Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen

Author:

Safeukui Innocent12,Buffet Pierre A.34,Deplaine Guillaume123,Perrot Sylvie12,Brousse Valentine5,Ndour Alioune34,Nguyen Marie6,Mercereau-Puijalon Odile12,David Peter H.12,Milon Geneviève7,Mohandas Narla8

Affiliation:

1. Institut Pasteur, Unité d'Immunologie Moléculaire des Parasites, Département de Parasitologie Mycologie, Paris, France;

2. Centre National de la Recherche Scientifique, Paris, France;

3. Inserm, Université Paris 6, Paris, France;

4. Department of Parasitology, Assistance Publique des Hôpitaux de Paris (AP-HP), Pitié Salpétrière Hospital, Paris, France;

5. Department of Pediatrics, AP-HP, Necker Hospital, Paris, France;

6. Institut Pasteur, Plate-Forme de Cytométrie, Imagopole, Paris France;

7. Département de Parasitologie Mycologie, Immunophysiologie et Parasitisme, Institut Pasteur, Paris, France; and

8. New York Blood Center, New York, NY

Abstract

AbstractSplenic sequestration of RBCs with reduced surface area and cellular deformability has long been recognized as contributing to pathogenesis of several RBC disorders, including hereditary spherocytosis. However, the quantitative relationship between the extent of surface area loss and splenic entrapment remains to be defined. To address this issue, in the present study, we perfused ex vivo normal human spleens with RBCs displaying various degrees of surface area loss and monitored the kinetics of their splenic retention. Treatment with increasing concentrations of lysophosphatidylcholine resulted in a dose-dependent reduction of RBC surface area at constant volume, increased osmotic fragility, and decreased deformability. The degree of splenic retention of treated RBCs increased with increasing surface area loss. RBCs with a > 18% average surface area loss (> 27% reduced surface area-to-volume ratio) were rapidly and completely entrapped in the spleen. Surface-deficient RBCs appeared to undergo volume loss after repeated passages through the spleen and escape from splenic retention. The results of the present study for the first time define the critical extent of surface area loss leading to splenic entrapment and identify an adaptive volume regulation mechanism that allows spherocytic RBCs to prolong their life span in circulation. These results have significant implications for understanding the clinical heterogeneity of RBC membrane disorders.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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