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
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.