Purpose: Red cells in hereditary spherocytosis are characterized by a reduc
ed surface area/volume ratio. The mechanisms leading to the loss of membran
e material and subsequent elimination of the cells have still not been clar
ified, It was the aim of the present study to analyze band 3 distribution i
n the red cell membrane and its putative role in red cell elimination. Meth
ods/Results: Immunogold histochemistry was performed to detect band 3 in re
d cell membranes. Band 3 density and distribution were visualized by electr
on microscopy. Unsplenectomized spherocytosis patients (n = 12) showed redu
ced band 3 density and aggregation compared to controls (n = 15) (density:
1.2 +/- 0.1 gold particles/mum circumference of red cell membrane vs 1.5 +/
- 0.07 gold particles/mum, chi +/- SEM; P < 0.05; aggregation: 0.26 +/- 0.0
2 aggregates/mum vs 0.3 +/- 0.02 aggregates/ mum). By contrast, band 3 dens
ity and aggregation were increased in spherocytosis patients who had underg
one splenectomy (density: 2.8 +/- 0.1 gold particles/mum vs 2.0 +/- 0.1 gol
d particles/mum; P < 0.05; aggregation: 1.5 +/- 0.1 aggregates/mum vs 0.5 /- 0.03 aggregates/mum; P < 0.01). Artificial ageing of red cells from heal
thy controls (n = 6) led to a significant increase in band 3 aggregation (2
.06 +/- 0.2 aggregates/mum vs 0.33 +/- 0.1 aggregates/mum; P-Wilicoxon < 0.
01) but no change in band 3 density. In hereditary spherocytosis (n 6), bot
h band 3 density and aggregation increased significantly after artificial a
geing of the red cells. The elevated band 3 aggregation was associated with
a stimulated erythrophagocytosis in vitro. Conclusion: Band 3 aggregation
characterizes the red cells in hereditary spherocytosis. It may be the caus
e of selective splenic phagocytosis of both spherocytes and senescent eryth
rocytes, (C) 2001 Academic Press.