An intrinsically semi-permeable PDMS nanosheet encapsulating adipose tissue-derived stem cells for enhanced angiogenesis

被引:2
|
作者
Takuma, Megumi [1 ]
Fujita, Hajime [1 ,4 ]
Zushi, Nanami [1 ]
Nagano, Hisato [2 ]
Azuma, Ryuichi [2 ]
Kiyosawa, Tomoharu [2 ]
Fujie, Toshinori [1 ,3 ]
机构
[1] Tokyo Inst Technol, Sch Life Sci & Technol, B-50,4259 Nagatsuta Cho,Midori Ku, Yokohama 2268501, Japan
[2] Natl Def Med Coll, Dept Plast & Reconstruct Surg, Tokorozawa, Saitama 3598513, Japan
[3] Inst Innovat Res, Tokyo Inst Technol, Res Ctr Autonomous Syst Mat ASMat, 4259 Nagatsuta Cho,Midori Ku, Yokohama 2268501, Japan
[4] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
ISLET; DEVICE; TRANSPLANTATION; DYNAMICS; NORPLANT; CULTURE; SIZE; THIN;
D O I
10.1039/d4bm00460d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cell encapsulation devices are expected to be promising tools that can control the release of therapeutic proteins secreted from transplanted cells. The protein permeability of the device membrane is important because it allows the isolation of transplanted cells while enabling the effectiveness of the device. In this study, we investigated free-standing polymeric ultra-thin films (nanosheets) as an intrinsically semi-permeable membrane made from polydimethylsiloxane (PDMS). The PDMS nanosheet with a thickness of 600 nm showed intrinsic protein permeability, and the device fabricated with the PDMS nanosheet showed that VEGF secreted from implanted adipose tissue-derived stem cells (ASCs) could be released for at least 5 days. The ASC encapsulation device promoted angiogenesis and the development of granulation tissue 1 week after transplantation to the subcutaneous area of a mouse. This cell encapsulation device consisting of PDMS nanosheets provides a new method for pre-vascularization of the subcutaneous area in cell transplantation therapy. Cell encapsulation devices are expected to be promising tools that can control the release of therapeutic proteins secreted from transplanted cells.
引用
收藏
页码:3401 / 3410
页数:10
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