The migratory response to platelet-derived growth factor of smooth muscle cells isolated from synthetic vascular grafts in a canine model

David J. Minion, Rudolph M. Snajdar, Maarten Paul Van De Kerkhove, John A. Van Aalst, Paul L. Fox, Linda M. Graham

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Objective: Previous studies on smooth muscle cells (SMCs) harvested from implanted synthetic grafts demonstrate increased production of platelet- derived growth factor (PDGF) but decreased proliferative response compared with aortic SMCs. The purpose of this study was to determine the migratory response of graft versus aortic SMCs. Methods: Thoracoabdominal grafts were implanted in beagles. The SMCs were harvested from the graft and infrarenal aorta. Migration was determined with the use of a razor-scrape assay and computerized image analysis. Results: The mean distance migrated and the number of cells that migrated were greater in graft SMCs at baseline (185 ± 18 μm and 108 ± 17 cells) compared with aortic cells (110 ± 10 μm and 42 ± 5 cells)(P < .05). Baseline differences persisted after treatment with antibodies to PDGF. The addition of PDGF (10 ng/mL) resulted in increased migration in both graft (229 ± 23 μm and 146 ± 20 cells) and aortic SMCs (130 ± 9 μm and 70 ± 5 cells) compared with baseline (P < .05). The relative increase in response to PDGF was similar between the two groups (P = not significant). Conclusions: Graft SMCs differ phenotypically from aortic SMCs; they exhibit increased basal migration that is independent of autocrine stimulation by PDGF. In contrast to their blunted proliferative response, graft SMCs have a similar migratory response to PDGF compared with aortic SMCs.

Original languageEnglish
Pages (from-to)953-959
Number of pages7
JournalJournal of Vascular Surgery
Volume31
Issue number5
DOIs
StatePublished - May 2000

Bibliographical note

Funding Information:
Supported by Grants from the NIH (HL41178) and the Department of Veterans Affairs.

Funding

Supported by Grants from the NIH (HL41178) and the Department of Veterans Affairs.

FundersFunder number
National Institutes of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)R01HL041178
U.S. Department of Veterans Affairs

    ASJC Scopus subject areas

    • Surgery
    • Cardiology and Cardiovascular Medicine

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