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. 2012 Apr 1;8(4):445–544. doi: 10.4161/auto.19496

graphic file with name auto-8-445-g20.jpg

Figure 20. Autophagosomes with recognizable cargo are rare in cells. (A) To assess relative rates of autophagosome formation, the fusion inhibitor bafilomycin A1 (10 nM) was applied for 2 h prior to fixation with 2% glutaraldehyde in order to trap newly formed autophagosomes. Two different PINK1 shRNA lines exhibit increased AV formation over 2 h compared with the control shRNA line. *p > 0.05 vs. Control. (B) Autophagosomes in bafilomycin A1-treated control cells contain a variety of cytoplasmic structures (left, arrow), while mitochondria comprise a prominent component of autophagosomes in A14 bafilomycin A1-treated (PINK1 shRNA) cells (right, arrow). Scale bar, 500 nm. These data indicate induction of selective mitophagy in PINK1-deficient cells. This figure was modified from Figure 2 published in Chu CT. A pivotal role for PINK1 and autophagy in mitochondrial quality control: implications for Parkinson disease. Hum Mol Genet 2010; 19:R28?37.