Shear stress effects on bacterial adhesion, leukocyte adhesion, and leukocyte oxidative capacity on a polyetherurethane

Citation
Ms. Shive et al., Shear stress effects on bacterial adhesion, leukocyte adhesion, and leukocyte oxidative capacity on a polyetherurethane, J BIOMED MR, 46(4), 1999, pp. 511-519
Citations number
47
Categorie Soggetti
Multidisciplinary
Journal title
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH
ISSN journal
00219304 → ACNP
Volume
46
Issue
4
Year of publication
1999
Pages
511 - 519
Database
ISI
SICI code
0021-9304(19990915)46:4<511:SSEOBA>2.0.ZU;2-J
Abstract
Infection of implanted cardiovascular biomaterials still occurs despite inh erent host defense mechanisms. Using a rotating disk system, we investigate d Staphylococcus epidermidis and polymorphonuclear leukocyte (PMN) adhesion to a polyetherurethane urea (PEUU-A') under shear stress (0-17.5 dynes/cm( 2)) for time periods up to 6 h. In addition, the superoxide (SO) release ca pacity of PMNs after transient exposure to PEUU-A' under shear stress was d etermined. Bacterial adhesion in phosphate-buffered saline (PBS) showed a l inear shear dependence, decreasing with increasing shear stress. Overall ad hesion in PBS decreased with time. However, bacterial adhesion in 25% human serum was similar for all time points up to 360 min. Adhesion was observed at all shear levels, displaying no shear dependence. In contrast, PMN adhe sion demonstrated a strong shear dependence similarly for times up to 240 m in, decreasing sharply with increasing shear stress. Although PMNs preexpos ed to shear stress showed a slightly diminished SO release response compare d to fresh cells for all stimuli, it was not statistically significant rega rdless of the stimulus. We conclude that circulating leukocytes are unable to adhere in regions of high shear which may contain adherent bacteria. In addition, exposure to PEUU-A' and shear stress (in the range 0-18 dynes/cm( 2)) is insufficient to cause a depression in the oxidative response of PMNs . (C) 1999 John Wiley & Sons, Inc.