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* Department of Cell Biology, Faculty of Medicine, We used an improved cryosectioning technique in combination with immunogold cytochemistry and morphometric analysis to study the convergence of the autophagic and endocytic pathways in
isolated rat hepatocytes. The endocytic pathway was
traced by continuous uptake of gold tracer for various time periods, up to 45 min, while the cells were
incubated in serum-free medium to induce autophagy. Endocytic structures involved in fusion with
autophagic vacuoles (AV) were categorized into
multivesicular endosomes (MVE) and vesicular endosomes (VE). Three types of AV The entry of tracer into AV, manifested as either
tracer-containing AV profiles (AV+) or fusion profiles (FP+) between AV and tracer-positive endosomal vesicles/vacuoles, was detected as early as 10 min
after endocytosis. The number of AV+ exhibited an
exponential increase with time. FP+ between MVE
or VE and all three types of AV were observed.
Among the 112 FP+ scored, 36% involved VE. Of
the AV types, AVi and AVi/d were found five to six
times more likely to be involved in fusions than AVd.
These fusion patterns did not significantly change
during the period of endocytosis (15-45 min). We
conclude that the autophagic and endocytic pathways
converge in a multistage fashion starting within 10 min of endocytosis. The nascent AV is the most upstream and preferred fusion partner for endosomes.
Department of Biochemistry, Faculty of Veterinary Medicine, Institute of
Biomembranes, Utrecht University, 3584 CX Utrecht, The Netherlands; and § Department of Anatomy, Chang Gung College of
Medicine and Technology, Taiwan, Republic of China
initial (AVi), intermediate (AVi/d), and degradative (AVd)
were
defined by morphological criteria and immunogold
labeling characteristics of marker enzymes.
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