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在猪肝切除模型中评估静脉注射同种异体多谱系分化应激耐受细胞的安全性和有效性。

The evaluation of the safety and efficacy of intravenously administered allogeneic multilineage-differentiating stress-enduring cells in a swine hepatectomy model.

机构信息

Department of Surgery, Tohoku University Graduate School of Medicine, 1-1 Seryo-machi, Aoba-ku, Sendai, Miyagi, 980-8574, Japan.

Department of Stem Cell Biology and Histology, Sendai, Japan.

出版信息

Surg Today. 2021 Apr;51(4):634-650. doi: 10.1007/s00595-020-02117-0. Epub 2020 Sep 11.

DOI:10.1007/s00595-020-02117-0
PMID:32915286
Abstract

INTRODUCTION

Multilineage-differentiating stress-enduring (Muse) cells are non-tumorigenic endogenous pluripotent-like cells residing in the bone marrow that exert a tissue reparative effect by replacing damaged/apoptotic cells through spontaneous differentiation into tissue-constituent cells. Post-hepatectomy liver failure (PHLF) is a potentially fatal complication. The main purpose of this study was to evaluate the safety and efficiency of allogeneic Muse cell administration via the portal vein in a swine model of PHLF.

METHODS

Swine Muse cells, collected from swine bone marrow-mesenchymal stem cells (MSCs) as SSEA-3(+) cells, were examined for their characteristics. Then, 1 × 10 allogeneic-Muse cells and allogeneic-MSCs and vehicle were injected via the portal vein in a 70% hepatectomy swine model.

RESULTS

Swine Muse cells exhibited characteristics comparable to previously reported human Muse cells. Compared to the MSC and vehicle groups, the Muse group showed specific homing of the administered cells into the liver, resulting in improvements in the control of hyperbilirubinemia (P = 0.04), prothrombin international normalized ratio (P = 0.05), and suppression of focal necrosis (P = 0.04). Integrated Muse cells differentiated spontaneously into hepatocyte marker-positive cells.

CONCLUSIONS

Allogeneic Muse cell administration may provide a reparative effect and functional recovery in a 70% hepatectomy swine model and thus may contribute to the treatment of PHLF.

摘要

简介

多谱系分化应激耐受(Muse)细胞是存在于骨髓中的非致瘤性内源性多能样细胞,通过自发分化为组织成分细胞来替代受损/凋亡细胞,从而发挥组织修复作用。肝切除术后肝衰竭(PHLF)是一种潜在的致命并发症。本研究的主要目的是评估同种异体 Muse 细胞通过门静脉输注在 PHLF 猪模型中的安全性和有效性。

方法

从猪骨髓间充质干细胞(MSCs)中收集的猪 Muse 细胞作为 SSEA-3(+)细胞,对其特性进行了研究。然后,通过门静脉在 70%肝切除的猪模型中注射 1×10 个同种异体 Muse 细胞、同种异体 MSC 和载体。

结果

猪 Muse 细胞表现出与先前报道的人类 Muse 细胞相当的特性。与 MSC 和载体组相比,Muse 组显示出所给予的细胞特异性归巢到肝脏,导致高胆红素血症的控制得到改善(P=0.04),国际标准化比值(P=0.05)得到改善,并且抑制了局灶性坏死(P=0.04)。整合的 Muse 细胞自发分化为肝细胞标志物阳性细胞。

结论

同种异体 Muse 细胞给药可能在 70%肝切除猪模型中提供修复作用和功能恢复,从而有助于 PHLF 的治疗。

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本文引用的文献

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Neurotrophic Factor Secretion and Neural Differentiation Potential of Multilineage-differentiating Stress-enduring (Muse) Cells Derived from Mouse Adipose Tissue.源自小鼠脂肪组织的多能诱导分化应激耐受细胞(Muse 细胞)的神经营养因子分泌和神经分化潜能。
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Muse Cells Are Endogenous Reparative Stem Cells.成体干细胞是内源性修复干细胞。
供者骨髓间充质干细胞治疗,无需 HLA 配型检测及免疫抑制剂治疗。
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Multilineage Differentiating Stress Enduring (Muse) Cells: A New Era of Stem Cell-Based Therapy.多谱系分化应激耐受(Muse)细胞:基于干细胞治疗的新时代。
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Multilineage-Differentiating Stress-Enduring Cells (Muse Cells): An Easily Accessible, Pluripotent Stem Cell Niche with Unique and Powerful Properties for Multiple Regenerative Medicine Applications.多谱系分化应激耐受细胞(Muse细胞):一种易于获取的多能干细胞龛,具有独特且强大的特性,适用于多种再生医学应用。
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Multilineage-Differentiating Stress-Enduring Cells (Muse Cells): The Future of Human and Veterinary Regenerative Medicine.多谱系分化应激耐受细胞(Muse细胞):人类和兽医再生医学的未来。
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Current evidence on posthepatectomy liver failure: comprehensive review.当前关于肝切除术后肝功能衰竭的证据:全面综述。
BJS Open. 2022 Nov 2;6(6). doi: 10.1093/bjsopen/zrac142.
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Randomized Trial of Spheroid Reservoir Bioartificial Liver in Porcine Model of Posthepatectomy Liver Failure.随机化试验:球体储液池型生物人工肝在肝切除术后肝功能衰竭猪模型中的应用。
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Stress and stem cells: adult Muse cells tolerate extensive genotoxic stimuli better than mesenchymal stromal cells.应激与干细胞:成人多能分化应激耐受细胞比间充质基质细胞更能耐受广泛的基因毒性刺激。
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Circ Res. 2018 Apr 13;122(8):1069-1083. doi: 10.1161/CIRCRESAHA.117.311648. Epub 2018 Feb 23.
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Mobilized Muse Cells After Acute Myocardial Infarction Predict Cardiac Function and Remodeling in the Chronic Phase.急性心肌梗死后动员的骨髓间充质细胞可预测慢性期心功能和重塑。
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