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The impact of stress on the transcriptomic signature of iNKT1 cells.

作者信息

Papadogianni Georgia, Ravens Inga, Hassan Ahmed, Dittrich-Breiholz Oliver, Bernhardt Günter, Georgiev Hristo

机构信息

Institute of Immunology, Hannover Medical School, 30625, Hannover, Germany.

Research Core Unit Genomics, Hannover Medical School, 30625, Hannover, Germany.

出版信息

Biochem Biophys Rep. 2021 Oct 29;28:101163. doi: 10.1016/j.bbrep.2021.101163. eCollection 2021 Dec.

DOI:10.1016/j.bbrep.2021.101163
PMID:34765746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8570944/
Abstract

Invariant natural killer T (iNKT) cells develop in thymus before emigrating and settling peripheral tissues and organs. In contrast to regular naïve T cells, most iNKT cells do not continuously recirculate but are rather sessile and can adopt phenotypically as well as functionally to their tissue environment. To explore this in more detail, we focused on the most widely distributed CD4iNKT1 cells and compared the transcriptome of cells isolated from liver and spleen. Whereas there are only very few genuine differences in the transcriptomes of CD4iNKT1 cells of these two organs, the mode of cell isolation left clear marks in the transcriptomic signature. In contrast to liver cell isolated in the cold, cells prepared by enzymatic tissue digestion upregulated quickly a series of genes known to respond to stress. Therefore, to avoid erroneous conclusions, a comparison of expression profiles must take into consideration the history of cell preparation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/8b9bca8f8859/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/2e4197193399/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/0bddc49d966d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/66bf44964608/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/8b9bca8f8859/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/2e4197193399/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/0bddc49d966d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/66bf44964608/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab73/8570944/8b9bca8f8859/gr4.jpg

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本文引用的文献

1
Impact of Aging on the Phenotype of Invariant Natural Killer T Cells in Mouse Thymus.衰老对小鼠胸腺中不变自然杀伤 T 细胞表型的影响。
Front Immunol. 2020 Oct 30;11:575764. doi: 10.3389/fimmu.2020.575764. eCollection 2020.
2
High Dimensional Single-Cell Analysis Reveals iNKT Cell Developmental Trajectories and Effector Fate Decision.高维单细胞分析揭示 iNKT 细胞的发育轨迹和效应器命运决定。
Cell Rep. 2020 Sep 8;32(10):108116. doi: 10.1016/j.celrep.2020.108116.
3
Tissue-specific shaping of the TCR repertoire and antigen specificity of iNKT cells.
iNKT 细胞 T 细胞受体库的组织特异性形成和抗原特异性。
Elife. 2019 Dec 16;8:e51663. doi: 10.7554/eLife.51663.
4
ARTC2.2/P2RX7 Signaling during Cell Isolation Distorts Function and Quantification of Tissue-Resident CD8 T Cell and Invariant NKT Subsets.在细胞分离过程中,ARTC2.2/P2RX7 信号会扭曲组织驻留 CD8 T 细胞和不变自然杀伤 T 细胞亚群的功能和定量分析。
J Immunol. 2019 Apr 1;202(7):2153-2163. doi: 10.4049/jimmunol.1801613. Epub 2019 Feb 18.
5
A common transcriptomic program acquired in the thymus defines tissue residency of MAIT and NKT subsets.在胸腺中获得的常见转录组程序定义了 MAIT 和 NKT 亚群的组织驻留。
J Exp Med. 2019 Jan 7;216(1):133-151. doi: 10.1084/jem.20181483. Epub 2018 Dec 5.
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Tissue-specific functions of invariant natural killer T cells.固有自然杀伤 T 细胞的组织特异性功能。
Nat Rev Immunol. 2018 Sep;18(9):559-574. doi: 10.1038/s41577-018-0034-2.
7
Runx3 programs CD8 T cell residency in non-lymphoid tissues and tumours.Runx3调控CD8 T细胞在非淋巴组织和肿瘤中的驻留。
Nature. 2017 Dec 14;552(7684):253-257. doi: 10.1038/nature24993. Epub 2017 Dec 6.
8
The P2X7 Receptor in Infection and Inflammation.P2X7 受体在感染和炎症中的作用。
Immunity. 2017 Jul 18;47(1):15-31. doi: 10.1016/j.immuni.2017.06.020.
9
Distinct gene expression patterns correlate with developmental and functional traits of iNKT subsets.不同的基因表达模式与 iNKT 亚群的发育和功能特征相关。
Nat Commun. 2016 Oct 10;7:13116. doi: 10.1038/ncomms13116.
10
Hobit and Blimp1 instruct a universal transcriptional program of tissue residency in lymphocytes.Hobit 和 Blimp1 指导淋巴细胞中组织驻留的通用转录程序。
Science. 2016 Apr 22;352(6284):459-63. doi: 10.1126/science.aad2035.