Affiliations: Department of Bioengineering and The Whitaker Institute of Biomedical Engineering, University of California, San Diego, La Jolla, California, USA
Note: [] Address for correspondence: Dr. Song Li, Department of Bioengineering University of California, Berkeley 459 Evans Hall #1762, Berkeley, CA 94720‐1762, USA. Tel. & Fax: +1 510 231 5631; E‐mail: [email protected].
Abstract: The migration of vascular endothelial cells (ECs) plays an important role in vascular remodeling. Here we studied the effects of cell morphology on the migration of bovine aortic ECs by culturing cells on micropatterned strips of collagen matrix (60‐, 30‐, and 15‐μm wide). The spreading areas of the cells on 15‐ and 30‐μm wide strips were 30% lower than those on 60‐ μm wide strips and unpatterned collagen. The cells on 15‐μm wide strips completely aligned in the direction of the strip, and had significantly lower shape index than those in all other groups. On strips of all widths, ECs tended to migrate in the direction of strips. ECs on 15‐μm wide strips had highest speed, particularly in the direction of the strip. Vinculin staining showed that the leading edge of ECs on 15‐μm wide strips had focal adhesions that were oriented with their lamellipodial protrusion and the direction of cell migration; this arrangement of the focal adhesions may promote EC migration. The present study provides direct evidence on the role of cell morphology in EC migration, and will help us to understand the mechanisms of EC migration during angiogenesis and wound healing.
