Enhanced proteolytic degradation of molecularly engineered PEG hydrogels in response to MMP-1 and MMP-2

J. Patterson, J. A. Hubbell

Research output: Contribution to journalArticle

263 Citations (Scopus)

Abstract

Bioactive hydrogels formed by Michael-type addition reactions of end-functionalized poly(ethylene glycol) macromers with cysteine-containing peptides have been described as extracellular matrix mimetics and tissue engineering scaffolds. Although these materials have shown favorable behavior in vivo in tissue repair, we sought to develop materials formulations that would be more rapidly responsive to cell-induced enzymatic remodeling. In this study, protease-sensitive peptides that have increased kcat values were characterized and evaluated for their effects on gel degradability. Biochemical properties for soluble peptides and hydrogels were examined for matrix metalloproteinase (MMP)-1 and MMP-2. The most efficient peptide substrates in some cases overlap and in other cases differ between the two enzymes tested, and a range of kcat values was obtained. For each enzyme, hydrogels formed using the peptides with higher kcat values degraded faster than a reference with lower kcat. Fibroblasts showed increased cell spreading and proliferation when cultured in 3D hydrogels with faster degrading peptides, and more cell invasion from aortic ring segments embedded in the hydrogels was observed. These faster degrading gels should provide matrices that are easier for cells to remodel and lead to increased cellular infiltration and potentially more robust healing in vivo.

Original languageEnglish
Pages (from-to)7836-7845
Number of pages10
JournalBiomaterials
Volume31
Issue number30
DOIs
StatePublished - Oct 1 2010
Externally publishedYes

Fingerprint

Matrix Metalloproteinase 1
Hydrogels
Matrix Metalloproteinase 2
Peptides
Polyethylene glycols
Degradation
Gels
Enzymes
Tissue Scaffolds
Addition reactions
Ethylene Glycol
Fibroblasts
Tissue Engineering
Scaffolds (biology)
Tissue engineering
Infiltration
Extracellular Matrix
Cysteine
Metalloproteases
Repair

Keywords

  • Biodegradation
  • Biomimetic material
  • Cell spreading
  • Hydrogel
  • Matrix metalloproteinase
  • Peptide

ASJC Scopus subject areas

  • Biomaterials
  • Bioengineering
  • Ceramics and Composites
  • Mechanics of Materials
  • Biophysics

Cite this

Enhanced proteolytic degradation of molecularly engineered PEG hydrogels in response to MMP-1 and MMP-2. / Patterson, J.; Hubbell, J. A.

In: Biomaterials, Vol. 31, No. 30, 01.10.2010, p. 7836-7845.

Research output: Contribution to journalArticle

Patterson, J. ; Hubbell, J. A. / Enhanced proteolytic degradation of molecularly engineered PEG hydrogels in response to MMP-1 and MMP-2. In: Biomaterials. 2010 ; Vol. 31, No. 30. pp. 7836-7845.
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