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三维分化的人骨髓间充质干细胞表现出强大的抗纤维化潜力,并改善了小鼠肝纤维化。

Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit Robust Antifibrotic Potential and Ameliorates Mouse Liver Fibrosis.

机构信息

Department of Internal Medicine, Catholic Kwandong University College of Medicine, International St. Mary's Hospital, Incheon, Republic of Korea.

Both the authors contributed equally to this article.

出版信息

Cell Transplant. 2021 Jan-Dec;30:963689720987525. doi: 10.1177/0963689720987525.

Abstract

Recently, three-dimensional (3D)-cultured adipose mesenchymal stem cells (ASCs) have provided an effective therapy for liver fibrosis. This study aimed to enhance the potential of human ASCs for antifibrosis or hepatocyte regeneration using a 3D culture system and investigate their therapeutic mechanism in experimental liver fibrosis. ASC-3Dc were generated in a 3D culture system and stimulated with four growth factors, namely epidermal growth factor, insulin-like growth factor (IGF)-1, fibroblast growth factor-2, and vascular endothelial growth factor-A. The expression levels of antifibrotic or hepatic regeneration factors were then measured using quantitative real-time polymerase chain reaction and enzyme-linked immunosorbent assay. The therapeutic effects of ASC-3Dc were determined using a liver fibrosis model induced by thioacetamide. Histological analysis was performed to elucidate the therapeutic mechanism. ASC-3Dc exhibited high levels of hepatocyte growth factor (HGF), IGF-1, stromal cell-derived factor (SDF)-1 genes, and protein expression. In addition, injecting ASC-3Dc significantly prevented hepatic fibrosis and improved liver function in vivo. Moreover, high numbers of ki-67-expressing hepatocytes were detected in the ASC-3Dc-injected livers. Albumin-expressing ASC-3Dc engrafted in fibrotic livers augmented HGF expression. Thus, short-term 3D-cultured ASCs may be a novel alternative to the conventional treatment for liver damage in clinical settings.

摘要

最近,三维(3D)培养的脂肪间充质干细胞(ASCs)为肝纤维化提供了有效的治疗方法。本研究旨在通过 3D 培养系统增强人 ASC 的抗纤维化或肝细胞再生潜力,并研究其在实验性肝纤维化中的治疗机制。在 3D 培养系统中生成 ASC-3Dc,并使用四种生长因子(表皮生长因子、胰岛素样生长因子(IGF)-1、成纤维细胞生长因子-2 和血管内皮生长因子-A)进行刺激。然后使用定量实时聚合酶链反应和酶联免疫吸附试验测量抗纤维化或肝再生因子的表达水平。使用硫代乙酰胺诱导的肝纤维化模型确定 ASC-3Dc 的治疗效果。进行组织学分析以阐明治疗机制。ASC-3Dc 表现出高水平的肝细胞生长因子(HGF)、IGF-1、基质细胞衍生因子(SDF)-1 基因和蛋白表达。此外,注射 ASC-3Dc 可显著预防肝纤维化并改善体内肝功能。此外,在注射 ASC-3Dc 的肝脏中检测到大量表达 ki-67 的肝细胞。在纤维化肝脏中植入表达白蛋白的 ASC-3Dc 可增强 HGF 表达。因此,短期 3D 培养的 ASC 可能是临床治疗肝损伤的一种新的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee93/7876751/1beb436019d9/10.1177_0963689720987525-fig1.jpg

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