Cell-cell affinity of senescent human erythrocytes
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作者:
Neu, B
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Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USAUniv So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
Neu, B
[1
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Sowemimo-Coker, SO
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Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USAUniv So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
Sowemimo-Coker, SO
[1
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Meiselman, HJ
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Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USAUniv So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
Meiselman, HJ
[1
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机构:
[1] Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
During their 120-day life span, human red blood cells (RBC) undergo several physicochemical changes, including an increased tendency to aggregate in plasma or polymer solutions. This study was designed to examine potential associations between age-related differences in RBC mobility, aggregation, and membrane glycocalyx properties for cells suspended in buffer and in 3 g/dl solutions of 70.3 kDa dextran. A recent model for depletion-mediated RBC aggregation was employed to calculate the changes of glycocalyx properties that were consistent with experimental electrophoretic mobility (EPM) and aggregation data. Young and old cells were obtained by density separation, after which aggregation and EPM were determined versus ionic strength; old cells exhibited a two- to threefold greater aggregation in dextran. EPM of old cells was identical to young cells in polymer-free media yet was 4% greater in dextran. The greater EPM for old RBC indicates a larger polymer depletion layer, which could be explained either by a 10-15% decrease of their glycocalyx thickness or a similar percentage decrease of polymer penetration into their glycocalyx. The larger depletion layer leads to markedly elevated cell-cell affinities for old cells, with the computed affinity increases consistent with enhanced old RBC aggregation. These results provide a rational explanation for the aggregation and EPM behavior of old RBC, and raise the possibility of depletion-mediated interactions contributing to senescent cell removal from the circulation.
机构:
Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Blagovic, Katarina
Gong, Emily S.
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Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Gong, Emily S.
Milano, Daniel F.
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Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Milano, Daniel F.
Natividad, Robert J.
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Northeastern Univ, Grad Program Bioengn, Boston, MA 02115 USANortheastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Natividad, Robert J.
Asthagiri, Anand R.
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Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Northeastern Univ, Grad Program Bioengn, Boston, MA 02115 USANortheastern Univ, Dept Chem Engn, Boston, MA 02115 USA