A tissue-engineered bioabsorbable nerve conduit created by three-dimensional culture of induced pluripotent stem cell-derived neurospheres

被引:17
|
作者
Uemura, Takuya [1 ]
Takamatsu, Kiyohito [2 ]
Ikeda, Mikinori
Okada, Mitsuhiro
Kazuki, Kenichi [2 ]
Ikada, Yoshito [3 ]
Nakamura, Hiroaki
机构
[1] Osaka City Univ, Grad Sch Med, Dept Orthopaed Surg, Abeno Ku, Osaka 5458585, Japan
[2] Osaka City Gen Hosp, Dept Orthopaed Surg, Osaka, Japan
[3] Nara Med Univ, Div Life Sci, Nara, Japan
关键词
Nerve conduits; induced pluripotent stem cells; tissue engineering; peripheral nerve; regenerative medicine; NEURAL STEM/PROGENITOR CELLS; SPINAL-CORD-INJURY; SCHWANN-CELLS; REGENERATION; REPAIR; MOUSE; FIBROBLASTS; GENERATION; RATS; MYC;
D O I
10.3233/BME-2012-0680
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We previously reported a bioabsorbable nerve conduit coated with Schwann cells for the treatment of peripheral nerve defects. Since there have been dramatic developments in induced pluripotent stem (iPS) cells in recent years, the purpose of the present study was to create a tissue-engineered nerve conduit coated with iPS cell-derived neurospheres. Such a conduit was constructed by three-dimensional (3D)-culture of these cells using a bioabsorbable polymer conduit as a scaffold. The nerve conduit was composed of a mesh of poly L-lactide, and a porous sponge of 50% poly L-lactide and 50% poly epsilon-caprolactone. The primary and secondary neurospheres (PNS and SNS, respectively) induced from iPS cells were suspended in individual conduits. The conduits were incubated for 7 or 14 days in vitro and then evaluated using immunohistochemistry. All of the 7- and 14-day differentiated PNS and SNS were observed to have adhered to the inner surface of the conduits and to have migrated into the inner porous sponge. The engrafted cells were positive for anti-Tuj1, -S-100 and -GFAP antibodies, indicating that their pluripotent ability to form neural or glial cells was maintained. These findings indicate the feasibility of creating nerve conduits coated with a 3D-culture of iPS cell-derived neurospheres for the treatment of peripheral nerve defects.
引用
收藏
页码:333 / 339
页数:7
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