Author
Listed:
- Mallory Paynich Murray
(La Jolla Institute for Immunology)
- Isaac Engel
(La Jolla Institute for Immunology)
- Grégory Seumois
(La Jolla Institute for Immunology)
- Sara Herrera-De la Mata
(La Jolla Institute for Immunology)
- Sandy Lucette Rosales
(La Jolla Institute for Immunology)
- Ashu Sethi
(La Jolla Institute for Immunology)
- Ashmitaa Logandha Ramamoorthy Premlal
(La Jolla Institute for Immunology)
- Goo-Young Seo
(La Jolla Institute for Immunology)
- Jason Greenbaum
(La Jolla Institute for Immunology)
- Pandurangan Vijayanand
(La Jolla Institute for Immunology
University of Southampton, Faculty of Medicine
University of California San Diego)
- James P. Scott-Browne
(La Jolla Institute for Immunology
National Jewish Health)
- Mitchell Kronenberg
(La Jolla Institute for Immunology
University of California San Diego)
Abstract
Invariant natural killer T cells (iNKT cells) differentiate into thymic and peripheral NKT1, NKT2 and NKT17 subsets. Here we use RNA-seq and ATAC-seq analyses and show iNKT subsets are similar, regardless of tissue location. Lung iNKT cell subsets possess the most distinct location-specific features, shared with other innate lymphocytes in the lung, possibly consistent with increased activation. Following antigenic stimulation, iNKT cells undergo chromatin and transcriptional changes delineating two populations: one similar to follicular helper T cells and the other NK or effector like. Phenotypic analysis indicates these changes are observed long-term, suggesting that iNKT cells gene programs are not fixed, but they are capable of chromatin remodeling after antigen to give rise to additional subsets.
Suggested Citation
Mallory Paynich Murray & Isaac Engel & Grégory Seumois & Sara Herrera-De la Mata & Sandy Lucette Rosales & Ashu Sethi & Ashmitaa Logandha Ramamoorthy Premlal & Goo-Young Seo & Jason Greenbaum & Pandur, 2021.
"Transcriptome and chromatin landscape of iNKT cells are shaped by subset differentiation and antigen exposure,"
Nature Communications, Nature, vol. 12(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21574-w
DOI: 10.1038/s41467-021-21574-w
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