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. 2011 May 15;14(10):1939–1951. doi: 10.1089/ars.2010.3779

Table 1.

Effect of Manipulations in Mitochondrial Proteins Opa1, Mfn1/2, Drp1, and Fis1 on Autophagy and Mitophagy

Manipulation Cell type Effect on mitophagy Reference Comments
Fis1 RNAi INS1 β-cells Reduction of 70% in APs containing mitochondria (110) No change in the mass of APs containing ER
Fis1 Overexpression HeLa cells, INS1 β-cells Reduces total mitochondrial volume by ∼50% (28, 83) No change in ER morphology or total ER area
  HeLa cells 50% increase in total APs mass. No direct assessment of mitophagy (30) Qualitative analysis suggests medium-high correlation between LC3 and mitochondrial markers
Drp1K38A INS1 β-cells Reduction of 75% in APs containing mitochondria (110) No change in the mass of APs containing ER
Drp1 RNAi HeLa cells Decrease in mitophagy (qualitative) (85) A general increase in autophagy.
Drp1 overexpression HeLa cells 70% decrease in mitochondrial mass (4) No specific tests for mitophagy
Opa1 Overexpression INS1 β-cells Reduction of 63% in APs containing mitochondria (110) No change in the mass of APs containing ER
Opa1 heterozygous mutant mice Retinal Ganglion cells An increase in general autophagy (120) No specific tests for mitophagy
Mfn1 overexpression INS1 β-cells 40% decrease in mitochondrial volume (83) No specific tests for mitophagy
Mfn1 loss of function (overexpression of Mfn1 DN) INS1 β-cells Unchanged mitochondrial mass (83) Insignificant slight decrease in mitochondrial volume. No specific tests for mitophagy.
Mfn2 KO MEFs Inhibition of autophagy (36) No specific tests for mitophagy

Note that in some works mitophagy was assessed directly by colocalization between mitochondrial and AP markers, indirectly as changes in mitochondrial mass, or not distinguished from autophagy.

AP, autophagosome; ER, endoplasmic reticulum; KO, knockout.