How do sickle cells become dehydrated?

2001 ◽  
Vol 2 (3) ◽  
pp. 200-205 ◽  
Author(s):  
Patrick Merciris ◽  
Françoise Giraud
Keyword(s):  
1986 ◽  
Vol 15 (2) ◽  
pp. 71-79
Author(s):  
Antoine K. Fomufod ◽  
Oswaldo Castro ◽  
Lynnard J. Slaughter ◽  
Laval N. Cothran ◽  
Norman R. Hayes ◽  
...  
Keyword(s):  

1988 ◽  
Vol 263 (9) ◽  
pp. 4338-4346
Author(s):  
W E Mickols ◽  
J D Corbett ◽  
M F Maestre ◽  
I Tinoco ◽  
J Kropp ◽  
...  

BMJ ◽  
1958 ◽  
Vol 1 (5075) ◽  
pp. 890-890 ◽  
Author(s):  
G. W. Storey
Keyword(s):  

1993 ◽  
Vol 264 (2) ◽  
pp. C251-C270 ◽  
Author(s):  
C. H. Joiner

Cellular dehydration is one of several pathological features of the sickle cell. Cation depletion is quite severe in certain populations of sickle cells and contributes to the rheological dysfunction that is the root cause of vascular occlusion in this disease. The mechanism of dehydration of sickle cells in vivo has not been ascertained, but three transport pathways may play important roles in this process. These include the deoxygenation-induced pathway that permits passive K+ loss and entry of Na+ and Ca2+; the K(+)-Cl- cotransport pathway, activated by acidification or cell swelling; and the Ca(2+)-activated K+ channel, or Gardos pathway, presumably activated by deoxygenation-induced Ca2+ influx. Recent evidence suggests that these pathways may interact in vivo. Heterogeneity exists among sickle cells as to the rate at which they become dense, suggesting that other factors may affect the activity or interactions of these pathways. Understanding the mechanism of dehydration of sickle cells may provide opportunities for pharmacological manipulation of cell volume to mitigate some of the symptoms of sickle cell disease.


1989 ◽  
Vol 565 (1 Sickle Cell D) ◽  
pp. 466-468
Author(s):  
J. STUART ◽  
P. C. W. STONE ◽  
M. PLAYER ◽  
Y. Y. BILTO

1958 ◽  
Vol 11 (5) ◽  
pp. 457-457 ◽  
Author(s):  
H. L. English
Keyword(s):  

Blood ◽  
1986 ◽  
Vol 68 (5) ◽  
pp. 1162-1166 ◽  
Author(s):  
DK Kaul ◽  
ME Fabry ◽  
RL Nagel

We have characterized the type of red cells from sickle cell patients that were trapped in the course of sickle-cell vaso-occlusion. In addition, the perfusion conditions (arterial perfusion pressure [Pa] and oxygen tension [PO2]) leading to experimentally induced vaso- occlusion in the artificially perfused, innervated mesocecum microvascular preparation were determined. Microvascular obstruction was induced by decrease in Pa; the lower the Pa, the greater the peripheral resistance as well as the extent of obstruction. The cells involved in the obstruction were recovered by vasodilation (secondary to denervation) and increase in Pa. Densitometric analysis of density gradient-separated infused and trapped cells was supplemented with morphological analysis to ascertain the involvement of density classes as well as morphological types seen in oxy and deoxy sickle blood. The trapping phenomenon was sensitive to PO2. Percentage of densest gradient classes, ie, fraction 3 (F3; mainly dense unsicklable SS discocytes [USDs]) and fraction 4 (F4; irreversibly sickled cells [ISCs] and the densest discocytes), showed a significant increase in trapping when perfusion was switched from oxy to deoxy perfusate. Morphological analysis revealed that unsicklable SS discocytes are more effectively trapped when deoxygenated. The deoxygenation of infused cells did not further change the percentage of ISCs trapped, suggesting that ISCs are equally capable of sequestration in the oxy and the deoxy states. The venous effluent showed a selective and significant depletion of dense cells (F4) and ISC counts at all Pa. We conclude that the progressive obstruction of the microcirculation by sickle cells involves selective sequestration of the densest classes of cells and that this mechanism might explain their partial disappearance during painful sickle cell crisis.


Blood ◽  
1986 ◽  
Vol 68 (2) ◽  
pp. 450-454 ◽  
Author(s):  
N Mohandas ◽  
ME Rossi ◽  
MR Clark

We hypothesized that the deoxygenation-induced increase in cation permeability of sickle cells was related to mechanical distention of the membrane by growing HbS polymer within the cell. To test this hypothesis, we determined the effect of deoxygenation on cation fluxes in sickle cells under conditions that restricted or permitted extensive growth of polymer, producing different degrees of membrane distention. Manipulation of suspending medium osmolality for density-isolated high and low mean cell hemoglobin concentration (MCHC) cells was used to regulate the extensional growth of polymer bundles and hence membrane distortion. For initially low MCHC cells, the deoxygenation-induced increase in both Na and K fluxes was markedly suppressed when the MCHC was increased by increasing the osmolality. This suppression corresponded to the inhibition of extensive morphologic cellular distortion. For initially high MCHC, ISC-rich cells, deoxygenation had minimal effect on K permeability. However, reduction of MCHC by a decrease in osmolality produced a concomitant increase in cation permeability and cellular distortion. These observations support the idea that the sickling-associated increase in membrane permeability is related to mechanical stress imposed on the membrane by bundles of HbS polymer.


Sign in / Sign up

Export Citation Format

Share Document