Formation of microvascular networks in vitro. Academic Article uri icon

Overview

abstract

  • This protocol describes how to form a 3D cell culture with explicit, endothelialized microvessels. The approach leads to fully enclosed, perfusable vessels in a bioremodelable hydrogel (type I collagen). The protocol uses microfabrication to enable user-defined geometries of the vascular network and microfluidic perfusion to control mass transfer and hemodynamic forces. These microvascular networks (μVNs) allow for multiweek cultures of endothelial cells or cocultures with parenchymal or tissue cells in the extra-lumen space. The platform enables real-time fluorescence imaging of living engineered tissues, in situ confocal fluorescence of fixed cultures and transmission electron microscopy (TEM) imaging of histological sections. This protocol enables studies of basic vascular and blood biology, provides a model for diseases such as tumor angiogenesis or thrombosis and serves as a starting point for constructing prevascularized tissues for regenerative medicine. After one-time microfabrication steps, the system can be assembled in less than 1 d and experiments can run for weeks.

publication date

  • August 29, 2013

Research

keywords

  • Microvessels
  • Tissue Engineering

Identity

Scopus Document Identifier

  • 84883342307

Digital Object Identifier (DOI)

  • 10.1038/nprot.2013.110

PubMed ID

  • 23989676

Additional Document Info

volume

  • 8

issue

  • 9