Mesenchymal stem cell-based therapy for paraquat-induced lung injury.

IF 5.3 2区 医学 Q2 CELL BIOLOGY
Xiaping Zhang, Ting Li, Yuan-Qiang Lu
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引用次数: 0

Abstract

Paraquat poisoning results in significant pulmonary damage, but current treatments are only minimally effective in repairing the injured lung tissues. Recent research has highlighted the promise of using stem cell therapy, namely mesenchymal stem cells, as a new method for treating paraquat toxicity. These cells have shown effectiveness in decreasing inflammation, apoptosis, and fibrosis in the mice lungs subjected to paraquat. The therapeutic implications of mesenchymal stem cells are believed to arise from their release of bioactive proteins and their capacity to regulate inflammatory responses. However, additional clinical study is required to validate these therapies' efficacy. This review thoroughly explores the pathophysiology of paraquat poisoning and the properties of mesenchymal stem cells. Additionally, it critically assesses the long-term safety and effectiveness of mesenchymal stem cell therapies, which is crucial for developing more dependable and effective treatment protocols. In summary, although mesenchymal stem cells offer promising prospects for treating lung injuries, more investigations are required to optimize their therapeutic promise and ensure their safe clinical application in the context of paraquat poisoning.

Abstract Image

基于间充质干细胞的百草枯肺损伤疗法。
百草枯中毒会导致严重的肺损伤,但目前的治疗方法对修复受伤的肺组织效果甚微。最近的研究强调,干细胞疗法(即间充质干细胞)有望成为治疗百草枯中毒的新方法。这些细胞在减少百草枯作用下小鼠肺部的炎症、细胞凋亡和纤维化方面显示出有效性。间充质干细胞的治疗意义被认为来自于其释放的生物活性蛋白及其调节炎症反应的能力。然而,要验证这些疗法的疗效,还需要更多的临床研究。这篇综述深入探讨了百草枯中毒的病理生理学和间充质干细胞的特性。此外,它还批判性地评估了间充质干细胞疗法的长期安全性和有效性,这对制定更可靠、更有效的治疗方案至关重要。总之,尽管间充质干细胞在治疗肺损伤方面前景广阔,但仍需进行更多研究,以优化其治疗前景,并确保其在百草枯中毒中的安全临床应用。
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
Cell Biology and Toxicology
Cell Biology and Toxicology 生物-毒理学
CiteScore
9.90
自引率
4.90%
发文量
101
审稿时长
>12 weeks
期刊介绍: Cell Biology and Toxicology (CBT) is an international journal focused on clinical and translational research with an emphasis on molecular and cell biology, genetic and epigenetic heterogeneity, drug discovery and development, and molecular pharmacology and toxicology. CBT has a disease-specific scope prioritizing publications on gene and protein-based regulation, intracellular signaling pathway dysfunction, cell type-specific function, and systems in biomedicine in drug discovery and development. CBT publishes original articles with outstanding, innovative and significant findings, important reviews on recent research advances and issues of high current interest, opinion articles of leading edge science, and rapid communication or reports, on molecular mechanisms and therapies in diseases.
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