AICAR induces autophagy in ARPE‐19 cells

• Published in: Acta ophthalmologica (Oxford, England) Vol. 89; no. s248
• Main Authors: KAARNIRANTA, K, VIIRI, J, AMADIO, M, HYTTINEN, J, PAIMELA, T, RYHÄNEN, T, MARCHESI, N, AKHTAR, S, PASCALE, A, PETROVSKI, G, SALMINEN, A
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-09-2011; Wiley Subscription Services, Inc
• Subjects: AMP; Autophagy; Cell culture; Confocal microscopy; Energy balance; Kinases; L-Lactate dehydrogenase; Lactic acid; Macular degeneration; Microscopy; Permeability; Phagocytosis; Phagosomes; Proteasome inhibitors; Proteasomes; Protein kinase; Proteins; Proteolysis; Retina; Transmission electron microscopy; Ubiquitin; Western blotting
• ISSN: 1755-375X; 1755-3768
• DOI: 10.1111/j.1755-3768.2011.2136.x

Purpose The pathogenesis of age‐related macular degeneration involves impaired protein degradation in retinal pigment epithelial (RPE) cells. The ubiquitin‐proteasome pathway and the lysosomal pathway including autophagy are the major proteolytic systems in eukaryotic cells. Recently, p62/sequestosome 1 (p62) has been shown to be a key player linking the proteasomal and lysosomal clearance systems. In the present study, the effects of AICAR (AICA ribonucleotide, 5‐aminoimidazole‐4‐carboxamide‐1‐β‐D‐ribofuranoside) and MG‐132 (proteasome inhibitor) on autophagy regulation in ARPE‐19 cells were evaluated.
Methods The AMP activated protein kinase (AMPK), p62 and ubiquitin protein levels were analyzed by western blotting. pDendra2‐hLC3 construct was used to detect macroautophagy in confocal microscopy analysis. Transmission electron microscopy was used to detect protein aggregates and autophagosomes. Cellular permeability was measured by analyzing lactate dehydrogenase levels in culture medium.
Results MG‐132 (5 microM) triggered the accumulation of perinuclear aggregates that strongly colocalized with p62 and ubiquitin. AICAR (2mM) induced autophagy clearance of p62 and ubiquitin positive protein aggregates without increasing cellular permeability. Cellular energy status regulator AMPK or p‐AMPK levels were not significantly changed in response to AICAR treatment.
Conclusion Our findings open new avenues for understanding the mechanisms of proteolytic processes and indicate that AICAR could be useful in the acceleration of protein clearance in RPE cells.