Endothelialized networks with a vascular geometry in microfabricated poly(dimethyl siloxane)

被引:172
作者
Shin, M
Matsuda, K
Ishii, O
Terai, H
Kaazempur-Mofrad, M
Borenstein, J
Detmar, M
Vacanti, JP [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
[3] Ctr Integrat Med & Innovat Technol, Cambridge, MA 02139 USA
[4] Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
[5] Massachusetts Gen Hosp, Dept Dermatol, Charlestown, MA 02129 USA
[6] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[7] Charles Stark Draper Lab Inc, MEMS Technol Grp, Cambridge, MA 02139 USA
关键词
tissue engineering; replica molding; biocompatible polymer; endothelialization;
D O I
10.1023/B:BMMD.0000048559.29932.27
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
One key challenge in regenerating vital organs is the survival of transplanted cells. To meet their metabolic requirements, transport by diffusion is insufficient, and a convective pathway, i.e., a vasculature, is required. Our laboratory pioneered the concept of engineering a vasculature using microfabrication in silicon and Pyrex. Here we report the extension of this concept and the development of a methodology to create an endothelialized network with a vascular geometry in a biocompatible polymer, poly(dimethyl siloxane) (PDMS). High-resolution PDMS templates were produced by replica-molding from micromachined silicon wafers. Closed channels were formed by bonding the patterned PDMS templates to flat PDMS sheets using an oxygen plasma. Human microvascular endothelial cells (HMEC-1) were cultured for 2 weeks in PDMS networks under dynamic flow. The HMEC-1 cells proliferated well in these confined geometries (channel widths ranging from 35 mum to 5 mm) and became confluent after four days. The HMEC-1 cells lined the channels as a monolayer and expressed markers for CD31 and von Willebrand factor (vWF). These results demonstrate that endothelial cells can be cultured in confined geometries, which is an important step towards developing an in vitro vasculature for tissue-engineered organs.
引用
收藏
页码:269 / 278
页数:10
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