Low immunogenicity of mouse induced pluripotent stem cell-derived neural stem/progenitor cells

被引：22
作者：
Itakura, Go [1 ,2 ]
Ozaki, Masahiro [1 ,2 ]
Nagoshi, Narihito [2 ]
Kawabata, Soya [1 ,2 ]
Nishiyama, Yuichiro [1 ,2 ]
Sugai, Keiko [1 ,2 ]
Iida, Tsuyoshi [1 ,2 ]
Kashiwagi, Rei [1 ,2 ]
Ookubo, Toshiki [1 ,2 ]
Yastake, Kaori [1 ,2 ]
Matsubayashi, Kohei [1 ,2 ]
Kohyama, Jun [1 ]
Iwanami, Akio [2 ]
Matsumoto, Morio [2 ]
Nakamura, Masaya [2 ]
Okano, Hideyuki [1 ]
机构：
[1] Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Orthopaed Surg, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan
来源：
SCIENTIFIC REPORTS | 2017年 / 7卷
基金：
日本科学技术振兴机构; 日本学术振兴会;
关键词：
TUMOR-ASSOCIATED MACROPHAGES; SPINAL-CORD-INJURY; IMMUNE PRIVILEGE; TGF-BETA; RESIST DESTRUCTION; TRANSPLANTATION; EXPRESSION; LYMPHOCYTES; ACTIVATION; INDUCTION;
D O I：
10.1038/s41598-017-13522-w
中图分类号：
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
Resolving the immunogenicity of cells derived from induced pluripotent stem cells (iPSCs) remains an important challenge for cell transplant strategies that use banked allogeneic cells. Thus, we evaluated the immunogenicity of mouse fetal neural stem/progenitor cells (fetus-NSPCs) and iPSC-derived neural stem/progenitor cells (iPSC-NSPCs) both in vitro and in vivo. Flow cytometry revealed the low expression of immunological surface antigens, and these cells survived in all mice when transplanted syngeneically into subcutaneous tissue and the spinal cord. In contrast, an allogeneic transplantation into subcutaneous tissue was rejected in all mice, and allogeneic cells transplanted into intact and injured spinal cords survived for 3 months in approximately 20% of mice. In addition, cell survival was increased after co-treatment with an immunosuppressive agent. Thus, the immunogenicity and post-transplantation immunological dynamics of iPSC-NSPCs resemble those of fetus-NSPCs.
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页数：13
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