dc.type | Journal Article | |
utslib.citation.volume | 29 | |
utslib.location.activity | United States | |
utslib.for | 11 Medical and Health Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
pubs.organisational-group | /University of Technology Sydney/Strength - CFI - Centre for Inflammation | |
utslib.copyright.status | open_access | * |
dc.date.updated | 2023-09-27T22:52:12Z | |
pubs.issue | 6 | |
pubs.publication-status | Published | |
pubs.volume | 29 | |
utslib.citation.issue | 6 |
Abstract:
Single-cell technologies have transformed our understanding of human tissues. Yet, studies typically capture only a limited number of donors and disagree on cell type definitions. Integrating many single-cell datasets can address these limitations of individual studies and capture the variability present in the population. Here we present the integrated Human Lung Cell Atlas (HLCA), combining 49 datasets of the human respiratory system into a single atlas spanning over 2.4 million cells from 486 individuals. The HLCA presents a consensus cell type re-annotation with matching marker genes, including annotations of rare and previously undescribed cell types. Leveraging the number and diversity of individuals in the HLCA, we identify gene modules that are associated with demographic covariates such as age, sex and body mass index, as well as gene modules changing expression along the proximal-to-distal axis of the bronchial tree. Mapping new data to the HLCA enables rapid data annotation and interpretation. Using the HLCA as a reference for the study of disease, we identify shared cell states across multiple lung diseases, including SPP1+ profibrotic monocyte-derived macrophages in COVID-19, pulmonary fibrosis and lung carcinoma. Overall, the HLCA serves as an example for the development and use of large-scale, cross-dataset organ atlases within the Human Cell Atlas.
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