Microscale multilayer cocultures for biomimetic blood vessels

J Biomed Mater Res A. 2005 Feb 1;72(2):146-60. doi: 10.1002/jbm.a.30182.

Abstract

Living tissues have complex and well-organized microstructures. Although microtechnology has been used to create in vivo-like cell microstructures in vitro, most available microscale systems are two-dimensional, and few three-dimensional (3D) systems have been explored. This article demonstrates a 3D hierarchical biomimetic multilayer microsystem created by a generally applicable technique. The technique employs layer-by-layer microfluidics to build layers of cells and biopolymers in microchannels, allowing controlled patterning of cells and their microenvironments in the x, y, and z-dimension. As a prototype, a multilayer system was created using three vascular cell types within heterogeneous types of biopolymers to mimic the structure and composition of a blood vessel wall. The effects of matrix composition and multilayer configurations on 3D cell-cell interactions and cell biology were revealed. Cell migration in the z-dimension, matrix remodeling, intercellular adhesion molecule expression and actin organization were examined under different 3D coculture conditions. A more biomimetic coculture was found to reproduce a more stable structure and in vivo-like function. This approach provides a method to fabricate microscale hierarchical "neotissues" with 3D configurations of matrix materials and multiple cell types, and an in vitro cell coculture model to understand 3D processes of cell-cell and cell-matrix interactions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Biomimetic Materials / chemistry*
  • Blood Vessels*
  • Cell Adhesion
  • Cell Movement
  • Cells, Cultured
  • Coculture Techniques
  • Collagen / pharmacology
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism
  • Microfluidics
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Tissue Engineering / methods*

Substances

  • Intercellular Adhesion Molecule-1
  • Collagen