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Cited by 257

The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.

Cell migration through defined, synthetic extracellular matrix analogues

Gobin, Andrea S., West, Jennifer L.·2002·The FASEB Journal

Abstract

We have developed synthetic hydrogel extracellular matrix (ECM) analogues that can be used to study mechanisms involved in cell migration, such as receptor‐ligand interactions and proteolysis. The biomimetic hydrogels consist of bioinert polyethylene glycol diacrylate derivatives with proteolytically degradable peptide sequences included in the backbone of the polymer and adhesive peptide sequences grafted to the network. Hydrogels have been developed that degrade as cells secrete proteolytic enzymes. Adhesive peptide sequences grafted to the hydrogel provide ligands that can interact with receptors on the cell surface to mediate adhesion and spreading. In this study, we have characterized the effects of adhesive ligand density on fibroblast migration through collagenase‐degradable and plasmin‐degradable hydrogels and on smooth muscle cell migration through elastase‐degradable hydrogels. In all three cases, we found that cell migration has a biphasic dependence on adhesion ligand concentration, with optimal migration at intermediate ligand levels. Furthermore, both adhesive and proteolytically degradable sequences were required for cell migration to occur. These synthetic ECM analogues may be useful for 3‐D mechanistic studies of many aspects of cell migration

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Metadata

Authors
Gobin, A. S., & West, J. L.
Venue
The FASEB Journal
Publisher
Wiley
Published
2002-03-26
Volume
16
Issue
7
Pages
751-753
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W1562490776
Cited by
257
References
23
FWCI
5.26
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Cell migration through defined, synthetic extracellular matrix analogues. https://app.cochat.ai/papers/10.1096/fj.01-0759fje
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Gobin, A. S., & West, J. L. (2002). Cell migration through defined, synthetic extracellular matrix analogues. The FASEB Journal. https://doi.org/10.1096/fj.01-0759fje

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