Abstract
In this work, we have examined the possible role of AMP-activated protein kinase (a key energy sensor) in regulating intracellular protein degradation. We have found that AICAR, a known activator of AMPK, has a dual effect. On one hand, it inhibits autophagy by a mechanism independent of AMPK activity; AICAR decreases class III PI3-kinase binding to beclin-1 and this effect counteracts and reverses the known positive effect of AMPK activity on autophagy. On the other hand, AICAR inhibits the proteasomal degradation of proteins by an AMPK-dependent mechanism. This is a novel function of AMPK that allows the regulation of proteasomal activity under conditions of energy demand.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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AMP-Activated Protein Kinases
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Aminoimidazole Carboxamide / analogs & derivatives
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Aminoimidazole Carboxamide / pharmacology
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Apoptosis Regulatory Proteins / antagonists & inhibitors
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Apoptosis Regulatory Proteins / metabolism
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Autophagy* / drug effects
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Beclin-1
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Cells, Cultured
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Down-Regulation
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Fibroblasts / drug effects
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Fibroblasts / enzymology
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Fibroblasts / metabolism
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Humans
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Membrane Proteins / antagonists & inhibitors
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Membrane Proteins / metabolism
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Multienzyme Complexes / metabolism*
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Phosphatidylinositol 3-Kinases / metabolism
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Phosphoinositide-3 Kinase Inhibitors
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Proteasome Endopeptidase Complex / metabolism*
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Proteasome Inhibitors
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Protein Serine-Threonine Kinases / metabolism*
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Ribonucleosides / pharmacology
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Vacuoles / drug effects
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Vacuoles / enzymology
Substances
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Apoptosis Regulatory Proteins
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BECN1 protein, human
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Beclin-1
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Membrane Proteins
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Multienzyme Complexes
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Phosphoinositide-3 Kinase Inhibitors
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Proteasome Inhibitors
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Ribonucleosides
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Aminoimidazole Carboxamide
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acadesine
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Protein Serine-Threonine Kinases
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AMP-Activated Protein Kinases
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Proteasome Endopeptidase Complex