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Related Experiment Video

Updated: Apr 14, 2026

Micropatterning and Assembly of 3D Microvessels
13:05

Micropatterning and Assembly of 3D Microvessels

Published on: September 9, 2016

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Fabrication of 3-dimensional multicellular microvascular structures.

Sebastian F Barreto-Ortiz1, Jamie Fradkin1, Joon Eoh1

  • 1*Department of Chemical and Biomolecular Engineering, Johns Hopkins Physical Sciences-Oncology Center and Institute for NanoBioTechnology, and Departments of Biomedical Engineering and Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland, USA; and Translational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|April 23, 2015
PubMed
Summary

Researchers developed 3D microfibers using hydrogel electrospinning to create microvasculature. This method enhances extracellular matrix deposition, enabling the formation of self-supporting, multilayered microvascular structures for regenerative medicine applications.

Keywords:
endothelial cellextracellular matrixfibrinmicrofiberperivascular cell

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Area of Science:

  • Biomaterials Engineering
  • Vascular Biology
  • Tissue Engineering

Background:

  • Limited research exists on developing microvasculature, the critical link between larger blood vessels and capillary beds.
  • Current tissue engineering strategies have focused on larger vessels or capillary networks, neglecting the intermediate microvasculature.
  • Developing functional microvasculature is essential for creating viable engineered tissues and organs.

Purpose of the Study:

  • To evaluate the efficacy of 3D microfibers fabricated by hydrogel electrospinning as templates for microvascular structure formation.
  • To investigate whether 3D microfibers enhance extracellular matrix (ECM) deposition by vascular cells.
  • To engineer freestanding, luminal multicellular microvasculature.

Main Methods:

  • Fabrication of 3D microfibers using hydrogel electrospinning.
  • Culture of vascular cells (endothelial colony-forming cells, pericytes, vascular smooth muscle cells) on fibrin microfibers.
  • Assessment of ECM deposition using confocal microscopy and RT-PCR.
  • Analysis of microvascular structure and lumen formation after microfiber core removal.

Main Results:

  • Fibrin microfibers significantly increased ECM protein deposition by vascular cells compared to 2D cultures.
  • Deposited ECM proteins included collagen types I, III, and IV, elastin, fibronectin, and laminin, forming layers of the vascular wall.
  • Successfully engineered multicellular microvascular structures with organized endothelium and a perivascular tunica media.
  • Achieved self-supporting, multilayered microvasculature with a distinct circular lumen post-core removal.

Conclusions:

  • 3D hydrogel electrospun microfibers serve as effective templates for engineering microvasculature.
  • This approach promotes enhanced ECM deposition and the formation of organized, self-supporting microvascular structures.
  • The method advances the development of human microvasculature for both basic research and translational applications in regenerative medicine.