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1 Division of Gastroenterology, University of Alberta, Edmonton, Alberta, Canada T6G 2C2; and 2 Human Genome Sciences, Rockville, Maryland 20850
Stanniocalcin (STC)
is an anti-hypercalcemic glycoprotein hormone previously identified in
the corpuscles of Stannius in bony fish and recently in the human
genome. This study undertook to express human STC in Chinese hamster
ovary (CHO) cells and to determine its effects on calcium and phosphate
absorption in swine and rat intestine. Unidirectional
mucosal-to-serosal
(Jm
s) and serosal-to-mucosal
(Js
m)
45Ca and
32P fluxes were measured in vitro
in duodenal tissue in voltage-clamped Ussing chambers. Addition of STC
(10-100 ng/ml) to the serosal surface of the duodenum resulted in
a simultaneous increase in calcium
Jm
s and
Js
m
fluxes, with a subsequent reduction in net calcium absorption. This was
coupled with an STC-stimulated increase in phosphate absorption.
Intestinal conductance was increased at the highest dose of STC (100 ng/ml) in swine tissue. The addition of STC to the mucosal surface had
no effect on calcium and phosphate fluxes. STC at doses of
10-1,000 ng/ml had no effect on short-circuit current in any
region of the rat intestine. In conclusion, human recombinant STC
decreases the absorption of calcium and stimulates the absorption of
phosphate in both swine and rat duodenum. STC is a novel regulatory
protein that regulates mammalian intestinal calcium and phosphate
transport.
duodenum
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