调节细胞死亡的机制:由特定蛋白质-A叙述检查诱导或抑制的结构和功能蛋白质通路
Diego Fernández-Lázaro1,2,3, Begoña Sanz3,4,5, Jesús Seco-Calvo3,4,6
1Department of Cellular Biology, Genetics, Histology and Pharmacology, Faculty of Health Sciences, University of Valladolid, Campus of Soria, 42004 Soria, Spain.
Proteomes
|January 22, 2024
概括
编程细胞死亡 (PCD) 平衡细胞分裂,以维持组织平衡. 本综述详细介绍了酶依赖和独立的PCD途径,这些途径对于理解生物调节和开发新疾病疗法至关重要.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生理学 生理学 生理学
背景情况:
- 细胞死亡是一种通过细胞分裂平衡的自然过程,防止组织缩.
- 编程细胞死亡 (PCD) 对于胚胎发育,组织平衡和去除受损细胞至关重要.
- 许多蛋白质介质和信号通路控制PCD.
研究的目的:
- 提供对酶依赖性和酶独立性PCD通路的叙述性综述.
- 阐明参与各种PCD机制的蛋白质和常见途径.
- 突出了解PCD对生物平衡和治疗发展的重要性.
主要方法:
- 对编程细胞死亡研究的文献综述.
- 将PCD分为酶依赖和酶独立的路径.
- 每个类别内的特定PCD类型的识别和描述.
主要成果:
- 详细的caspase-依赖的PCD的审查:阿诺伊基斯,灾难性菌,热,帝,帕尔塔纳托斯,角化.
- 详细的caspase-independent PCD的综述:瓦勒里亚退化,铁,帕拉,内,甲,ETosis (包括NETosis和EETosis).
- 重点是共同的途径和参与多种PCD机制的蛋白质媒介.
结论:
- 了解多种PCD途径对于理解生物平衡至关重要.
- 识别PCD中的特定蛋白质对于发现生物标志物和治疗点至关重要.
- 调节PCD反应为各种疾病的新型治疗干预提供了潜力.
相关概念视频
Overview of Cell Death
7.3K
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...
7.3K
The Intrinsic Apoptotic Pathway
6.6K
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...
6.6K
The Extrinsic Apoptotic Pathway
6.4K
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...
6.4K
Apoptosis
11.5K
Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
11.5K
Regulated Protein Degradation
7.3K
It is vital to regulate the activity of enzymatic as well as non-enzymatic proteins inside the cell. This can be achieved either through creating a balance between their rate of synthesis and degradation or regulating the intrinsic activity of the protein. Both these regulation mechanisms play an essential role in the normal functioning of cells.
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
7.3K
Regulation of the Unfolded Protein Response
2.4K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.4K


