急性肺损伤中的自噬作用

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Danjuan Liu, Shuoyun Weng, Chunjin Fu, Rongjie Guo, Min Chen, Bingbing Shi, Junting Weng
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引用次数: 0

摘要

急性肺损伤(ALI)是由于广泛炎症和肺血管通透性增加而导致的快速呼吸衰竭,通常会发展为急性呼吸窘迫综合征(ARDS),死亡率很高。自噬是一种细胞降解过程,对清除受损细胞器和蛋白质至关重要,在调节肺损伤和修复方面发挥着关键作用。本综述探讨了自噬在 ALI 中维持细胞功能、减轻炎症和氧化应激方面的保护作用。它强调了精确调控的必要性,以充分利用自噬在这方面的治疗潜力。我们总结了自噬影响肺损伤和修复的机制,讨论了自噬和细胞凋亡之间的相互作用,并研究了潜在的治疗策略,包括自噬诱导剂、靶向自噬信号通路、抗氧化剂、抗炎药物、基因编辑和干细胞疗法。了解自噬在ALI中的作用有助于开发新的干预措施,改善患者预后,降低与这种严重疾病相关的死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autophagy in Acute Lung Injury.

Acute lung injury (ALI) is a critical condition marked by rapid-onset respiratory failure due to extensive inflammation and increased pulmonary vascular permeability, often progressing to acute respiratory distress syndrome (ARDS) with high mortality. Autophagy, a cellular degradation process essential for removing damaged organelles and proteins, plays a crucial role in regulating lung injury and repair. This review examines the protective role of autophagy in maintaining cellular function and reducing inflammation and oxidative stress in ALI. It underscores the necessity of precise regulation to fully harness the therapeutic potential of autophagy in this context. We summarize the mechanisms by which autophagy influences lung injury and repair, discuss the interplay between autophagy and apoptosis, and examine potential therapeutic strategies, including autophagy inducers, targeted autophagy signaling pathways, antioxidants, anti-inflammatory drugs, gene editing, and stem cell therapy. Understanding the role of autophagy in ALI could lead to novel interventions for improving patient outcomes and reducing mortality rates associated with this severe condition.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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