iPS cell sheets created by a novel magnetite tissue engineering method for reparative angiogenesis.
iPS cell sheets created by a novel magnetite tissue engineering method for reparative angiogenesis.
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DOI:
10.1038/srep01418
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发表时间:
2013
影响因子:
4.6
通讯作者:
Murohara, Toyoaki
中科院分区:
文献类型:
--
作者:
Kito, Tetsutaro;Shibata, Rei;Ishii, Masakazu;Suzuki, Hirohiko;Himeno, Tatsuhito;Kataoka, Yoshiyuki;Yamamura, Yumiko;Yamamoto, Takashi;Nishio, Naomi;Ito, Sachiko;Numaguchi, Yasushi;Tanigawa, Tohru;Yamashita, Jun K.;Ouchi, Noriyuki;Honda, Hiroyuki;Isobe, Kenichi;Murohara, Toyoaki
Angiogenic cell therapy represents a novel strategy for ischemic diseases, but some patients show poor responses. We investigated the therapeutic potential of an induced pluripotent stem (iPS) cell sheet created by a novel magnetite tissue engineering technology (Mag-TE) for reparative angiogenesis. Mouse iPS cell-derived Flk-1+ cells were incubated with magnetic nanoparticle-containing liposomes (MCLs). MCL-labeled Flk-1+ cells were mixed with diluted extracellular matrix (ECM) precursor and a magnet was placed on the reverse side. Magnetized Flk-1+ cells formed multi-layered cell sheets according to magnetic force. Implantation of the Flk-1+ cell sheet accelerated revascularization of ischemic hindlimbs relative to the contralateral limbs in nude mice as measured by laser Doppler blood flow and capillary density analyses. The Flk-1+ cell sheet also increased the expressions of VEGF and bFGF in ischemic tissue. iPS cell-derived Flk-1+ cell sheets created by this novel Mag-TE method represent a promising new modality for therapeutic angiogenesis.
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DOI:
10.1161/atvbaha.111.231100
发表时间:
2011-10-01
影响因子:
8.7
作者:
Ishii, Masakazu;Shibata, Rei;Murohara, Toyoaki
通讯作者:
Murohara, Toyoaki
影响因子:
3.3
作者:
Kajiguchi, Masahiro;Kondo, Takahisa;Murohara, Toyoaki
通讯作者:
Murohara, Toyoaki
影响因子:
37.8
作者:
Higashi, Y;Kimura, M;Yoshizumi, M
通讯作者:
Yoshizumi, M
影响因子:
6.2
作者:
Miyagawa, S;Sawa, Y;Matsuda, H
通讯作者:
Matsuda, H
影响因子:
15.9
作者:
Murohara, T;Asahara, T;Isner, JM
通讯作者:
Isner, JM