Dynamics of neutrophil rolling over stimulated endothelium in vitro

• Published in: Biophysical journal Vol. 66; no. 6; pp. 2202 - 2209
• Main Authors: Goetz, D.J., el-Sabban, M.E., Pauli, B.U., Hammer, D.A.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.06.1994
• Subjects: Animals; Aorta, Thoracic; Cattle; Cell Adhesion Molecules - pharmacology; Cell Movement - drug effects; Cells, Cultured; Endothelium, Vascular - physiology; Kinetics; Neutrophils - cytology; Neutrophils - drug effects; Neutrophils - physiology; P-Selectin; Platelet Membrane Glycoproteins - pharmacology; Space life sciences; Stress, Mechanical
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(94)81016-1

Prior to extravasation at sites of acute inflammation, neutrophils roll over activated endothelium. Neutrophil rolling is often characterized by the average rolling velocity. An additional dynamic feature of rolling that has been identified but not extensively studied is the fluctuation in the rolling velocity about the average. To analyze this characteristic further, we have measured the instantaneous velocity of bovine neutrophils interacting with lipopolysaccharide-stimulated bovine aortic endothelium at shear stresses of 1, 2, 3, and 4 dynes/cm2. The average velocities are quantitatively similar to those reported for human neutrophils rolling over reconstituted P-selectin at a surface density of 400 sites/microns 2. At all shear stresses tested, the population average variance in the instantaneous velocity is at least 2 orders of magnitude higher than the theoretical variance generated from experimental error, indicating that the neutrophils translate with a nonconstant velocity. Possible sources of the variance are discussed. These include "macroscopic" sources such as topological heterogeneity in the endothelium and microscopic sources, such as inherent stochastic formation and breakage of the receptor-ligand bonds that mediate the rolling. Regardless of the ultimate source of the variance, these results justify the use of mathematical models that incorporate stochastic processes to describe bond formation and breakage between the neutrophil and the endothelium and hence are able to generate variable velocity trajectories.