Histone deacetylase 3 is required for iNKT cell development
Abstract NKT cells are a distinct subset that have developmental requirements that often differ from conventional T cells. Here, we show that NKT-specific deletion of Hdac3 results in a severe reduction in the number of iNKT cells, particularly of NKT1 cells. In addition, there is decreased cytokine...
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Nature Portfolio
2017
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oai:doaj.org-article:bb0b26a9f24f4d3983eb28ce34699aa42021-12-02T15:06:17ZHistone deacetylase 3 is required for iNKT cell development10.1038/s41598-017-06102-52045-2322https://doaj.org/article/bb0b26a9f24f4d3983eb28ce34699aa42017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-06102-5https://doaj.org/toc/2045-2322Abstract NKT cells are a distinct subset that have developmental requirements that often differ from conventional T cells. Here, we show that NKT-specific deletion of Hdac3 results in a severe reduction in the number of iNKT cells, particularly of NKT1 cells. In addition, there is decreased cytokine production by Hdac3-deficient NKT2 and NKT17 cells. Hdac3-deficient iNKT cells have increased cell death that is not rescued by transgenic expression of Bcl-2 or Bcl-xL. Hdac3-deficient iNKT cells have less Cyto-ID staining and lower LC3A/B expression, indicative of reduced autophagy. Interestingly, Hdac3-deficient iNKT cells also have lower expression of the nutrient receptors GLUT1, CD71 and CD98, which would increase the need for autophagy when nutrients are limiting. Therefore, Hdac3 is required for iNKT cell development and differentiation.Puspa ThapaSinibaldo Romero ArochaJi Young ChungDerek B. Sant’AngeloVirginia Smith ShapiroNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017) |
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Medicine R Science Q Puspa Thapa Sinibaldo Romero Arocha Ji Young Chung Derek B. Sant’Angelo Virginia Smith Shapiro Histone deacetylase 3 is required for iNKT cell development |
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Abstract NKT cells are a distinct subset that have developmental requirements that often differ from conventional T cells. Here, we show that NKT-specific deletion of Hdac3 results in a severe reduction in the number of iNKT cells, particularly of NKT1 cells. In addition, there is decreased cytokine production by Hdac3-deficient NKT2 and NKT17 cells. Hdac3-deficient iNKT cells have increased cell death that is not rescued by transgenic expression of Bcl-2 or Bcl-xL. Hdac3-deficient iNKT cells have less Cyto-ID staining and lower LC3A/B expression, indicative of reduced autophagy. Interestingly, Hdac3-deficient iNKT cells also have lower expression of the nutrient receptors GLUT1, CD71 and CD98, which would increase the need for autophagy when nutrients are limiting. Therefore, Hdac3 is required for iNKT cell development and differentiation. |
format |
article |
author |
Puspa Thapa Sinibaldo Romero Arocha Ji Young Chung Derek B. Sant’Angelo Virginia Smith Shapiro |
author_facet |
Puspa Thapa Sinibaldo Romero Arocha Ji Young Chung Derek B. Sant’Angelo Virginia Smith Shapiro |
author_sort |
Puspa Thapa |
title |
Histone deacetylase 3 is required for iNKT cell development |
title_short |
Histone deacetylase 3 is required for iNKT cell development |
title_full |
Histone deacetylase 3 is required for iNKT cell development |
title_fullStr |
Histone deacetylase 3 is required for iNKT cell development |
title_full_unstemmed |
Histone deacetylase 3 is required for iNKT cell development |
title_sort |
histone deacetylase 3 is required for inkt cell development |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/bb0b26a9f24f4d3983eb28ce34699aa4 |
work_keys_str_mv |
AT puspathapa histonedeacetylase3isrequiredforinktcelldevelopment AT sinibaldoromeroarocha histonedeacetylase3isrequiredforinktcelldevelopment AT jiyoungchung histonedeacetylase3isrequiredforinktcelldevelopment AT derekbsantangelo histonedeacetylase3isrequiredforinktcelldevelopment AT virginiasmithshapiro histonedeacetylase3isrequiredforinktcelldevelopment |
_version_ |
1718388539017658368 |