GSTDTAP  > 地球科学
DOI10.1126/science.aau9072
Choline acetyltransferase-expressing T cells are required to control chronic viral infection
Cox, Maureen A.1; Duncan, Gordon S.1; Lin, Gloria H. Y.1,13; Steinberg, Benjamin E.1,2,14; Yu, Lisa X.3; Brenner, Dirk1,4,5,6; Buckler, Luke N.1; Elia, Andrew J.1; Wakeham, Andrew C.1; Nieman, Brian3,7,8; Dominguez-Brauer, Carmen1; Elford, Alisha R.1; Gill, Kyle T.1; Kubli, Shawn P.1; Haight, Jillian1; Berger, Thorsten1; Ohashi, Pamela S.1,9; Tracey, Kevin J.10; Olofsson, Peder S.10,11; Mak, Tak W.1,7,8,9,12
2019-02-08
发表期刊SCIENCE
ISSN0036-8075
EISSN1095-9203
出版年2019
卷号363期号:6427页码:639-+
文章类型Article
语种英语
国家Canada; Luxembourg; Denmark; USA; Sweden; Peoples R China
英文摘要

Although widely studied as a neurotransmitter, T cell-derived acetylcholine (ACh) has recently been reported to play an important role in regulating immunity. However, the role of lymphocyte-derived ACh in viral infection is unknown. Here, we show that the enzyme choline acetyltransferase (ChAT), which catalyzes the rate-limiting step of ACh production, is robustly induced in both CD4(+) and CD8(+) T cells during lymphocytic choriomeningitis virus (LCMV) infection in an IL-21-dependent manner. Deletion of Chat within the T cell compartment in mice ablated vasodilation in response to infection, impaired the migration of antiviral T cells into infected tissues, and ultimately compromised the control of chronic LCMV clone 13 infection. Our results reveal a genetic proof of function for ChAT in T cells during viral infection and identify a pathway of T cell migration that sustains antiviral immunity.


领域地球科学 ; 气候变化 ; 资源环境
收录类别SCI-E
WOS记录号WOS:000458114200051
WOS关键词IL-21 ; EFFECTOR
WOS类目Multidisciplinary Sciences
WOS研究方向Science & Technology - Other Topics
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/200715
专题地球科学
资源环境科学
气候变化
作者单位1.Univ Hlth Network, Campbell Family Inst Breast Canc Res, Princess Margaret Canc Ctr, Toronto, ON M5G 2M9, Canada;
2.Univ Toronto, Dept Anesthesia, Toronto, ON M5G 1E2, Canada;
3.Hosp Sick Children, Mouse Imaging Ctr, Toronto, ON M5T 3H7, Canada;
4.Luxembourg Inst Hlth, Dept Infect & Immun, L-4354 Esch Sur Alzette, Luxembourg;
5.Univ Southern Denmark, Odense Univ Hosp, ORCA, Dept Dermatol, Odense, Denmark;
6.Univ Southern Denmark, Odense Univ Hosp, Allergy Ctr, Odense, Denmark;
7.Univ Toronto, Ontario Inst Canc Res, Toronto, ON M5G 2C1, Canada;
8.Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2C1, Canada;
9.Univ Toronto, Dept Immunol, Toronto, ON M5G 2C1, Canada;
10.Feinstein Inst Med Res, Lab Biomed Sci, Manhasset, NY 11030 USA;
11.Karolinska Inst, Karolinska Univ Hosp, Dept Med, Ctr Bioelect Med, S-17176 Stockholm, Sweden;
12.Univ Hong Kong, Dept Pathol, Hong Kong, Peoples R China;
13.Trillium Therapeut Inc, Mississauga, ON L5L 1J9, Canada;
14.Hosp Sick Children, Dept Anesthesia & Pain Med, Toronto, ON M5G 1X8, Canada
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GB/T 7714
Cox, Maureen A.,Duncan, Gordon S.,Lin, Gloria H. Y.,et al. Choline acetyltransferase-expressing T cells are required to control chronic viral infection[J]. SCIENCE,2019,363(6427):639-+.
APA Cox, Maureen A..,Duncan, Gordon S..,Lin, Gloria H. Y..,Steinberg, Benjamin E..,Yu, Lisa X..,...&Mak, Tak W..(2019).Choline acetyltransferase-expressing T cells are required to control chronic viral infection.SCIENCE,363(6427),639-+.
MLA Cox, Maureen A.,et al."Choline acetyltransferase-expressing T cells are required to control chronic viral infection".SCIENCE 363.6427(2019):639-+.
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