The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling

Abstract The efficient induction and long-term persistence of pathogen-specific memory CD8 T cells are pivotal to rapidly curb the reinfection. Recent studies indicated that long-noncoding RNAs expression is highly cell- and stage-specific during T cell development and differentiation, suggesting th...

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Main Authors: Yanyan Zhang, Baohua Li, Qiang Bai, Pengcheng Wang, Gang Wei, Zhirong Li, Li Hu, Qin Tian, Jing Zhou, Qizhao Huang, Zhiming Wang, Shuai Yue, Jialin Wu, Liuqing Yang, Xinyuan Zhou, Lubin Jiang, Ting Ni, Lilin Ye, Yuzhang Wu
Format: Article
Language:English
Published: Nature Publishing Group 2021-03-01
Series:Signal Transduction and Targeted Therapy
Online Access:https://doi.org/10.1038/s41392-021-00492-9
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spelling doaj-ccb3befdc2754c018ded748254cf1d302021-03-28T11:17:33ZengNature Publishing GroupSignal Transduction and Targeted Therapy2059-36352021-03-016111410.1038/s41392-021-00492-9The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signalingYanyan Zhang0Baohua Li1Qiang Bai2Pengcheng Wang3Gang Wei4Zhirong Li5Li Hu6Qin Tian7Jing Zhou8Qizhao Huang9Zhiming Wang10Shuai Yue11Jialin Wu12Liuqing Yang13Xinyuan Zhou14Lubin Jiang15Ting Ni16Lilin Ye17Yuzhang Wu18Institute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityHuman Phenome Institute, Fudan UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer CenterInstitute of Immunology PLA, Third Military Medical UniversityInstitute Pasteur of Shanghai, Chinese Academy of Sciences (CAS)Human Phenome Institute, Fudan UniversityInstitute of Immunology PLA, Third Military Medical UniversityInstitute of Immunology PLA, Third Military Medical UniversityAbstract The efficient induction and long-term persistence of pathogen-specific memory CD8 T cells are pivotal to rapidly curb the reinfection. Recent studies indicated that long-noncoding RNAs expression is highly cell- and stage-specific during T cell development and differentiation, suggesting their potential roles in T cell programs. However, the key lncRNAs playing crucial roles in memory CD8 T cell establishment remain to be clarified. Through CD8 T cell subsets profiling of lncRNAs, this study found a key lncRNA-Snhg1 with the conserved naivehi-effectorlo-memoryhi expression pattern in CD8 T cells of both mice and human, that can promote memory formation while impeding effector CD8 in acute viral infection. Further, Snhg1 was found interacting with the conserved vesicle trafficking protein Vps13D to promote IL-7Rα membrane location specifically. With the deep mechanism probing, the results show Snhg1-Vps13D regulated IL-7 signaling with its dual effects in memory CD8 generation, which not just because of the sustaining role of STAT5-BCL-2 axis for memory survival, but more through the STAT3-TCF1-Blimp1 axis for transcriptional launch program of memory differentiation. Moreover, we performed further study with finding a similar high-low-high expression pattern of human SNHG1/VPS13D/IL7R/TCF7 in CD8 T cell subsets from PBMC samples of the convalescent COVID-19 patients. The central role of Snhg1-Vps13D-IL-7R-TCF1 axis in memory CD8 establishment makes it a potential target for improving the vaccination effects to control the ongoing pandemic.https://doi.org/10.1038/s41392-021-00492-9
collection DOAJ
language English
format Article
sources DOAJ
author Yanyan Zhang
Baohua Li
Qiang Bai
Pengcheng Wang
Gang Wei
Zhirong Li
Li Hu
Qin Tian
Jing Zhou
Qizhao Huang
Zhiming Wang
Shuai Yue
Jialin Wu
Liuqing Yang
Xinyuan Zhou
Lubin Jiang
Ting Ni
Lilin Ye
Yuzhang Wu
spellingShingle Yanyan Zhang
Baohua Li
Qiang Bai
Pengcheng Wang
Gang Wei
Zhirong Li
Li Hu
Qin Tian
Jing Zhou
Qizhao Huang
Zhiming Wang
Shuai Yue
Jialin Wu
Liuqing Yang
Xinyuan Zhou
Lubin Jiang
Ting Ni
Lilin Ye
Yuzhang Wu
The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
Signal Transduction and Targeted Therapy
author_facet Yanyan Zhang
Baohua Li
Qiang Bai
Pengcheng Wang
Gang Wei
Zhirong Li
Li Hu
Qin Tian
Jing Zhou
Qizhao Huang
Zhiming Wang
Shuai Yue
Jialin Wu
Liuqing Yang
Xinyuan Zhou
Lubin Jiang
Ting Ni
Lilin Ye
Yuzhang Wu
author_sort Yanyan Zhang
title The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
title_short The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
title_full The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
title_fullStr The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
title_full_unstemmed The lncRNA Snhg1-Vps13D vesicle trafficking system promotes memory CD8 T cell establishment via regulating the dual effects of IL-7 signaling
title_sort lncrna snhg1-vps13d vesicle trafficking system promotes memory cd8 t cell establishment via regulating the dual effects of il-7 signaling
publisher Nature Publishing Group
series Signal Transduction and Targeted Therapy
issn 2059-3635
publishDate 2021-03-01
description Abstract The efficient induction and long-term persistence of pathogen-specific memory CD8 T cells are pivotal to rapidly curb the reinfection. Recent studies indicated that long-noncoding RNAs expression is highly cell- and stage-specific during T cell development and differentiation, suggesting their potential roles in T cell programs. However, the key lncRNAs playing crucial roles in memory CD8 T cell establishment remain to be clarified. Through CD8 T cell subsets profiling of lncRNAs, this study found a key lncRNA-Snhg1 with the conserved naivehi-effectorlo-memoryhi expression pattern in CD8 T cells of both mice and human, that can promote memory formation while impeding effector CD8 in acute viral infection. Further, Snhg1 was found interacting with the conserved vesicle trafficking protein Vps13D to promote IL-7Rα membrane location specifically. With the deep mechanism probing, the results show Snhg1-Vps13D regulated IL-7 signaling with its dual effects in memory CD8 generation, which not just because of the sustaining role of STAT5-BCL-2 axis for memory survival, but more through the STAT3-TCF1-Blimp1 axis for transcriptional launch program of memory differentiation. Moreover, we performed further study with finding a similar high-low-high expression pattern of human SNHG1/VPS13D/IL7R/TCF7 in CD8 T cell subsets from PBMC samples of the convalescent COVID-19 patients. The central role of Snhg1-Vps13D-IL-7R-TCF1 axis in memory CD8 establishment makes it a potential target for improving the vaccination effects to control the ongoing pandemic.
url https://doi.org/10.1038/s41392-021-00492-9
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