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1,4GlcNAc
1,2Man
-specific Receptor from
Rat Liver
(Received for publication, March 7, 1997)
From the Department of Pathology, Washington University School of
Medicine, St. Louis, Missouri 63110
Glycoproteins, such as the glycoprotein
hormone lutropin (LH), bear oligosaccharides terminating with the
sequence SO4-4GalNAc
1,4GlcNAc
1,2Man
(S4GGnM)
and are rapidly removed from the circulation by a receptor present in hepatic endothelial cells and Kupffer cells. Rapid removal
from the circulation is essential for attaining maximal hormone
activity in vivo. We have isolated a protein from rat liver
which has the properties expected for the S4GGnM-specific receptor
(S4GGnM-R). The S4GGnM-R is closely related to the macrophage mannose
receptor (Man-R) both antigenically and structurally. At least 12 peptides prepared from the S4GGnM-R have amino acid sequences that are
identical to those of the Man-R. Nonetheless, the ligand binding
properties of the S4GGnM-R and the Man-R differ in a number of
respects. The S4GGnM-R binds to immobilized LH but not to immobilized
mannose, whereas the Man-R binds to immobilized mannose but not to
immobilized LH. When analyzed using a binding assay that precipitates
receptor ligand complexes with polyethylene glycol, the S4GGnM-R is
able to bind S4GGnM-bovine serum albumin (S4GGnM-BSA) conjugates
whereas the Man-R is not. In contrast both the S4GGnM-R and the Man-R
are able to bind Man-BSA. Monosaccharides that inhibit binding of
Man-BSA by the Man-R enhance binding by the S4GGnM-R. Oligosaccharides
terminating with S4GGnM and those terminating with Man are bound at
independent sites on the S4GGnM-R. The S4GGnM-R present in hepatic
endothelial cells may account for clearance of glycoproteins bearing
oligosaccharides terminating with S4GGnM and glycoproteins bearing
oligosaccharides terminating with either mannose, fucose, or
N-acetylglucosamine.
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