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Herbert Meiselman

2008 Recipient of the Jean-Leonard-Marie Poiseuille Award

Outstanding Research on Red Cell Rheology in Health and Disease

 

Herbert J. Meiselman was recognized as the recipient of the Poiseuille Gold Medal at the 13th Congress.   During his Professorship at USC, Herb became one of the most prolific and important experimental scientists in the field of blood rheology.  His studies encompassed many aspects of red blood and leukocyte cell rheology, exploring the factors underlying the flow and deformation of red and white cells (e.g. cell deformation, aggregation, viscoelasticity).  Much of his work has been concerned with the changes in cellular mechanics that occur in the neonatal and in the abnormal pathophysiological circulation and result in clinically relevant phenomena.  This has taken him into fields as diverse as the effect of dextran, polyvinylpyrrolidone and other polymers on red cell rheology (important for subsequent work on the mechanism of red cell aggregation), hemorhological factors (including those of polymorphonuclear leukocytes) in cerebral ischemia, coronary artery disease and aspects of blood cell abnormalities in diabetes mellitus, sickle cell disease and hypertension. 

In subsequent years, his laboratory undertook a major study of the mechanism underlying red cell aggregation by polymers.  It has been shown that the depletion model rather than the bridging model is in qualitative and quantitative agreement with the measured cell-cell affinity and red cell aggregation.  This model proposes that RBC cell aggregation occurs as a result of a lower localized protein or polymer concentration near the cell surface as compared with the suspending medium (i.e., relative depletion near the cell surface). This exclusion of macromolecules near the cell surface leads to an osmotic gradient and thus depletion interaction. As with the bridging model, disaggregation forces are electrostatic repulsion, membrane strain, and mechanical shearing.  Herb intends to apply this model to unresolved aspects of human red cell aggregation, such as the more than 100% increase of aggregation for old versus young red cells when suspended in autologous plasma or polymer solutions (
Clinical Hemorheology 13:575-592, 1993), or the reduced aggregation of neonatal red cells in plasma or in polymer solutions (Pediatric Research, 18:1356-1360, 1984). Application of this model may also be of potential value in human disease.

His award lecture was titled "In vitro and in vivo aspects of red blood cell aggregation".

 


 


 









 

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