自反应性CD8+T细胞上的KIR表达是由T细胞受体参与控制的
1The R.W. Johnson Pharmaceutical Research Institute, San Diego, California 92121, USA. huard@cmu.unige.ch
Nature
|February 5, 2000
概括
在没有T细胞受体 (TCR) 参与的情况下,T细胞上的杀手抑制受体 (KIR) 被下调. TCR参与维持KIR表达,这表明T细胞对自我抗原的耐受性具有动态的KIR调节.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 分子医学是分子医学.
背景情况:
- 自然杀手 (NK) 细胞的耐受性依赖于杀手抑制受体 (KIRs) 与自我主要基因相容性复合体 (MHC) I 类分子相互作用.
- 在T细胞上类似的抑制受体的作用仍然不完全理解.
研究的目的:
- 研究KIR表达在CD8+T细胞上的调节和功能意义.
- 为了确定T细胞受体 (TCR) 参与如何影响KIR表达和功能.
主要方法:
- 研究了CD8+ T细胞上的KIR表达与抗原呈现细胞上的KIR配体存在的关系.
- 评估了TCR参与对KIR表达和抑制功能的影响.
- 在体内抗原接触的背景下研究动态KIR表达.
主要成果:
- 当TCR不被激活时,CD8+ T细胞上的KIR被KIR配体下调.
- TCR参与维持KIR表达并恢复在带诱导下调后的功能.
- 动态KIR表达可以通过持续的抗原暴露来维持.
结论:
- CD8+ T 细胞上的动态 KIR 表达,由 TCR 参与和抗原暴露调节,在 T 细胞耐受性中起作用.
- 这种调节机制可能会节省自我反应性T细胞,使它们能够对各种抗原进行必要的免疫功能.
相关概念视频
Receptor Downregulation in MVBs
3.0K
Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
3.0K
Regulation of Hematopoietic Stem Cells
4.4K
All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
4.4K
Receptor Tyrosine Kinases
21.2K
Receptor tyrosine kinases or RTKs are membrane-bound receptors that phosphorylate specific tyrosine on protein substrates. RTKs regulate cellular growth, differentiation, survival, and migration. They contain an extracellular ligand binding domain, a transmembrane domain, and a cytosolic tail with intrinsic kinase activity. Several extracellular signaling molecules activate RTKs in one or more ways and relay the signal downstream. Ligands such as platelet-derived growth factor (PDGF) or...
21.2K
T Cell Activation and Clonal Selection
17.8K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
17.8K
T Cell Types and Functions
3.5K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
3.5K
Cytotoxic T Cells-mediated Immune Response
8.4K
Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
8.4K


