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用于治疗脂肪肝疾病的创新性间充质干细胞疗法。

Innovative mesenchymal stem cell treatments for fatty liver disease.

作者信息

Gao Fei-Qiong, Zhu Jia-Qi, Feng Xu-Dong

机构信息

Department of Endocrinology, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou 310003, Zhejiang Province, China.

Laboratory Medicine Center, Department of Clinical Laboratory, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou 310014, Zhejiang Province, China.

出版信息

World J Stem Cells. 2024 Sep 26;16(9):846-853. doi: 10.4252/wjsc.v16.i9.846.

DOI:10.4252/wjsc.v16.i9.846
PMID:39351260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11438732/
Abstract

The incidence of non-alcoholic fatty liver disease (NAFLD) and alcohol-associated liver disease (ALD) is increasing year by year due to changes in the contemporary environment and dietary structure, and is an important public health problem worldwide. There is an urgent need to continuously improve the understanding of their disease mechanisms and develop novel therapeutic strategies. Mesenchymal stem cells (MSCs) have shown promise as a potential therapeutic strategy in therapeutic studies of NAFLD and ALD. NAFLD and ALD have different triggers and their specific mechanisms of disease progression are different, but both involve disease processes such as hepatocellular steatosis and potential fibrosis, cirrhosis, and even hepatocellular carcinoma. MSCs have metabolic regulatory, anti-apoptotic, antioxidant, and immunomodulatory effects that together promote liver injury repair and functional recovery, and have demonstrated positive results in preclinical studies. This editorial is a continuum of Jiang 's review focusing on the advantages and limitations of MSCs and their derivatives as therapeutics for NAFLD and ALD. They detail how MSCs attenuate the progression of NAFLD by modulating molecular pathways involved in glucolipid metabolism, inflammation, oxidative stress, endoplasmic reticulum stress, and fibrosis. Based on recent advances, we discuss MSCs and their derivatives as therapeutic strategies for NAFLD and ALD, providing useful information for their clinical application.

摘要

由于当代环境和饮食结构的变化,非酒精性脂肪性肝病(NAFLD)和酒精性肝病(ALD)的发病率逐年上升,是全球重要的公共卫生问题。迫切需要不断加深对其发病机制的认识,并开发新的治疗策略。间充质干细胞(MSCs)在NAFLD和ALD的治疗研究中已显示出作为一种潜在治疗策略的前景。NAFLD和ALD有不同的触发因素,其疾病进展的具体机制也不同,但两者都涉及肝细胞脂肪变性以及潜在的纤维化、肝硬化甚至肝细胞癌等疾病过程。MSCs具有代谢调节、抗凋亡、抗氧化和免疫调节作用,共同促进肝损伤修复和功能恢复,并在临床前研究中取得了积极成果。这篇社论是蒋氏综述的延续,重点关注MSCs及其衍生物作为NAFLD和ALD治疗方法的优缺点。他们详细阐述了MSCs如何通过调节参与糖脂代谢、炎症、氧化应激、内质网应激和纤维化的分子途径来减轻NAFLD的进展。基于最近的进展,我们讨论了MSCs及其衍生物作为NAFLD和ALD的治疗策略,为其临床应用提供有用信息。

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Innovative mesenchymal stem cell treatments for fatty liver disease.用于治疗脂肪肝疾病的创新性间充质干细胞疗法。
World J Stem Cells. 2024 Sep 26;16(9):846-853. doi: 10.4252/wjsc.v16.i9.846.
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本文引用的文献

1
Current perspectives on mesenchymal stem cells as a potential therapeutic strategy for non-alcoholic fatty liver disease.间充质干细胞作为非酒精性脂肪性肝病潜在治疗策略的当前观点。
World J Stem Cells. 2024 Jul 26;16(7):760-772. doi: 10.4252/wjsc.v16.i7.760.
2
Tumor necrosis factor-inducible gene 6 protein and its derived peptide ameliorate liver fibrosis by repressing CD44 activation in mice with alcohol-related liver disease.肿瘤坏死因子诱导基因 6 蛋白及其衍生肽通过抑制酒精性肝病小鼠 CD44 活化改善肝纤维化。
J Biomed Sci. 2024 May 24;31(1):54. doi: 10.1186/s12929-024-01042-5.
3
RNF31 alleviates liver steatosis by promoting p53/BNIP3-related mitophagy in hepatocytes.RNF31 通过促进肝细胞中 p53/BNIP3 相关的线粒体自噬来减轻肝脂肪变性。
Free Radic Biol Med. 2024 Jul;219:163-179. doi: 10.1016/j.freeradbiomed.2024.04.214. Epub 2024 Apr 13.
4
Mesenchymal stem/stromal cells armored by FGF21 ameliorate alcohol-induced liver injury through modulating polarization of macrophages.成纤维细胞生长因子 21 包裹的间充质干细胞/基质细胞通过调节巨噬细胞极化改善酒精性肝损伤。
Hepatol Commun. 2024 Mar 29;8(4). doi: 10.1097/HC9.0000000000000410. eCollection 2024 Apr 1.
5
Human umbilical cord mesenchymal stem cells attenuate diet-induced obesity and NASH-related fibrosis in mice.人脐带间充质干细胞可减轻饮食诱导的小鼠肥胖及非酒精性脂肪性肝炎相关纤维化。
Heliyon. 2024 Feb 1;10(3):e25460. doi: 10.1016/j.heliyon.2024.e25460. eCollection 2024 Feb 15.
6
Strategies to improve the therapeutic efficacy of mesenchymal stem cell-derived extracellular vesicle (MSC-EV): a promising cell-free therapy for liver disease.提高间充质干细胞衍生细胞外囊泡(MSC-EV)治疗效果的策略:一种有前景的肝病无细胞疗法。
Front Bioeng Biotechnol. 2023 Dec 13;11:1322514. doi: 10.3389/fbioe.2023.1322514. eCollection 2023.
7
Recent Advances in Mesenchymal Stem/Stromal Cell-Based Therapy for Alcohol-Associated Liver Disease and Non-alcoholic Fatty Liver Disease.间质干细胞/基质细胞治疗酒精相关性肝病和非酒精性脂肪性肝病的最新进展。
Stem Cells Transl Med. 2024 Feb 14;13(2):107-115. doi: 10.1093/stcltm/szad082.
8
Human umbilical cord mesenchymal stem cell-derived exosomes ameliorate liver steatosis by promoting fatty acid oxidation and reducing fatty acid synthesis.人脐带间充质干细胞来源的外泌体通过促进脂肪酸氧化和减少脂肪酸合成来改善肝脏脂肪变性。
JHEP Rep. 2023 Mar 28;5(7):100746. doi: 10.1016/j.jhepr.2023.100746. eCollection 2023 Jul.
9
MSC-sEV Treatment Polarizes Pro-Fibrotic M2 Macrophages without Exacerbating Liver Fibrosis in NASH.MSC-sEV 治疗不会加重 NASH 中的肝纤维化,反而使促纤维化 M2 巨噬细胞极化。
Int J Mol Sci. 2023 Apr 30;24(9):8092. doi: 10.3390/ijms24098092.
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Curcumin preconditioned mesenchymal stem cells derived exosomes transplantation ameliorate and protect against non- alcoholic steatohepatitis by regulation the expression of key genes of inflammation and oxidative stress.姜黄素预处理间充质干细胞来源的外泌体移植通过调节炎症和氧化应激关键基因的表达改善和保护非酒精性脂肪性肝炎。
Transpl Immunol. 2023 Jun;78:101837. doi: 10.1016/j.trim.2023.101837. Epub 2023 Apr 7.