Biomedical Microdevices

, Volume 6, Issue 4, pp 269–278

Endothelialized Networks with a Vascular Geometry in Microfabricated Poly(dimethyl siloxane)

Authors

  • Michael Shin
    • Department of SurgeryMassachusetts General Hospital and Harvard Medical School
    • Center for Integration of Medicine and Innovative Technology
  • Kant Matsuda
    • Cutaneous Biology Research Center and Department of DermatologyMassachusetts General Hospital and Harvard Medical School
  • Osamu Ishii
    • Department of SurgeryMassachusetts General Hospital and Harvard Medical School
    • Center for Integration of Medicine and Innovative Technology
  • Hidetomi Terai
    • Department of SurgeryMassachusetts General Hospital and Harvard Medical School
    • Center for Integration of Medicine and Innovative Technology
  • Mohammed Kaazempur-Mofrad
    • Center for Integration of Medicine and Innovative Technology
  • Jeffrey Borenstein
    • Center for Integration of Medicine and Innovative Technology
  • Michael Detmar
    • Cutaneous Biology Research Center and Department of DermatologyMassachusetts General Hospital and Harvard Medical School
  • Joseph P. Vacanti
    • Department of SurgeryMassachusetts General Hospital and Harvard Medical School
    • Center for Integration of Medicine and Innovative Technology
Article

DOI: 10.1023/B:BMMD.0000048559.29932.27

Cite this article as:
Shin, M., Matsuda, K., Ishii, O. et al. Biomedical Microdevices (2004) 6: 269. doi:10.1023/B:BMMD.0000048559.29932.27

Abstract

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 μm 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.

tissue engineeringreplica moldingbiocompatible polymerendothelialization
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Copyright information

© Kluwer Academic Publishers 2004