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Updated: Jul 11, 2026

Analysis of Cell Migration within a Three-dimensional Collagen Matrix
Published on: October 5, 2014
Extracellular matrix molecules regulate endothelial cell migration stimulated by lysophosphatidic acid
T S Panetti1, D F Hannah, C Avraamides
1Department of Microbiology and Immunology, Sol Sherry Thrombosis Research Center, Temple University School of Medicine, Philadelphia, PA 19140, USA. tpanetti@temple.edu
Lysophosphatidic acid (LPA) stimulates endothelial cell transmigration through specific extracellular matrix proteins like collagen and gelatin, unlike sphingosine 1-phosphate (S1P). This process involves the protein Hic-5 and adhesion strength, highlighting matrix-dependent cell migration.
Area of Science:
- Cell biology
- Biochemistry
- Extracellular matrix research
Background:
- Lysophosphatidic acid (LPA) and sphingosine 1-phosphate (S1P) are bioactive lipids.
- These lipids signal through G-protein coupled receptors.
- They differentially regulate endothelial cell transmigration.
Purpose of the Study:
- To investigate if endothelial cell transmigration induced by LPA, but not S1P, is contingent on the extracellular matrix.
- To elucidate the role of extracellular matrix in LPA-mediated endothelial cell migration.
Main Methods:
- Bovine pulmonary artery endothelial cell (BPAE) transmigration assessed using a modified Boyden chamber.
- Cell locomotion dynamics observed via video microscopy.
- Analysis of cell adhesion strength and focal adhesion protein localization (Hic-5, paxillin).
Main Results:
- LPA promoted BPAE transmigration through gelatin- and collagen-coated filters, but not fibronectin, vitronectin, or fibrinogen.
- Cell adhesion was weaker to collagen and gelatin compared to fibronectin.
- LPA induced distinct cell morphologies and Hic-5 localization differences on various matrix substrates.
Conclusions:
- Endothelial cell transmigration stimulated by LPA is dependent on the extracellular matrix composition.
- Hic-5 localization and adhesion strength correlate with LPA-induced transmigration.
- These findings differentiate LPA and S1P signaling in endothelial cell migration.
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