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A canine liver fibrosis model to develop a therapy for liver cirrhosis using cultured bone marrow–derived cells

机译:犬肝纤维化模型使用培养的骨髓源性细胞开发治疗肝硬化的方法

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摘要

We have been developing a therapy for liver cirrhosis using cultured autologous bone marrow–derived mesenchymal stem cells (BMSCs). Before human clinical trials can be considered, the safety and efficacy of BMSC infusion in medium to large animals must be confirmed; thus, we developed a canine liver fibrosis model. A small amount of bone marrow fluid was aspirated from the canine humerus to assess the characteristics of BMSCs. We implanted a venous catheter in the stomach and a subcutaneous infusion port in the back of the neck of each canine. Repeated injection of CCl4 through the catheter was performed to induce liver cirrhosis. After 10 weeks of CCl4 injection, eight canines were equally divided into two groups: no cell infusion (control group) and autologous BMSC infusion through the peripheral vein (BMSC group). A variety of assays were carried out before and 4 weeks after the infusion. The area of liver fibrosis stained with sirius red was significantly reduced in the BMSC group 4 weeks after BMSC infusion, consistent with a significantly shortened half‐life of indocyanine green and improved liver function. Conclusion: We established a useful canine liver fibrosis model and confirmed that cultured autologous BMSC infusion improved liver fibrosis without adverse effects. (Hepatology Communications 2017;1:691–703)
机译:我们正在开发一种使用培养的自体骨髓源性间充质干细胞(BMSCs)治疗肝硬化的方法。在可以考虑进行人类临床试验之前,必须确认BMSC在大中型动物中的安全性和有效性。因此,我们建立了犬肝纤维化模型。从犬肱骨中吸出少量骨髓液以评估BMSCs的特征。我们将静脉导管植入胃中,并在每个犬的颈部背面植入皮下输液端口。通过导管重复注射CCl4以诱发肝硬化。注射CCl4 10周后,将八个犬平均分为两组:不进行细胞输注(对照组)和通过外周静脉自体BMSC输注(BMSC组)。在输注之前和输注后4周进行了各种测定。输注骨髓间充质干细胞4周后,骨髓间充质干细胞组肝纤维化区域染有天狼星红,明显减少了吲哚菁绿的半衰期并改善了肝功能。结论:我们建立了有用的犬肝纤维化模型,并证实自体自体骨髓间充质干细胞灌注可改善肝纤维化而无不良影响。 (肝病通讯2017; 1:691–703)

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