LFA-1 Activation in T-Cell Migration and Immunological Synapse Formation.

LFA-1 Activation in T-Cell Migration and Immunological Synapse Formation.
复制标题

DOI:
10.3390/cells12081136
复制
发表时间:
2023-04-12
期刊:
影响因子:
6
通讯作者:
--
中科院分区:
生物学2区
文献类型:
--
作者:

文献摘要

参考文献

相似文献

整合素LFA-1在t细胞迁移和免疫突触的形成中起关键作用。LFA-1通过与不同亲和度的配体相互作用发挥作用:低、中、高。先前的研究大多是研究LFA-1在高亲和力状态下如何调节T细胞的运输和功能。LFA-1也以中间亲和状态存在于T细胞上,然而,激活LFA-1到中间亲和状态的信号通路以及LFA-1在这种亲和状态中的作用在很大程度上仍然是未知的。本文就LFA-1在调节t细胞迁移和免疫突触形成中的作用及其与不同配体结合亲和力作一综述。
Integrin LFA-1 plays a critical role in T-cell migration and in the formation of immunological synapses. LFA-1 functions through interacting with its ligands with differing affinities: low, intermediate, and high. Most prior research has studied how LFA-1 in the high-affinity state regulates the trafficking and functions of T cells. LFA-1 is also presented in the intermediate-affinity state on T cells, however, the signaling to activate LFA-1 to the intermediate-affinity state and the role of LFA-1 in this affinity state both remain largely elusive. This review briefly summarizes the activation and roles of LFA-1 with varied ligand-binding affinities in the regulation of T-cell migration and immunological synapse formation.
DOI: 10.1371/journal.pone.0005403
发表时间: 2009
期刊: PloS one
影响因子: 3.7
作者:
Rossy J;Schlicht D;Engelhardt B;Niggli V
通讯作者: Niggli V
DOI: 10.1084/jem.20111493
发表时间: 2012-02-13
期刊: The Journal of experimental medicine
影响因子: --
作者:
Block H;Herter JM;Rossaint J;Stadtmann A;Kliche S;Lowell CA;Zarbock A
通讯作者: Zarbock A
DOI: 10.1083/jcb.201406120
发表时间: 2015-02-16
期刊: The Journal of cell biology
影响因子: --
作者:
Comrie WA;Li S;Boyle S;Burkhardt JK
通讯作者: Burkhardt JK
DOI: 10.1083/jcb.201406121
发表时间: 2015-02-16
期刊: The Journal of cell biology
影响因子: --
作者:
Comrie WA;Babich A;Burkhardt JK
通讯作者: Burkhardt JK
DOI: 10.1126/scitranslmed.3005930
发表时间: 2013-03-20
影响因子: 17.1
作者:
Brentjens RJ;Davila ML;Riviere I;Park J;Wang X;Cowell LG;Bartido S;Stefanski J;Taylor C;Olszewska M;Borquez-Ojeda O;Qu J;Wasielewska T;He Q;Bernal Y;Rijo IV;Hedvat C;Kobos R;Curran K;Steinherz P;Jurcic J;Rosenblat T;Maslak P;Frattini M;Sadelain M
通讯作者: Sadelain M