Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking

Abstract T cell receptor (TCR) signaling is important for T cell homeostasis and function. However, how surface TCR levels are regulated and its biological significance on T cells remains largely unknown. Here, we show that the T cell-specific deletion of Arpc2, a component of Arp2/3 complex, result...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Ye Zhang, Hao Shen, Haifeng Liu, Haiyun Feng, Yan Liu, Xiaoyan Zhu, Xiaolong Liu
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/ae3bc8bd6ab84d138b7f827da4167c83
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ae3bc8bd6ab84d138b7f827da4167c83
record_format dspace
spelling oai:doaj.org-article:ae3bc8bd6ab84d138b7f827da4167c832021-12-02T16:06:01ZArp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking10.1038/s41598-017-08357-42045-2322https://doaj.org/article/ae3bc8bd6ab84d138b7f827da4167c832017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08357-4https://doaj.org/toc/2045-2322Abstract T cell receptor (TCR) signaling is important for T cell homeostasis and function. However, how surface TCR levels are regulated and its biological significance on T cells remains largely unknown. Here, we show that the T cell-specific deletion of Arpc2, a component of Arp2/3 complex, results in compromised peripheral T cell homeostasis. Arp2/3 complex-nucleated actin filaments are essential for maintaining surface TCR levels by regulating TCR+ endosome trafficking in resting state and controlling polarization of TCR+ endosomes during immune synapse formation in T cells. Additionally, Arpc2-TKO T cells are unable to form immune synapse. Interestingly, defected T cell homeostasis is caused by reduced surface TCR levels but not impaired immune synapse formation. Collectively, our findings suggest that Arp2/3 complex-nucleated actin filaments are required for maintaining surface TCR levels via regulating TCR+ endosome trafficking which is essential for T cell homeostasis.Ye ZhangHao ShenHaifeng LiuHaiyun FengYan LiuXiaoyan ZhuXiaolong LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Ye Zhang
Hao Shen
Haifeng Liu
Haiyun Feng
Yan Liu
Xiaoyan Zhu
Xiaolong Liu
Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
description Abstract T cell receptor (TCR) signaling is important for T cell homeostasis and function. However, how surface TCR levels are regulated and its biological significance on T cells remains largely unknown. Here, we show that the T cell-specific deletion of Arpc2, a component of Arp2/3 complex, results in compromised peripheral T cell homeostasis. Arp2/3 complex-nucleated actin filaments are essential for maintaining surface TCR levels by regulating TCR+ endosome trafficking in resting state and controlling polarization of TCR+ endosomes during immune synapse formation in T cells. Additionally, Arpc2-TKO T cells are unable to form immune synapse. Interestingly, defected T cell homeostasis is caused by reduced surface TCR levels but not impaired immune synapse formation. Collectively, our findings suggest that Arp2/3 complex-nucleated actin filaments are required for maintaining surface TCR levels via regulating TCR+ endosome trafficking which is essential for T cell homeostasis.
format article
author Ye Zhang
Hao Shen
Haifeng Liu
Haiyun Feng
Yan Liu
Xiaoyan Zhu
Xiaolong Liu
author_facet Ye Zhang
Hao Shen
Haifeng Liu
Haiyun Feng
Yan Liu
Xiaoyan Zhu
Xiaolong Liu
author_sort Ye Zhang
title Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
title_short Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
title_full Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
title_fullStr Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
title_full_unstemmed Arp2/3 complex controls T cell homeostasis by maintaining surface TCR levels via regulating TCR+ endosome trafficking
title_sort arp2/3 complex controls t cell homeostasis by maintaining surface tcr levels via regulating tcr+ endosome trafficking
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/ae3bc8bd6ab84d138b7f827da4167c83
work_keys_str_mv AT yezhang arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT haoshen arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT haifengliu arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT haiyunfeng arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT yanliu arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT xiaoyanzhu arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
AT xiaolongliu arp23complexcontrolstcellhomeostasisbymaintainingsurfacetcrlevelsviaregulatingtcrendosometrafficking
_version_ 1718385167950675968