Abstract
Red blood cell (RBC) deformability is an essential component of
microcirculatory function that appears to be enhanced by physiological
shear stress, while being negatively affected by supraphysiological
shears and/or free radical exposure. Given that blood contains RBCs with
non-uniform physical properties, whether all cells equivalently
tolerate mechanical and oxidative stresses remains poorly understood. We
thus partitioned blood into old and young RBCs which were exposed to
phenazine methosulfate (PMS) that generates intracellular superoxide
and/or specific mechanical stress. Measured RBC deformability was lower
in old compared to young RBCs. PMS increased total free radicals in both
sub-populations, and RBC deformability decreased accordingly. Shear
exposure did not affect reactive species in the sub-populations but
reduced RBC nitric oxide synthase (NOS) activation and intriguingly
increased RBC deformability in old RBCs. The co-application of PMS and
shear exposure also improved cellular deformability in older cells
previously exposed to reactive oxygen species (ROS), but not in younger
cells. Outputs of NO generation appeared dependent on cell age; in
general, stressors applied to younger RBCs tended to induce
S-nitrosylation of RBC cytoskeletal proteins, while older RBCs tended to
reflect markers of nitrosative stress. We thus present novel findings
pertaining to the interplay of mechanical stress and redox metabolism in
circulating RBC sub-populations.
Originalsprache | Englisch |
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Aufsatznummer | 47 |
Zeitschrift | Biology |
Jahrgang | 10 |
Ausgabenummer | 1 |
Seiten (von - bis) | 1-13 |
Seitenumfang | 13 |
ISSN | 2079-7737 |
DOIs | |
Publikationsstatus | Veröffentlicht - 11.01.2021 |