Cargando…

Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin

Naked mole-rats (NMR) are subterranean rodents characterized by an unusual longevity coupled with an unexplained resistance to aging. In the present study, we performed extensive in situ analysis and single-cell RNA-sequencing comparing young and older animals. At variance with other species, NMR ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Savina, Aleksandra, Jaffredo, Thierry, Saldmann, Frederic, Faulkes, Chris G., Moguelet, Philippe, Leroy, Christine, Marmol, Delphine Del, Codogno, Patrice, Foucher, Lucy, Zalc, Antoine, Viltard, Mélanie, Friedlander, Gérard, Aractingi, Selim, Fontaine, Romain H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134947/
https://www.ncbi.nlm.nih.gov/pubmed/35507806
http://dx.doi.org/10.18632/aging.204054
_version_ 1784713862760628224
author Savina, Aleksandra
Jaffredo, Thierry
Saldmann, Frederic
Faulkes, Chris G.
Moguelet, Philippe
Leroy, Christine
Marmol, Delphine Del
Codogno, Patrice
Foucher, Lucy
Zalc, Antoine
Viltard, Mélanie
Friedlander, Gérard
Aractingi, Selim
Fontaine, Romain H.
author_facet Savina, Aleksandra
Jaffredo, Thierry
Saldmann, Frederic
Faulkes, Chris G.
Moguelet, Philippe
Leroy, Christine
Marmol, Delphine Del
Codogno, Patrice
Foucher, Lucy
Zalc, Antoine
Viltard, Mélanie
Friedlander, Gérard
Aractingi, Selim
Fontaine, Romain H.
author_sort Savina, Aleksandra
collection PubMed
description Naked mole-rats (NMR) are subterranean rodents characterized by an unusual longevity coupled with an unexplained resistance to aging. In the present study, we performed extensive in situ analysis and single-cell RNA-sequencing comparing young and older animals. At variance with other species, NMR exhibited a striking stability of skin compartments and cell types, which remained stable over time without aging-associated changes. Remarkably, the number of stem cells was constant throughout aging. We found three classical cellular states defining a unique keratinocyte differentiation trajectory that were not altered after pseudo-temporal reconstruction. Epidermal gene expression did not change with aging either. Langerhans cell clusters were conserved, and only a higher basal stem cell expression of Igfbp3 was found in aged animals. In accordance, NMR skin healing closure was similar in young and older animals. Altogether, these results indicate that NMR skin is characterized by peculiar genetic and cellular features, different from those previously demonstrated for mice and humans. The remarkable stability of the aging NMR skin transcriptome likely reflects unaltered homeostasis and resilience.
format Online
Article
Text
id pubmed-9134947
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Impact Journals
record_format MEDLINE/PubMed
spelling pubmed-91349472022-06-01 Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin Savina, Aleksandra Jaffredo, Thierry Saldmann, Frederic Faulkes, Chris G. Moguelet, Philippe Leroy, Christine Marmol, Delphine Del Codogno, Patrice Foucher, Lucy Zalc, Antoine Viltard, Mélanie Friedlander, Gérard Aractingi, Selim Fontaine, Romain H. Aging (Albany NY) Research Paper Naked mole-rats (NMR) are subterranean rodents characterized by an unusual longevity coupled with an unexplained resistance to aging. In the present study, we performed extensive in situ analysis and single-cell RNA-sequencing comparing young and older animals. At variance with other species, NMR exhibited a striking stability of skin compartments and cell types, which remained stable over time without aging-associated changes. Remarkably, the number of stem cells was constant throughout aging. We found three classical cellular states defining a unique keratinocyte differentiation trajectory that were not altered after pseudo-temporal reconstruction. Epidermal gene expression did not change with aging either. Langerhans cell clusters were conserved, and only a higher basal stem cell expression of Igfbp3 was found in aged animals. In accordance, NMR skin healing closure was similar in young and older animals. Altogether, these results indicate that NMR skin is characterized by peculiar genetic and cellular features, different from those previously demonstrated for mice and humans. The remarkable stability of the aging NMR skin transcriptome likely reflects unaltered homeostasis and resilience. Impact Journals 2022-05-04 /pmc/articles/PMC9134947/ /pubmed/35507806 http://dx.doi.org/10.18632/aging.204054 Text en Copyright: © 2022 Savina et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Savina, Aleksandra
Jaffredo, Thierry
Saldmann, Frederic
Faulkes, Chris G.
Moguelet, Philippe
Leroy, Christine
Marmol, Delphine Del
Codogno, Patrice
Foucher, Lucy
Zalc, Antoine
Viltard, Mélanie
Friedlander, Gérard
Aractingi, Selim
Fontaine, Romain H.
Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title_full Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title_fullStr Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title_full_unstemmed Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title_short Single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
title_sort single-cell transcriptomics reveals age-resistant maintenance of cell identities, stem cell compartments and differentiation trajectories in long-lived naked mole-rats skin
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134947/
https://www.ncbi.nlm.nih.gov/pubmed/35507806
http://dx.doi.org/10.18632/aging.204054
work_keys_str_mv AT savinaaleksandra singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT jaffredothierry singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT saldmannfrederic singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT faulkeschrisg singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT mogueletphilippe singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT leroychristine singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT marmoldelphinedel singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT codognopatrice singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT foucherlucy singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT zalcantoine singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT viltardmelanie singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT friedlandergerard singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT aractingiselim singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin
AT fontaineromainh singlecelltranscriptomicsrevealsageresistantmaintenanceofcellidentitiesstemcellcompartmentsanddifferentiationtrajectoriesinlonglivednakedmoleratsskin