间充质干细胞治疗肺纤维化的潜力。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
DNA and cell biology Pub Date : 2022-11-01 Epub Date: 2022-10-26 DOI:10.1089/dna.2022.0327
Zhihou Guo, Yaping Zhang, Furong Yan
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引用次数: 3

摘要

肺纤维化(Pulmonary fibrosis, PF)是急慢性炎症性肺部疾病的常见病理特征,目前尚无有效的临床治疗方法。间充质干细胞(MSCs)被认为是再生损伤组织的理想细胞来源,因为它们易于提取和扩增,具有有限的致瘤风险,并且缺乏免疫原性。最近,以MSC为基础的治疗方法被认为是减轻PF的潜在治疗策略。尽管MSCs的给药在PF中具有抗炎和抗纤维化作用,但还需要进一步的研究来优化MSC的来源和剂量、给药时间和给药途径,以提高其保护作用。此外,基于msc的PF治疗机制仍然难以捉摸。在这里,我们回顾了最近发表的MSC给药治疗PF的数据,以深入了解MSC给药程序和来源的治疗影响。此外,我们讨论了MSC管理对PF影响的潜在机制,并强调了改善MSC有益作用的有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential of Mesenchymal Stem Cell-Based Therapies for Pulmonary Fibrosis.

Pulmonary fibrosis (PF) is a common pathological feature of acute and chronic inflammatory lung diseases that currently has no effective clinical treatment. Mesenchymal stem cells (MSCs) are considered to be an ideal cell source for regenerating injured tissues, as they are easily extracted and expanded, have a limited risk of tumorigenicity, and lack immunogenicity. Recently, MSC-based therapies have been suggested as potential therapeutic strategies for attenuating PF. Although the administration of MSCs has been reported to have anti-inflammatory and anti-fibrotic effects in PF, further studies are required to optimize the MSC source and dose, delivery time, and route of administration to improve their protective effects. Moreover, the mechanisms underlying MSC-based therapies for PF remain elusive. Here, we review recently published data on MSC administration for the treatment of PF to provide insights into the therapeutic impact of MSC delivery procedures and sources. In addition, we discuss the potential mechanisms underlying the effects of MSC administration on PF and highlight promising strategies for improving the beneficial effects of MSCs.

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来源期刊
DNA and cell biology
DNA and cell biology 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
93
审稿时长
1.5 months
期刊介绍: DNA and Cell Biology delivers authoritative, peer-reviewed research on all aspects of molecular and cellular biology, with a unique focus on combining mechanistic and clinical studies to drive the field forward. DNA and Cell Biology coverage includes: Gene Structure, Function, and Regulation Gene regulation Molecular mechanisms of cell activation Mechanisms of transcriptional, translational, or epigenetic control of gene expression Molecular Medicine Molecular pathogenesis Genetic approaches to cancer and autoimmune diseases Translational studies in cell and molecular biology Cellular Organelles Autophagy Apoptosis P bodies Peroxisosomes Protein Biosynthesis and Degradation Regulation of protein synthesis Post-translational modifications Control of degradation Cell-Autonomous Inflammation and Host Cell Response to Infection Responses to cytokines and other physiological mediators Evasive pathways of pathogens.
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