siRNA silencing reveals role of vascular cell adhesion molecule-1 in vascular smooth muscle cell migration

Erik J. Petersen, Toru Miyoshi, Zuobiao Yuan, Satoshi Hirohata, Jin Zhong Li, Weibin Shi, John F. Angle

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Vascular cell adhesion molecule-1 (VCAM-1) is an adhesion molecule expressed by endothelial cells for recruitment of leukocytes during inflammation. It is also abundantly expressed by smooth muscle cells in atherosclerotic lesions and in injured arteries. In this study, we examined the role of VCAM-1 in smooth muscle cell migration. Smooth muscle cells were isolated from the aorta of C57BL/6 mice and transfected with short interfering RNAs (siRNAs) targeting VCAM-1. Inhibition on VCAM-1 expression by siRNAs was assessed by Western blot analysis, RT-PCR and by measuring soluble VCAM-1 concentrations in the incubation medium. One siRNA that showed greater suppression on VCAM-1 expression was used for migration assay. A single scratch wound was made on 70% confluent cells and cells migrated from wounded monolayer were counted 24 and 48 h after injury. Treatment with VCAM-1 siRNA resulted in a significant reduction in the number of migrated cells. This siRNA also exhibited a minor effect on smooth muscle cell proliferation. Thus, our findings indicate that VCAM-1 is necessary for the migration of smooth muscle cells and interfering VCAM-1 expression could be an effective approach to prevention and treatment of atherosclerosis and restenosis.

Original languageEnglish (US)
Pages (from-to)301-306
Number of pages6
JournalAtherosclerosis
Volume198
Issue number2
DOIs
StatePublished - Jun 2008
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by the National Institutes of Health grant HL71844 and the Society of Interventional Radiology seed grant. Appendix A

Keywords

  • Migration
  • Smooth muscle cells
  • VCAM-1
  • siRNA

Fingerprint

Dive into the research topics of 'siRNA silencing reveals role of vascular cell adhesion molecule-1 in vascular smooth muscle cell migration'. Together they form a unique fingerprint.

Cite this