Growth factor delivery from self-assembling nanofibers to facilitate islet transplantation

被引:94
作者
Stendahl, John C. [1 ,3 ]
Wang, Ling-Jia [2 ]
Chow, Lesley W. [3 ]
Kaufman, Dixon B. [1 ,2 ]
Stupp, Samuel I. [1 ,3 ,4 ,5 ]
机构
[1] Northwestern Univ, Inst BioNanotechnol Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Surg, Chicago, IL 60611 USA
[3] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL USA
[5] Northwestern Univ, Dept Med, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
islet transplantation; omentum; peptide amphiphile nanofibers; fibroblast growth factor-2; vascular endothelial growth factor;
D O I
10.1097/TP.0b013e3181806d9d
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances in nanotechnology and molecular self-assembly may provide novel solutions to current cell transplantation deficiencies. Heparin-binding peptide amphiphiles (HBPAs) self-assemble from aqueous media into nanofibers that bind growth factors through interactions with the bioactive polymer heparin. In this report, we demonstrate that delivery of vascular endothelial growth factor and fibroblast growth factor-2 from HBPA scaffolds significantly increases blood vessel density in the mouse omentum over control scaffolds without growth factors (P<0.0005) and significantly enhances islet engraftment. Diabetic recipients transplanted with 250 isologous islets and HBPA scaffolds containing vascular endothelial growth factor/fibroblast growth factor-2 achieved normoglycemia at a higher rate (78%) than control animals receiving identical scaffolds without growth factors (30%; P<0.05) or growth factors alone (20%). These data indicate that the enhanced engraftment can be attributed to specific growth factor effects that were made possible by the delivery mechanism of HBPA nanostructures.
引用
收藏
页码:478 / 481
页数:4
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