CD4 与 CD8 T 细胞命运的决定:一个基于多基因组的观点
Zoë Steier1,2,3, Esther Jeong Yoon Kim4, Dominik A Aylard4
1Department of Bioengineering and Center for Computational Biology, University of California, Berkeley, California, USA.
Annual review of immunology
|January 25, 2024
概括
发育中的T细胞在CD4+辅助细胞或CD8+细胞毒性命运之间进行选择. 我们的研究使用CITE-seq来绘制RNA和蛋白质在分化过程中的变化,为T细胞谱系选择提出了一个新的顺序选择模型.
科学领域:
- 免疫学 免疫学 免疫学
- 发展生物学 发展生物学
- 分子生物学分子生物学
背景情况:
- 胸细胞分化成CD4+辅助细胞或CD8+细胞毒性T细胞对于适应性免疫至关重要,但不完全理解.
- 之前的研究缺乏足够的分辨率来充分阐明控制这种血统决定的分子机制.
研究的目的:
- 在CD4+和CD8+T细胞分化过程中提供RNA和蛋白质表达的高分辨率时间图.
- 研究T细胞受体信号与关键血统转录因子 (ThPOK和RUNX3) 的表达之间的关系.
- 为T细胞谱系承诺提出一种新型模型.
主要方法:
- 转录组和表皮细胞的利用细胞索引 (CITE-seq) 用于小鼠胸细胞的多组学分析.
- 在T细胞发育过程中分析了基因和蛋白质表达动态.
主要成果:
- 在CD8与CD4T细胞分化过程中RNA和蛋白质表达变化的详细时间表.
- 重新评估了T细胞受体信号与ThPOK/RUNX3表达之间的联系.
- 确定了推动血统承诺的关键分子事件.
结论:
- 提出了一种序列选择模型来解释MHC识别与T细胞谱系选择之间的联系.
- 这个模型整合了动力信号,指导和随机/选择模型的元素.
- 提供了对T细胞分化途径的精细理解.
关键词:
CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD4 CD7 CD7 CD7 CD7 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD9 CD8 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD8 CD9 CD8 CD8 CD8 CD9 CD9 CD8 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 CD9 是一个字体的字体的字体是什么意思在T细胞抗原受体抗原受体.单细胞基因表达分析分析甲状腺细胞 (thymocytes) 是一种细胞.胸腺 (thymus) 是一个神经系统.相关概念视频
T Cell Activation and Clonal Selection
735
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...
735
T Cell Types and Functions
1.0K
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...
1.0K
Multipotency of Hematopoietic Stem Cells
3.1K
The hematopoietic stem cells or HSCs are multipotent, meaning they can differentiate and give rise to all blood and immune cells. HSCs are maintained in the quiescent stage until an external stimulus initiates their differentiation. The multipotent HSCs exist as two heterogeneous populations, long-term repopulating cells (LTRC) and short-term repopulating cells (STRC). The two HSC populations have different surface markers or receptors and are classified based on quiescence and long-term...
3.1K
Lineage Commitment
3.0K
Commitment is the process whereby stem cells:
3.0K
B Cell Activation and Differentiation
1.7K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
1.7K
Cells of the Adaptive Immune Response
988
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
988


