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1 Departments of Pediatrics and Medicine and 2 Division of Pediatric Nephrology, University of Rochester School of Medicine, Rochester 14642; and 3 Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, New York 10032
Carbonic anhydrase (CA) IV is a
membrane-bound enzyme that catalyzes the dehydration of carbonic acid
to CO2 and water. Using peptides from each end of the
deduced rabbit CA IV amino acid sequence, we generated a goat
anti-rabbit CA IV antibody, which was used for immunoblotting and
immunohistochemical analysis. CA IV was expressed in a variety of
organs including spleen, heart, lung, skeletal muscle, colon, and
kidney. Rabbit kidney CA IV had two N-glycosylation sites and
was sialated, the apparent molecular mass increasing by at least 11 to
~45 kDa in the cortex. Medullary CA IV was much more heavily
glycosylated than CA IV from cortex or any other organ, such
modifications increasing the molecular mass by at least 20 kDa. CA IV
was expressed on the apical and basolateral membranes of proximal
tubules with expression levels on the order of S2 > S1 > S3 = 0. Because CA IV is believed to be anchored to the apical membrane by
glycosylphosphatidylinositol, the presence of basolateral CA IV
suggests an alternative mechanism. CA IV was localized on the apical
membranes of outer medullary collecting duct cells of the inner stripe
and inner medullary collecting duct cells, as well as on
-intercalated cells. However, CA IV was not expressed by
-intercalated cells, glomeruli, distal tubule, or Henle's loop
cells. Thus CA IV was expressed by H+-secreting cells of
the rabbit kidney, suggesting an important role for CA IV in urinary acidification.
organs; intercalated cells; proximal tubule; medullary collecting duct; immunohistochemistry; Western blot
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