细胞死亡,IL-1细胞因子和瘤进展
1Key Laboratory of Cell Proliferation and Differentiation of the Ministry of Education, School of Life Sciences, Peking University, Beijing 100871, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.
Cancer cell
|April 18, 2025
概括
瘤细胞死亡影响癌症生长和免疫力. 阻断死细胞释放interleukin-1α (IL-1α) 和巨细胞吞apoptotic细胞的途径,从而激活IL-33-调节T细胞 (Treg) 信号,可以改善免疫疗法.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 细胞生物学 细胞生物学
背景情况:
- 瘤细胞死亡是影响癌症发展和身体对癌症免疫反应的关键因素.
- 最近的研究突出了不同类型的瘤细胞死亡影响瘤微环境和免疫规避的特定机制.
研究的目的:
- 阐明瘤类细胞死亡和瘤类细胞细胞灭绝在塑造瘤微环境中的不同作用.
- 研究由这些细胞死亡过程激活的下游信号通路.
- 评估阻断这些已识别的途径以增强抗癌免疫疗法的潜力.
主要方法:
- 在死细胞样细胞死亡后,细胞因子释放的分析 (介质素-1α).
- 研究瘤细胞的巨细胞衰变的研究.
- 对介质蛋白-33 (IL-33) 和调控性T细胞 (Treg) 轴激活的评估.
- 在临床前癌症模型中评估涉及阻断这些途径的治疗策略.
主要成果:
- 经证明,瘤类瘤细胞死亡会释放中白素-1α (IL-1α),促进髓质衍生免疫抑制.
- 研究人员发现,中枢鼻腔巨细胞 (MSM) 对亡性瘤细胞的化作用会激活IL-33-Treg轴.
- 这种IL-33-Treg轴激活与加速瘤生长有关.
- 阻断这些特定的与细胞死亡相关的途径表明,有可能提高现有的癌症免疫疗法的有效性.
结论:
- 不同的瘤细胞死亡模式对抗瘤免疫力产生明显和显著的影响.
- 向从死细胞释放的IL-1α和通过细胞吞活动激活的IL-33-Treg轴是一个有前途的战略.
- 干扰这些免疫抑制机制可以提高癌症免疫治疗的疗效,提供新的治疗途径.
相关概念视频
The Extrinsic Apoptotic Pathway
5.5K
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...
5.5K
Overview of Cell Death
5.6K
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...
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...
5.6K
The Intrinsic Apoptotic Pathway
5.7K
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...
5.7K
Caspases
11.5K
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...
11.5K
T Cell Types and Functions
689
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...
689
Phagocytosis of Apoptotic Cells
3.1K
Cells undergoing apoptosis form apoptotic bodies that must be removed immediately to prevent inflammation, autoimmune diseases, and necrosis. Phagocytosis is carried out by professional phagocytes such as macrophages or immature dendritic cells. Non-professional phagocytes such as epithelial cells and fibroblasts also take part in this process; however, they are not as effective as professional phagocytes.
Normal cells contain receptors that prevent them from being recognized...
Normal cells contain receptors that prevent them from being recognized...
3.1K


