Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

Mitochondrial fusion is selective

We hypothesized that mitochondrial fusion is a selective process and tested the prediction that a subpopulation of mitochondria with low fusion capacity could be identified. Our goal was to follow these mitochondria and examine their metabolic function, source and fate. Fusion in INS1 cells was determined by the spread of mitochondrial matrix-targeted photoactivatable GFP (mtPA-GFP) from a subset of mitochondria throughout the mitochondrial network. In each cell, an area comprising approximately 10% of the cell cross-section area in a single focal plane was exposed to the two-photon laser stimulation, resulting in the labeling of 10–20% of the mitochondrial volume (square in Figure 1A). As a result of fusion, activated mtPA-GFP molecules spread to unlabeled mitochondria, resulting in a decrease in GFP fluorescence intensity (FI) of the mitochondria containing activated mtPA-GFP (Figure 1B; see ‘Mitochondrial fusion assay' in the Supplementary data). Dilution of mtPA-GFP reached a steady state after 10–30 min. If mitochondria were non-selectively fusing with the network, we would expect to see a homogeneous distribution and dilution of the GFP signal. However, in 32% of the INS1 cells, a subpopulation of mitochondria failed to dilute their activated mtPA-GFP and carried the same GFP FI measured immediately after photoconversion (n=22). Similar results were obtained in primary mouse β-cells (60%, n=10; Figure 1D). The number of defined non-fusing mitochondrial structures detected in each cell was 3.1±1.1. This represents the number of non-fusing mitochondria within the mitochondrial population that was labeled at the beginning of the experiment. (Therefore, if normalized per cell these would amount to ∼20 mitochondria per cell.)

Compared with the average cellular Δψ_m, determined by TMRE FI, the non-fusing mitochondria were depolarized. Quantitative analysis found a 26%±5.3 reduction in TMRE FI, equivalent to 7.8±1.6 mV (Figure 1C; P<0.001, unpaired t-test).

Fusion and fission are paired consecutive events

To determine if segregation is upstream or downstream of depolarization, we characterized the life cycle of mitochondria in non-apoptotic INS1 and COS7 cells. Individual mitochondria were tagged and tracked with mtPA-GFP to temporally map fusion and fission events (Figure 2). Fusion and fission were paired and occurred most commonly as fusion quickly followed by fission (Figure 2A and B). Cumulative probability analysis indicates that fusion triggers fission, but fission has no effect on the timing of the following fusion (Figure 2C and D). In INS1 and COS7 cells we found that mitochondria spent the majority of their time in the post-fission, ‘single state' (defined as the time interval from fission to fusion) and only 5.4–7.2% of the time in the post-fusion, ‘fused state' (defined as the time interval between fusion and fission).

Membrane potential changes during fusion and fission

Double labeling of a single mitochondrion with mtPA-GFP and TMRE was used to determine the bioenergetic profile of the individual fission events (Figure 3A). Detailed description of measures taken in order to avoid imaging artifacts and laser-induced damage is provided in the Supplementary data. Changes in the ratio between TMRE and mtPA-GFP of the individual mitochondria were used to calculate deviations in Δψ_m as previously described (Twig et al, 2006). We found that during the intervals between pairs of fusion–fission events, Δψ_m of both INS1 and COS7 mitochondria was stable; spending 95% of the recording period within ±2.7 mV of the average baseline (Figure 3C; Supplementary Figure S1). During fission, mtPA-GFP molecules redistributed and equilibrated between the two daughter mitochondria, and had GFP FI similar to the pre-fission mitochondrion (Δ_{pre-andpost-fission}=2.2±1.2%; Δ_{daughters1and2}=1.6±1.1%). Immediately after a fission event, however, large changes in Δψ_m were measured (Figure 3A–C). We observed the following patterns in 48 fission events:

1. In 85% of fission events, one daughter mitochondrion depolarized (criterion=2 mV) to a maximal amplitude of +5.9±3.7 mV, while the other daughter hyperpolarized (criterion=2 mV) to a maximal amplitude of −6.5±3.8 mV compared to pre-fission potential (Figure 3Bi). In 22% of these fission events, the post-fission depolarization phase was sustained without recovery (Figure 3Bii). The depolarized units were followed for additional 10–30 min. Fisher's one-sided probability analysis indicates that this pattern (Figure 3Bii) of Δψ_m change did not occur preferentially in de novo fission events as compared with those that followed fusion events (P=0.34).

2. In 4% of fission events, one daughter had similar Δψ_m as before fission while the other daughter hyperpolarized (Figure 3Biii). In these cases, the mother mitochondrion was relatively depolarized by 7–10 mV relative to the average cellular Δψ_m. These patterns were significantly associated with de novo fission, not preceded by fusion (two-sided, P=0.049).

3. In 11% of fission events, both daughters had no change in Δψ_m.

Potential mechanisms for the observed depolarization were tested and ruled out:

1. Generation of a pore during fission; no leakage of mtPA-GFP was observed;

2. Increase in ATP synthase activity; depolarization was observed with 1 μM oligomycin, n=4;

3. Reduced fuel availability or Krebs cycle function; depolarization was observed in the presence of methyl succinate, a membrane-permeable fuel, n=3;

4. Opening of the permeability transition pore; depolarization was observed with 1 μM cyclosporin A, n=4;

5. Translocation of mitochondrion (from perinuclear to sub-plasmalemmal and vice versa; see Supplementary data);

6. Engulfment of the daughter mitochondrion by an autophagosome (AP); autophagy occurs hours after depolarization and depolarized mitochondria are more frequent when autophagy is inhibited (Supplementary Figure S4; Figure 7E).

Depolarized daughter mitochondrion is unlikely to fuse

To test whether fission-induced changes in Δψ_m orchestrate subsequent fusion events, we followed the depolarized and the hyperpolarized daughters and recorded subsequent fusion events (Figure 4). The probability that a hyperpolarized daughter mitochondrion would fuse within 3 min post-fission was six times higher than that of a depolarized daughter mitochondrion, with a mean time interval of 105 s between fission and fusion (range 40–620 s; n=8). Representative schematic illustrations of these events are shown in Figure 4A. Fisher's two-sided probability analysis indicates that the depolarized daughter mitochondrion has a significantly lower probability of undergoing a fusion within 150 s after fission (P=0.03). In two experiments, depolarized mitochondria with Δψ_m 9–10 mV below the cell Δψ_m average were observed to undergo fission and generate a hyperpolarized daughter that went through subsequent fusion (data not shown).

Δψ_m Depolarization occurs hours before autophagy

It has previously been suggested that metabolically impaired mitochondria are preferably targeted by autophagy (Elmore et al, 2001; Priault et al, 2005). The time interval between depolarization and autophagy would indicate whether the isolation membrane of the early AP contributes to the segregation of depolarized daughter mitochondria and to their reduced fusion probability. Mitochondria, lysosomes, APs and autophagolysosomes (late APs) were imaged in the presence and absence of proteolytic enzyme inhibitors, E64d and pepstatin A. We found that unless digestion of late APs content is pharmacologically arrested, colocalization of mitochondria with AP markers is rarely captured (Supplementary Figure S2). Inhibition of proteolysis in late APs results in the accumulation of 15–30 APs within 30 min, indicating a high turnover rate of APs and fast removal of mitochondria after autophagy has started (Supplementary Figure S2).

To reveal whether mitochondria depolarize before or after the onset of autophagy, we determined the Δψ_m of autophagocytosed mitochondria at different time points before autophagy (Figure 4B; Supplementary Figure S10). Δψ_m was determined by pulsing the cells with Δψ_m-dependent dye, mitotracker red (MTR), at different time points. Mitochondria that were pulse labeled 24 h before detection of autophagy had bright MTR staining, indicative of intact Δψ_m during the staining period (Figure 4B and C). However, those pulsed 1–3 h before detection of autophagy had dim MTR staining, indicating that depolarization occurred one or more hours before their engulfment. To ascertain that MTR itself does not induce or inhibit autophagy, the effect of MTR on the conversion of LC3-I to LC3-II, a marker for the activation of autophagy, was tested in INS1 cells treated with MTR for 24 h. MTR at the concentrations used for the above experiment had no effect on autophagy (data not shown). To verify that the observed aggregates of LC3:GFP are formed by APs and do not represent an expression artifact, LC3:GFP expressing cells were treated with the autophagy inhibitor 3-MA and aggregates were quantified. No aggregates were observed under these conditions.

This sequence of events was also supported by the following observations: (a) after 50 min of tracking individual mitochondria with reduced Δψ_m, there was no reduction in mtPA-GFP intensity as would be expected if these units were consumed and digested (Supplementary Figure S3), and (b) inhibition of autophagy does not result in the recovery of depolarized mitochondria but rather in their accumulation as observed in INS1 (Figure 7E, n=6), MEF (Supplementary Figure S4C, n=10) or rat liver H4 (Supplementary Figure S4A, n=5). Together, these results indicate that reduced fusion capacity of the depolarized daughter is unlikely due to engulfment by APs.

Reduced OPA1 characterizes non-fusing and autophagocytosed mitochondria

The long time gap between depolarization and autophagy suggested that mitochondria spend a long period of time as non-fusing mitochondria prior to autophagy. It was therefore hypothesized that before autophagy mitochondria lose their fusion capacity potentially by degradation of a fusion protein such as OPA1. To test this hypothesis, we performed an immunoreactivity study of non-fusing mitochondria (Figure 5A) and of mitochondria inside APs (Figure 5B). To determine the protein level of OPA1 in non-fusing mitochondria, cells expressing mtPA-GFP and mtDsRed were subjected to fusion assays as described in Figure 1A. Two hours after photoconversion, cells were fixed, permeabilized and immunostained using a monoclonal antibody to the C-terminus of OPA1 (amino acids 708–830 in hOPA1; Alavi et al, 2007). Non-fusing mitochondria were identified as those that did not equilibrate their photoconverted mtPA-GFP with the unlabeled mitochondria over a period of 2–3 h, so that their GFP FI was over two folds higher as compared with the average mitochondria in the same cell. The ratio of OPA1 to mtDsRed was determined and was reduced in mitochondria that maintained high intensity of mtPA-GFP (Figure 5A), indicating that non-fusing mitochondria are characterized by reduced OPA1 immunoreactivity. Next, we determined OPA1 immunoreactivity in mitochondria inside APs (Figure 5B). Proteolytic activity was inhibited for 2–4 h using pepstatin A and E64d in cells expressing LC3:GFP and the matrix protein mtDsRed, both introduced by lentiviral transduction. The efficiency of the antiproteolytic activity was verified by the intact fluorescence of both the matrix protein mtDsRed and LC3:GFP. As compared with mitochondria outside APs, those inside had significantly reduced OPA1 immunoreactivity (P=0.003), but unchanged mtDsRed FI (P=0.38). To control for a potential artifact that might arise from partial proteolytic activity, we repeated this experiment this time inhibiting lysosomal V-ATPase with bafilomycin, which inhibits the fusion of lysosome with the early AP and preserves the mitochondrial morphology inside the AP (for electron microscopy of bafilomycin-treated APs, see Supplementary Figure S8). Similar reduction in OPA1 immunoreactivity was observed under these conditions (P<0.001; Figure 5B).

To determine if the observed reduction in OPA1 contributed to the targeting of mitochondria to AP, OPA1 was overexpressed by transduction with adenoviruses in INS1 cells stably expressing LC3:GFP and mtDsRed. Mitophagy (mitochondrial autophagy) was determined by counting mitochondria-containing APs under conditions in which proteolysis inside the APs was pharmacologically arrested for 1 h. Mitophagy was found to be reduced by 64% in OPA1-overexpressing cells as compared with control cells transduced with mtPA-GFP adenovirus (Figure 5C, P<0.001). Total number of APs was not significantly different (APs per cell: control, 47.4±19; OPA1 OE, 35.1±21). As previously reported, OPA1 overexpression can result in either a decrease or an increase in mitochondrial size (Cipolat et al, 2004; Griparic et al, 2004; Chen et al, 2005). Similar to MEF cells, OPA1 overexpression in INS1 cells resulted in a general but relatively homogenous reduction in mitochondrial size, while mitochondrial fusion activity remained intact (Chen et al, 2005). These observations rule out that decreased autophagy was solely due to increased mitochondrial size.

Inhibition of fission reduces mitochondrial autophagy

The reciprocal dependence of fusion and autophagy on Δψ_m suggests that mitochondrial fission may play a key role in segregating and uncoupling mitochondria from the network, thereby enabling depolarization and autophagy of dysfunctional daughter units. The role of fission in mitochondrial autophagy was evaluated in INS1 cells expressing low levels of FIS1, the rate-limiting protein in the mitochondrial fission process (Yoon et al, 2003; Okamoto and Shaw, 2005) and in cells expressing a dominant-negative form of the fission protein DRP1 (DRP1^K38A, or DRP1-DN). Both were introduced by lentiviral transduction and tested within 10 days of the infection (see Supplementary Figure S5A and B; Stojanovski et al, 2004). Expression of DRP1-DN resulted in the transformation of mitochondrial architecture to the characteristic elongated tubules with enlarged circular ends (Figure 7B; Supplementary Figure S9). The effect of FIS1 RNAi on mitochondrial morphology is milder and was verified by morphometric analysis (Supplementary Figure S5C). Inhibition of mitochondrial fission resulted in reduction of the number of mitochondria-containing APs (P<0.001; Figure 6A and B) but not in the number of ER-containing APs (FIS1 RNAi group, P=0.51; Figure 6C). The total number of lysosomes (Figure 6C) and the total number of APs remained without a significant change (DRP1-DN group: n=11, P=0.53; FIS1 RNAi group: n=12, P=0.59).

While mitochondrial autophagy was inhibited, the assembly of the isolation membrane and the propagation of the AP to late AP was not affected by FIS1 RNAi, as indicated by (a) unchanged maximal AP formation capacity detected by long-term exposure to E64d and pepstatin A (control 24±5, FIS1 RNAi 21±7), (b) resumption of AP digestion in <1 min after E64d and pepstatin A were removed from the media (data not shown), (c) no difference in lysosome formation capacity between the control and the FIS1 RNAi groups as indicated by counting lysosomes stained with lysosensor blue dye (Figure 6C; Supplementary Figure S6) and (d) electron micrographs showing normal appearance of early and late APs as obtained by treatment with the protease inhibitors pepstatin A and E64d, or with the lysosomal V-ATPase inhibitor bafilomycin (Supplementary Figure S8).

Fission-deficient mitochondria have more oxidized protein but less ROS

We hypothesized that inhibition of fission would reduce segregation and degradation of dysfunctional mitochondria and thus result in accumulation of damaged mitochondrial proteins. Levels of mitochondrial protein oxidation in cells expressing FIS1 RNAi were 1.7-fold higher than in control RNAi (Figure 7A, n=4). Similar effect was found in DRP1-DN-treated cells where both carbonylated protein and nitrotyrosine were accumulated (Figure 7A and B). To test the possibility that the latter finding arose from overproduction of ROS in FIS1 RNAi cells, ROS generation was assessed using dihydroethidium (DHE) (Figure 7C). There was an insignificant decrease in ROS production in cells expressing FIS1 RNAi compared with control RNAi under normal culture conditions (11 mM glucose; P=0.50). This decrease became significant using 22 mM glucose (P<0.001). These results suggest that the observed increase in oxidized protein in fission-deficient cells is the result of accumulation rather than excess generation of damage. To test if inhibition of autophagy affects the accumulation of oxidized proteins in mitochondria, we inhibited fusion between lysosomes and APs with bafilomycin A1 (0.1 μM) and determined carbonylated proteins (Figure 7D). Treatment with bafilomycin A1 for as short as 3 h resulted in increased levels of oxidized proteins in mitochondria and in the accumulation of early APs as revealed by increased LC3-II band. Treatment with 3-MA (2 mM, 5 days), which inhibits the initiation of the early AP, resulted in increased subcellular heterogeneity in Δψ_m and the appearance of small depolarized mitochondria (Figure 7E). A similar effect was observed in two autophagy deficient cell lines, Beclin1 RNAi H4 and ATG5−/− MEF cells (Supplementary Figure S4A and C).

FIS1 knockdown affects metabolism and insulin secretion

The effects of attenuated fission and reduced mitochondrial autophagy on mitochondrial respiratory function were assessed by measuring cellular oxygen consumption (Figure 8). An uncoupler, FCCP (5 μM) or DNP (100 μM), was added to collapse Δψ_m and assess maximal respiration capacity of the cell. It was found that the respiratory capacity of INS1 cells expressing FIS1 RNAi or DRP1-DN was reduced by 48% (n=4) and 32% (n=4), respectively (P<0.001 in both the groups) (Figure 8A). Overexpression of RNAi-resistant FIS1 together with FIS1 RNAi (n=3) restored maximal respiration to the same level of INS1 cells expressing control RNAi (n=3, P=0.72).

To determine if a FIS1 knockdown affected mitochondrial protein synthesis, we measured the expression levels of the mtDNA-encoded subunit I of COX. We found that FIS1 knockdown for 10 days had no effect on subunit I expression (Figure 8B). The antiapoptotic effect of FIS1 RNAi treatment was validated to exclude technical artifacts as a cause for the metabolic phenotype (Supplementary Figure S7).

To determine if a reduction in autophagy by itself can affect OXPHOS activity, oxygen consumption was monitored in INS1 cells, C2C12 cells and MEF cells, where autophagy was inhibited by two different mechanisms. Autophagy inhibition with 2 mM 3-MA over 5 days in INS1 cells reduced maximal respiration to ∼50% of the control condition (P<0.001, Figure 8A). ATG5 is an essential component for the assembly of the isolation membrane of the APs (Pyo et al, 2005). ATG5-deficient MEF cells had maximal respiration reduced by ∼40% (Figure 8A). Treatment of C2C12 mouse myoblasts cells with 3-MA (1 mM) resulted in a ∼16% reduction in maximal oxygen consumption (P=0.04).

The INS1 cells used here were derived from rat insulinoma (pancreatic tumor β-cells) and are characterized by a linear relationship between insulin secretion and glucose concentration within a range of 2–10 mM (Hohmeier et al, 2000). At basal glucose concentration (2 mM), there was no significant difference in insulin secretion between FIS1 RNAi and the control RNAi cells (n=5, P=0.57; Figure 8C). Elevation of media glucose concentration to 8 mM increased insulin secretion in both cell types (P<0.001; Figure 8C). However, in FIS1 RNAi the magnitude of glucose-stimulated insulin secretion (GSIS) was smaller than control RNAi cells (n=5, P=0.02).

Mitochondrial fusion is selective

Fusion was determined to be a selective process using two different approaches. First, a group of mitochondria was tagged by photoactivation of mtPA-GFP. A subpopulation was identified that did not exchange mtPA-GFP with unlabeled units (Figure 1). Second, daughters of mitochondrial fission were tracked and found to possess unequal probabilities of undergoing subsequent fusion (Figure 4). In both cases, a similar level of Δψ_m depolarization was identified in the non-fusing mitochondria.

While previous studies have demonstrated that uncoupling drugs cause overall mitochondrial fragmentation and arrest fusion (Legros et al, 2002; Ishihara et al, 2003; Meeusen et al, 2004; Malka et al, 2005), the relevance of these observations to fusion in the undisturbed cell has not been addressed. The present study is the first demonstration in living cells that mitochondrial fusion occurs preferentially between mitochondria with higher Δψ_m, and generates an isolated subpopulation of non-fusing mitochondria. Moreover, these results demonstrate that a physiologically relevant reduction in Δψ_m impacts the prevalence of fusion. As each fusing mitochondrion requires intact Δψ_m to achieve matrix fusion, the process is unlikely to rescue dysfunctional units with altered Δψ_m. Yet, the selectivity of the fusion process does not rule out the view that mitochondrial fusion serves as an inter-mitochondrial complementary route for metabolites and mtDNA between mitochondria with intact Δψ_m (Nakada et al, 2001).

Conversely, Δψ_m is influenced when fusion is inhibited (Olichon et al, 2003; Chen et al, 2005), suggesting that reduced fusion capacity could be either the cause or the result of Δψ_m depolarization. Experiments presented here conclude that depolarization occurs immediately subsequent to fission and not as a delayed consequence of reduced fusion capacity. The stability of Δψ_m of the individual mitochondria at all times other than the immediate post-fission period, as reported here, further supports the conclusion that reduced fusion over a period of an hour does not compromise the bioenergetic parameters of the individual unit.

OPA1 as a mechanism for selective fusion

In addition to having reduced Δψ_m, non-fusing mitochondria were characterized by depletion in OPA1 immunoreactivity, providing a possible explanation for the reduced fusion capacity (Figure 5). Recently, a protonophore-induced complete collapse of Δψ_m of the entire cell mitochondria was shown to trigger proteolytic cleavage or degradation of OPA1 long (l-)isoforms (Griparic et al, 2004; Duvezin-Caubet et al, 2006; Ishihara et al, 2006; Song et al, 2007). Here we show that minute and physiological depolarization of the individual mitochondrion in the context of the intact cell is accompanied by reduced OPA1 levels and diminished fusion capacity. These results further emphasize that depletion of OPA1 in the individual mitochondrion within the intact cell may preclude fusion and metabolic complementation even if surrounded by fusion-competent mitochondria (Figure 1). The dependency of OPA1 proteolysis on ATP concentration may explain how small changes in Δψ_m may lead to such profound reduction in fusion capacity (Herlan et al, 2004). Given that a depolarization of 14 mV can drop ATP synthesis by up to 10-fold (Nicholls, 2004), a depolarization of ∼7 mV, as found in the non-fusing mitochondria, may alter fusion through ATP depletion or processing of OPA1.

The attenuated OPA1 staining seen in non-fusing mitochondria in this study reflects mainly the degradation of OPA1 and not their proteolytic cleavage, since the antibody used here targeted the common region for the l- and s-isoforms. This finding is in accordance with Song et al (2007) showing that complete degradation (rather than proteolytic cleavage) is the principal route of processing of the long isoforms (splice 1 and 2) of OPA1, and is therefore likely to be an underestimation of the actual depletion in OPA1 long isoforms.

Metabolic consequences of single fission events

We found that mitochondrial fission results in predictive and asymmetric changes in Δψ_m of the two daughters (Figures 2 and 3). This is the first measurement of a metabolic consequence of single fission event. It demonstrates for the first time that although the mitochondrial network permits diffusion and equilibration of matrix and membrane components, fission results in the separation of metabolically uneven daughters. The asymmetrical nature of the fission event may have a role in directing different segments of the mitochondrial network to disparate fates and in endowing a functional specificity to a sorting mechanism of any kind.

A number of potential mechanisms underlying the uneven Δψ_m of the daughter mitochondria were ruled out, including PTP opening, disruption of membrane integrity and increased ATP synthase activity. Although the mechanism is yet to be resolved, EM studies of cells treated with agents that impose immediate and extensive mitochondrial fragmentation observed neighboring fragments with disparate cristae structures, suggesting the possibility that fission of mitochondria might yield daughters with unequal membranous structures (Barsoum et al, 2006).

Is autophagy preventing subsequent fusion of the depolarized daughter unit?

The reduced probability of depolarized mitochondria to proceed into a consecutive fusion raised the possibility that fusion is prevented by an isolation membrane of forming APs.

Our observations indicate that in the absence of a stress-related death signal, mitochondria depolarize hours before being engulfed by the isolation membrane of the APs (Figure 4). These suggest that autophagy does not contribute to the observed depolarization of the daughter unit or its segregation from the fusing population. The time interval between mitochondrial depolarization and colocalization with lysosomes was reported to be ∼20 min (Elmore et al, 2001). However, the time gap estimated by Elmore and co-workers was measured under autophagy inducers (starvation and glucagon) and by the detection of lysosomal rather than AP isolation membrane markers.

The decreased OPA1 immunoreactivity in mitochondria that have been targeted by autophagy and in non-fusing mitochondria (Figure 5) provides a potential link between depolarization, reduced fusion capacity and removal by autophagy. The ability of OPA1 overexpression to reduce mitochondrial autophagy indicates that OPA1 plays a role in determining the fate of mitochondria. This may be direct, by preventing AP targeting, or indirect, by either increasing bioenergetic efficiency or increasing the mitochondrial fusion probability, leading to a more homogenous network and reduced chance for the generation of depolarized mitochondria.

Mitochondrial fission is essential for autophagy

This study and others have demonstrated that depolarized mitochondria are targeted by autophagy. We showed here that the main source of depolarized mitochondria is the fission event. Together, these observations raise the possibility that fission might be essential for mitochondrial autophagy.

Indeed, inhibition of fission resulted in the inhibition of mitochondrial, but not ER, autophagy (Figure 6). Formation of APs, lysosomes mass, generation of the autophagolysosomes and digestion of their content were not affected. We conclude that mitochondrial autophagy is inhibited before assembly of the isolation membrane, and implicate mitochondrial fission as a mediator of mitochondrial turnover. However, the role fission play is in reducing mitochondrial size may only be permissive and is unlikely to function as a trigger for autophagy, since overexpression of OPA1, which we found to inhibit mitochondrial autophagy, is accompanied by segmentation of the mitochondrial network, as reported by others and observed here in INS1 cells (Griparic et al, 2004; Chen et al, 2005).

In summary, mitochondrial fission is the occasional producer of daughter mitochondria that are characterized by three features found in autophagocytosed mitochondria: reduced Δψ_m, decreased OPA1 and reduced size. Before being targeted by autophagy, these mitochondria have reduced fusion capacity and are less likely to be recruited by fusion into a polarized network (Figure 9).

Mitochondrial dynamics and insulin secretion

Defective GSIS observed in diabetic models has been strongly associated with mitochondrial dysfunction and specifically with abnormal respiratory chain activity (Maechler et al, 1999; Lowell and Shulman, 2005). Inhibition of fission reduced maximal respiratory chain capacity, an observation that could explain the suppression of GSIS (Figure 8) as well as the reduction in ROS production in the FIS1 RNAi cells.

The accumulation of oxidized mitochondrial protein in the absence of increased ROS in FIS1 RNAi cells suggests that inhibition of fission results in reduced mitochondrial turnover (Figure 7). This is in line with experiments in which removal of mitochondria by autophagy was arrested, leading to a comparable decrease in respiratory chain activity. ATG5−/− fibroblasts and cells treated with the autophagy inhibitor 3-MA, two mechanistically distinct cellular models for autophagy inhibition, were found to have reduced respiratory capacity, similar to FIS1 RNAi and DRP1-DN-treated cells. This agrees with studies on fibroblasts in which inhibition of autophagy by 3-MA or by targeting of ATG7 resulted in the accumulation of mitochondria with lowered Δψ_m in the former and in alteration of mitochondrial morphology in the latter (Stroikin et al, 2004; Komatsu et al, 2005). However, additional studies will be required to determine what is the isolated contribution of the FIS1 RNAi and DRP1-DN-induced inhibition of autophagy to the accumulation of damaged mitochondrial proteins and mitochondrial dysfunction.

The combination of fission, selective fusion and autophagy described here may represent a quality control mechanism of the mitochondrial population (Figure 9). Why this mechanism fails to select against dysfunctional units or promotes respiratory compromised mitochondria under certain circumstances remains unclear. A defect in the quality control mechanism would lead to a progressive, diverse and insult-dependent decrease in function such as found in metabolic diseases and aging. In this context, the quality control checkpoint presented here may provide a potential mechanism for the induced senescence observed in cells in which fission has been hampered (Yoon et al, 2006; Lee et al, 2007).

Animals

Twelve-week-old male C57BL6 mice were used.

Islet isolation, primary cells and cell line culture

Islets were isolated, dispersed and plated as previously described (Heart et al, 2006).

Cell lines

ATG5+/+ and ATG5−/− mouse embryonic fibroblasts (MEFs) transfected with pEF321-T, and an SV40 large T antigen expression vector were a generous gift from N Mizushima and were previously described (Kuma et al, 2004).

DNA plasmids, constructs

Construction of viruses delivering mtPA-GFP, DRP1-DN, pWPI, FIS1 shRNA, control shRNA, LC3:GFP, mtDsRed and OPA1 OE is described in detail in the Supplementary data.

Confocal microscopy

Confocal microscopy was performed using a Zeiss LSM 510 Meta microscope. Detailed description of imaging protocols and controls for imaging artifacts is found in the Supplementary data.

Measurement of ROS production

Cells were loaded with 1 μM DHE (Invitrogen, Carlsbad, CA, USA) for 20 min at 37°C. Images were analyzed Using Metamorph imaging software (Molecular Devices, Sunnyvale, CA, USA).

O₂ consumption

Oxygen consumption in INS1 (expressing DRP1-DN) and in C2C12 cells was measured by an XF24 bioenergetic assay (Seahorse Bioscience, Billerica, MA, USA). Assays have been previously described in detail (Wu et al, 2007) and explained in the Supplementary data.

Oxygen consumption in INS1 (expressing FIS1 RNAi) and in ATG5 MEF null cells was measured as previously described (Corkey et al, 1986) (see Supplementary data).

Immunostaining

Cells were fixed with 4% paraformaldehyde for 15 min, washed, permeabilized in 0.5% Triton-X for 15 min, washed, blocked with 1% BSA/PBS for 15 min, incubated with primary antibody for 1 h, washed, incubated with the secondary antibody for 1 h, and washed and mounted with mowiol mounting media. All washes were with PBS and all procedures were performed at room temperature. The following primary antibodies were used: OPA1 (BD, USA, cat no. 612606; 1:100) and anti-nitrotyrosine (Upstate, MA; 1:500). Secondary antibodies were from Zymed (Invitrogen, Carlsbad, CA).

Insulin secretion from INS-1 cells

The above procedure was performed as previously described (Noel et al, 1997) (see also Supplementary data).

Protein oxidation detection

Mitochondrial isolation was performed using a mitochondrial isolation kit (Pierce, cat no. 89801), followed by using the Oxyblot™ protein oxidation detection kit (Chemicon International) (see Supplementary data).

Statistics

Unless stated otherwise error bars indicate SD and unpaired t-test was used to validate statistical differences.