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1 Institute of Molecular Biology and Physiology, University of Copenhagen, Copenhagen Muscle Research Centre, Copenhagen, Denmark
2 Rigshospitalet, Copenhagen Muscle Research Centre, Copenhagen, Denmark
* To whom correspondence should be addressed. E-mail: cjuel{at}aki.ku.dk.
The present study investigated the effects of injected darbepoetin (Novel Erythropoietin Stimulating Protein, NESP) on the density of three erythrocyte membrane transport proteins: the lactate/H+ co-transporter (MCT1), the chloride-bicarbonate exchanger 1 (AE1), and the water channel aquaporin 1 (AQP1). Thirteen subjects were injected with NESP once a week for four weeks. Blood samples were obtained before, during, and after the injection period, and the erythrocyte transport proteins were determined by western blotting. The NESP injections induced a transient increase in hematocrit, red cell volume, and reticulocyte fraction. The density of AQP1 protein was higher (maximal increase +59 %)(P<0.01) during the injection period compared to the pre-injection value, and lower (P<0.01) after the injection period. The density of AE1 protein was higher (maximal increase +15 %)(P<0.05) during the injection period compared to the pre-injection value, and tended (P=0.06) to be lower after the injection period than before the injection period. The density of the erythrocyte MCT1 protein was higher (maximal increase +43 %)(P<0.05) during the injection period than in the pre-injection period. Age-separation experiments using self-creating Percoll gradients demonstrated a higher density of membrane transport proteins in young red blood cells. These data suggest that the NESP-induced increase in membrane transport proteins is caused by a higher fraction of newly formed erythrocytes (and reticulocytes), which have a higher density of membrane transport proteins. However, increased incorporation of membrane proteins during erythrocyte formation may also be involved. We suggest that NESP improves the quality of erythrocyte membrane transport through these mechanisms.
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