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Extracellular α-synuclein levels are regulated by neuronal activity

Molecular Neurodegeneration201813:9

https://doi.org/10.1186/s13024-018-0241-0

©  The Author(s). 2018

  • Received: 23 October 2017
  • Accepted: 6 February 2018
  • Published:

Abstract

Background

α-Synuclein is a presynaptic protein abundant in the cytoplasmic compartment of neurons, whereas its presence in the extracellular space has also been observed under physiological conditions. Extracellular α-synuclein has pathological significance, exhibiting cellular toxicity and impairment of synaptic transmission. Notably, misfolded α-synuclein drives the cell-to-cell propagation of pathology via the extracellular space. However, the primary mechanism that regulates the extracellular levels of α-synuclein remains to be determined.

Methods

Using several mechanistically distinct methods to modulate neuronal/synaptic activities in primary neuronal culture and in vivo microdialysis, we examined the involvement of neuronal/synaptic activities on α-synuclein release.

Results

We demonstrate here that physiological release of endogenous α-synuclein highly depends on intrinsic neuronal activities. Elevating neuronal activity rapidly increased, while blocking activity decreased, α-synuclein release. In vivo microdialysis experiments in freely moving mice revealed that ~ 70% of extracellular α-synuclein arises from neuronal activity-dependent pathway. Selective modulation of glutamatergic neurotransmission altered extracellular α-synuclein levels, implicating this specific neuronal network in the mechanism of activity-dependent release of α-synuclein. While neuronal activity tightly regulated α-synuclein release, elevated synaptic vesicle exocytosis per se was capable to elicit α-synuclein release. We also found that extracellular α-synuclein exists as high molecular weight species.

Conclusions

The present study uncovers a novel regulatory pathway associated with α-synuclein release, whose dysregulation might affect various pathological actions of extracellular α-synuclein including its trans-synaptic propagation.

Keywords

  • α-synuclein
  • Parkinson’s disease
  • Propagation
  • Neuronal activity

Background

The pathological aggregation of α-synuclein characterizes Parkinson’s disease, dementia with Lewy bodies and multiple system atrophy collectively referred to as α-synucleinopathies [1, 2]. While α-synuclein aggregates intracellularly, accumulating evidence suggests that extracellular α-synuclein also has pathological significance [3]: studies have demonstrated that aggregated forms of extracellular α-synuclein trigger trans-cellular spreading of α-synuclein pathology [4–7]. Extracellular α-synuclein oligomers impairs long-term potentiation (LTP), alters the glutamatergic synaptic transmission and α3-Na+/K+-ATPase activity [8, 9], and also activates inflammatory response in microglia [10]. Secreted monomeric α-synuclein has been also shown to exhibit toxicity to cells [11], perturb calcium homeostasis [12] and induce fragmentation of lipid rafts [13].

α-Synuclein is present in media of various cells overexpressing α-synuclein and peripheral neurons [6, 11, 14, 15], brain interstitial fluid (ISF) [16] and also in cerebrospinal fluid [17, 18], suggesting that its release occurs independently of cell death. Now the phenomenon of α-synculein release has been well documented, whereas the underlying mechanism that regulates α-synuclein release has remained poorly investigated. To better understand the physiological release of α-synuclein, we have examined the relationship between neuronal activity and α-synuclein release both in cultured neurons and living mice.

Results

Neuronal activity drives de novo release of α-synuclein from neurons

We hypothesized that neuronal activity regulates physiological release of α-synuclein. Due to the artificial influences of over-expressed α-synuclein on the secretory mechanism [19] as well as basal synaptic transmission [20, 21], we sought to measure release of endogenous α-synuclein from cultured neurons.

Consistent with the hypothesis, we found that tetrodotoxin (TTX), a sodium channel blocker that inhibits the generation of action potential, significantly decreased α-synuclein levels released in media (Fig. 1a).
Fig. 1
Fig. 1

Modulating neuronal activity alters α-synuclein release from neurons. a TTX (1 μM, 30 min) decreased α-synuclein in the media. N = 12–16. b Glutamate (10 μM, 30 min) increased α-synuclein in the media, which was blocked by 50 μM AP5 and 10 μM NBQX. N = 8–20. c Cellular α-synuclein levels were not altered by glutamate. N = 8. d LDH activities in the media after indicated pharmacological treatments. N = 8–28. mean ± SEM, **p < 0.01, ***p < 0.001, ****p < 0.0001 using unpaired t test (a, c) or one-way ANOVA (b, d)

The expression of α-synuclein at the synapses of excitatory neurons [22, 23] led us to examine the involvement of excitatory neurotransmission. Thirty minutes exposure of glutamate increased extracellular α-synuclein levels. Pre-incubation with a specific NMDA receptor antagonist, AP5, and an AMPA receptor antagonist, NBQX, abolished both basal and glutamate-evoked α-synuclein release (Fig. 1b). The increase in α-synuclein release by glutamate was not associated with changes in cellular α-synuclein levels (Fig. 1c). While prolonged exposure of glutamate at higher dose (2.5 h treatment of 100 μM glutamate) increased the non-specific release of lactate dehydrogenase (LDH) in the media likely due to excitotoxicity, such increase was not observed in 30 min exposure of 20 μM glutamate and other treatment groups (Fig. 1d). This demonstrates that neuronal activity influenced extracellular α-synuclein levels by modulating the release, not by augmenting excitotoxicity or altering its expression level.

Neuronal activity alters the steady-state levels of extracellular α-synuclein in vivo

We reasoned if neuronal activity is a major regulator of α-synuclein release, altering activity would also change its steady state levels in ISF. To test this in the context of intact neuronal network, we performed in vivo microdialysis that allows the measurement of real-time changes in ISF endogenous α-synuclein on an hourly basis in freely moving mice. Following the collection of basal α-synuclein, picrotoxin (PTX), a GABAA receptor antagonist, was locally and continuously administered to hippocampus through the microdialysis probes with 1000 kDa cut-off membranes by reverse microdialysis to stimulate neurons. PTX significantly enhanced ISF α-synuclein levels (Fig. 2a, b) in a dose dependent manner, suggesting that the degree of neuronal activation determines its levels (Fig. 2c). Consistent with the report that low dose of PTX only produces occasional spikes and does not cause any excitotoxicity [24], PTX did not increase ISF LDH activities (Fig. 2d, e), while the same dose significantly elevated ISF α-synuclein levels.
Fig. 2
Fig. 2

ISF α-synuclein is present as high molecular weight species and its steady-state levels are dynamically regulated by neuronal activity. a Picrotoxin (PTX, 50 μM) increased ISF α-synuclein compared to vehicle treatment. N = 4–5. b ISF α-synuclein concentrations were increased by 50 μM PTX from baseline. N = 5. c The mean ISF α-synuclein levels after 25 μM or 50 μM PTX or vehicle (0 μM) infusion were elevated dose dependently N = 4–7. d % ISF LDH activities did not alter by 50 μM PTX. N = 4. e ISF LDH activities did not change by 50 μM PTX from baseline. N = 4. f Tetrodotoxin (5 μM, TTX) decreased ISF α-synuclein N = 4. g ISF α-synuclein concentrations were decreased by TTX from baseline. N = 4. h 50 μM AP5 and 10 μM NBQX decreased ISF α-synuclein. N = 6. i ISF α-synuclein concentrations were decreased by AP5 and NBQX from baseline. N = 6. j 300 μM LY341495 increased ISF α-synuclein without changing LDH activities N = 4. k ISF α-synuclein concentrations were increased by LY341495 from baseline. N = 4. The effect of drug treatment was assessed between baseline α-synuclein levels and mean α-synuclein levels in the entire treatment period. l Absolute concentration of ISF α-synuclein collected at 1.0 μl/min through either 30 kDa membranes or 1000 kDa membranes. N = 4–6. m Absolute concentration of ISF lactate collected at 1.0 μl/min through either 30 kDa membranes or 1000 kDa membranes. N = 4–6. n α-Synuclein concentrations in dialysate collected at the different flow rate by in vitro microdialysis with 30 kDa membranes. o ISF samples obtained from wild-type mice through 1000 kDa membranes were separated by a size exclusion chromatography using a Superdex75 column. α-Synuclein levels in eluted fractions were quantified by α-synuclein ELISA (N = 4). Mean ± SEM, *p < 0.05, **p < 0.01, using one-way ANOVA (c) or using ratio paired t test (b, e, g, i, k) or unpaired t test (l, m)

In contrast to PTX, inhibiting neuronal activity by TTX significantly decreased ISF α-synuclein levels by a maximum of ~ 70% (Fig. 2f, g). TTX reduced ISF α-synuclein not only in hippocampus but also in striatum (data not shown). This striking reduction in ISF α-synuclein levels suggests that the majority of extracellular α-synuclein arises from neuronal activity-dependent mechanisms.

Blocking glutamate receptors by AP5 and NBQX also significantly decreased ISF α-synuclein levels (Fig. 2h, i). Metabotropic glutamate receptors 2/3 negatively regulate glutamate release at the pre-synaptic terminal [24]. Thus, its inhibition enhances glutamate release. Infusion of a highly specific metabotropic receptor 2/3 antagonist, LY341495 slightly but significantly elevated ISF α-synuclein levels without changing LDH activities (Fig. 2j, k).

In order to examine the molecular weight size of ISF α-synuclein, we performed in vivo microdialysis using probes with 30 kDa cut-off membrane, which will predominantly collect monomeric α-synuclein (~ 14 kDa) and possibly a dimeric form (~ 28 kDa). Surprisingly, α-synculein was not detected in ISF collected through 30 kDa membranes although ISF lactate levels were not decreased with 30 kDa compared to 1000 kDa membranes (Fig. 2l, m). Recombinant α-synuclein was detectable by in vitro microdialysis with 30 kDa membranes in a flow rate-dependent manner as indicated by an inverse relationship between concentration and flow rate [25], suggesting that at least monomeric α-synuclein can pass through 30 kDa membranes (Fig. 2n). To further verify whether ISF α-synculein exists in a form larger than 30 kDa, we separated ISF samples collected through 1000 kDa cut-off membranes by a size-exclusion chromatography and measured the α-synuclein levels in individual fractions. ISF α-synuclein was eluted as a single sharp peak with an apparent molecular weight of 60 kDa (Fig. 2o). Although it is uncertain whether this represents α-synuclein oligomer or α-synuclein monomer bound to other proteins, it suggests that α-synuclein forms a high molecular weight complex in ISF.

Synaptic vesicle exocytosis per se is sufficient to enhance α-synuclein release

Collectively, the results suggest that neuronal activity is one mechanism regulating α-synuclein release. Glutamate activates post-synaptic receptors, depolarizes neurons and increases synaptic vesicle exocytosis. To further define which cellular process is associated with α-synuclein release, we performed pharmacological experiments in neurons.

α-Latrotoxin (αLTX) binds to neurexin receptors on the presynaptic terminals and enhanced synaptic vesicles release through calcium influx independently of pre-synaptic depolarization [26, 27] (Fig. 3a). αLTX increased α-synuclein release, which was blocked in the presence of EGTA (Fig. 3b). Next, to separately assess the effects of synaptic vesicle exocytosis and neuronal activity on α-synuclein release, we treated neurons with αLTX in the presence of TTX, AP5 and NBQX to enhance synaptic vesicle release while simultaneously blocking depolarization and post-synaptic glutamate receptor activation. The inhibitor mixture containing TTX, AP5 and NBQX in the absence of αLTX significantly decreased α-synuclein release. Interestingly, αLTX still enhanced α-synuclein release in the presence of the inhibitor mixture (Fig. 3c), with no changes in LDH activities and cellular α-synuclein levels (Fig. 3d, e). This suggests that pre-synaptic vesicle exocytosis is a critical downstream event associated with α-synuclein release and post-synaptic receptor activation is not the prerequisite.
Fig. 3
Fig. 3

Synaptic vesicle exocytosis is associated with α-synuclein release. a Schematic illustration of target molecules for the compounds used in the experiment. b α-Latrotoxin (αLTX, 0.5 nM) increased α-synuclein release, which was blocked by 4 mM EGTA. N = 8. c αLTX significantly increased α-synuclein release in the presence or absence of 1 μM TTX, 50 μM AP5 and 10 μM NBQX. N = 16–32. d LDH activities in the media were not altered by indicated pharmacological treatments. N = 16–24. e Cellular α-synuclein levels were not altered by indicate pharmacological treatments. N = 8. mean ± SEM, ***p < 0.001, ****p < 0.0001 using one-way ANOVA

Discussion

Prior studies overexpressing α-synuclein have reported multiple pathways that influence α-synuclein release such as proteasomal stress, lysosomal dysfunction, mitochondrial dysfunction [14, 28], and sulfonylurea receptor 1 mediated mechanism [23]. While the studies have shown that cells under external stress release more α-synuclein, the intrinsic mechanism that mediates endogenous α-synuclein release from healthy neurons in brain have not been empirically investigated to date. In the present study, using several mechanistically distinct methods to modulate neuronal activity, we provided substantial evidence that de novo release of endogenous α-synuclein highly depends on neuronal activity. More importantly, by measuring its real-time changes in freely moving wild-type mice, we also demonstrated that neuronal activity impacts the steady-state levels of extracellular α-synuclein in vivo.

Previous studies have suggested that secreted soluble α-synuclein exerts multiple effects. Intriguingly, many of its reported actions are associated with perturbation in neuronal/synaptic function at various levels, such as partitioning of voltage-gated calcium channels [29] or impairment in LTP [8] or alteration in synaptic activity [12] or increase in the susceptibility to depolarization by interacting with α3-Na+/K+-ATPase [9]. Thus, activity-dependent release of α-synuclein may participate in a dynamic feedback mechanism on neuronal/synaptic function.

Extracellular α-synuclein levels appear to highly rely on intrinsic neuronal activity compared to other secretory proteins released via an activity-dependent manner. For example, TTX only suppressed ISF Aβ levels by ~ 30% despite its complete inhibition of action potentials, suggesting that remaining ~ 70% pool of Aβ release arises from activity-independent mechanisms [27].

The steady-state levels of extracellular α-synuclein are maintained based on the balance between release and clearance. The rapid decrease in ISF α-synuclein by TTX also unveils that α-synuclein is normally cleared rapidly from ISF. Such clearance might be mediated by extracellular protease such as neurosin, which has been shown to degrade α-synuclein in culture media [30]. This is in sharp contrast to tau protein, which has a longer half-life in ISF, despite the common regulatory mechanism of release in an activity dependent manner [24, 31].

Our data suggests the link between synaptic activity and α-synuclein release; nonetheless this is not necessarily equated to its release via synaptic vesicles. Alternatively, it is certainly possible that synaptic activity drives other associated secretory process directly responsible for α-synuclein release.

α-Synuclein release has been shown to occur via an exosome-mediated pathway [5, 11]. Although detection of α-synuclein directly by ELISA in this study suggested the presence of α-synuclein not embedded in extracellular vesicles, it is unknown whether exosome-mediated release also occurs. Currently, the molecular mechanisms for exosome-independent α-synuclein release remains largely unknown and should be explored in the future studies.

Although the current study focuses on the physiological release of α-synuclein, it should further be investigated whether activity-dependent release promotes transmission of α-synuclein pathology. Although it is uncertain that α-synuclein forms oligomers in ISF, our study suggests that extracellular α-synuclein exists as a high molecular weight complex. Given that α-synuclein is capable of oligomerizing in the extracellular space [6], it is tempting to speculate that when local concentration of extracellular α-synuclein at synapses is abnormally elevated by neuronal activation, it may culminate in the chronic accumulation of oligomeric α-synuclein, which could ultimately facilitate the trans-synaptic spreading of α-synuclein pathology. Similar concept has been proposed for the cell-to-cell propagation of tau pathology [32]. From this perspective, the present microdialysis technique with 1000-kDa cut-off membranes might serve as a valuable tool to measure extracellular pathogenic α-synuclein and directly test the efficacy of potential pharmacological treatments in vivo.

Conclusions

We have demonstrated that neuronal/synaptic activity regulates α-synuclein release in vivo. Trans-synaptic spreading of pathology through neuronal network has been only reported in a certain class of pathogenic cytoplasmic proteins such as α-synuclein and tau. Of note, tau release is also dynamically regulated by synaptic activity [24, 33]. Our findings on the activity-dependent release of α-synuclein may underscore the common mechanistic link between trans-synaptic propagation and the synaptic activities in different types of neurodegenerative disorders.

Methods

Compounds

α-Latrotoxin and TTX were purchased from Alamone Labs and Wako Pure Chemical Industries respectively. Glutamate and picrotoxin were purchased from Sigma-Aldrich. D-AP5, NBQX and LY341495 were purchased from Abcam.

Culture of mouse primary neurons and measurements of α-synculein release from primary neurons

Primary cortical neurons were prepared from embryonic day 14 C57B6/J mouse embryos and plated on dishes coated with poly-D-lysine. Neurons were maintained in Neurobasal medium (Life technologies) containing 1% Glutamax I (Life technologies), 2% B-27 supplement (Life technologies), penicillin, streptomycin and cytosine arabinofuranoside to restrict proliferation of non-neuronal cells. Neurons cultured 14 days in vitro were rinsed once with DPBS and then incubated with Neurobasal phenol red minus medium or artificial CSF (aCSF; 1.3 mM CaCl2, 1.2 mM MgSO4, 3 mM KCl, 0.4 mM KH2PO4, 25 mM NaHCO3, and 122 mM NaCl, pH 7.4) containing 1% Glutamax I, 2% B-27 supplement with or without indicated chemicals for 30 min at 37 °C (treatment period). To maximize the inhibitory effects of TTX, AP5 and NBQX on the neuronal activity, these inhibitors were added both in treatment period and pre-incubation period (for 2 h at 37 °C). At the end of the experiments, collected media was centrifuged to remove cell debris and the supernatant was used for the further analysis. Neurons were lysed with RIPA (150 mM NaCl, 50 mM Tris, 0.5% deoxycholic acid, 1% Triton X-100, and 0.5% SDS, 25 mM EDTA, pH 8.0) supplemented with Complete (Roche) and PhosSTOP (Roche). α-Synuclein levels were normalized by cellular protein levels determined with BCA assay. To minimize inter-experiment variations, α-synuclein levels/total protein were further normalized by untreated control samples in the same experiment.

In vivo microdialysis

In vivo microdialysis using 1000 kDa cut-off Atmos microdialysis probes (Eicom microdialysis) was performed with slight modifications from the previously described method [24, 25]. A guide cannula was stereotaxically implanted in the hippocampus (bregma − 3.1 mm, 2.5 mm lateral to midline, 1.2 mm below dura at a 12.5° angle) or the striatum (bregma + 0.5 mm, 1.8 mm lateral to midline, 1.4 mm below dura at a 0° angle) under anesthesia and cemented. A Syringe pump (KDS-101, KD scientific) and a roller pump (ERP-10, Eicom microdialysis) were operated simultaneously for a push-pull microdialysis [34]. As a perfusion buffer, 4% BSA solution in aCSF was made fresh on the day and filtered through a 0.1 μm membrane. The probe was inserted through a guide cannula and perfused at 10 μl/min for 1 h and then ISF was collected at 1.0 μl/min by refrigerated fraction collectors (Univentor 820 microsampler, Univentor). Microdialysis with 30 kDa cut-off membranes (BR-2 probes, BASi) was operated only by a syringe pump. To ensure the stable collection of α-synuclein, the first 9 h fractions were excluded from analysis. The inclusion of chemicals in the perfusion buffer allows them to diffuse out to ISF. This technique is called reverse microdialysis. Reverse microdialysis was performed in hippocampus unless specifically mentioned. To infuse chemicals via reverse microdialysis, a normal perfusion buffer was switched to a perfusion buffer containing various chemicals. As a vehicle control for picrotoxin, a perfusion buffer containing 0.05% DMSO was administered. To assess the maximal effect of TTX or AP5 + NBQX, the mean α-synuclein or LDH levels during the final 3 h of treatment were compared.

In vitro microdialysis

In vitro microdialysis with 30 kDa cut-off membranes (BR-2 probes, BASi) was also operated by a syringe pump. Recombinant α-synuclein from SensoLyte α-synuclein ELISA kit (Anaspec) was dissolved in aCSF at 1 μg/ml and prepared in an Axygen maximum recovery tube. During microdialysis, flow rate varied from 0.2–1.2 μl/min and α-synuclein concentration in each flow rate was determined by α-synuclein ELISA.

Size exclusion chromatography

ISF samples were pooled and separated by a size exclusion chromatography using Superdex 75 column (GE healthcare). PBS was run at 0.5 ml/min with an AKTA explorer 10S (GE healthcare). α-Synuclein levels in each fraction were determined α-synuclein ELISA. LMW calibration kit to determine molecular weights was purchased from GE healthcare.

α-Synuclein ELISA

α-Synuclein levels in media or dialysates were determined at the end of collection by SensoLyte α-synuclein ELISA kit (Anaspec).

Lactate assay

Lactate levels in ISF were determined by lactate assay kit (Biovision).

LDH assay

LDH activities were measured by cytotoxicity detection kit (Roche). A reference absorbance at 600 nm (A600) was measured and subtracted from absorbance at 490 nm (A490). Maximum LDH release (100%) was induced by adding 5% lysis buffer from a cytotoxicity detection kit to media and % cell toxicity was calculated.

Statistical analysis

All statistical analysis was performed using Prism 6 (Graph Pad software). The comparison between baseline and treatment was done by two-tailed ratio paired t test. The comparison of two groups and multiple groups were done by two-tailed unpaired t test and one-way ANOVA with Tukey’s post-hoc test respectively.

Animals

All animal studies were reviewed and approved by the Institutional Animal Care and Use Committee of the Graduate School of Medicine at the University of Tokyo. 2–6 month old wild type male mice on C57B6/J background were purchased from Japan SLC (Hamamatsu, Shizuoka, Japan).

Abbreviations

GAPDH: 

Glyceraldehyde 3-phosphate dehydrogenase

ISF: 

Brain interstitial fluid

LDH: 

Lactate dehydrogenase

PTX: 

Picrotoxin

TTX: 

Tetrodotoxin

αLTX: 

α-latrotoxin

Declarations

Acknowledgements

We thank all members in Iwatsubo’s lab for helpful suggestions and discussion.

Funding

This work was supported by JSPS KAKENHI, Grant-in-Aid for Research Activity Start-up (K.Y.)(Grant number: 26890009) and Grant-in-Aid for Young Scientists (B) (K.Y.)(Grant number: 16 K20969). This research is partially supported by the program for Brain Mapping by Integrated Neurotechnologies for Disease Studies (Brain/MINDS) from Japan Agency for Medical Research and development, AMED (T.I.) (JP17dm0207014h0004).

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article.

Authors’ contributions

KY conceived, designed the experiments and performed all experiments. KY and TI wrote the manuscript. Both authors read and approved the final manuscript.

Ethics approval

All animal studies were reviewed and approved by the Institutional Animal Care and Use Committee of the Graduate School of Medicine at the University of Tokyo.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Department of Neuropathology, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

References

  1. Spillantini MG, Schmidt ML, Lee VM, Trojanowski JQ, Jakes R, Goedert M. Alpha-synuclein in Lewy bodies. Nature. 1997;388:839–40.View ArticlePubMedGoogle Scholar
  2. Horowitz NH, Bonner D, Mitchell HK, Tatum EL, Beadle GW. Genic control of biochemical reactions in Neurospora. Am Nat. 1945;79:304–17.View ArticleGoogle Scholar
  3. Lee HJ, Bae EJ, Lee SJ. Extracellular α-synuclein-a novel and crucial factor in Lewy body diseases. Nat Rev Neurol. 2014;10:92–8.View ArticlePubMedGoogle Scholar
  4. Volpicelli-Daley LA, Luk KC, Lee VM-Y. Addition of exogenous α-synuclein preformed fibrils to primary neuronal cultures to seed recruitment of endogenous α-synuclein to Lewy body and Lewy neurite–like aggregates. Nat Protoc. 2014;9:2135–46.View ArticlePubMedPubMed CentralGoogle Scholar
  5. Danzer KM, Kranich LR, Ruf WP, Cagsal-Getkin O, Winslow AR, Zhu L, Vanderburg CR, McLean PJ. Exosomal cell-to-cell transmission of alpha synuclein oligomers. Mol Neurodegener. 2012;7:42.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Danzer KM, Ruf WP, Putcha P, Joyner D, Hashimoto T, Glabe C, Hyman BT, McLean PJ. Heat-shock protein 70 modulates toxic extracellular α-synuclein oligomers and rescues trans-synaptic toxicity. FASEB J. 2011;25:326–36.View ArticlePubMedPubMed CentralGoogle Scholar
  7. Luk KC, Kehm V, Carroll J, Zhang B, O’Brien P, Trojanowski JQ, Lee VM. Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice. Science. 2012;338:949–53.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Diógenes MJ, Dias RB, Rombo DM, Miranda HV, Maiolino F, Guerreiro P, Näsström T, Franquelim HG, Oliveira LMA, Castanho MARB, Lannfelt L, Bergström J, Ingelsson M, Quintas A, Sebastião AM, Lopes LV, Outeiro TF. Extracellular alpha-Synuclein oligomers modulate synaptic transmission and impair LTP via NMDA-receptor activation. J Neurosci. 2012;32:11750–62.View ArticlePubMedGoogle Scholar
  9. Shrivastava AN, Redeker V, Fritz N, Pieri L, Almeida LG, Spolidoro M, Liebmann T, Bousset L, Renner M, Léna C, Aperia A, Melki R, Triller A. α-synuclein assemblies sequester neuronal α3-Na+/K+-ATPase and impair Na+ gradient. EMBO J. 2015;34:2408–23.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Kim C, Ho D-H, Suk J-E, You S, Michael S, Kang J, Joong Lee S, Masliah E, Hwang D, Lee H-J, Lee S-J. Neuron-released oligomeric α-synuclein is an endogenous agonist of TLR2 for paracrine activation of microglia. Nat Commun. 2013;4:1562.View ArticlePubMedPubMed CentralGoogle Scholar
  11. Emmanouilidou E, Melachroinou K, Roumeliotis T, Garbis SD, Ntzouni M, Margaritis LH, Stefanis L, Vekrellis K. Cell-produced alpha-synuclein is secreted in a calcium-dependent manner by exosomes and impacts neuronal survival. J Neurosci. 2010;30:6838–51.View ArticlePubMedPubMed CentralGoogle Scholar
  12. Melachroinou K, Xilouri M, Emmanouilidou E, Masgrau R, Papazafiri P, Stefanis L, Vekrellis K. Deregulation of calcium homeostasis mediates secreted α-synuclein-induced neurotoxicity. Neurobiol Aging. 2013;34:2853–65.View ArticlePubMedGoogle Scholar
  13. Emanuele M, Esposito A, Camerini S, Antonucci F, Ferrara S, Seghezza S, Catelani T, Crescenzi M, Marotta R, Canale C, Matteoli M, Menna E, Chieregatti E. Exogenous alpha-Synuclein alters pre- and post-synaptic activity by fragmenting lipid rafts. EBioMedicine. 2016;7:191–204.View ArticlePubMedPubMed CentralGoogle Scholar
  14. Lee H-J, Patel S, Lee S-J. Intravesicular localization and exocytosis of alpha-synuclein and its aggregates. J Neurosci. 2005;25:6016–24.View ArticlePubMedGoogle Scholar
  15. Paillusson S, Clairembault T, Biraud M, Neunlist M, Derkinderen P. Activity-dependent secretion of alpha-synuclein by enteric neurons. J Neurochem. 2013;125:512–7.View ArticlePubMedGoogle Scholar
  16. Emmanouilidou E, Elenis D, Papasilekas T, Stranjalis G, Gerozissis K, Ioannou PC, Vekrellis K. Assessment of α-synuclein secretion in mouse and human brain parenchyma. PLoS One. 2011;6:1–9.View ArticleGoogle Scholar
  17. Kang JH, Irwin DJ, Chen-Plotkin AS, Siderowf A, Caspell C, Coffey CS, Waligórska T, Taylor P, Pan S, Frasier M, Marek K, Kieburtz K, Jennings D, Simuni T, Tanner CM, Singleton A, Toga AW, Chowdhury S, Mollenhauer B, Trojanowski JQ, Shaw LM. Association of cerebrospinal fluid β-amyloid 1-42, t-tau, p-tau <inf>181</inf>, and α-synuclein levels with clinical features of drug-naive patients with early parkinson disease. JAMA Neurol. 2013;70:1277–87.PubMedPubMed CentralGoogle Scholar
  18. Mollenhauer B, Locascio JJ, Schulz-Schaeffer W, Sixel-Döring F, Trenkwalder C, Schlossmacher MG. α-Synuclein and tau concentrations in cerebrospinal fluid of patients presenting with parkinsonism: a cohort study. Lancet Neurol. 2011;10:230–40.View ArticlePubMedGoogle Scholar
  19. Simón D, García-García E, Gómez-Ramos A, Falcón-Pérez JM, Díaz-Hernández M, Hernández F, Avila J. Tau overexpression results in its secretion via membrane vesicles. Neurodegener Dis. 2012;10:73–5.View ArticlePubMedGoogle Scholar
  20. Wu N, Joshi PR, Cepeda C, Masliah E, Levine MS. Alpha-Synuclein overexpression in mice alters synaptic communication in the corticostriatal pathway. J Neurosci Res. 2010;88:1764–76.PubMedPubMed CentralGoogle Scholar
  21. Lundblad M, Decressac M, Mattsson B, Björklund A. Impaired neurotransmission caused by overexpression of α-synuclein in nigral dopamine neurons. Proc Natl Acad Sci U S A. 2012;109:3213–9.View ArticlePubMedPubMed CentralGoogle Scholar
  22. Taguchi K, Watanabe Y, Tsujimura A, Tatebe H, Miyata S, Tokuda T, Mizuno T, Tanaka M. Differential expression of alpha-synuclein in hippocampal neurons. PLoS One. 2014;9:e89327.View ArticlePubMedPubMed CentralGoogle Scholar
  23. Emmanouilidou E, Minakaki G, Keramioti MV, Xylaki M, Balafas E, Chrysanthou-Piterou M, Kloukina I, Vekrellis K. GABA transmission via ATP-dependent K+ channels regulates α-synuclein secretion in mouse striatum. Brain. 2016;139:871–90.View ArticlePubMedGoogle Scholar
  24. Yamada K, Holth JK, Liao F, Stewart FR, Mahan TE, Jiang H, Cirrito JR, Patel TK, Hochgräfe K, Mandelkow E-M, Holtzman DM. Neuronal activity regulates extracellular tau in vivo. J Exp Med. 2014;211:387–93.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Yamada K, Cirrito JR, Stewart FR, Jiang H, Finn MB, Holmes BB, Binder LI, Mandelkow E-M, Diamond MI, Lee VM-Y, Holtzman DM. In vivo microdialysis reveals age-dependent decrease of brain interstitial fluid tau levels in P301S human tau transgenic mice. J Neurosci. 2011;31:13110–7.View ArticlePubMedPubMed CentralGoogle Scholar
  26. Südhof TC. Alpha-Latrotoxin and its receptors: neurexins and CIRL/latrophilins. Annu Rev Neurosci. 2001;24:933–62.View ArticlePubMedGoogle Scholar
  27. Cirrito JR, Yamada KA, Finn MB, Sloviter RS, Bales KR, May PC, Schoepp DD, Paul SM, Mennerick S, Holtzman DM. Synaptic activity regulates interstitial fluid amyloid-beta levels in vivo. Neuron. 2005;48:913–22.View ArticlePubMedGoogle Scholar
  28. Jang A, Lee HJ, Suk JE, Jung JW, Kim KP, Lee SJ. Non-classical exocytosis of α-synuclein is sensitive to folding states and promoted under stress conditions. J Neurochem. 2010;113:1263–74.PubMedGoogle Scholar
  29. Ronzitti G, Bucci G, Emanuele M, Leo D, Sotnikova TD, Mus LV, Soubrane CH, Dallas ML, Thalhammer A, Cingolani LA, Mochida S, Gainetdinov RR, Stephens GJ, Chieregatti E. Exogenous α-Synuclein decreases raft partitioning of Cav2.2 channels inducing dopamine release. J Neurosci. 2014;34:10603–15.View ArticlePubMedGoogle Scholar
  30. Tatebe H, Watanabe Y, Kasai T, Mizuno T, Nakagawa M, Tanaka M, Tokuda T. Extracellular neurosin degrades α-synuclein in cultured cells. Neurosci Res. 2010;67:341–6.View ArticlePubMedGoogle Scholar
  31. Yamada K, Patel TK, Hochgräfe K, Mahan TE, Jiang H, Stewart FR, Mandelkow E-M, Holtzman DM. Analysis of in vivo turnover of tau in a mouse model of tauopathy. Mol Neurodegener. 2015;10:55.View ArticlePubMedPubMed CentralGoogle Scholar
  32. Wu JW, Hussaini SA, Bastille IM, Rodriguez GA, Mrejeru A, Rilett K, Sanders DW, Cook C, Fu H, Boonen RACM, Herman M, Nahmani E, Emrani S, Figueroa YH, Diamond MI, Clelland CL, Wray S, Duff KE. Neuronal activity enhances tau propagation and tau pathology in vivo. Nat Neurosci. 2016;19:1085–92.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Pooler AM, Phillips EC, Lau DHW, Noble W, Hanger DP. Physiological release of endogenous tau is stimulated by neuronal activity. EMBO Rep. 2013;14:389–94.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Yamada K. In vivo microdialysis of brain interstitial fluid for the determination of extracellular tau levels. Methods Mol Biol. 2017;1523:285–96.View ArticlePubMedGoogle Scholar

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Molecular Neurodegeneration

ISSN: 1750-1326