Cargando…

Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells

Innate T cells, including CD1d-restricted invariant natural killer T (iNKT) cells, are characterized by their rapid activation in response to non-peptide antigens, such as lipids. While the transcriptional profiles of naive, effector, and memory adaptive T cells have been well studied, less is known...

Descripción completa

Detalles Bibliográficos
Autores principales: Kane, Harry, LaMarche, Nelson M, Ní Scannail, Áine, Garza, Amanda E, Koay, Hui-Fern, Azad, Adiba I, Kunkemoeller, Britta, Stevens, Brenneth, Brenner, Michael B, Lynch, Lydia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831610/
https://www.ncbi.nlm.nih.gov/pubmed/36458691
http://dx.doi.org/10.7554/eLife.76586
_version_ 1784867880362311680
author Kane, Harry
LaMarche, Nelson M
Ní Scannail, Áine
Garza, Amanda E
Koay, Hui-Fern
Azad, Adiba I
Kunkemoeller, Britta
Stevens, Brenneth
Brenner, Michael B
Lynch, Lydia
author_facet Kane, Harry
LaMarche, Nelson M
Ní Scannail, Áine
Garza, Amanda E
Koay, Hui-Fern
Azad, Adiba I
Kunkemoeller, Britta
Stevens, Brenneth
Brenner, Michael B
Lynch, Lydia
author_sort Kane, Harry
collection PubMed
description Innate T cells, including CD1d-restricted invariant natural killer T (iNKT) cells, are characterized by their rapid activation in response to non-peptide antigens, such as lipids. While the transcriptional profiles of naive, effector, and memory adaptive T cells have been well studied, less is known about the transcriptional regulation of different iNKT cell activation states. Here, using single-cell RNA-sequencing, we performed longitudinal profiling of activated murine iNKT cells, generating a transcriptomic atlas of iNKT cell activation states. We found that transcriptional signatures of activation are highly conserved among heterogeneous iNKT cell populations, including NKT1, NKT2, and NKT17 subsets, and human iNKT cells. Strikingly, we found that regulatory iNKT cells, such as adipose iNKT cells, undergo blunted activation and display constitutive enrichment of memory-like cMAF(+) and KLRG1(+) populations. Moreover, we identify a conserved cMAF-associated transcriptional network among NKT10 cells, providing novel insights into the biology of regulatory and antigen-experienced iNKT cells.
format Online
Article
Text
id pubmed-9831610
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-98316102023-01-11 Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells Kane, Harry LaMarche, Nelson M Ní Scannail, Áine Garza, Amanda E Koay, Hui-Fern Azad, Adiba I Kunkemoeller, Britta Stevens, Brenneth Brenner, Michael B Lynch, Lydia eLife Computational and Systems Biology Innate T cells, including CD1d-restricted invariant natural killer T (iNKT) cells, are characterized by their rapid activation in response to non-peptide antigens, such as lipids. While the transcriptional profiles of naive, effector, and memory adaptive T cells have been well studied, less is known about the transcriptional regulation of different iNKT cell activation states. Here, using single-cell RNA-sequencing, we performed longitudinal profiling of activated murine iNKT cells, generating a transcriptomic atlas of iNKT cell activation states. We found that transcriptional signatures of activation are highly conserved among heterogeneous iNKT cell populations, including NKT1, NKT2, and NKT17 subsets, and human iNKT cells. Strikingly, we found that regulatory iNKT cells, such as adipose iNKT cells, undergo blunted activation and display constitutive enrichment of memory-like cMAF(+) and KLRG1(+) populations. Moreover, we identify a conserved cMAF-associated transcriptional network among NKT10 cells, providing novel insights into the biology of regulatory and antigen-experienced iNKT cells. eLife Sciences Publications, Ltd 2022-12-02 /pmc/articles/PMC9831610/ /pubmed/36458691 http://dx.doi.org/10.7554/eLife.76586 Text en © 2022, Kane et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Kane, Harry
LaMarche, Nelson M
Ní Scannail, Áine
Garza, Amanda E
Koay, Hui-Fern
Azad, Adiba I
Kunkemoeller, Britta
Stevens, Brenneth
Brenner, Michael B
Lynch, Lydia
Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title_full Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title_fullStr Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title_full_unstemmed Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title_short Longitudinal analysis of invariant natural killer T cell activation reveals a cMAF-associated transcriptional state of NKT10 cells
title_sort longitudinal analysis of invariant natural killer t cell activation reveals a cmaf-associated transcriptional state of nkt10 cells
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831610/
https://www.ncbi.nlm.nih.gov/pubmed/36458691
http://dx.doi.org/10.7554/eLife.76586
work_keys_str_mv AT kaneharry longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT lamarchenelsonm longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT niscannailaine longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT garzaamandae longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT koayhuifern longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT azadadibai longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT kunkemoellerbritta longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT stevensbrenneth longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT brennermichaelb longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells
AT lynchlydia longitudinalanalysisofinvariantnaturalkillertcellactivationrevealsacmafassociatedtranscriptionalstateofnkt10cells