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J Biol Chem, Vol. 274, Issue 19, 13547-13555, May 7, 1999
From the Unité de Neuroendocrinologie et Biologie Cellulaire
Digestives, Institut National de la Santé et de la Recherche
Médicale, U410, Faculté de Médecine Xavier Bichat, 16 Rue Henri Huchard, 75018 Paris, France
In hepatocellular carcinoma HepG2 cells, free
polymannose-type oligosaccharides appearing in the cytosol during the
biosynthesis and quality control of glycoproteins are rapidly
translocated into lysosomes by an as yet poorly defined process
(Saint-Pol, A., Bauvy, C., Codogno, P., and Moore, S. E. H. (1997)
J. Cell Biol. 136, 45-59). Here, we demonstrate an
ATP-dependent association of
[2-3H]mannose-labeled Man5GlcNAc with
isolated rat liver lysosomes. This association was only observed in the
presence of swainsonine, a mannosidase inhibitor, which was required
for the protection of sedimentable, but not nonsedimentable,
Man5GlcNAc from degradation, indicating that
oligosaccharides were transported into lysosomes. Saturable high
affinity transport (Kuptake, 22.3 µM, Vmax, 7.1 fmol/min/unit of
-hexosaminidase) was dependent upon the hydrolysis of ATP but
independent of vacuolar H+/ATPase activity. Transport was
inhibited strongly by NEM and weakly by vanadate but not by sodium
azide, and, in addition, the sugar transport inhibitors phloretin,
phloridzin, and cytochalasin B were without effect on transport.
Oligosaccharide import did not show absolute specificity but was
selective toward partially demannosylated and dephosphorylated
oligosaccharides, and, furthermore, inhibition studies revealed that
the free reducing GlcNAc residue of the oligosaccharide was of critical
importance for its interaction with the transporter. These results
demonstrate the presence of a novel lysosomal free oligosaccharide
transporter that must work in concert with cytosolic
hydrolases in order to clear the cytosol of endoplasmic
reticulum-generated free oligosaccharides.
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