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通过移植诱导多能干细胞来源的Flk-1阳性细胞进行治疗性血管生成。

Therapeutic angiogenesis by transplantation of induced pluripotent stem cell-derived Flk-1 positive cells.

作者信息

Suzuki Hirohiko, Shibata Rei, Kito Tetsutaro, Ishii Masakazu, Li Ping, Yoshikai Toru, Nishio Naomi, Ito Sachiko, Numaguchi Yasushi, Yamashita Jun K, Murohara Toyoaki, Isobe Kenichi

机构信息

Department of Cardiology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi 466-8560, Japan.

出版信息

BMC Cell Biol. 2010 Sep 22;11:72. doi: 10.1186/1471-2121-11-72.

Abstract

BACKGROUND

Induced pluripotent stem (iPS) cells are the novel stem cell population induced from somatic cells. It is anticipated that iPS will be used in the expanding field of regenerative medicine. Here, we investigated whether implantation of fetal liver kinase-1 positive (Flk-1+) cells derived from iPS cells could improve angiogenesis in a mouse hind limb model of ischemia.

RESULTS

Flk-1+ cells were induced from iPS cells after four to five days of culture. Hind limb ischemia was surgically induced and sorted Flk-1+ cells were directly injected into ischemic hind limbs of athymic nude mice. Revascularization of the ischemic hind limb was accelerated in mice that were transplanted with Flk-1+ cells compared with control mice, which were transplanted with vehicle, as evaluated by laser Doppler blood flowmetry. Transplantation of Flk-1+ cells also increased expression of VEGF mRNA in ischemic tissue compared to controls.

CONCLUSIONS

Direct local implantation of iPS cell-derived Flk-1+ cells would salvage tissues from ischemia. These data indicate that iPS cells could be valuable in the therapeutic induction of angiogenesis.

摘要

背景

诱导多能干细胞(iPS细胞)是从体细胞诱导产生的新型干细胞群体。预计iPS细胞将在不断发展的再生医学领域得到应用。在此,我们研究了植入源自iPS细胞的胎儿肝激酶-1阳性(Flk-1+)细胞是否能改善小鼠后肢缺血模型中的血管生成。

结果

培养四至五天后,从iPS细胞诱导出Flk-1+细胞。通过手术诱导后肢缺血,并将分选的Flk-1+细胞直接注射到无胸腺裸鼠的缺血后肢中。与注射赋形剂的对照小鼠相比,通过激光多普勒血流仪评估,移植了Flk-1+细胞的小鼠缺血后肢的血管再通加速。与对照相比,Flk-1+细胞移植还增加了缺血组织中VEGF mRNA的表达。

结论

直接局部植入iPS细胞来源的Flk-1+细胞可挽救缺血组织。这些数据表明,iPS细胞在血管生成的治疗诱导中可能具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ba3/2955572/61059b9caa20/1471-2121-11-72-1.jpg

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