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J Biol Chem. 2013 May 3;288(18):13093-109. doi: 10.1074/jbc.M112.437061. Epub 2013 Mar 18.

Agonist-induced down-regulation of endogenous protein kinase c α through an endolysosomal mechanism.

Author information

1
The Eppley Institute, University of Nebraska Medical Center, Omaha, Nebraska 68198-5950, USA.

Abstract

Protein kinase C (PKC) isozymes undergo down-regulation upon sustained stimulation. Previous studies have pointed to the existence of both proteasome-dependent and -independent pathways of PKCα processing. Here we demonstrate that these down-regulation pathways are engaged in different subcellular compartments; proteasomal degradation occurs mainly at the plasma membrane, whereas non-proteasomal processing occurs in the perinuclear region. Using cholesterol depletion, pharmacological inhibitors, RNA interference, and dominant-negative mutants, we define the mechanisms involved in perinuclear accumulation of PKCα and identify the non-proteasomal mechanism mediating its degradation. We show that intracellular accumulation of PKCα involves at least two clathrin-independent, cholesterol/lipid raft-mediated pathways that do not require ubiquitination of the protein; one is dynamin-dependent and likely involves caveolae, whereas the other is dynamin- and small GTPase-independent. Internalized PKCα traffics through endosomes and is delivered to the lysosome for degradation. Supportive evidence includes (a) detection of the enzyme in EEA1-positive early endosomes, Rab7-positive late endosomes/multivesicular bodies, and LAMP1-positive lysosomes and (b) inhibition of its down-regulation by lysosome-disrupting agents and leupeptin. Only limited dephosphorylation of PKCα occurs during trafficking, with fully mature enzyme being the main target for lysosomal degradation. These studies define a novel and widespread mechanism of desensitization of PKCα signaling that involves endocytic trafficking and lysosome-mediated degradation of the mature, fully phosphorylated protein.

KEYWORDS:

Caveolae; Endocytosis; Lipid Raft; Lysosomal; Lysosomes; PKCα Degradation; Protein Degradation; Protein Kinase C (PKC)

PMID:
23508961
PMCID:
PMC3642351
DOI:
10.1074/jbc.M112.437061
[Indexed for MEDLINE]
Free PMC Article
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