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Unité de Neuroendocrinologie et Biologie Cellulaire Digestives, Institut National de la Santé et de la Recherche Médicale,
U410, Faculté de Médecine Xavier Bichat, 75018 Paris, France
Large, free polymannose oligosaccharides
generated during glycoprotein biosynthesis rapidly appear in the cytosol of HepG2 cells where they undergo
processing by a cytosolic endo H-like enzyme and a
mannosidase to yield the linear isomer of Man5GlcNAc (Man[
1-2]Man[
1-2]Man[
1-3][Man
1-6]Man[
14]GlcNAc). Here we have examined the fate of these
partially trimmed oligosaccharides in intact HepG2
cells. Subsequent to pulse-chase incubations with d-[2-
3H]mannose followed by permeabilization of cells with
streptolysin O free oligosaccharides were isolated from
the resulting cytosolic and membrane-bound compartments. Control pulse-chase experiments revealed that
total cellular free oligosaccharides are lost from HepG2
cells with a half-life of 3-4 h. In contrast use of the vacuolar H+/ATPase inhibitor, concanamycin A, stabilized
total cellular free oligosaccharides and enabled us to
demonstrate a translocation of partially trimmed oligosaccharides from the cytosol into a membrane-bound
compartment. This translocation process was unaffected by inhibitors of autophagy but inhibited if cells
were treated with either 100 µM swainsonine, which
provokes a cytosolic accumulation of large free oligosaccharides bearing 8-9 residues of mannose, or
agents known to reduce cellular ATP levels which
lead to the accumulation of the linear isomer of
Man5GlcNAc in the cytosol. Subcellular fractionation
studies on Percoll density gradients revealed that the
cytosol-generated linear isomer of Man5GlcNAc is degraded in a membrane-bound compartment that cosediments with lysosomes.
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