Mechanical properties, proteolytic degradability and biological modifications affect angiogenic process extension into native and modified fibrin matrices in vitro

Lukas Urech, Anne Greet Bittermann, Jeffrey A. Hubbell, Heike Hall

Research output: Contribution to journalArticle

67 Citations (Scopus)

Abstract

During initial stages of wound healing, fibrin clots provide a three-dimensional scaffold that induces cell infiltration and regeneration. Here, L1Ig6, a ligand for αvβ3 integrin was covalently incorporated within fibrin matrices to explore it as a matrix-immobilized angiogenic factor. Incorporation at concentrations greater than 1μg/ml reduced the fibrin crosslink density, as reflected by measurements of elastic modulus and swelling. The influence of crosslink density on endothelial cell process extension was characterized by modulating factor XIII concentrations in the coagulation mixture. At low incorporated concentrations of L1Ig6, it was possible to compensate gel elastic modulus via increased factor XIII, but not at high concentrations of L1Ig6. Similar findings were found when matrix swelling was analyzed. Fibrin crosslink density strongly influenced endothelial cell process extension, fewer and shorter processes were observed at high crosslink density. Matrix metalloproteinases (MMPs) were required for process extension and zymography and Western blots identified MMP-2 but not MMP-9. The amount of active MMP-2 increased for endothelial cells cultured in native and L1Ig6-modified matrices or when stimulated with VEGF-A165. The data indicate that distinct matrix properties can be tailored such that they become biologically stimulating and respond to cellular proteolytic activities, being a prerequisite for potential use of such matrices in biomedical applications.

Original languageEnglish
Pages (from-to)1369-1379
Number of pages11
JournalBiomaterials
Volume26
Issue number12
DOIs
StatePublished - Apr 1 2005
Externally publishedYes

Fingerprint

Fibrin
Endothelial cells
Factor XIII
Mechanical properties
Endothelial Cells
Elastic Modulus
Matrix Metalloproteinase 2
Swelling
Elastic moduli
Angiogenesis Inducing Agents
Matrix Metalloproteinase 9
Coagulation
Matrix Metalloproteinases
Infiltration
Scaffolds
Integrins
Wound Healing
Vascular Endothelial Growth Factor A
Regeneration
Gels

Keywords

  • Angiogenesis
  • Endothelial cell
  • Fibrin
  • Hydrogels
  • Matrix metalloproteinases
  • Mechanical properties

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Biomedical Engineering

Cite this

Mechanical properties, proteolytic degradability and biological modifications affect angiogenic process extension into native and modified fibrin matrices in vitro. / Urech, Lukas; Bittermann, Anne Greet; Hubbell, Jeffrey A.; Hall, Heike.

In: Biomaterials, Vol. 26, No. 12, 01.04.2005, p. 1369-1379.

Research output: Contribution to journalArticle

Urech, Lukas ; Bittermann, Anne Greet ; Hubbell, Jeffrey A. ; Hall, Heike. / Mechanical properties, proteolytic degradability and biological modifications affect angiogenic process extension into native and modified fibrin matrices in vitro. In: Biomaterials. 2005 ; Vol. 26, No. 12. pp. 1369-1379.
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