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Propionic acid induces dendritic spine loss by MAPK/ERK signaling and dysregulation of autophagic flux

Molecular Brain volume 13, Article number: 86 (2020) Cite this article

Abstract

Propionic acid (PPA) is a short-chain fatty acid that is an important mediator of cellular metabolism. It is also a by-product of human gut enterobacteria and a common food preservative. A recent study found that rats administered with PPA showed autistic-like behaviors like restricted interest, impaired social behavior, and impaired reversal in a T-maze task. This study aimed to identify a link between PPA and autism phenotypes facilitated by signaling mechanisms in hippocampal neurons. Findings indicated autism-like pathogenesis associated with reduced dendritic spines in PPA-treated hippocampal neurons. To uncover the mechanisms underlying this loss, we evaluated autophagic flux, a functional readout of autophagy, using relevant biomedical markers. Results indicated that autophagic flux is impaired in PPA-treated hippocampal neurons. At a molecular level, the mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) pathway was activated and autophagic activity was impaired. We also observed that a MAPK inhibitor rescued dendritic spine loss in PPA-treated hippocampal neurons. Taken together, these results suggest a previously unknown link between PPA and autophagy in spine formation regulation in hippocampal neurons via MAPK/ERK signaling. Our results indicate that MAPK/ERK signaling participates in autism pathogenesis by autophagy disruption affecting dendritic spine density. This study may help to elucidate other mechanisms underlying autism and provide a potential strategy for treating ASD-associated pathology.

Introduction

The human microbiome represents a diverse ecosystem of microbes. Reports on its influences on the immune system [1], metabolic processes [2], gene expression [3, 4], and nervous system [5] have led to increased recognition of the importance of the gut microbiome in human health and disease. The relationship between the gut microbiome and nervous system as a significant component of the gut-brain axis has also attracted increasing interest in recent years [6]. The gut microbiome possesses significant metabolic capacity, and certain microbe-derived metabolites are released into circulation and can cross the blood–brain barrier [7, 8]. Fermentation of dietary fiber by the colonic microbiome is the primary source of short-chain fatty acids (SCFAs), such as acetic acid, propionic acid (PPA), and butyric acid [9, 10]. PPA is used as a preservative in many processed foods, such as milk and cheese, and naturally occurs in yogurt [11, 12]. At appropriate levels, PPA improves immune function, facilitates cell signaling, and reduces food intake [9]. However, recent studies have reported that PPA is also associated with negative effects on health and behavior. Rats treated with PPA demonstrate impaired social behavior and inflammatory responses in the brain [13, 14]. High levels of PPA, but not other SCFAs, have been reported in the stools of autistic spectrum disorder (ASD) individuals [15]. Studies have demonstrated that intraventricular infusions of PPA caused abnormal behavioral patterns, such as abnormal social interaction and anxiety-like behavior in rats similar to those seen in humans with ASD [14, 16]. Although there is growing evidence that PPA can affect behavioral development, the direct effects of PPA on neuronal cells remain poorly understood.

It was previously published that SCFAs may modulate the levels of neurotransmitters [17]. For instance, neurogenesis-relevant signaling molecules such as brain-derived neurotrophic factor (BDNF) are shown to be modulated by change actions of SCFAs in the brain [18,19,20]. These data could reveal some clues about how SCFAs could regulate neuronal development. In neuronal circuits, dendrites from an individual neuron may have a thousand or more spines that participate in the establishment of excitatory synapses. Spines and synapses are produced in excess numbers during development that are later pruned via activity-dependent stabilization or elimination [21]. Dendritic spines are highly dynamic and undergo constant turnover and morphological plasticity depending on developmental stage and activity, and defective synapse formation or development has been implicated in many neurological diseases. However, whether PPA regulates the development of spine has not been experimentally tested. Changes in the number, formation, or elimination of dendritic spines depend on different molecules including actin [22], the cytoskeleton [23], cell surface receptors [24], and signaling pathways such as Ras and Rap kinase [25]. Moreover, activation of autophagy has also been reported to be related to spine morphology [26].

Macroautophagy is a cellular pathway, wherein damaged organelles are degraded, particularly those produced during oxidative stress, and metabolic precursors are regenerated [27]. In the initial step of autophagy, organelles are engulfed inside a double-membraned vesicle called an autophagosome. The autophagosome then fuses with an autolysosome to degrade organelles with lysosomal enzymes. Components are thereby recycled to produce energy and maintain synthesis [28]. Disruption of autophagy has been associated with several cellular pathologies, including tumors and neurological diseases [29, 30]. Impaired autophagy significantly reduces the size of synapses and number of boutons in Drosophila [31]. A previous study found that deletion of the vital autophagy gene Atg7 resulted in increased immature dendritic filopodia and defects in synaptic refinement [32]. Evidence points to a relationship between autophagy and dendritic spine defects, but the mechanistic basis for these defects remains elusive.

Autophagy is regulated by a range of signaling pathways such as mammalian target of rapamycin (mTOR), ERK, and protein kinase B (AKT) [33]. ERK signaling is central to the MAPK pathway that regulates many cellular processes such as proliferation, differentiation, development, learning, and apoptosis [34]. The MAPK/ERK pathway is also a key regulator of autophagy, and starvation, a stimulator of autophagy, transiently activates MAPK/ERK to stimulate the maturation of the autophagosome [35]. Inhibition of MAPK/ERK activation by MAPK inhibitor pretreatment abolishes starvation-induced autophagy [36]. While it is difficult to draw a firm conclusion about the relationship of ERK to autophagy, it is clear that the MAPK/ERK pathway is an important factor therein.

We examined autophagic activity and the MAPK/ERK pathway to characterize the biological effects of PPA on hippocampal neurons. Results suggest that spine defects are associated with autophagy impairment and activation of the MAPK/ERK signaling pathway.

Methods

Primary culture

Primary cultures of rat hippocampal neurons were prepared from the brains of day 18 embryonic rats. Briefly, the hippocampus was dissected in free HBSS and incubated with a 0.125% trypsin solution for 15 min at 37 °C. The resulting cell suspensions were diluted in neurobasal medium (#21103–049, Gibco), supplemented with SM1 components (#05711, Stemcell), and plated onto 100 μg/mL poly-D-lysine (#P0899, Sigma-Aldrich) and 2 μg/mL laminin (#11–243–217-001, Roche)-coated plates or coverslips.

Pharmacological treatment of hippocampal neuron

Propionic acid (#402907) and bafilomycin A1 (B1793) were purchased from Sigma-Aldrich, USA, and PD98059 (#513000) was purchased from Calbiochem. PPA was dissolved in phosphate-buffered saline (PBS) for treatment (100 μmole/mL). Bafilomycin A1 (2 nmole/mL) and PD98059 (10 μmole/mL) were dissolved in dimethyl sulfoxide and stored in aliquots at − 20 °C until the experiments. Vehicle (PBS), bafilomycin A1 (2 nmole/mL), and PD98059 (10 μmole/mL) were simultaneously treated with PPA (100 μmole/mL). PPA treatment was denoted as DIV 18, and cells were harvested on DIV 21.

Western blotting analysis

Cultured neurons were harvested by scraping in ice-cold radio-immunoprecipitation assay buffer (#89900, Thermo Scientific) solution containing a protease inhibitor (A32963, Thermo Scientific) and phosphatase cocktail inhibitors (#5970, Cell Signaling) to avoid phosphorylation and degradation of proteins. After incubation, all lysates were centrifuged at 15,000 g at 4 °C for 30 min. The supernatant was then evaluated for total protein concentration using a BCA protein assay kit (#23225, ThermoFisher). Equal amounts of protein samples were incubated with 5X SDS sample loading buffer (CBSS-9005, CHEM-BIO) at 95 °C for 5 min. The samples (10 μg) were subjected to SDS-polyacrylamide gel electrophoresis on precast, 4–15% gradient mini-gels (#456–1085, Bio-rad). Following transfer to PVDF membranes (#1620177, Bio-rad), the membranes were blocked in Tris-buffered saline (#CBTB-9110, CHEM-BIO) containing 3% BSA (#9048-4-8, GENEray Biotechnology) and 0.1% Tween 20 (H5152, Promega) for 1 h. Membranes were then washed with TBST and incubated overnight at 4 °C with primary antibodies against phosphorylated ERK1/2 (#4370, Cell Signaling), phosphorylated AKT (#4060, Cell Signaling), LC3A/B (#12741, Cell Signaling), p62 (ab56416, Abcam), and beclin-1 (#3495, Cell Signaling). Membranes were then probed with horse radish peroxidase-conjugated secondary antibody (1:5000) for 1 h and developed using an enhanced chemiluminescence immunoblot detection system (Fusion FX7, VILBER). Immunoblots for phosphorylated ERK1/2 and phosphorylated AKT were subsequently stripped and re-probed with anti-ERK1/2 (#4692, Cell Signaling) and anti-AKT (#4691, Cell Signaling) antibodies. Immunoblots were analyzed by densitometry using ImageJ software (National Institutes of Health). Only film exposures that were in the linear range of the ECL reaction (#32106, Thermo Scientific) were used for quantification analysis.

Immunofluorescence staining

Cultured neurons were fixed with 1% paraformaldehyde in PBS containing 4% sucrose for 5 min at room temperature. Without washing, neurons were then permeabilized and blocked simultaneously in 100% methanol for 7 min at − 20 °C. Primary antibodies against LC3A/B (#12741, Cell Signaling), p62 (ab56416, Abcam), lysosomal-associated membrane protein (LAMP1) (H4A3, Santa Cruz), and ubiquitin (P4D1, Santa Cruz) were added to blocking solution containing 0.1% gelatin, 0.3% Triton X-100, 16 mM sodium phosphate, and 450 mM NaCl and incubated overnight at 4 °C. After washing with PBS, coverslips were incubated with AlexaFluor488 (#4412, Cell Signaling) or AlexaFluor594 (#8890, Cell Signaling)-conjugated secondary antibodies for 1 h at room temperature and then washed extensively with PBS and distilled water. Subsequently, coverslips were mounted with mounting medium (H-1000, Vector Laboratories). The samples were imaged with a confocal laser-scanning microscope (Nikon, Japan) using a 60X oil lens and 488 nm and 594 nm emission lasers.

Confocal microscopy for dendritic spines

Cells were maintained in an incubator with 5% CO2 at 37 °C. The neurons were transfected with 2 μg of GFP construct with 2 μL of lipofectamine 2000 (Invitrogen). Then, cells were stained by immunofluorescence labeling with anti-GFP antibody (A11122, Invitrogen). The samples were imaged with a confocal laser-scanning microscope (Nikon, Japan) using a 60X oil lens and 488 nm laser. Our data indicate that all spine categories were represented in pyramidal neurons. Dendritic spine densities were assessed by analyzing high-resolution digital images with ImageJ software (National Institutes of Health). Dendritic spines were counted manually using the point picker function in ImageJ particle analysis. The dendritic field was estimated to be 10 μm in length.

Detection of autophagic flux

The formation of autophagosomes and autolysosomes in hippocampal neurons of control and PPA-treated cells was detected using a Premo™ Autophagy Tandem Sensor RFP-GFP-LC3B Kit (P36239, Invitrogen), according to the manufacturer’s instructions. The RFP-GFP-LC3B sensor enables the detection of LC3B-positive, neutral pH autophagosomes in green fluorescence (GFP), and LC3B-positive acidic pH autolysosome in red fluorescence (RFP). Cells were grown on coverslips and incubated with 10 μL of BacMam reagents containing RFP-GFP-LC3B for 16 h. Cells were then washed in PBS three times. Coverslips were mounted with mounting medium (H-1000, Vector Laboratories), and fluorescent images were taken using confocal microscopy (Nikon, Japan). LC3B-positive autophagosomes (GFP and YFP) and LC3B-positive autolysosomes (RFP only) were analyzed and quantified using ImageJ software (National Institutes of Health).

Transmission electron microscopy for autophagy

Neuron cells were treated with 100 μM of PPA for 3 days and then fixed at 4 °C in 2.5% glutaraldehyde (#16210, EMS) and 2% paraformaldehyde (#19210, EMS); cells were then post-fixed with 2% osmium tetroxide (#19150, Sigma-Aldrich) for 30 min at 4 °C. Then, the cells were stained en bloc with 0.1 mg TCH (T1136, TCI) in 10 mL distilled water and 1% uranyl acetate (#22400, EMS) and dehydrated via a graded ethanol series. Samples were then embedded with an EMBed-812 embedding kit (#14120, EMS). Embedded samples were sectioned (60 nm) with an ultra-microtome (Leica, Germany), and the sections were then viewed on a Tecnai 20 transmission electron microscope (TEM) (ThermoFisher, USA) at 120 kV. Numbers of autophagosomes and autolysosomes per 100 μm2 were measured, as well as the size of the ultrastructure, using ImageJ software (National Institutes of Health).

Statistical analysis

All data are represented as mean ± standard error of the mean (SEM) of at least three individual experiments. Statistical analysis was performed using one-way analysis of variance, and statistical significance (p-value) was calculated with GraphPad Prism 5 (GraphPad Software). Results at the 95% confidence level were considered significant.

Results

PPA induces the dendritic spine defects in hippocampal neurons

We evaluated the effect of PPA on hippocampal neurons using pH and cell viability assays. The viability of hippocampal neurons treated with PPA was assessed with a CCK-8 assay. Hippocampal neurons were treated with PPA at concentrations of 0, 0.01, 0.1, 1, 10, and 100 mM. For hippocampal neurons treated with PPA at different doses, culture medium pH was decreased from the 10 mM PPA-treated group (Fig. 1a). Viability was decreased only in the 100 mM PPA-treated group (Fig. 1b). These results indicated that a 100 μM PPA concentration is not toxic to hippocampal neurons, and this was used in PPA treatments to investigate PPA’s effect on cellular organelle structure in hippocampal neurons.

Fig. 1
figure 1

PPA decreases density of dendritic spines in hippocampal neurons (a) pH. b Cell viability. pH was measured in cultured media. Hippocampal neurons were incubated with PPA in concentrations ranging from 0 to 100 mM for 72 h. Viability was measured by CCK-8 assay. Results are expressed as percentage of viable cells and represent mean ± SEM of three samples (n = 3). c Top shows representative pyramidal neurons transfected with PLV-GFP and treated with vehicle (PBS) and PPA (100 μM) for 72 h. Bottom shows high magnification of representative secondary dendrites. Scale bar of top panel is 20 μm; scale bar of bottom panel is 1 μm. d Bar graph showing mean ± SEM for dendritic spine numbers of the representative groups (n = 50). ***p < 0.0005, ****p < 0.0001

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We assessed the effect of PPA on hippocampal neuron morphology by investigating whether PPA affects dendritic spine formation. Hippocampal neurons were transfected with GFP plasmid DNA at DIV 17, and neuronal morphology was observed at DIV 21, a stage wherein highly dynamic dendritic spines gradually increase and become stable [37]. At DIV 21, neurons were fixed, stained, and imaged with confocal microscopy. Neurons were identified by green fluorescence, which diffusely filled the transfected hippocampal neurons and highlighted cellular morphology. We then analyzed these transfected pyramidal neurons by measuring secondary dendritic spine density. PPA-treated cells had visibly decreased dendritic spine density at both low and high magnifications of representative neurons and dendrites as shown by microscopic analysis (Fig. 1c). After treatment with PPA, the number of dendritic spines was 1.828 ± 0.1794, whereas that of untreated neurons was 4.671 ± 0.1818 in 10 μm. Quantitative analyses showed 39.13% lesser dendritic spine density in treated neurons than in controls (Fig. 1d). These findings indicate that PPA induces dendritic spine loss in hippocampal neurons.

PPA upregulates biochemical markers of autophagy initiation in hippocampal neurons

We addressed the impact of PPA on induction of autophagy by assessing several autophagy markers, such as intracellular microtubule-associated protein 1 light chain 3 (LC3), beclin-1, and LAMP1. As lipidation of LC3 and its association with autophagosome membranes is an indicator of autophagy [38], we detected LC3 by immunoblot and fluorescence microscopy. LC3-I was modified to the PE-conjugated form, LC3-II, because LC3-II is associated with mature autophagosomes upon autophagy induction. LC3 conversion from I to II is a measurement of autophagic activity [39]. We detected a significant increase in LC3-II/LC3-I ratio in PPA-treated cells compared with control, as shown by western blot (Fig. 2a, b). The number of LC3 puncta in PPA-treated cells was visibly increased as shown by immunofluorescence (Fig. 2c). After treatment with PPA, the number of puncta was 89.6 ± 6.765, whereas that of untreated neurons was 43.42 ± 5.549 (Fig. 2d). We then measured protein levels of beclin-1 by western blot (Fig. 2e). The beclin-1 protein is a tumor suppressor and a central regulator of autophagy critical to the nucleation phase of autophagy [40]. Wong and colleagues used beclin-1 antibody to visualize the formation of the autophagosome complex of protein aggregates to elucidate the autophagosome formation process [41]. After PPA treatment, beclin-1 was elevated by 27% compared with control neurons (Fig. 2f).

Fig. 2
figure 2

PPA upregulates biochemical markers of autophagy in hippocampal neurons (a) Representative western blot of LC3 after PPA treatment. b Quantification of LC3-II levels with respect to LC3-I levels (n = 4). c) Representative immunofluorescence images showing LC3 staining in hippocampal neurons and PPA-treated cells. d Quantification of number of LC3 puncta from images in (C) (n = 10). e Representative Western blot showing increased expression of beclin-1 for 72 h after PPA treatment. f Quantification of beclin-1 levels with respect to GAPDH levels (n = 4). g Representative immunofluorescence images showing LAMP1 staining in hippocampal neurons and PPA-treated cells. h Quantification of the number of LAMP1 puncta from images in (G) (n = 12). i Representative Immunofluorescence images showing poly-ubiquitin staining in hippocampal neurons and PPA-treated cells. j Quantification of the number of poly-ubiquitin puncta from the images in (I) (n = 10). Bar graph showing mean ± SEM of the representative groups. Scale bar is 10 μm. *p < 0.05, **p < 0.01, ****p < 0.0001

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We next assessed the impact of PPA on protein aggregation-lysosome state levels of autophagic markers. PPA markedly increased the number of LAMP-1 and poly-ubiquitin puncta (Fig. 2g, i). After treatment with PPA, the number of LAMP-1 puncta was 188 ± 22.65, whereas that of the untreated neurons was 100.8 ± 8.645 (Fig. 2h). After treatment, the number of poly-ubiquitin puncta was 90.8 ± 16.91, whereas that of untreated neurons was 2.667 ± 0.9482 (Fig. 2j). These findings strongly suggest PPA as an inducer of autophagy throughout the process, from protein aggregation to autophagosome initiation.

Autophagic degradation is impaired by PPA

The interaction between LC3 and p62 was assessed by measuring protein levels of p62, a selective substrate of autophagy; p62 binds directly to LC3 at a short LC3 interaction region [42], and the induction of autophagic activity leads to p62 expression decline [43]. However, our immunoblot (Fig. 3a) and immunofluorescence (Fig. 3c) results showed a significant increase in p62 in PPA-treated cells compared with control. Specific immunoblot results showed a significant increase (30.8%) in p62 in PPA-treated cells over controls (Fig. 3b). After treatment with PPA, the number of p62 puncta was 158 ± 6.525, whereas that of untreated neurons was 112.3 ± 9.66 (Fig. 3d). PPA treatment was associated with elevated levels of p62, a protein degraded by autophagy that accumulates when autophagy is impaired. This finding indicated that the increase in LC3-II levels was not caused by enhanced formation but rather impaired clearance of the autophagosome. An increased LC3-II/LC3-I ratio (Fig. 2b, d) and an accumulation of p62 protein (Fig. 3b, d) were indicative of impaired autophagy in PPA-treated cells.

Fig. 3
figure 3

Autophagic degradation impaired by PPA (a) Representative western blot of p62 after PPA treatment. b Quantification of p62 levels with respect to GAPDH (n = 4). c Representative immunofluorescence images showing p62 staining in hippocampal neurons and PPA-treated cells. d Quantification of number of p62 puncta from images in (C) (n = 8). Bar graph showing mean ± SEM of representative groups. Scale bar is 10 μm. *p < 0.05, **p < 0.01

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To understand the autophagy defect better, we investigated by transfecting hippocampal neurons with a marker gene, tandem fluorescent-tagged LC3 (GFP-RFP-LC3) in a baculoviral vector to monitor LC3 translocation. Results in Fig. 4a show that there is no significant change in autophagosome (GFP+ and YFP+ puncta) (Fig. 4b). After treatment with PPA, the number of RFP+ only puncta was 592 ± 104.4, whereas in the absence of PPA treatment, it was 1097 ± 109.4. A quantification analysis revealed a 50.2% decrease in red fluorescence expression (Fig. 4c), suggesting that PPA dysregulates the fusion of autophagosome to autolysosome.

Fig. 4
figure 4

PPA dysregulates fusion from autophagosome to autolysosome (a) Representative fluorescent images after transfection with RFP-GFP-LC3B in control hippocampal neurons and PPA-treated cells. Scale bar is 20 μm. b, c Quantification of number of GFP and YFP puncta (autophagosome) and RFP only puncta (autolysosome) from images in (A) (n = 5). d Black box shows representative TEM images in control hippocampal neurons and PPA-treated cells. Red box shows representative TEM high magnification images of autolysosome and autophagosome (black arrow indicates autophagosome and red arrow indicates autolysosome). Black scale bar is 500 μm. e, f Quantification of autophagosome and autolysosome number per area (n = 35). Bar graph showing mean ± SEM of the representative groups. g Top shows representative pyramidal neurons transfected with PLV-GFP and treated with bafilomycin A1 (2 nM) and PPA (100 μM) for 72 h. Bottom shows high magnification of representative secondary dendrites. Scale bar of top panel is 20 μm; scale bar of bottom panel is 1 μm. h Bar graph showing mean ± SEM for dendritic spine numbers of the representative groups (n = 50). *p < 0.05, ***p < 0.0005, ****p < 0.0001

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We then further assessed fusion inhibition by analyzing the number of autolysosomes using TEM in control and PPA-treated cells (Fig. 4d). The number of autolysosomes was significantly decreased in PPA-treated cells, indicating inefficient fusion associated with PPA (Fig. 4f). These results strongly suggest that PPA dysregulates autolysosome fusion.

Moreover, to investigate whether autophagy defects by PPA are critical for spine loss, we investigated the effect of bafilomycin A1 in hippocampal neurons. Bafilomycin A1 is a well-known drug that disrupts autophagic flux by preventing cargo degradation [44]. Bafilomycin A1-treated cells visibly decreased dendritic spine density at both low and high magnifications of representative neurons and dendrites, as shown by microscopic analysis (Fig. 4g). After treatment with bafilomycin A1, the number of dendritic spines was 2.161 ± 0.5523, whereas that of untreated neurons was 4.726 ± 0.1715 in 10 μm. Quantitative analyses showed 45.72% lesser dendritic spine density in treated neurons than in controls (Fig. 4h). The reduction of spine density in bafilomycin A1-treated hippocampal neurons is similar compared with PPA-treated cells. These results show that PPA induces dendritic spine loss in hippocampal neurons by dysregulating autolysosome fusion, similar to bafilomycin A1.

ERK signaling pathway is involved in PPA-induced autophagy defects in hippocampal neurons

MAPK/ERK signaling regulates the expression of autophagic and lysosomal genes and stimulates autophagy by interacting with LC3. We investigated whether PPA exposure changes ERK1/2 signaling in hippocampal neurons by detecting phospho-ERK1/2 and total-ERK1/2 using immunoblot assays (Fig. 5a). As shown in Fig. 5b, we observed a significant increase (30.2%) in the p-ERK/ERK ratio in PPA-treated cells compared with controls (Fig. 5b). We then assessed whether PPA changes AKT signaling in hippocampal neurons by detecting phospho-AKT and total AKT using immunoblot assays (Fig. 5c). Compared with the level of p-AKT/AKT, no significant change in p-AKT/AKT ratio in PPA-treated hippocampal neurons was observed (Fig. 5d). These results suggest that the MAPK/ERK pathway is more associated with autophagy impairment than the AKT pathway in this study.

Fig. 5
figure 5

PPA activates MAPK/ERK pathway associated with autophagy impairment a Representative western blot of p-ERK and ERK after PPA treatment. b Quantification of p-ERK levels compared to ERK levels (n = 3). c Representative western blot of p-AKT and AKT after PPA treatment. d Quantification of p-AKT levels compared to AKT (n = 3). Bar graph showing mean ± SEM of the representative groups. *p < 0.05

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Inhibition of MAPK/ERK signaling rescues PPA phenotypes in vitro

Finally, we analyzed the impact of PD98059, a MAPK inhibitor, on dendritic spine loss and autophagic flux in hippocampal neurons. PD98059 treatment rescued dendritic spine density in PPA-treated neurons, an effect that was visible at both low and high magnification of representative neurons and dendrites (Fig. 6a). Quantitative analyses showed a 42.2% rescue of dendritic spine density in PD98059-treated neurons over PPA-treated-only neurons (Fig. 6b). In addition, to investigate whether PPA-induced MAPK/ERK activation is involved in autophagy regulation, we observed fusion activity by analyzing the number of autolysosomes using TEM. PD98059 treatment rescued the number of autolysosome in PPA-treated neurons (Fig. 6c). The number of autolysosomes was significantly increased (40.9%) in PPA and PD98059-treated neurons than in only PPA-treated neurons (Fig. 6d). Taken together, our data showed that inhibition of MAPK/ERK signaling rescued dendritic spine loss and autophagic disruption by PPA.

Fig. 6
figure 6

PD98059 rescues spine density and autophagy disruption in PPA-treated hippocampal neurons a Top shows representative pyramidal neurons transfected with PLV-GFP and treated with PPA (100 μM) and PD98059 (10 μM) for 72 h. Bottom shows high magnification of representative secondary dendrites. Scale bar of top panel is 20 μm; scale bar of bottom panel is 1 μm. b Bar graph showing mean ± SEM for dendritic spine numbers of the representative groups (n = 50). c Top shows representative TEM images in PPA (100 μM) and PD98059 (10 μM) for 72 h (white arrow is autolysosome). Bottom shows high magnification of representative images of autolysosome. d Quantification of autolysosome number per cell (n = 10). Bar graph showing mean ± SEM of the representative groups. *p < 0.05, **p < 0.01, ****p < 0.0001

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Discussion

Recent studies have demonstrated that autophagy is involved in synaptic remodeling in Drosophila melanogaster and mice [45]. Autophagy dysfunction is associated with reduced synaptic plasticity and dendritic spine deficiency [46]. Autophagic activity is required for BDNF-mediated synaptic plasticity in the hippocampus [47]. Auerbach and colleagues demonstrated that TSC1/2 deficiency associated with decreased autophagy leads to synaptic plasticity impairment in the hippocampus [48]. Another study showed that cortical neuron dendritic spine density was reduced in TSC1 knockout mice [49]. Goo et al. reported that lysosome inhibition alters lysosome trafficking in dendrites; furthermore, it decreases dendritic spine density [50]. In our study, PPA treatment of hippocampal neurons resulted in increased autophagy initiation but impaired autolysosome fusion. Electron and immunofluorescence microscopy analyses indicated that PPA-induced autophagosomes had not matured. They were double membrane-enclosed vesicles containing organelles, but the subsequent fusion with the outer membrane of lysosomes indicating autophagosome maturation, wherein the inner contents of autolysosomes are degraded for synthesis of new molecules and organelles, did not occur. Our findings suggest that PPA induces spine loss by disrupting the maturation of autophagosomes into functional autolysosomes. An increase in autophagosomes without a concomitant increase in autolysosomes provided valuable information for identifying signaling events. PPA was found to selectively disrupt autolysosomal maturation. This impairment of autophagy led to a decrease in dendritic spine density. We also showed the dendritic spine loss in bafilomycin A1-treated hippocampal neurons (Fig. 4g, h). Our results suggest that the mature of autolysosome in the spine helps to maintain cellular homeostasis and remodel synapse.

What is the delineation of signals that control autophagy? One report provides evidence that MAPK/ERK tightly regulates the maturation of autophagosomes [35]. Activation of the MAPK/ERK pathway was sufficient to arrest the autophagic maturation step with characteristic accumulation of autophagosomes and abolishment of autophagic degradation [36]. For instance, ERK cascade components colocalize with autophagosome, suggesting that aberrant autophagy is associated with ERK hyper-phosphorylation [51]. Consistent with this report, our results showed that the MAPK/ERK pathway is activated during autophagy maturation impairment in PPA-induced cells. We further found that the inhibition of MAPK/ERK signaling restored the autolysosome-represent autophagic flux (Fig. 6d). These findings indicate that MAPK/ERK activation is involved in autophagy defects. The AKT signaling pathway also regulates autophagy [33]; however, we observed that activation of this pathway did not significantly affect dendrites (Fig. 5d), implicating the MAPK/ERK pathway, but not the AKT pathway, in autophagy impairment. Spine density and disruption of autophagic flux were rescued when a MAPK inhibitor and PPA were co-treatment. It indicates that inhibition of the pathway specifically may affect maturation and not autophagy initiation.

A growing number of studies have implicated gut microbiota dysbiosis in behavioral and neurologic pathologies, such as in Alzheimer’s, Parkinson’s disease and ASD [17]. PPA administration has been proposed as a target for ASDs [52, 53]. Dendritic spines may serve as a common substrate for many neuropsychiatric disorders, particularly those that involve cognitive deficits, and dysregulation in spine morphology has been implicated in ASD [54]. There are two types of dendritic spine modifications in animal models of ASD-related genes. For example, SHANK3-mutated mice and PTEN transgenic mice models of ASD show a decrease in spine density. However, FMRP, MeCP2, neuroligin-3/4, and neurexin1 ASD models show an increase in spine density [55]. Our results illustrated a possible link between PPA and reduction of dendritic spine density in ASD animal model.

Taken together, we speculate that autophagy degradation disruption and MAPK/ERK signaling pathway activation induce dendritic spine defects and may affect synapse function and plasticity, leading to autistic-like phenotypes in PPA-treated hippocampal neurons. It will be of interest to determine if altered autophagy function and MAPK/ERK inhibition is a contributing factor to ASD. Our study represents the first empirical data supporting MAPK/ERK signaling pathway involvement in autophagic degradation disruption and the resulting pathologies associated with ASD.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Abbreviations

PPA:

Propionic acid

MAPK:

Mitogen-activated protein kinase

ERK:

Extracellular signal-regulated kinase

mTOR:

Mammalian target of rapamycin

AKT:

Protein kinase B

ASD:

Autism spectrum disorder

BDNF:

Brain-derived neurotrophic factor

PBS:

Phosphate-buffered saline

DIV:

Days in vitro

GFP:

Green fluorescent protein

YFP:

Yellow fluorescent protein

RFP:

Red fluorescent protein

LC3:

Intracellular microtubule-associated protein 1 light chain 3

LAMP1:

Lysosomal-associated membrane protein 1

TEM:

Transmission electron microscope

SEM:

Standard error of the mean

References

  1. Johnson CC, Ownby DR. Allergies and asthma: do atopic disorders result from inadequate immune homeostasis arising from infant gut dysbiosis? Expert Rev Clin Immunol. 2016;12(4):379–88.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  2. Nicholson JK, Holmes E, Kinross J, Burcelin R, Gibson G, Jia W, et al. Host-gut microbiota metabolic interactions. Science. 2012;336(6086):1262–7.

    CAS  PubMed  Article  Google Scholar 

  3. Cureau N, AlJahdali N, Vo N, Carbonero F. Epigenetic mechanisms in microbial members of the human microbiota: current knowledge and perspectives. Epigenomics. 2016;8:1259–73.

    CAS  PubMed  Article  Google Scholar 

  4. Woo V, Alenghat T. Host–microbiota interactions: epigenomic regulation. Curr Opin Immunol. 2017;44:52–60.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  5. Bourassa MW, Alim I, Bultman SJ, Ratan RR. Butyrate, neuroepigenetics and the gut microbiome: can a high fiber diet improve brain health? Neurosci Lett. 2016;625:56–63.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  6. Mayer EA, Knight R, Mazmanian SK, Cryan JF, Tillisch K. Gut microbes and the brain: paradigm shift in neuroscience. J Neurosci. 2014;34(46):15490–6.

    PubMed  PubMed Central  Article  Google Scholar 

  7. Stilling RM, Dinan TG, Cryan JF. Microbial genes, brain & behaviour - epigenetic regulation of the gut-brain axis. Genes Brain Behav. 2014;13(1):69–86.

    CAS  PubMed  Article  Google Scholar 

  8. Karuri A, Dobrowsky E, Tannock I. Selective cellular acidification and toxicity of weak organic acids in an acidic microenvironment. Br J Cancer. 1993;68(6):1080.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  9. Al-Lahham SH, Peppelenbosch MP, Roelofsen H, Vonk RJ, Venema K. Biological effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms. Biochim Biophys Acta. 2010;1801(11):1175–83.

    CAS  PubMed  Article  Google Scholar 

  10. Hsu ST, Yang ST. Propionic acid fermentation of lactose by Propionibacterium acidipropionici: effects of pH. Biotechnol Bioeng. 1991;38(6):571–8.

    CAS  PubMed  Article  Google Scholar 

  11. Rook J, Balch C. The effects of intraruminal infusions of acetic, propionic and butyric acids on the yield and composition of the milk of the cow. Br J Nutr. 1961;15(3):361–9.

    CAS  PubMed  Article  Google Scholar 

  12. Dengate S, Ruben A. Controlled trial of cumulative behavioural effects of a common bread preservative. J Paediatr Child Health. 2002;38(4):373–6.

    CAS  PubMed  Article  Google Scholar 

  13. MacFabe DF, Cain NE, Boon F, Ossenkopp KP, Cain DP. Effects of the enteric bacterial metabolic product propionic acid on object-directed behavior, social behavior, cognition, and neuroinflammation in adolescent rats: relevance to autism spectrum disorder. Behav Brain Res. 2011;217(1):47–54.

    CAS  PubMed  Article  Google Scholar 

  14. Choi J, Lee S, Won J, Jin Y, Hong Y, Hur T-Y, et al. Pathophysiological and neurobehavioral characteristics of a propionic acid-mediated autism-like rat model. PLoS One. 2018;13(2):e0192925.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  15. Wang L, Christophersen CT, Sorich MJ, Gerber JP, Angley MT, Conlon MA. Elevated fecal short chain fatty acid and ammonia concentrations in children with autism spectrum disorder. Dig Dis Sci. 2012;57(8):2096–102.

    CAS  PubMed  Article  Google Scholar 

  16. MacFabe D. Autism: metabolism, mitochondria, and the microbiome. Glob Adv Health Med. 2013;2(6):52–66.

    PubMed  PubMed Central  Article  Google Scholar 

  17. Silva YP, Bernardi A, Frozza RL. The role of short-chain fatty acids from gut microbiota in gut-brain communication. Front Endocrinol. 2020;11:25.

    Article  Google Scholar 

  18. Maqsood R, Stone TW. The gut-brain axis, BDNF, NMDA and CNS disorders. Neurochem Res. 2016;41(11):2819–35.

    CAS  PubMed  Article  Google Scholar 

  19. Barichello T, Generoso JS, Simões LR, Faller CJ, Ceretta RA, Petronilho F, et al. Sodium butyrate prevents memory impairment by re-establishing BDNF and GDNF expression in experimental pneumococcal meningitis. Mol Neurobiol. 2015;52(1):734–40.

    CAS  PubMed  Article  Google Scholar 

  20. Binder DK, Scharfman HE. Brain-derived neurotrophic factor. Growth factors (Chur, Switzerland). 2004;22(3):123.

    CAS  Article  Google Scholar 

  21. Changeux J-P, Danchin A. Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks. Nature. 1976;264(5588):705.

    CAS  PubMed  Article  Google Scholar 

  22. Osterweil E, Wells DG, Mooseker MS. A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis. J Cell Biol. 2005;168(2):329–38.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  23. Tada T, Sheng M. Molecular mechanisms of dendritic spine morphogenesis. Curr Opin Neurobiol. 2006;16(1):95–101.

    CAS  PubMed  Article  Google Scholar 

  24. Washbourne P, Dityatev A, Scheiffele P, Biederer T, Weiner JA, Christopherson KS, et al. Cell adhesion molecules in synapse formation. J Neurosci. 2004;24(42):9244–9.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  25. Vazquez LE, Chen H-J, Sokolova I, Knuesel I, Kennedy MB. SynGAP regulates spine formation. J Neurosci. 2004;24(40):8862–72.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  26. Shen D-N, Zhang L-H, Wei E-Q, Yang Y. Autophagy in synaptic development, function, and pathology. Neurosci Bull. 2015;31(4):416–26.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  27. Mizushima N, Levine B, Cuervo AM, Klionsky DJ. Autophagy fights disease through cellular self-digestion. Nature. 2008;451(7182):1069–75.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  28. Levine B, Klionsky DJ. Development by self-digestion: molecular mechanisms and biological functions of autophagy. Dev Cell. 2004;6(4):463–77.

    CAS  PubMed  Article  Google Scholar 

  29. Hara T, Nakamura K, Matsui M, Yamamoto A, Nakahara Y, Suzuki-Migishima R, et al. Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice. Nature. 2006;441(7095):885.

    CAS  PubMed  Article  Google Scholar 

  30. Rubinsztein DC, Gestwicki JE, Murphy LO, Klionsky DJ. Potential therapeutic applications of autophagy. Nat Rev Drug Discov. 2007;6(4):304.

    CAS  PubMed  Article  Google Scholar 

  31. Shen W, Ganetzky B. Autophagy promotes synapse development in Drosophila. J Cell Biol. 2009;187(1):71–9.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  32. Kim H, Cho M, Shim W, Kim J, Jeon E, Kim D, et al. Deficient autophagy in microglia impairs synaptic pruning and causes social behavioral defects. Mol Psychiatry. 2017;22(11):1576–84.

    CAS  Article  PubMed  Google Scholar 

  33. Petiot A, Pattingre S, Arico S, Meley D, Codogno P. Diversity of signaling controls of macroautophagy in mammalian cells. Cell Struct Funct. 2002;27(6):431–41.

    PubMed  Article  Google Scholar 

  34. Shaul YD, Seger R. The MEK/ERK cascade: from signaling specificity to diverse functions. Biochimica et Biophysica Acta (BBA)-molecular. Cell Res. 2007;1773(8):1213–26.

    CAS  Google Scholar 

  35. Corcelle E, Djerbi N, Mari M, Nebout M, Fiorini C, Fénichel P, et al. Control of the autophagy maturation step by the MAPK ERK and p38: lessons from environmental carcinogens. Autophagy. 2007;3(1):57–9.

    CAS  PubMed  Article  Google Scholar 

  36. Corcelle E, Nebout M, Bekri S, Gauthier N, Hofman P, Poujeol P, et al. Disruption of autophagy at the maturation step by the carcinogen Lindane is associated with the sustained mitogen-activated protein kinase/extracellular signal–regulated kinase activity. Cancer Res. 2006;66(13):6861–70.

    CAS  PubMed  Article  Google Scholar 

  37. Nwabuisi-Heath E, LaDu MJ, Yu C. Simultaneous analysis of dendritic spine density, morphology and excitatory glutamate receptors during neuron maturation in vitro by quantitative immunocytochemistry. J Neurosci Methods. 2012;207(2):137–47.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  38. He C, Klionsky DJ. Regulation mechanisms and signaling pathways of autophagy. Annu Rev Genet. 2009;43:67–93.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  39. Kabeya Y, Mizushima N, Ueno T, Yamamoto A, Kirisako T, Noda T, et al. LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing. EMBO J. 2000;19(21):5720–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  40. Wirawan E, Lippens S, Vanden Berghe T, Romagnoli A, Fimia GM, Piacentini M, et al. Beclin1: a role in membrane dynamics and beyond. Autophagy. 2012;8(1):6–17.

    CAS  PubMed  Article  Google Scholar 

  41. Wong E, Bejarano E, Rakshit M, Lee K, Hanson HH, Zaarur N, et al. Molecular determinants of selective clearance of protein inclusions by autophagy. Nat Commun. 2012;3:1240.

    PubMed  Article  CAS  Google Scholar 

  42. Komatsu M, Waguri S, Koike M, Sou YS, Ueno T, Hara T, et al. Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice. Cell. 2007;131(6):1149–63.

    CAS  PubMed  Article  Google Scholar 

  43. Jiang P, Mizushima N. LC3-and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells. Methods. 2015;75:13–8.

    CAS  PubMed  Article  Google Scholar 

  44. Klionsky DJ, Elazar Z, Seglen PO, Rubinsztein DC. Does bafilomycin A1 block the fusion of autophagosomes with lysosomes? Taylor & Francis; 2008; 849-50. .

  45. Rowland AM, Richmond JE, Olsen JG, Hall DH, Bamber BA. Presynaptic terminals independently regulate synaptic clustering and autophagy of GABAA receptors in Caenorhabditis elegans. J Neurosci. 2006;26(6):1711–20.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  46. Lieberman OJ, McGuirt AF, Tang G, Sulzer D. Roles for neuronal and glial autophagy in synaptic pruning during development. Neurobiol Dis. 2019;122:49–63.

    PubMed  Article  Google Scholar 

  47. Nikoletopoulou V, Sidiropoulou K, Kallergi E, Dalezios Y, Tavernarakis N. Modulation of autophagy by BDNF underlies synaptic plasticity. Cell Metab. 2017;26(1):230–42 e5.

    CAS  PubMed  Article  Google Scholar 

  48. Auerbach BD, Osterweil EK, Bear MF. Mutations causing syndromic autism define an axis of synaptic pathophysiology. Nature. 2011;480(7375):63–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  49. Meikle L, Pollizzi K, Egnor A, Kramvis I, Lane H, Sahin M, et al. Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function. J Neurosci. 2008;28(21):5422–32.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  50. Goo MS, Sancho L, Slepak N, Boassa D, Deerinck TJ, Ellisman MH, et al. Activity-dependent trafficking of lysosomes in dendrites and dendritic spines. J Cell Biol. 2017;216(8):2499–513.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  51. Martinez-Lopez N, Athonvarangkul D, Mishall P, Sahu S, Singh R. Autophagy proteins regulate ERK phosphorylation. Nat Commun. 2013;4:2799.

    PubMed  Article  CAS  Google Scholar 

  52. Dinan TG, Cryan JF. Microbes, immunity, and behavior: psychoneuroimmunology meets the microbiome. Neuropsychopharmacology. 2017;42(1):178–92.

    CAS  PubMed  Article  Google Scholar 

  53. Shultz SR, Aziz NA, Yang L, Sun M, MacFabe DF, O’Brien TJ. Intracerebroventricular injection of propionic acid, an enteric metabolite implicated in autism, induces social abnormalities that do not differ between seizure-prone (FAST) and seizure-resistant (SLOW) rats. Behav Brain Res. 2015;278:542–8.

    CAS  PubMed  Article  Google Scholar 

  54. Fiala JC, Spacek J, Harris KM. Dendritic spine pathology: cause or consequence of neurological disorders? Brain Res Rev. 2002;39(1):29–54.

    PubMed  Article  Google Scholar 

  55. Penzes P, Cahill ME, Jones KA, VanLeeuwen J-E, Woolfrey KM. Dendritic spine pathology in neuropsychiatric disorders. Nat Neurosci. 2011;14(3):285.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

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Acknowledgments

Transmission electron microscopy and confocal microscopy data were acquired at Brain Research Core Facilities in KBRI.

Funding

This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. 2019R1A2C1010634) and KBRI basic research program through Korea Brain Research Institute funded by Ministry of Science and ICT (20-BR-04-01).

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Authors and Affiliations

  1. BK21 Plus Program, Department of Senior Healthcare, Graduate School, Eulji University, Daejeon, South Korea

    Hyosun Choi & In Sik Kim

  2. Neural Circuit Research Group, Korea Brain Research Institute, Daegu, 41068, Republic of Korea

    Hyosun Choi & Ji Young Mun

  3. Department of Biomedical Laboratory Science, Eulji University School of Medicine, Daejeon, South Korea

    In Sik Kim

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  1. Hyosun Choi
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J.Y.M, I.S.K and H.C. designed research. H. C performed research and analyzed data. J.Y.M and. H.C. wrote the paper. All authors read and approved the final manuscript.

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Correspondence to Ji Young Mun.

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All animal experiments were carried out in compliance with the Guide for Care and Use of Laboratory Animals of the National Institutes of Health and were approved by the Institutional Animal Care and Use Committee of Korea Brain Research Institute (IACUC-18-00013).

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Choi, H., Kim, I.S. & Mun, J.Y. Propionic acid induces dendritic spine loss by MAPK/ERK signaling and dysregulation of autophagic flux. Mol Brain 13, 86 (2020). https://doi.org/10.1186/s13041-020-00626-0

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  • DOI: https://doi.org/10.1186/s13041-020-00626-0

Keywords

  • Propionic acid
  • Short-chain fatty acid
  • Autophagy
  • MAPK/ERK signaling
  • Spine density

Molecular Brain

ISSN: 1756-6606