Impact of age on T cell signaling: A general defect or specific alterations?

被引:73
作者
Larbi, Anis [1 ]
Pawelec, Graham [2 ]
Wong, Siew Cheng [1 ]
Goldeck, David [2 ]
Tai, June Jing-Yi [1 ]
Fulop, Tamas [3 ]
机构
[1] ASTAR, Singapore Immunol Network SIgN, Singapore 138648, Singapore
[2] Univ Tubingen, Med Res Ctr, Tuebingen Aging & Tumor Immunol Grp, D-72074 Tubingen, Germany
[3] Univ Sherbrooke, Immunol Lab, Res Ctr Aging, Sherbrooke, PQ J1K 2R1, Canada
关键词
TCR; Signaling; Lipid rafts; Functionality; Flow cytometry; NF-KAPPA-B; LIPID RAFTS; TYROSINE PHOSPHORYLATION; ANTIGEN RECEPTOR; DOWN-REGULATION; IN-VITRO; IMMUNOLOGICAL SYNAPSE; CD28; COSTIMULATION; ALTERED FUNCTIONS; ELDERLY HUMANS;
D O I
10.1016/j.arr.2010.09.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Decreased immune responsiveness associated with aging is generally termed "immunosenescence". Several theories have been proposed to explain age-related declines in immune responses. Here, we will focus on and describe potential defects in T cell signal transduction from the membrane to the nucleus, leading to changes in the type, intensity and duration of the response as a major factor contributing to immunosenescence. We will first detail T cell signaling through the T cell receptor (TCR), CD28 and IL-2 receptor (IL-2R) and then discuss the observed age-related alterations to these signaling pathways. The role of membrane rafts in T cell signaling and T cell aging will be described. These factors will be considered in the context of the notion that age-related changes to T cell signaling may be attributed to changes in the functionality of the T cells due to shifts in T cell subpopulations with age. For this reason, we conclude by highlighting the application of multiparametric signaling analysis in leukocyte subsets using flow cytometry as a means to obtain a clearer picture with respect to age-related changes to immune signaling. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:370 / 378
页数:9
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