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一种用于开发使用培养的骨髓来源细胞治疗肝硬化疗法的犬肝纤维化模型。

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

作者信息

Matsuda Takashi, Takami Taro, Sasaki Ryo, Nishimura Tatsuro, Aibe Yuki, Paredes Bruno Diaz, Quintanilha Luiz Fernando, Matsumoto Toshihiko, Ishikawa Tsuyoshi, Yamamoto Naoki, Tani Kenji, Terai Shuji, Taura Yasuho, Sakaida Isao

机构信息

Department of Gastroenterology & Hepatology Yamaguchi University Graduate School of Medicine Yamaguchi Japan.

Department of Oncology and Laboratory Medicine Yamaguchi University Graduate School of Medicine Yamaguchi Japan.

出版信息

Hepatol Commun. 2017 Jul 17;1(7):691-703. doi: 10.1002/hep4.1071. eCollection 2017 Sep.

Abstract

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 CCl through the catheter was performed to induce liver cirrhosis. After 10 weeks of CCl 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. : We established a useful canine liver fibrosis model and confirmed that cultured autologous BMSC infusion improved liver fibrosis without adverse effects. ( 2017;1:691-703).

摘要

我们一直在研发一种使用培养的自体骨髓间充质干细胞(BMSCs)治疗肝硬化的方法。在考虑进行人体临床试验之前,必须证实向中大型动物输注BMSCs的安全性和有效性;因此,我们建立了犬肝纤维化模型。从犬的肱骨抽取少量骨髓液以评估BMSCs的特性。我们在每只犬的胃中植入静脉导管,并在其颈部后方植入皮下输注端口。通过导管反复注射四氯化碳(CCl)以诱导肝硬化。在注射CCl 10周后,将8只犬平均分为两组:不进行细胞输注(对照组)和通过外周静脉输注自体BMSCs(BMSC组)。在输注前和输注后4周进行了各种检测。BMSC输注4周后,BMSC组中用天狼星红染色的肝纤维化面积显著减小,这与吲哚菁绿的半衰期显著缩短和肝功能改善一致。我们建立了一种有用的犬肝纤维化模型,并证实培养的自体BMSC输注可改善肝纤维化且无不良影响。(2017;1:691 - 703)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7df4/5721436/33704a832c51/HEP4-1-691-g001.jpg

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