Mitochondrial aconitase 1 regulates age‐related memory impairment via autophagy/mitophagy‐mediated neural plasticity in middle‐aged flies

1 INTRODUCTION

Age-related memory impairment (AMI) refers to a significant decrease in learning and memory ability with age (Gkikas et al., 2014). Approximately 40% of people over 60 years of age experience AMI. Notably, AMI results in decreased acumen to encode working memories of new events or facts (Klencklen et al., 2017). Moreover, AMI also can appear in middle age (Kwon et al., 2016). The known causes of AMI in humans are age-related changes in the levels of cortisol, and estrogen (Jacobs et al., 1998; Lupien et al., 1998), cerebral vascular supply (Martin et al., 1991), oxidative stress (Lu et al., 2004), and a deficiency in the histone-binding protein RbAp48 (Pavlopoulos et al., 2013).

AMI occurs in most animals, including nematodes, fruit flies, mice, and chimpanzees. In fruit flies, the AMI phenotype has been described as a decrease in learning (3-min memory; Fresquet & Médioni, 1993), short-term memory (<1 h; Yamazaki et al., 2014), middle-term memory (3–7 h; Haddadi et al., 2014), or long-term memory (>24 h; Tonoki & Davis, 2015). DC0 (cAMP-dependent protein kinase) (Yamazaki et al., 2007), pyruvate decarboxylase (Yamazaki et al., 2014), and insulin-like growth factor signaling molecules (Tanabe et al., 2017) in energy metabolism; antioxidant SOD1 (Haddadi et al., 2014) in oxidative stress; and TORC2 and UNC-51 (Huang et al., 2013; Mochizuki et al., 2011) in autophagy have been reported as Drosophila AMI regulators. However, the mechanisms of AMI that emerge in middle-aged individuals before the aging traits remain largely unknown.

There are two isoforms of aconitase: mitochondrial aconitase (m-aconitase) and cytosolic aconitase (c-aconitase). The human homolog of mitochondrial Acon1 (mAcon1; m-aconitase in Drosophila) is aconitase 2 (ACO2). mAcon1 converts citrate to isocitrate in the tricarboxylic acid (TCA) cycle in the mitochondrial matrix (Beinert & Kennedy, 1993). When mAcon1 activity decreases, cellular respiration and ATP levels also decrease. These changes are associated with the dysfunction or senescence of cells. In addition, the iron–sulfur [4Fe-4S] cluster of mAcon1 is involved in regulating iron homeostasis (Lauble et al., 1992) and interacts with PTEN-induced kinase 1 (Pink1) (Esposito et al., 2013). In Drosophila, homozygous mutants of mAcon1 are lethal. RNA interference (RNAi)-mediated knockdown of mAcon1 resulted in reduced locomotor activity, shortened lifespan, and increased cell death in the developing brain (Cheng et al., 2013). Thus, mAcon1 plays an essential role in mitochondrial activity, energy metabolism, and aging.

Neurons maintain proteostasis to fulfill high metabolic demands and manage various stresses (Yin et al., 2016). Autophagy is an essential mechanism to manage the homeostasis of proteins and organelles; decreased autophagy with aging contributes to brain aging (Aman et al., 2021; Rubinsztein et al., 2011). In autophagy, autophagy-related proteins (ATGs) form autophagosomes and combine with lysosomes to degrade target organelles or proteins. Of them, ATG8 (Drosophila homolog of light chain 3, LC3) plays an important role in autophagosome maturation (lipidation), and p62 (ubiquitin-binding scaffold protein) recognizes ubiquitinated proteins and interacts with ATG8, leading to elimination via autophagy (Pankiv et al., 2007). Therefore, p62 aggregates accumulate when autophagy is absent, and p62 level decreases when autophagy is induced.

Mitophagy is a selective form of autophagy that removes dysfunctional mitochondria to reorganize specific mitochondrial networks and to improve mitochondrial quality (Ashrafi & Schwarz, 2013). Mitophagy also eliminates superfluous healthy mitochondria in certain physiological conditions, such as the maturation of erythrocytes and removal of paternal mitochondria in fertilized oocytes (Sandoval et al., 2008). Pink1 and Park (E3 ubiquitin ligase) are necessary factors for mitophagy to occur (Lazarou et al., 2015). The suppression of pink1 and park expression in Drosophila induces the accumulation of swollen and clumped mitochondria in dopamine neurons owing to the absence of proper mitophagy (Cornelissen et al., 2018). Interestingly, mAcon1 is a dominant suppressor of Pink1, and its expression levels are reduced in pink1 mutants (Esposito et al., 2013). Therefore, mAcon1 likely regulates AMI through autophagy and mitophagy.

A recent report suggested that synaptic plasticity, rather than the loss of neurons, causes age-related cognitive decline (Morrison & Baxter, 2012). Bruchpilot (BRP), a structural protein in the presynaptic active zone (AZ), regulates synaptic plasticity by controlling the release of synaptic vesicles into the synaptic cleft (Böhme et al., 2016). BRP content increases with age in Drosophila due to decreased autophagy (Gupta et al., 2016). This condition sets the upper limit of the operational range of AZ, limiting synaptic plasticity and contributing to impairment of memory formation. Interestingly, increased autophagy reduces brain BRP levels and improves AMI in Drosophila (Gupta et al., 2016). Hence, autophagy is closely related to synaptic plasticity, and autophagy induced by mAcon1 expression is likely to regulate AMI.

Herein, we report that the metabolic regulator mAcon1 alters autophagic and mitophagic activities and induces further changes in synaptic plasticity to regulate AMI in middle-aged flies.

2 RESULTS 2.1 AMI impairs learning in middle-aged wild-type fruit flies

The lifespan curve reveals the level of progression of aging, wherein the premortality plateau is regarded as old age (Tamura et al., 2003). The lifespan of w1118 is longer than that of Canton-S-related strains used in other AMI studies (Tanabe et al., 2017; Yamazaki et al., 2014). In this study, the median lifespan (MLS) of wild-type Drosophila (w1118) combined with men and women was 64 days (d) (Figure 1a). This was much longer than that of Canton-S-related strains (wCS10, 33 d) (Paik et al., 2012). The mortality rate of Canton-S increased 20 d after eclosion (DAE) (Tamura et al., 2003); however, this rate increased after 50 DAE for w1118 (Figure 1b). Since w1118 reached a premortality plateau at 56 d in men and 61 d in women, these flies can be considered middle aged before 50 DAE. Expression of antioxidant genes, such as cat and sod1, is decreased in old flies compared to young flies (Haddadi et al., 2014). However, cat and sod1 mRNA expression levels in w1118 did not decrease until 30 DAE (Figure S1e,f). Because no evident aging phenotypes in mortality and expression of antioxidant genes appeared at 30 DAE, we considered w1118 flies at 10 DAE as young flies and 30 DAE as middle-aged flies.

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AMI appears in middle-aged wild-type flies, and the neuronal expression of mAcon1 controls the lifespan and AMI. (a) Lifespan curve of w1118. The median lifespan (MLS) is 64 d, and the maximum lifespan (MaxLS) is 92 d (n = 712). (b) The mortality rate of w1118 increases after 40 d after eclosion (DAE) (F(4, 25) = 6.34, p < 0.01). (c) Compared to young flies, learning is significantly reduced in middle-aged flies (F(4, 35) = 125.2, p < 0.001). (d) Memory retention curve of w1118. The learning, and 1, 3, and 7 h memory of middle-aged flies are significantly reduced, compared to the values from young flies (age effect [F(1, 72) = 71.17, p < 0.001], time effect [F(3, 72) = 76.62, p < 0.001], and interaction [F(3, 72) = 1.62, p = 0.191]). (e and f) In w1118 fly heads, the mAcon1 mRNA and protein expression levels decrease significantly in middle-aged flies, compared to young flies. (g and h) When mAcon1 expression in neurons is reduced in adult stage, MLS decreases (g, RU-: 71 d, n = 679; RU+: 65 d, n = 664; χ2 = 44.47, df = 1, p < 0.001). When mAcon1 expression increases, MLS also increases (h, RU-: 63 d, n = 694; RU+: 73 d, n = 700; χ2 = 74.52, df = 1, p < 0.001). (I and J) When mAcon1 expression decreases in neurons in adulthood, AMI worsens (I; age effects [F(1, 28) = 114.7, p < 0.001], RU effects [F(1, 28) = 4.86, p < 0.05], and interaction [F(1, 28) = 5.99, p < 0.05]). When mAcon1 expression increases, AMI is alleviated (J, age effect [F(1, 28) = 254.1, p < 0.0001], RU effect [F(1, 28) = 25.87, p < 0.0001], and interaction [F(1, 28) = 10.36, p < 0.01]). (K) Feeding w1118 middle-aged flies with isocitrate (50 µg/ml) for 30 d significantly improves learning (n = 8)

Using the aversive olfactory learning/memory paradigm, we examined the AMI phenotype in learning at 10-d intervals from 10 to 50 DAE in w1118. Learning (3-min memory) ability decreased significantly after 30 DAE (Figure 1c). There was no difference in the odor-sensing ability to benzaldehyde (BEN) or 3-octanol (OCT) and reactivity to electric shock between w1118 at 10 and w1118 at 30 DAE (Figure S1a-c). Anti-geotactic locomotor activity was slightly reduced at 30 DAE than at 10 DAE (Figure S1dd). However, as no difference was observed in the avoidance tests at both 10 and 30 DAE, reduced anti-geotactic locomotor activity at 30 DAE did not affect the learning tests.

After learning, memory retention ability decreased significantly over time (Figure 1d). The performance index (PI) of 10 DAE young flies was significantly higher than that of 30 DAE middle-aged flies. Notably, the slope of the memory retention curve of the young flies was similar to that of the middle-aged flies. Therefore, the AMI appearing in the middle-aged w1118 flies was not a memory impairment but rather a learning (3-min memory) impairment.

2.2 mAcon1 regulates longevity

In the heads of w1118 flies, the expression levels of mAcon1 mRNA (Figure 1e) and protein (Figure 1fa-fb) significantly decreased as aging progressed. mAcon1 transcript and protein levels in isolated heads of the actin-GeneSwitch [GS]-Gal4 > mAcon1 RNAi (RU486-positive [RU+]) were reduced by almost 50% and 60% compared to controls (RU-), respectively (Figure S3a,c,d). The mAcon1 overexpression efficiency increased 5.6-fold at the mRNA level and 1.6-fold at the protein level, compared to that in control flies (Figure S3b,c,e). To determine whether mAcon1 expression affects lifespan, we measured the lifespan of genetically modified adult flies in which mAcon1 expression was modulated by an inducible pan-neuronal Gal4 driver and its inducer RU continuously after eclosion. When the neuronal expression of mAcon1 was suppressed, MLS significantly decreased in adult flies (8.45%, Figure 1g). When mAcon1 expression was upregulated, MLS significantly increased (15.87%, Figure 1h). Thus, mAcon1 is an aging- and longevity-regulating gene.

2.3 Neuronal expression of mAcon1 regulates AMI in w1118 flies

In young flies, the neuronal increase or decrease in mAcon1 expression levels did not affect learning (Figure 1i-j). In middle-aged flies, downregulating mAcon1 expression in neurons led to a significant decrease in learning (Figure 1i). Conversely, neuronal overexpression of mAcon1 increased learning (Figure 1j). Therefore, the neuronal control of mAcon1 expression after eclosion regulated AMI in middle-aged flies.

2.4 Feeding isocitrate, a metabolic product of mAcon1, improves AMI

If mAcon1 is an essential factor in AMI, it is plausible that isocitrate, a catalytic product of mAcon1, may also affect AMI. To assess this, we fed the middle-aged w1118 with various concentrations of isocitrate and measured learning afterward. Learning was significantly improved when the middle-aged flies were fed 50 µg/ml isocitrate (Figure 1k and Figure S2a). However, there was no improvement in learning at the same concentration in young flies (Figure S2b). Moreover, feeding isocitrate improved AMI, even when mAcon1 expression levels decreased in the mushroom body (MB) (Figure 2j and Figure S2c). Feeding isocitrate for 7 d to flies with overexpressed mAcon1 in the MB did not improve AMI (Figure S2d). However, feeding it for 30 d further improved AMI (Figure 2k). Hence, AMI could be improved through the supplementation of isocitrate.

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Modulation of mAcon1 expression in Kenyon cells (KCs) regulates AMI. (a–c) Mitochondria of KCs labeled with (a, MB-GS >mito-GFP, scale bar: 10 µm) GFP and mAcon1 labeled with (b) mAcon1-specific antibodies colocalized (c, 74.95 ± 3.91%, n = 5). (d and e) Survival curve patterns and MLS are not changed by reducing (d, RU-: 60 d, n = 703; RU+: 63 d, n = 670; χ2 = 2.709, df = 1, p = 0.1) or increasing (e, RU-: 63 d, n = 700; RU+: 61 d, n = 698; χ2 = 2.50, df = 1, p = 0.114) mAcon1 expression in the KCs. (f and g) Reducing mAcon1 expression in KCs during the adult period of middle-aged flies significantly reduces learning (f, age effect [F(1, 28) = 205.1, p < 0.001], RU effect [F(1, 28) = 7.916, p < 0.01], and interaction [F(1, 28) = 3.81, p = 0.061]). Increasing mAcon1 expression improves learning (g, age effect [F(1, 28) = 257.4, p < 0.01]). (h) Reinforcing the intensity of mAcon1 knockdown in KCs of the young flies decreased learning (age effect [F(1, 28) = 226.5, p < 0.001], and RU effect [F(1, 28) = 57.64, p < 0.001]). (I) Reinforcing the intensity of mAcon1 overexpression in KCs of the young flies increases learning (age effect [F(1, 28) = 578.8, p < 0.001], RU effect [F(1, 28) = 60.53, p < 0.001], and interaction [F(1, 28) = 11.66, p < 0.01]). (j and k) Feeding isocitrate (50 µg/ml) for 30 d improves AMI, regardless of mAcon1 expression levels in the KCs of middle-aged flies (j, F(2,29) = 19.46, p < 0.001; k, F(2,29) = 28.2, p < 0.001)

2.5 Changes in mAcon1 expression in the MB do not affect lifespan

The mAcon1 encodes one of the TCA cycle enzymes in the mitochondria. The enzyme is present in all neural cells (Beinert & Kennedy, 1993). Immunohistochemistry (IHC) using mAcon1-specific antibody demonstrated that mAcon1 was expressed in the whole brain (Figure S3d-f). The protein colocalized with the mitochondria of the Kenyon cells (KCs) (Figure 2a-c); KCs construct MB neuropils and function in olfactory learning and memory in fruit flies (Aso et al., 2014). Unlike the neuronal effects of mAcon1 on longevity (Figure 1g-h), changes in mAcon1 expression in the MB during adulthood did not affect MLS or the patterns of survival curves (Figure 2d,e).

2.6 mAcon1 expression levels in the MB regulate AMI

To determine whether mAcon1 expression levels in the KCs are related to AMI, we evaluated learning of a mAcon1 mutant and flies with modulated mAcon1 expression using MB247-Gal4. Young mAcon1 mutant flies (mAcon1mb09176) displayed significantly reduced learning (Figure S4a). Learning was not affected in Gal4 heterozygotes (MB247-Gal4/+ > RNAi/+ or > UAS/+). In contrast, Gal4 homozygotes (MB247-Gal4/MB247-Gal4 > RNAi/+ or > UAS/+) demonstrated decreased learning in young flies (Figure S4b). In middle-aged flies, learning was reduced even in Gal4 heterozygotes (Figure S4c). Next, we measured AMI after modulating mAcon1 mRNA levels in the KCs throughout the adult stage using inducible Gal4 (MB-GS-Gal4). In the case of heterozygotes, the increase or decrease in mAcon1 expression in the KCs of young flies did not affect learning. However, in middle-aged flies, the decrease in mAcon1 expression significantly worsened AMI and increased mAcon1 expression improved learning (Figure 2f,g). When we increased the working intensity by constructing the homozygous Gal4/UAS system (MB-GS-Gal4/MB-GS-Gal4 > RNAi/RNAi or >UAS/UAS), the learning ability was regulated according to the mAcon1 expression levels in the KCs, even in young flies (Figure 2h-i). To determine whether short-term control of mAcon1 could affect learning, we limited RU feeding to 7 d. There was no significant difference in learning between heterozygotes (Figure S5a,b). Short-term feeding of RU significantly decreased learning in the homozygous young flies but not in middle-aged flies (Figure S5c,d). These results suggest that both the expression levels and the available duration of mAcon1 were essential for learning, and mAcon1 in KCs could affect the learning of the young and middle-aged flies.

2.7 Aging and MB mAcon1 expression levels control ATP production

As the expression of mAcon1 and other TCA cycle enzymes decreases with aging, the amount of ATP produced should also decrease. To verify this, we estimated the change in ATP levels in KCs using AT1.03NL, an ATP reporter (Tsuyama et al., 2013). As aging progressed, the amount of ATP in the KCs decreased significantly in middle-aged flies compared to young flies (Figure 3a,d,g). Next, we investigated whether the regulation of mAcon1 expression affects ATP production. In young flies, the amount of ATP significantly decreased (Figure 3b,g) or increased (Figure 3c,g), depending on the expression levels of mAcon1. Similarly, when mAcon1 expression in the KCs increased, ATP significantly increased in the middle-aged flies (Figure 3f-g). However, the reduction in mAcon1 expression did not decrease ATP levels in the middle-aged flies (Figure 3e,g). This discrepancy might have reflected the detection limit of AT1.03NL.

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Expression levels of mAcon1 affect citrate, acetyl-CoA, and ATP contents. (a–g) ATP in KCs of young or middle-aged flies estimated by normalizing the FRET signal of ATP reporter (MB-GS >AT1.03NL) to CFP (ATP unbinding form) (a–f, scale bar: 10 µm). ATP content decreases significantly in middle-aged flies compared to that in KCs of young flies. mAcon1 overexpression significantly increases ATP production (g, age effect [F(1, 22) = 80.52, p < 0.001], genotype effect [F(2, 22) = 89.26, p < 0.001], and interaction [F(2, 22) = 12.40, p < 0.001]). (h) No significant difference in the amount of mitochondrial DNA in the heads of the w1118 young and middle-aged flies. (i) Acetyl-CoA and citrate levels are significantly increased in the heads of middle-aged flies compared to that in w1118 young flies (age [F(1,32) = 29.72, p < 0.001] and metabolite effects [F(7,32) = 3.34, p < 0.01]). (j and k) Reducing mAcon1 expression in neurons during the adult stage of young flies significantly increases the levels of acetyl-CoA and citrate in the head (j, age [F(1,32) = 16.58, p < 0.001] and metabolite effects [F(7,32) = 3.25, p < 0.05]), whereas increasing mAcon1 expression significantly decreases acetyl-CoA and citrate levels (k, metabolite effect [F(7,32) = 4.66, p < 0.01])

2.8 Aging and mAcon1 expression do not affect mitochondrial DNA content

To determine whether the changes in the amount of ATP are related to the copy number of mitochondria in the KCs, we estimated the mitochondrial copy number by quantifying mitochondrial genes. The genes included mitochondrial cytochrome c oxidase subunit I (mt:CoI), mitochondrial cytochrome c oxidase subunit III (mt:CoIII), and mitochondrial cytochrome b (mt:Cyt-b). We observed no difference in the number of these mitochondrial genes in the heads of young and middle-aged w1118 flies (Figure 3i). Next, after labeling mitochondria with the fluorescent protein mt-Keima, mAcon1 expression was regulated in the KCs. The KCs expressing the mt-Keima signal were collected using fluorescence-activated cell sorting (FACS), and the mitochondrial genes were quantified. Aging and mAcon1 expression levels caused no significant difference in mitochondrial DNA copy number between the control and experimental groups where mAcon1 expression levels were modulated (Figure S7a-c).

2.9 Aging and neuronal mAcon1 expressions are associated with acetyl-CoA and citrate levels

Because mAcon1 expression decreased with aging, we speculated that reducing TCA cycle metabolites plausibly decrease ATP production. To verify this, we quantified these metabolites in fly heads using liquid chromatography-mass spectrometry (LC-MS). Only acetyl-CoA and citrate concentrations were significantly enriched in the head of middle-aged flies and not in young flies (Figure 3i). Levels of other TCA cycle metabolites were not different between the young and middle-aged flies. Interestingly, neuronal suppression of mAcon1 in young flies significantly increased the levels of acetyl-CoA and citrate (Figure 3j). These results were similar to the metabolite patterns observed in the middle-aged w1118 flies (Figure 3i). Conversely, increasing mAcon1 expression significantly reduced acetyl-CoA and citrate levels (Figure 3k) in young flies. Thus, the expression level of mAcon1 may be essential for maintaining acetyl-CoA, citrate, and ATP levels in middle-aged flies.

2.10 mAcon1 expression in the MB regulates mitophagy

The findings that mAcon1 controls ATP production without changing the total mitochondrial DNA content in KCs prompted an experiment to verify the relationship between changes in ATP production and mitochondrial quality control via mitophagy (Ashrafi & Schwarz, 2013). The mt-Keima protein was expressed in KCs to visualize mitophagy in vivo (Sun et al., 2015). The yellow-orange signal of mt-Keima decreased with aging (Figure 4a,d,g). Moreover, when the expression level of mAcon1 decreased, the mt-Keima signal was significantly reduced in both young and middle-aged flies (Figure 4b,e,g). Similarly, when the expression level of mAcon1 increased, the mt-Keima signal significantly increased in young and middle-aged flies (Figure 4c,f,g).

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Aging and mAcon1 regulates autophagy and mitophagy. (a–f) mt-Keima emission signals from Drosophila (MB-GS >mt-Keima) expressing the mitophagy reporter mt-Keima protein in KCs (scale bar: 10 µm). (g) Yellow-orange mt-Keima signal (low pH) decreases significantly with aging but significantly increases as mAcon1 expression increases (age effect [F(1, 56) = 207.9, p < 0.001], genotype effect [F(2, 56) = 709.6, p < 0.001], and interaction [F(2, 56) = 53.94, p < 0.001]). (h–j) In the KCs of middle-aged flies, mitophagy induced by increased mAcon1 expression disappears when pink1 expression is suppressed (h, scale bar: 10 µm; k, F(2, 27) = 662.5, p < 0.001). (l) When pink1 is knocked down in middle-aged flies, no improvement in AMI is observed because of mAcon1 overexpression (F(2, 21) = 8.15, p < 0.01). (m) Immunostaining of protein expression levels of ATG8a-II and p62 reveals changes according to age and expression level of mAcon1 in the heads of w1118 flies and neuronal modulation of mAcon1. (n-w) Expression levels of Atg8a-II and p62 proteins according to aging and expression level of mAcon1 (n = 4–6; using t-test). (n and s) Expression of Atg8a-II (n) and p62 (s) in the head of w1118 flies significantly reduces in middle-age. (o–r and t-w) Regulation of Atg8a-II and p62 levels by the neuronal expression of mAcon1 in young (o–r) and middle-aged (t–w) flies. The results are normalized to β-actin levels

The mAcon1 expression was modulated in KCs labeled with mt-Keima to investigate the correlation between mAcon1 and various mitophagy regulators (Gkikas et al., 2018). KCs emitting the mt-Keima signal were collected using FACS. The mRNA levels of mitophagy regulatory genes, such as AMP-activated protein kinase alpha subunit (AMPKα), target of rapamycin (tor), and the sirtuin family members, were measured. Only AMPKα mRNA levels changed according to mAcon1 expression (Figure S8a-g).

2.11 The pink1 is required for mitophagy induction and AMI improvement

The pink1 is necessary for mitophagy induction (Lazarou et al., 2015), and mAcon1 is a dominant suppressor of pink1 (Esposito et al., 2013). Therefore, we investigated whether mitophagy induction by mAcon1 was related to pink1. The mRNA expression level of pink1 in the heads of w1118 flies decreased with age (Figure S9a). When the expression of pink1 in Drosophila heads was modulated using actin-GS-Gal4, the expression level of mAcon1 did not change (Figure S9b,c). Conversely, even when mAcon1 expression was manipulated under the same conditions, the expression levels of pink1 remained unchanged (Figure S9d,e). Mitophagy significantly decreased when the expression of pink1 was suppressed after controlling mAcon1 expression in the KCs of middle-aged flies (Figure 4h-k). Furthermore, mAcon1 expression levels showed no significant deterioration or improvement effects on AMI in middle-aged flies when pink1 expression was repressed (Figure 4l). These results imply that the pink1 pathway is required to induce mitophagy and improve AMI through mAcon1.

2.12 Aging and mAcon1 modulate autophagy

Next, the expression levels of ATG8a and p62 proteins were quantified using Western blotting to determine whether aging and the regulation of mAcon1 expression affect autophagy. Regarding autophagy activity, the level of ATG8a-II, a lipidated form of ATG8a, was significantly lower in middle-aged flies than in young flies (Figure 4m,n). When mAcon1 expression decreased in neurons, the amount of ATG8a-II also decreased in both young and middle-aged flies (Figure 4m,o,p). Similarly, when mAcon1 expression increased in neurons, the amount of ATG8a-II also increased in both aged flies (Figure 4m,q,r). To estimate autophagic flux, we also measured the expression level of the ubiquitin-binding scaffold protein p62 (Drosophila homolog, Ref(2)P). Expression levels of p62 significantly increased in middle-aged flies compared to young flies (Figure 4m,s). When mAcon1 expression decreased in neurons, p62 also increased in young and middle-aged flies (Figure 4m,t,u). When mAcon1 expression increased in neurons, the amount of p62 decreased in both aged flies (Figure 4m,v,w). Thus, neuronal mAcon1 expression can regulate the production and degradation of autophagosome during autophagy. Considering the mitophagy results (Figure 4a-g), it could be concluded that mAcon1 regulates both autophagy and mitophagy in the Drosophila brain.

2.13 Neuronal mAcon1 expression regulates BRP protein levels in whole brain

Reduction in autophagic activity in the Drosophila brain results in a learning decline because of decreased synaptic plasticity (Bhukel et al., 2017). Moreover, the activity of synaptic plasticity can be estimated by the amount of the presynaptic structural protein BRP (Bhukel et al., 2019). Thus, we measured BRP levels to understand the possible role of mAcon1 in synaptic plasticity after manipulating mAcon1 expression in young and middle-aged flies. As aging progressed, BRP expression increased significantly in the brain (Figure 5a,c,e,g,I,h). When mAcon1 expression decreased in neurons, the BRP expression levels increased significantly in young and middle-aged flies (Figure 5b,d,i). Conversely, an increase in mAcon1 expression significantly decreased the expression of BRP protein in both the young and middle-aged flies (Figure 5f,h,j).

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Aging and mAcon1 regulate the expression of the presynaptic structural protein BRP in the whole brain. (a–h) Neuronal expression levels of mAcon1 were controlled. BRP expression visualized using IHC (a and e, scale bar: 10 µm). (i–j) BRP expression increases significantly with aging and is inversely proportional to mAcon1 expression levels (I, age [F(1, 20) = 58.63, p < 0.001] and genotype effects [F(1, 20) = 81.78, p < 0.001]; j, age effect [F(1, 20) = 28.76, p < 0.001], genotype effect [F(1, 20) = 68.12, p < 0.001], and interaction [F(1, 20) = 4.53, p < 0.05]). (k–o) mAcon1 expression levels were controlled in the MB KCs. Visualization of brain BRP distribution (k and o, scale bar: 10 µm). (s–t) Although mAcon1 expression is controlled only in KCs, changes in BRP signals appear in the whole brain. The pattern is inversely proportional to mAcon1 expression levels shown in panels i–j. (s, age [F(1, 20) = 31.96, p < 0.001] and genotype effects [F(1, 20) = 91.61, p < 0.001]; t, age [F(1, 20) = 54.08, p < 0.001] and genotype effects [F(1, 20) = 48.32, p < 0.001])

2.14 The mAcon1 expression in the MB also regulates BRP protein levels in whole brain

When autophagy is controlled only in the MB, a synaptic phenotype appears in the whole fly brain in a non-cell-autonomous manner (Bhukel et al., 2019). We controlled mAcon1 expression levels in the MB and measured BRP expression in the whole brain to determine the non-cell-autonomous effects of mAcon1. Flies in which mAcon1 expression decreased in the KCs displayed significantly increased BRP expression with age (Figure 5k,m,o,q,s,t). Moreover, as in the case where mAcon1 expression decreased in neurons, the reduction in mAcon1 expression only in the MB significantly increased BRP levels in the whole brain (Figure 5l,n,s). Furthermore, when mAcon1 expression increased, BRP levels decreased (Figure 5p,r,t). These results indicate that mAcon1 expression in all neurons or only the MB can regulate a non-cell-autonomous effect on the synaptic plasticity of the whole brain.

3 DISCUSSION

AMI is affected by energy metabolism, autophagy/mitophagy, and synaptic plasticity. The results of this study demonstrate that AMI, defined as a learning impairment in middle-aged flies, is regulated by mAcon1, a mitochondrial TCA cycle enzyme. In addition to the findings by Gupta et al. (2013) who proposed that lowering the neuronal autophagic clearance by aging is related to AMI, we reveal that mAcon1 regulates autophagy/mitophagy and further neural plasticity to control AMI.

We observed an increase in acetyl-CoA and citrate levels in fly heads with aging and upon mAcon1 suppression (Figure 3i-j). When the expression of mAcon1 increased, the contents of citrate and acetyl-CoA decreased in the fly heads (Figure 3k). The increased citrate moves into the cytoplasm via citrate carriers and is converted to acetyl-CoA and oxaloacetate by ATP-citrate lyase. Therefore, inhibition of mAcon1 expression increases the amount of cytosolic acetyl-CoA (Wellen et al., 2009). Increased cytosolic acetyl-CoA decreases autophagy. Conversely, when acetyl-CoA decreased, autophagy increased (Figure 4a-g,m-w). Acetyl-CoA acts as a cellular energy sensor to regulate autophagy in the nucleus and cytoplasm through three mechanisms. First, increased acetyl-CoA in the nucleus promotes histone acetylation through the action of lysine acetyltransferases (KATs) to inhibit ATG gene expression and thereby inhibits autophagy (Eisenberg et al., 2014). Moreover, p300/CBP inhibits autophagy by acetylation of FOXOs in the nucleus (Bánréti et al., 2013). Second, when acetyl-CoA level in the cytoplasm increases, the acetylation of several proteins, including autophagy mediator proteins, through p300/CBP increases, and autophagy is inhibited (Mariño et al., 2014; McEwan & Dikic, 2011). Several enzyme groups, including GNAT, p300/CBP, Rtt109, and MYST, acetylate cellular proteins (Dancy & Cole, 2015). However, the enzymes that mediate cellular acetyl-CoA levels to induce autophagy are unknown. The third mechanism involves the histone deacetylase 6 (HDAC6) pathway through which acetyl-CoA also affects autophagy. When acetyl-CoA levels increase, deacetylation of α-tubulin by HDAC6 decreases, mitochondrial transport through microtubules is improved, and subsequently, mitophagy is reduced (Lee et al., 2010). HDAC6 promotes autophagosome–lysosomal fusion by deacetylation of cortactin to activate F-actin remodeling (Lee et al., 2010). The expression of ecdysone-induced protein 74EF (Eip74EF), a target gene of nejire (Drosophila homolog of p300/CBP) (Bodai et al., 2012), was significantly increased in mAcon1-knockdown flies and decreased in mAcon1-overexpressing flies (Figure S10). These findings imply that cellular acetyl-CoA should regulate the activity of the nuclear p300/CBP. How the changes in cellular acetyl-CoA levels by mAcon1 regulate autophagy needs to be studied.

The ongoing structural reorganization of neuronal circuits through neuronal plasticity is essential for acquiring knowledge and consolidation of memory (Fleming & Rubinsztein, 2020). In the presynaptic AZ, scaffold proteins, such as BRP, control synaptic plasticity by regulating synaptic vesicle (SV) release factors like unc-13 (Böhme et al., 2016). Autophagy plays an important role in synaptic plasticity (Kulkarni & Maday, 2018). The size of AZ increases as aging progresses or autophagy decreases (Gupta et al., 2016). The operational range of synapse reaches the upper limit (metaplasticity), the synapse is gradually strengthened, and plasticity decreases; eventually learning ability is reduced (Bhukel et al., 2017). Autophagy and BRP expression are closely related. For example, spermidine inhibits AMI by decreasing the size of presynaptic AZ and SV release, which increases with aging (Gupta et al., 2016). Additionally, knockdown of atg5 and atg9 among autophagy machinery genes increases BRP level and decreases memory capacity in presynaptic AZ (Bhukel et al., 2019). In our study, although we could not measure the amount of BRP after direct autophagy control, autophagy/mitophagy activity in the head and KCs decreased with aging (Figure 4), and BRP level in the brain increased (Figure 5). Conversely, when mAcon1 expression increased, autophagy activity increased, and the amount of BRP decreased (Figures 4 and 5). These results suggest that autophagy induced by mAcon1 promotes neuronal plasticity through the micro-processes mentioned above and further regulates age-related memory.

The mAcon1 transcript and protein levels decreased during middle age in Drosophila (Figure 1e,f). It is important to elucidate the mechanism for the decrease in mAcon1 with aging to determine the fundamental cause of AMI. As aging progresses, the expression of genes encoding some TCA cycle enzymes was significantly reduced (Figure S6). These enzymes included citrate synthase (kdn), isocitrate dehydrogenase (idh3a), succinate dehydrogenase (SdhA), and oxoglutarate dehydrogenase (Nc73EF). In addition, some mitochondria-related proteins and mAcon1 change (Manczak et al., 2005). The function of the mitochondrial oxidative phosphorylation complex and the expression of related genes also reduce with age in humans (Emelyanova et al., 2018). Recently, it was reported that when oxidative stress increased following SOD mutation, the mRNA and protein levels of aconitase decreased in Salmonella enterica, with increased expression of proteins involved in oxidative stress response and DNA damage repair (Noster et al., 2019). Therefore, the increase in oxidative stress due to aging may be one of the causes of decreasing aconitase mRNA and protein expression in Drosophila.

Since mAcon1 is one of the TCA cycle enzymes, its deficiency can cause various problems. In particular, inhibited mAcon1 expression in all cells at the developmental stage affects locomotor activity, cell death, and lifespan (Cheng et al., 2013). To avoid the widespread effect of mAcon1, we used the inducible Gal4 system only for 10 or 30 DAE. Expression sites were also limited to neurons and MB KCs, and feeding 150 µM of RU does not affect the lifespan (Tricoire et al., 2009). Experimentally, the expression of mAcon1 using the MB-GS-Gal4 driver did not change the Drosophila lifespan (Figure 2d,e). However, even under the same conditions, flies showed a significant difference in learning ability without any difference in sensory ability (Figures S1a,c and S2f-k). Thus, we could avoid the adverse effects of mAcon1 in this study. In humans, patients with mAcon1 deficiency have cardiac palpations and various myopathies (Mochel & Haller, 1993). These symptoms appear to be related to the loss of control of iron–sulfur homeostasis by mAcon1. Although we mainly studied the metabolic effect of mAcon1, it would be interesting to study the function of mAcon1 in iron–sulfur homeostasis.

Well-known lifespan signaling pathways, such as insulin-like signaling, mitochondrial stress, and hypoxic response, operate through non-cell-autonomous signaling mechanisms (Miller et al., 2020). A neuron-specific knockdown of mAcon1 also extended the lifespan of Drosophila (Figure 1g). When aging progresses, the activity of mAcon1 in the thoracic flight muscles of Drosophila decreases (Yan et al., 1997). Feeding citrate increases the lifespan of Drosophila (Patel et al., 2016). Thus, the expression effect of mAcon1 may appear through acetyl-CoA or citrate, even in peripheral tissues. In addition, since neuronal senescence can be promoted when autophagy is reduced (Kang et al., 2011; Moreno-Blas et al., 2019), decreased expression of mAcon1 in neurons reduces autophagy to promote senescence. These senescent neurons may induce peripheral tissue aging via the senescence-associated secretory phenotype. Thus, the effect of neuronal mAcon1 expression may be transmitted to the peripheral tissues that consequently affect the lifespan.

Using the mt-Keima protein, we observed that local induction of mAcon1 expression in the KCs modulated mitophagy (Figure 4f-l). Furthermore, the expression of ATG8a-II, an autophagosome-forming protein, was regulated by mAcon1 expression (Figure 4a-e). In our IHC experiments, we labeled mitochondria with green fluorescent protein (GFP) and ATG8a using red fluorescent protein. Less than 6% of the signals were colocalized, and colocalization of morphologically intact mitochondria with ATG8a signal clumps was not observed (Figure S11a,b). It is possible that the mitochondria could be degraded rapidly within the autophagosome and that the GFP signal could be underestimated because GFP is not as stable as the mt-Keima protein, especially in acidic lysosomes. Nevertheless, these results imply that mAcon1 induces both selective and non-selective autophagy.

We selected mAcon1 from the screening studies to identify novel genes controlling longevity by measuring the lifespan of EP lines with a long-lived w1118 genetic background (Paik et al., 2012) and performed DNA microarray analysis with short-lived cantonized w1118 (wCS10). mAcon1 expression decreases with age in humans (Emelyanova et al., 2018); the amount of cytosolic acetyl-CoA increases in human U2OS cells, and autophagy decreases (Mariño et al., 2014). In mice, increased autophagy improves synaptic plasticity and suppresses age-related memory decline (Glatigny et al., 2019). Thus, decreased expression of mAcon1 with aging may occur in other Drosophila strains and other species. Confirming mAcon1 functions in autophagy and synaptic plasticity in other species would be exciting.

In conclusion, we found that AMI is a learning (3-min memory) impairment in middle-aged flies using wild-type Drosophila (w1118) and demonstrated that mAcon1, a TCA enzyme, is a novel regulator of aging and AMI. The findings also reveal the interconnection of energy metabolism, autophagy, mitophagy, and synaptic plasticity and their involvements in AMI regulation through mAcon1. It would be interesting to determine the roles of mAcon1 in neurodegenerative and pathological conditions.

4 EXPERIMENTAL PROCEDURES

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