在T细胞激活后,编程细胞死亡所需的Fas ((CD95) /FasL相互作用
1Arthritis Center, Boston University School of Medicine, Massachusetts 02118.
Nature
|February 2, 1995
概括
受体交联激活T细胞,导致细胞死亡. 这个过程涉及Fas连接体和Fas,触发细胞死亡程序,揭示T细胞亡的关键分子机制.
科学领域:
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 通过受体交叉连接激活T细胞会导致细胞亡.
- 调解这种激活诱导细胞死亡 (AICD) 的特定基因产物以前未被确定.
- AICD需要新的RNA和蛋白质合成.
研究的目的:
- 为了确定在受体交叉连接后导致T细胞死亡的特定基因产物.
- 为了阐明底层激活诱导的T细胞死亡的分子机制.
主要方法:
- 在实验模型中利用T细胞杂交瘤.
- 研究了Fas连接体和Fas上调在受体交叉连接上的作用.
- 使用可溶性Fas-免疫球蛋白融合蛋白来阻止Fas介导的信号传递.
主要成果:
- 发现受体交联诱导Fas联接体,并对T细胞上调Fas表达.
- 证明Fas连接体和Fas之间的相互作用可以激活细胞死亡途径.
- 一种可溶性Fas-免疫球蛋白融合蛋白选择性地抑制了细胞死亡,但没有初始激活.
结论:
- 联体和Fas是关键的死亡基因产物,调解激活诱导的T细胞死亡.
- Fas by Fas 连接体的参与代表了AICD的核心分子机制.
- 这些发现澄清了刺激后导致T细胞亡的途径.
相关概念视频
Overview of Cell Death
Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...
Caspases
Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside cells.
The Extrinsic Apoptotic Pathway
The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
The Intrinsic Apoptotic Pathway
Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
T Cell Activation and Clonal Selection
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...
Cytotoxic T Cells-mediated Immune Response
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...


