A porous photocurable elastomer for cell encapsulation and culture

被引:99
作者
Gerecht, Sharon
Townsend, Seth A.
Pressler, Heather
Zhu, Han
Nijst, Christiaan L. E.
Bruggeman, Joost P.
Nichol, Jason W.
Langer, Robert
机构
[1] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Chem, Cambridge, MA 02139 USA
[4] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[5] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[6] Eindhoven Univ Technol, Dept Biomed Engn, NL-5600 MB Eindhoven, Netherlands
[7] Erasmus MC, Dept Plast & Reconstruct Surg, NL-3000 CA Rotterdam, Netherlands
关键词
biocompatibility; cell encapsulation; elastomer; nerve; scaffold; stem cell;
D O I
10.1016/j.biomaterials.2007.07.039
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Encapsulating cells within a polymer matrix creates a three-dimensional (3D) scaffold that may more accurately represent the native microenvironment and cell organization. Here we report a porous scaffold prepared from a photocurable elastomer, poly(glycerolcosebacate)-acrylate (PGSA). The scaffold porosity, swelling, mass loss, toxicity and mechanical properties, suggest that porous PGSA could be used to support the growth and differentiation of encapsulated cells. Neuroblastoma (NB) and human embryonic stem cells (hESCs) were encapsulated into the matrix and found to adhere to the material and interact with each other within 24h. After 7 days, encapsulated NB cells were found to grow, and form matrix fibrils and tissue. Undifferentiated hESCs proliferated and differentiated in the PGSA scaffold. In vivo experiments showed that both porous scaffolds have similar biocompatibility profiles as non-porous PGSA, but porous PGSA promotes tissue ingrowth, as compared to non-porous PGSA. We therefore propose that porous PGSA scaffolds can provide a logistical template for 3D growth of cells and tissue engineering. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4826 / 4835
页数:10
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