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Detection of Duffy antigen in the plasma membranes and caveolae of vascular
endothelial and epithelial cells of nonerythroid organs
A Chaudhuri, S Nielsen, ML Elkjaer, V Zbrzezna, F Fang and AO Pogo
Laboratory of Cell Biology, Lindsley F. Kimball Research Institute of the
New York Blood Center, NY 10021, USA.
The nonerythroid expression of the Duffy blood group protein (gp-Fy) was
confined to certain cell types. Immunocytochemistry studies of the kidney
showed gp-Fy in the endothelium of glomeruli, peritubular capillaries, vasa
recta, and the principal cells (epithelial) of collecting ducts. Gp-Fy was
also produced in the endothelial cells of large venules and epithelial
cells (type-I) of pulmonary alveoli. In the thyroid, only the endothelial
cells of capillaries produced gp-Fy. In the spleen, the endothelial cells
of capillaries, high endothelial venule, and sinusoids produced abundant
gp-Fy. Ultrastructural studies showed that apical and basolateral plasma
membrane domains, including caveolae, had gp-Fy. Immunoblot analysis showed
substantially less gp- Fy in nonerythroid cells than in erythrocytes.
Moreover, the analyzed nonerythroid organs of Duffy-negative individuals
did not produce more gp-Fy to compensate for the lack of this protein in
their erythrocytes. The nucleotide sequence and the size of kidney mRNA
from a Duffy- positive individual were the same as that of bone marrow. It
is assumed, therefore, that nonerythroid Duffy protein is the product of
the same gene as that of bone marrow. This notion is reinforced by the fact
that nonerythroid and erythroid gp-Fy have the same antigenic domains.
Volume 89,
Issue 2,
pp. 701-712,
01/15/1997
Copyright © 1997 by The American Society of Hematology

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