Evolving methodologies for identification and differentiation of regulated cell death modalities.

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Anmol Kaur, Urvi, Rajeev Kumar Pandey, Sanjana Mehrotra
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引用次数: 0

Abstract

Cell death is a crucial evolutionary adaptation for multicellular organisms through which they can systematically eliminate cells that are no longer needed, potentially harmful, or are damaged beyond repair. Over the past few decades, our understanding of the cell death mechanisms has expanded significantly revealing a diverse, and interconnected array of regulated cell death (RCD) pathways that includes apoptosis, necroptosis, pyroptosis, cuproptosis etc. While the complexities of these pathways have incrementally increased with the evolution of multicellularity, many core components associated with cell death have remained conserved. This points towards the essential function of cell death in maintenance of homeostasis at the cellular, organismal and individual level. It is thus not a surprise that their dysregulation can manifest in the form of several pathologies. Therefore, the ability to accurately detect and distinguish different forms of cell death is essential not only for advancing our understanding of the fundamental cellular and molecular processes but also for elucidating their role in disease pathogenesis, where their dysregulation contributes to various pathological conditions. However, detecting and differentiating various forms of cell death is a challenging task. Since there are multiple cell death modalities, many of their characteristics overlap, such as a condensed nucleus being observed in both secondary necrosis and apoptosis. Further, a cell can undergo more than one kind of cell death simultaneously, a process known as "cell death continuum" further complicating detection and classification. This chapter provides an overview of the conventional methods used for detecting cell death, highlighting both probe-based and non-probe-based techniques. Recent advancements in high-throughput strategies, AI based predictive modelling and other such novel techniques that offer greater specificity in cell death characterization are particularly emphasized.

鉴定和分化受调节细胞死亡模式的不断发展的方法。
细胞死亡是多细胞生物的一种重要的进化适应,通过这种适应,它们可以系统地消除不再需要的、潜在有害的或受损无法修复的细胞。在过去的几十年里,我们对细胞死亡机制的理解已经大大扩展,揭示了多种相互关联的调节细胞死亡(RCD)途径,包括凋亡、坏死坏死、焦亡、铜坏死等。虽然这些通路的复杂性随着多细胞进化而逐渐增加,但许多与细胞死亡相关的核心成分仍然是保守的。这指出了细胞死亡在维持细胞、组织和个体水平上的稳态中的基本功能。因此,它们的失调可以表现为几种病理形式也就不足为奇了。因此,准确检测和区分不同形式的细胞死亡的能力不仅对于提高我们对基本细胞和分子过程的理解至关重要,而且对于阐明它们在疾病发病机制中的作用至关重要,其中它们的失调导致了各种病理状况。然而,检测和区分各种形式的细胞死亡是一项具有挑战性的任务。由于存在多种细胞死亡方式,它们的许多特征重叠,例如在继发性坏死和细胞凋亡中都观察到细胞核凝聚。此外,一个细胞可以同时经历一种以上的细胞死亡,这一过程被称为“细胞死亡连续体”,进一步使检测和分类复杂化。本章概述了用于检测细胞死亡的传统方法,重点介绍了基于探针和非基于探针的技术。高通量策略、基于人工智能的预测建模和其他新技术的最新进展特别强调了细胞死亡表征的更大特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.00
自引率
0.00%
发文量
110
审稿时长
4-8 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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