|The Ca(2+)/Mn(2+) ion-pump PMR1 links elevation of cytosolic Ca(2+) levels to α-synuclein toxicity in Parkinson's disease models.|
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|PMID: 23154387 Owner: NLM Status: Publisher|
|Parkinson's disease (PD) is characterized by the progressive loss of dopaminergic neurons, which arises from a yet elusive concurrence between genetic and environmental factors. The protein α-synuclein (αSyn), the principle toxic effector in PD, has been shown to interfere with neuronal Ca(2+) fluxes, arguing for an involvement of deregulated Ca(2+) homeostasis in this neuronal demise. Here, we identify the Golgi-resident Ca(2+)/Mn(2+) ATPase PMR1 (plasma membrane-related Ca(2+)-ATPase 1) as a phylogenetically conserved mediator of αSyn-driven changes in Ca(2+) homeostasis and cytotoxicity. Expression of αSyn in yeast resulted in elevated cytosolic Ca(2+) levels and increased cell death, both of which could be inhibited by deletion of PMR1. Accordingly, absence of PMR1 prevented αSyn-induced loss of dopaminergic neurons in nematodes and flies. In addition, αSyn failed to compromise locomotion and survival of flies when PMR1 was absent. In conclusion, the αSyn-driven rise of cytosolic Ca(2+) levels is pivotal for its cytotoxicity and requires PMR1.Cell Death and Differentiation advance online publication, 16 November 2012; doi:10.1038/cdd.2012.142.|
|S Büttner; L Faes; W N Reichelt; F Broeskamp; L Habernig; S Benke; N Kourtis; D Ruli; D Carmona-Gutierrez; T Eisenberg; P D'hooge; R Ghillebert; V Franssens; A Harger; T R Pieber; P Freudenberger; G Kroemer; S J Sigrist; J Winderickx; G Callewaert; N Tavernarakis; F Madeo|
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|Type: JOURNAL ARTICLE Date: 2012-11-16|
|Title: Cell death and differentiation Volume: - ISSN: 1476-5403 ISO Abbreviation: Cell Death Differ. Publication Date: 2012 Nov|
|Created Date: 2012-11-16 Completed Date: - Revised Date: -|
Medline Journal Info:
|Nlm Unique ID: 9437445 Medline TA: Cell Death Differ Country: -|
|Languages: ENG Pagination: - Citation Subset: -|
|Institute of Molecular Biosciences; University of Graz; Graz, Austria.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Cell Death Differ
Journal ID (iso-abbrev): Cell Death Differ
Publisher: Nature Publishing Group
Copyright © 2013 Macmillan Publishers Limited
Received Day: 29 Month: 03 Year: 2012
Revision Received Day: 07 Month: 09 Year: 2012
Accepted Day: 09 Month: 10 Year: 2012
Print publication date: Month: 03 Year: 2013
Electronic publication date: Day: 16 Month: 11 Year: 2012
pmc-release publication date: Day: 1 Month: 3 Year: 2013
Volume: 20 Issue: 3
First Page: 465 Last Page: 477
PubMed Id: 23154387
Publisher Item Identifier: cdd2012142
|The Ca2+/Mn2+ ion-pump PMR1 links elevation of cytosolic Ca2+ levels to α-synuclein toxicity in Parkinson's disease models Alternate Title:PMR1 regulates α-synuclein toxicity|
|W N Reichelt112|
|T R Pieber5|
|S J Sigrist11|
1Institute of Molecular Biosciences; University of Graz; Graz, Austria
2Research Group Neurodegeneration; Katholieke Universiteit Leuven Campus Kortrijk, Kortrijk,Belgium
3Functional Biology; Katholieke Universiteit Leuven, Leuven, Belgium
4Institute of Molecular Biology and Biotechnology; Foundation for Research and Technology-Hellas, Crete, Greece
5Department of Internal Medicine, Medical University Graz, Graz, Austria
6INSERM, U848, 94805 Villejuif, France
7Metabolomics Platform, Institut Gustave Roussy, Villejuif, France
8Centre de Recherche des Cordeliers, Paris, France
9Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP, Paris, France
10Université Paris Descartes, Sorbonne Paris Cité, Paris, France
11Institute for Biology/Genetics; Freie Universität Berlin; Berlin, Germany
|*Research Group Neurodegeneration; Katholieke Universiteit Leuven Campus Kortrijk, Kortrijk, Belgium. Tel: +32 5624 6224; Fax: +32 5624 6994; E-mail: Greet.Callewaert@med.kuleuven.be
*Institute of Molecular Biosciences University of Graz, Humboldtstrasse 50/EG, Graz 8010, Austria. Tel: +43 316 3808878; Fax: +43 316 3809898; E-mail: Frank.Madeo@uni-graz.at
12These authors contributed equally to this work.
α-Synuclein (αSyn) is a small, natively unfolded protein that is abundantly expressed in the central nervous system. It constitutes the major structural component of the intracellular protein inclusions termed Lewy bodies that define a pathological hallmark of Parkinson's disease (PD).1 Mutations in or duplication and triplication of the gene coding for αSyn all result in familial PD.2, 3, 4, 5, 6 An increasing body of evidence points towards a role for Ca2+ ions and Ca2+-dependent processes in the pathology of PD in general7, 8 and αSyn-mediated neuronal death during PD in particular.9, 10, 11, 12 The underlying mechanisms, however, remain enigmatic. A valuable tool to explore such pending questions are humanized yeast models based on heterologous expression of human αSyn and pathogenic mutants, as they have not only recapitulated several features of PD but have also allowed to identify novel and evolutionary-conserved mediators and processes involved in the cytocidal consequences of αSyn.13, 14, 15, 16, 17 As the regulation of Ca2+ homeostasis is highly conserved between yeast and mammals – with the advantage of reduced complexity and redundancy in yeast18, 19, 20 – we heterologously expressed human αSyn in yeast to elucidate its effect on Ca2+ homeostasis and cell death. We could identify the Golgi-resident Ca2+/Mn2+ ATPase PMR1 (plasma membrane-related Ca2+-ATPase 1) as mediator of αSyn -driven changes in Ca2+ homeostasis and cytotoxicity in yeast, nematodes and flies.
We first quantified the basal cytosolic Ca2+ levels in yeast cells equipped with the Ca2+-dependent reporter protein aequorin at standard external [Ca2+] of ∼1 mM in the culture medium. In this setting, heterologous expression of αSyn provoked an elevation of the cytosolic Ca2+- concentration, [Ca2+]cyt, within the first 24 h of expression that subsided after 2 days of culturing (Figure 1a). Simultaneous determination of oxidative stress based on the superoxide-driven conversion of dihydroethidium to fluorescent ethidium (DHE→Eth) demonstrated that the rise in [Ca2+]cyt triggered by αSyn (Figure 1a) coincided with an increase in oxidative stress. However, the [Ca2+]cyt boost developed well before the massive production of reactive oxygen species (ROS), which started after 24 h of αSyn expression (Figure 1b), and subsequent cell death (Figure 1c). This points towards a sequential course of events, where αSyn-directed [Ca2+]cyt increase occurs upstream of ROS generation and death. Immunoblot analysis revealed that αSyn (driven by a galactose-promoter) was well expressed throughout the experiment, accumulating around 8 h after promoter induction (Figure 1e). The transient, αSyn-induced increase in [Ca2+]cyt was not related to a different localization of the protein itself, as – in line with previous studies15 – green fluorescent protein (GFP)-tagged αSyn was prominently detectable at the plasma membrane within the first 2 days of expression (Figure 1f).
In addition to the disturbance in basal [Ca2+]cyt, αSyn altered the cellular response to high extracellular Ca2+ pulses. Upon challenge with 150 mM Ca2+, a rapid and transient increase in [Ca2+]cyt was detectable that was largely amplified upon expression of αSyn (Figure 1d).
Addition of 2 mM ethylene glycol tetraacetic acid (a Ca2+ chelator) to the culture medium partly inhibited the increase in basal [Ca2+]cyt and at the same time ameliorated αSyn-induced accumulation of ROS and cell death (Figures 1g–i). Similar results were obtained using another Ca2+ chelator, BAPTA-AM (1,2-bis-(o-Aminophenoxy)-ethane-N,N,N',N'-tetraacetic acid, tetraacetoxymethyl ester), which is cell-permeable and acts as intracellular Ca2+ sponge (Supplementary Figures S1A and B). Thus, inhibition of the rise in basal [Ca2+]cyt attenuates subsequent ROS accumulation and death, indicating a causal link between disturbances in Ca2+ homeostasis and αSyn-inflicted cellular demise.
Oxidative stress and concomitant oxidation of DNA, proteins and lipids are essentially involved in neuronal cell death in various models of PD.21, 22, 23 Therefore, we tested whether the thiolic antioxidant N-acetylcysteine (NAC), a precursor of glutathione that has been shown to be protective in several PD-associated neurodegenerative scenarios,24, 25, 26, 27 could block αSyn-induced generation of ROS and eventual cell death. Although supplementation with NAC did not prevent the first increase in ROS generation detectable within 24 h, it clearly inhibited massive ROS production and subsequent cell death occurring after 2 days of αSyn expression (Figures 2a–c). Basal [Ca2+]cyt levels were largely unaffected by the addition of NAC (Figure 2d). By contrast, overexpression of cytosolic or mitochondrial superoxide dismutase (Sod1p or Sod2p, respectively) had no effect on αSyn-induced oxidative stress (Supplementary Figures S2A and B), arguing in favour of a rather broad pattern of cellular oxidative stress (that cannot by antagonized by overexpression of superoxid dismutases) as a cause of αSyn-induced cell death.
To identify molecular determinants for αSyn toxicity and dysregulation of Ca2+ homeostasis, we monitored αSyn-induced consequences in numerous deletion mutants known to influence Ca2+ transport or signalling. Yeast codes for various homologues of mammalian Ca2+ channels, transporters, sensors and buffers, including the plasma membrane-located voltage-dependent Ca2+ channel Cch1p/Mid1p, the secretory pathway and Golgi-resident Ca2+-ATPase Pmr1p, the sarcoendoplasmic reticulum Ca2+-ATPase Cod1p, the vacuolar H+/Ca2+ exchanger Vcx1p, the plasma membrane Ca2+-ATPase Pmc1p, the vacuolar cation channel Yvc1p – a putative homologue of the mammalian transient receptor potential canonical channels – or the general calcium sensor calmodulin as well as calcineurin and calmodulin-dependent kinases.18, 19, 20 Using deletion mutants of these calcium-related regulators and automated quantification of ROS production, we evaluated the contribution of these proteins to αSyn cytotoxicity. This approach identified PMR1 as a mediator of αSyn-triggered ROS production (Figures 3a and b). In addition, the αSyn-driven development of apoptotic and necrotic markers – assessed using AnnexinV/propidium iodide (PI) co-staining, which allows the discrimination between early apoptotic (AnnV+), late apoptotic/secondary necrotic (AnnV+/PI+) and necrotic (PI+) cells – demonstrated that deletion of PMR1 completely inhibited αSyn-driven increase in apoptotic and necrotic populations (Figures 3c and d). By contrast, the absence of CCH1, MID1, PMC1, VCX1, YVC1, or COD1 did neither alter αSyn-instigated ROS-accumulation nor cell death markers as compared with wild type (WT; Figures 3a–d). Notably, deletion of these genes did not compromise αSyn expression (Figure 3e). Determination of survival using clonogenic survival plating assays showed that the absence of Pmr1p potently inhibited αSyn-induced cell death (Figure 3f). In addition, we generated a conditional PMR1 mutant by replacement of the promoter region of PMR1 with a tetO promoter that is active in the absence of doxycycline and prevents gene expression upon addition of 10 μg/ml of the chemical.28 Treatment of cells with doxycycline and thus depletion of Pmr1p largely reduced αSyn-induced ROS production, confirming that Pmr1p is essentially involved in αSyn cytotoxicity (Figures 3g and h).
To test whether αSyn has any effect on the localization and/or expression levels of Pmr1p, we performed fluorescence microscopy as well as immunoblot analyses of yeast cells endogenously expressing a Pmr1p-GFP fusion protein. No obvious effect on Pmr1p protein levels or Golgi localization was apparent (Figures 4a and b). Using reverse transcription quantitative PCR, we could detect a slight upregulation of PMR1 mRNA (normalized to actin mRNA) after 14 h of αSyn expression (Figure 4c).
We next analysed whether the rise in basal [Ca2+]cyt triggered by αSyn is connected to the upregulation of a specific Ca2+ influx system that has been shown to be stimulated in scenarios such as the accumulation of misfolded proteins in the endoplasmic reticulum,29 different defects in vesicular trafficking30, 31 and depletion of Ca2+ from the endoplasmic reticulum, for example, upon PMR1 deficiency.32, 33 In all of these cases, a high rate of Ca2+ uptake via upregulation/activation of a high-affinity Ca2+ influx system that involves Cch1p and Mid1p is triggered.34 Resultant elevated basal [Ca2+]cyt levels lead to the activation of Ca2+ signalling pathways essential for initiation of compensatory mechanisms and subsequent cell survival.34
Using quantitative PCR, we could indeed detect that after 14 h of expression, αSyn significantly amplified CCH1 mRNA levels and slightly upregulated MID1 mRNA (Figure 4d). As shown for PMR1 mRNA levels (Figure 4c), this effect faded after 24 h (Figure 4d). Given these results, we tested whether proteins involved in the calmodulin/calcineurin pathway and thus responsible for cellular Ca2+ sensing might alter αSyn-instigated cytotoxicity. Determination of ROS production demonstrated that αSyn toxicity was mostly unaffected by deletion of genes coding for the calcineurin-responsive zinc finger transcription factor Crz1p and the calmodulin-dependent kinases Cmk1p and Cmk2p, while the absence of Cnb1p, the regulatory subunit of calcineurin (and to some extent the absence of Cna2p, one of two isoforms of the catalytic subunit of calcineurin), did aggravate and expedite αSyn-induced oxidative stress (Figure 4e). Thus, an intact and functional Ca2+ signalling pathway that essentially involves calcineurin might contribute to a compensatory mechanism that partly counteracts and/or delays the toxic consequences of αSyn expression.
Next, we analysed whether the absence of proteins mediating cellular Ca2+ transport modified the αSyn-induced raise in cytosolic Ca2+ levels. Consistent with a link between αSyn-mediated toxicity and dysregulation of Ca2+-homeostasis, expression of αSyn increased basal [Ca2+]cyt in all deletion mutants except in Δpmr1 cells (Figure 5a). In line with previous studies,35 deletion of PMR1 already caused increased basal [Ca2+]cyt as visible in the baseline recordings in Figure 5b. Furthermore, the absence of Pmr1p largely inhibited αSyn-induced amplification of rapid, transient cytosolic Ca2+ peaks upon addition of 150 mM Ca2+ (Figure 5b). Although this remained mostly unaffected upon deletion of MID1, PMC1, VCX1 and YVC1, the absence of CCH1 or COD1 elevated the cellular response to external Ca2+ pulses per se and prevented further peak amplification by αSyn (Supplementary Figures S3A–F). Similar expression levels of aequorin were observed in all mutants (Figure 5c). Moreover, measurement of the transient elevation of [Ca2+]cyt following the addition of glucose to glucose-starved cells demonstrated that again αSyn provoked an increase in [Ca2+]cyt peak amplitude, which was inhibited in Δpmr1 cells (Figure 5d) but present in all other deletion mutants tested (Figure 5e). Thus, Pmr1p is crucially involved in the cellular consequences following αSyn expression, including (i) elevation of basal [Ca2+]cyt, (ii) deregulation of the rapid cellular response to sudden external glucose or high Ca2+ pulses, and (iii) accumulation of ROS and subsequent death.
The primarily Golgi-resident pump Pmr1p not only supplies Ca2+ to both the Golgi complex and the endoplasmic reticulum but also constitutes an important route to detoxify excess manganese, providing Mn2+ for protein glycosylation in the Golgi complex.36 Thus, deletion of PMR1 results in (i) depletion of endoplasmic reticulum Ca2+ stores,33 which in turn causes elevated [Ca2+]cyt via increased Ca2+ uptake, as well as in (ii) hypersensitivity to manganese.36 Defects in cellular manganese homeostasis as well as exposure to manganese have been associated with PD and PD-like syndroms in humans37, 38 and several model systems.39, 40, 41, 42, 43 Thus, we performed spotting assays on galactose plates containing high levels of manganese, demonstrating that exposure to manganese slightly aggravated αSyn-instigated cytotoxicity in concentrations that did not affect isogenic control cells (2 mM and 4 mM Mn2+ ions, respectively; Figure 6a). Upon PMR1 deletion, Mn2+ was highly toxic (Figures 6a and b).
Furthermore, we generated strains that overexpress Pmr1p alone or in combination with αSyn and subjected these strains to spotting and clonogenic survival assays on galactose plates with and without manganese. Notably, high levels of Pmr1p were per se toxic to yeast cells, and combined overexpression of Pmr1p and αSyn killed >95% of all cells (Figures 6b and c). Complementation analyses in PMR1-deficient cells demonstrated that expression of Pmr1p could (i) restore αSyn cytotoxicity and (ii) supress manganese toxicity (Figures 6b and c).
To further investigate the contribution of Ca2+versus Mn2+ transport activity of Pmr1p to the toxic consequences of αSyn expression, we additionally transfected WT and PMR1-deficient cells with two point mutants of Pmr1p that were defective for transport of either Ca2+ ions (Pmr1pD53A) or Mn2+ ions (Pmr1pQ783A).36, 44 Compared with native Pmr1p, the overexpression of these point mutants in the background of WT cells still was less toxic than that of native Pmr1p, and both mutated variants were slightly less effective in enforcing αSyn cytotoxicity as determined in spotting assays and survival plating on galactose plates with and without addition of Mn2+ (Figures 7a and b). Conducting the same experiments in PMR1-deleted cells demonstrated that native Pmr1p and Pmr1pQ783A, which displays a selective loss of Mn2+ transport, both efficiently reinstated αSyn toxicity, whereas the Pmr1pD53A variant deficient in Ca2+ transport partly lost this ability (Figures 7a and b). Native Pmr1p as well as Pmr1pD53A expectedly suppressed manganese toxicity of PMR1-deficient cells, whereas Pmr1pQ783A did not (Figures 7a and b). Expression of the Pmr1p variants and αSyn was confirmed in all strains (Figure 7c). These data indicate that the Ca2+ transport activity of Pmr1p – rather than that of Mn2+ – contributes to αSyn-induced cell killing.
To test and challenge our finding in vivo, we analysed the effects of PMR1 depletion on αSyn neurotoxicity in the nematode Caenorhabditis elegans and in the fruit fly Drosophila melanogaster. Nematodes expressing human αSyn directed by the dopamine transporter (dat-1) promoter were examined for survival of dopaminergic neurons. In WT nematodes, expression of αSyn resulted in the death of ∼40% of the dopaminergic neurons, while only ∼20% died in PMR1-deficient (pmr-1(tm1840)) animals (Figure 8a). Quantification of cytosolic Ca2+ levels in αSyn-expressing dopaminergic neurons using the Ca2+-sensitive fluorescent reporter protein GCaMP2.045 revealed that αSyn elevated the resting [Ca2+]cyt in WT nematodes but not in pmr-1(tm1840) mutants (Figure 8b). In flies, the pan-neuronal elav-GAL4-driven expression of human αSyn significantly enhanced organismal death of male and female animals upon treatment with manganese. This effect was largely revised by RNA interference (RNAi)-mediated depletion of the Drosophila homologue of PMR1 (SPoCk) (Figures 8c and d). The absence of SPoCk did not affect the expression of αSyn (Figure 8e). As αSyn is known to provoke locomotive deficits and the selective loss of tyrosine hydroxylase-positive dopaminergic neurons in Drosophila PD models,16, 46 we tested for a possible involvement of SPoCk in these neurotoxic consequences. The αSyn-induced decline in negative geotaxis (which drives flies to walk upwards after being tapped to the bottom of a vial) was prevented by depletion of SPoCk (Figure 8f). Furthermore, expression of αSyn caused a significant loss of dopaminergic neurons in defined clusters of the brain, and this effect was absent when SpoCk was depleted (Figures 8g and h). Thus, the toxic consequences of αSyn expression in yeast, nematodes and flies essentially involve the Ca2+ ATPase PMR1.
Diverse Ca2+ signals govern a myriad of vital functions, including mechanisms of fundamental neuronal biology such as synaptic transmission, plasticity, regulated neurite outgrowth and synaptogenesis as well as pivotal generic processes like proliferation, transcription, differentiation and apoptosis. In particular, the mitochondrial cell death pathway is susceptible to elevated calcium concentrations.47 Here, we establish that αSyn cytotoxicity is governed through sequentially occurring events, where the PMR1-dependent generation of a [Ca2+]cyt increase precedes a burst of oxidative radicals that ultimately triggers cell death. In fact, the cytocidal effects of αSyn are reduced by treatment of cells with Ca2+ chelators or by PMR1 deletion as well as via treatment with the generic antioxidant NAC. Thus, whether αSyn is able to trigger elevated basal cytosolic Ca2+ levels appears crucial for the subsequent cellular death. However, the transient [Ca2+]cyt peaks following high external Ca2+ or glucose pulses in αSyn-expressing cells, while remaining a good predictor of toxicity, are not fully stringent, as under specific conditions (e.g., upon deletion of COD1 or CCH1), high Ca2+ pulses were able to trigger massive transient [Ca2+]cyt peaks without αSyn expression (Figure 5 and Supplementary Figure S3). The prominent role of Ca2+ in αSyn-triggered cell death predicts that cellular Ca2+ sensing/signalling mechanisms may modulate the detrimental effects of αSyn expression. In fact, disruption of calcineurin signalling results in exacerbated toxicity, suggesting a compensatory mechanism based on the recognition of abnormal Ca2+ levels that partly counteracts the toxic consequences of αSyn. Cellular survival depends on tightly controlled Ca2+ fluxes between cellular organelles as well as across the plasma membrane. Impaired Ca2+ homeostasis and dysfunctional Ca2+ signalling are implicated in a broad variety of neurodegenerative diseases besides PD, including Alzheimer's disease, Huntington's disease, Glaucoma, Amyotrophic Lateral Sclerosis, Epilepsy and even the psychiatric disorder Schizophrenia.48 Upon Ca2+ overload, mitochondria readily sequester and accumulate Ca2+, which leads to enhanced production of ROS, and subsequently to dissipation of mitochondrial transmembrane potential, opening of the mitochondrial permeability transition pore and cellular demise.47 For αSyn-induced cell death in particular, where the lethal role of mitochondria has been clearly established,14, 49, 50, 51 the molecular axis of toxicity might therefore converge in this organelle.
Our findings establish Pmr1p as a conserved mediator of αSyn cytotoxicity in yeast, nematodes and flies and indicate a toxic role for Ca2+ in the pathology of PD. Enhancement of cytosolic calcium levels upon αSyn expression seems crucial for subsequent toxicity, a deadly road that requires PMR1.
Experiments were carried out in BY4741 (MATa his3Δ1 leu2Δ0 met15Δ0 ura3Δ0) and corresponding null mutants Δpmr1, Δpmc1, Δcch1, Δmid1, Δcod1, Δvcx1, Δyvc1, Δcnb1, Δcna1, Δcna2, Δcrz1, Δcmk1 and Δcmk2 as well as in BY4741 harbouring endogenously GFP-tagged PMR1 (Euroscarf, Frankfurt, Germany). Strains were grown on SC medium containing 0.17% yeast nitrogen base (Difco, BD Biosciences, Schwechat, Austria), 0.5% (NH4)2SO4 and 30 mg/l of all amino acids (except 80 mg/l histidine and 200 mg/l leucine), 30 mg/l adenine and 320 mg/l uracil with 2% glucose (SCD) or 2% galactose (SCG). Previously described αSyn-constructs in pESC-His (galactose promoter) or pUG23-His (methionine-repressible promoter)14 or pGGE181 (constitutive promoter)17 were deployed. To monitor cytosolic Ca2+ levels, strains were transformed with the pYX212 vector encoding cytosolic aequorin (pYX212-cytAEQ) (kind gift from E. Martegani, Department of Biotechnology and Biosciences, University of Milano-Bicocca, Milan, Italy). To construct a conditional PMR1 mutant, the promoter region of PMR1 has been replaced by a tetO promoter (which prevents gene expression upon addition of ≥10 μg/ml doxycycline) following the protocol described by Yen et al.28 Briefly, the KanMX-tetO7 cassette has been amplified using pCM325 as template and the following primers: 5′-CAT TTT GTT ACA TCA AGA CAA GAT TCT CTA TTT AAA GAA GTA CGT ACG CTG CAG GTC GAC GG-3′ (forward) and 5′-AAT TAT CTT ATC TTT TAC TTA CAC TTA AGC TTA CGT CTG TGC TGG CAT AGG CCA CTA GTG GAT CTG-3′ (reverse). The amplified cassette has been integrated into the parental strain CML476 via homologous recombination.28 To generate SOD1 and SOD2 constructs, inserts were amplified by PCR with primers 5′-ATC TGA ATT CAT GGT TCA AGC AGT CGC AG-3′ and 5′-ATC TAT CGA TGT TGG TTA GAC CAA TGA CAC C-3′ for SOD1 and 5′-ATC TGA ATT CAT GTT CGC GAA AAC AGC AGC-3′ and 5′-ATC TAT CGA TGA TCT TGC CAG CAT CGA ATC TTC-3′ for SOD2, cut with EcoRI and ClaI (Fermentas, Thermo Scientific, Vienna, Austria) and ligated into pUG35-Ura.52 To generate PMR1 and the two point mutants PMR1D53A and PMR1Q783A in pESC-Ura (Stratagene, Agilent Technologies, Vienna, Austria), previously described plasmids coding for Pmr1p or respective point mutants were used as templates36, 44 (kind gift of R. Rao, Johns Hopkins University, Baltimore, Maryland, USA). Inserts were amplified by PCR with the primers 5′-ATC TGC GGC CGC ATG AGT GAC AAT CCA TTT AAT GC-3′ and 5′-ATC TAC TAG TGT AAC ATT TGA GAA ATA CGT TGA GTC-3′, cut with NotI and SpeI (Fermentas) and ligated into pESC-Ura.
To determine survival, oxidative stress, phosphatidylserine externalization and loss of membrane integrity upon expression of αSyn, cells from overnight cultures were inoculated in SCD to OD600 0.1, grown to midlog phase and shifted to SCG for induction of αSyn expression. Clonogenic survival plating was performed as previously described.53, 54 Briefly, a CASY cell counter (Schärfe System, Reutlingen, Germany) was used to measure the cell counts and 500 cells were either plated on full-media YEPD (1% yeast extract, 2% Bacto peptone, 4% glucose; Difco) agar plates (to repress further galactose-driven expression of αSyn and/or Pmr1p and point mutants) or on selective galactose agar plates (to induce expression of αSyn and/or Pmr1p) supplemented or not with 1 mM, 2 mM or 4 mM MnCl2 as indicated. Colony-forming units were quantified after 2 days (YEPD plates) or 3 days (galactose plates) of growth using a Scanalyser Colony Counter (LemnaTec, Wuerselen, Germany). To measure the level of cellular oxidative stress, cultures were subjected to DHE staining at indicated time points, followed by quantification using a fluorescence reader or flow cytometry as previously described.55 Externalization of phosphatidylserine and loss of membrane integrity was quantified after 48 h of αSyn expression using Annexin V/propidium iodide co-staining as previously described.55 For quantifications using flow cytometry (FACSAria, BD Biosciences, Schwechat, Austria), 30 000 cells were evaluated and analysed with BD FACSDiva software. Same cells were visualized via epifluorescence microscopy on a Zeiss Axioskop microscope (Zeiss, Vienna, Austria). Notably, at least four different clones were tested after plasmid transformation to rule out clonogenic variations. For experiments with the Ca2+ chelators ethylene glycol tetraacetic acid and BAPTA-AM (Sigma, Vienna, Austria) and the antioxidant NAC (Sigma), cultures were either grown for 7 h after the shift on SCG for induction of αSyn expression and then supplemented with 2 mM ethylene glycol tetraacetic acid or 380 μM BAPTA-AM or treated with 20 mM and 30 mM NAC directly after the shift. For spotting assays, cells were grown in SCG for 24 h, adjusted to 5·106 cells/ml and spotted in fivefold serial dilutions onto glucose (expression repressed) and galactose (expression induced) agar plates supplemented or not with indicated concentrations of Mn2+.
[Ca2+]cyt were measured using yeast strains carrying the vector pYX212 encoding the bioluminescent protein aequorin under the control of a TPI promoter. For analysis of resting, basal [Ca2+]cyt and of the cellular response to high doses of external Ca2+, cells expressing αSyn under a galactose-inducible promoter (pESC-His) and equipped with pYX212-cytAEQ were inoculated in SCD to OD600 0.1, grown to midlog phase and shifted to SCG for induction of αSyn expression. At indicated time points, an equivalent of 6·106 cells was transferred into a 96 well plate and harvested by centrifugation. The pellets were resuspended in 200 μl SCG containing 4 μM coelenterazine and incubated for 1 h in the dark. To remove excess coelenterazine, the cells were washed once with fresh SCG and subsequently incubated for further 30 min. A LUMIstar Galaxy Luminometer (BMG Labtechnologies, Offenburg, Germany) was used to measure basal [Ca2+]cyt as well as the response of [Ca2+]cyt to external Ca2+ shocks. The basal luminescence was measured per well in 0.5-s intervals for 25 s, whereas for kinetic luminescence measurements the signal was recorded for 70 s. In order to investigate the kinetics of the cellular response to an external Ca2+ shock, a pump injected 40 μl of a 0.8 M CaCl2 solution into each well. During all measurements, the plate was shaken and incubated at 28 °C. The luminescence signal was normalized to the OD600 of each well and reported in relative luminescence units.
For analysis of glucose-induced transients after glucose starvation, yeast cells constitutively expressing αSyn (using the pGGE181 plasmid) transformed with pYX212-cytAEQ were grown in selective medium with 2% glucose. Cells taken from stationary-phase pre-cultures were used to inoculate a new culture. When cultures reached an OD600 of±1.2, one OD600 unit of cells was plated on concanavaline A-coated coverslips and incubated at 30 °C for 1 h. Cells were subsequently washed with 0.1 M 2-(N-morpholino) ethanesulphonic acid (MES)/Tris, pH 6.5, which is a nutrient-free buffer, and again incubated for 1 h at 30 °C with 0.1 M MES/Tris pH 6.5 supplemented with 5 μM wt coelenterazine (Promega, Mannheim, Germany). Excess of coelenterazine was removed by washing the cells three times with 0.1 M MES/Tris pH 6.5, and coverslips were mounted in a thermostated perfusion chamber (30 °C). Cells were initially perfused with 0.1 M MES/Tris pH 6.5, followed by 0.1 M MES/Tris pH 6.5 supplemented with 10 mM CaCl2. Cells were then stimulated by addition of 80 mM glucose to induce a transient elevation of cytosolic Ca2+ (TECC response) after glucose starvation.56 At the end of the experiment, cells were lysed in a Ca2+-rich hypotonic medium (10 mM CaCl2 in H2O) containing 0.5% Triton X-100. The recorded aequorin luminescence data were calibrated offline into cytosolic Ca2+ values using the following algorithm [Ca2+]cyt=((L'Lmax)1/3+[118(L'Lmax)1/3−1])/(7 × 106−[7 × 106(L'Lmax)1/3)]), where L is the luminescence intensity at any time point and Lmax is the integrated luminescence.57
Immunoblot analysis of whole-cell extracts was performed as described.53 Blots were probed with monoclonal antibodies against FLAG-epitope (Sigma), GFP (Sigma), glyceraldehyd-3-phosphate dehydrogenase (Sigma) and Aequorin (Abcam, Cambridge, UK) and the respective peroxidase-conjugated affinity-purified secondary antibodies (Sigma).
To determine mRNA levels in yeast, total RNA was extracted from respective strains using Qiagen RNeasy kit (Qiagen, Hilden, Germany) with 5·108 cells per extraction. Contaminating DNA was removed by DNase I digestion using Qiagen RNase-Free DNase Set and RNA was cleaned up according to the Qiagen RNA cleanup and concentration protocol. RNA concentrations were determined with a NanoDrop Spectrophotometer (NanoDrop Technologies, Thermo Scientific, Vienna, Austria), and 100 ng were used for detection of mRNA levels of PMR1, CCH1 and MID1 and of actin mRNA (as endogenous housekeeping gene) via reverse transcription and quantitative PCR amplification using SensiMixTM SYBR one-Step Kit (Bioline, Wiener Neudorf, Austria) and a Corbett Research RG6000 PCR machine (Qiagen). The following primers were used at a concentration of 300 nM: PMR1 primers 5′-TCCTTAGCGGTTGCTGCTAT-3′ (forward) and 5′-TCCTTAGCGGTTGCTGCTAT-3′ (reverse), CCH1 primers 5′-GCTACGGTAATGGGTTCAGC-3′ (forward) and 5′-CGCCTTTTCCTCAATGGTAA-3′ (reverse), MID1 primers 5′-CGAACGCTACCTCCACGTAT-3′ (forward) and 5′-GGCCTTACATCCCACTGAAA-3′ (reverse) and actin primers 5′-GCCTTCTACGTTTCCATCCA-3′ (forward) and 5′-GGCCAAATGATTCTCAAAA-3′ (reverse), all amplifying a length between 150 and 160 bp. Cycling conditions were 10 min at 42 °C and 10 min at 95 °C, followed by 40 cycles of 15 s at 95 °C, 15 s at 60 °C and 15 s at 72 °C. The obtained mRNA levels were normalized to the mRNA levels of the actin housekeeping gene within the same sample.
A one-way ANOVA followed by a Bonferroni post-hoc test was used to calculate P-values. For survival of Drosophila, a two-way ANOVA with time and strain as independent factors followed by a Bonferroni post-hoc test was used.
We followed standard procedures for C. elegans strain maintenance.58 Nematode-rearing temperature was kept at 20 °C, unless noted otherwise. The following strains were used in this study: N2: WT Bristol isolate (wt), pmr-1(tm1840), Ex[pdat-1GCamP2.0], pmr-1(tm1840)X;Ex[pdat-1GCamP2.0], BZ555: egIs1[pdat-1GFP], UA44: baIn11[pdat-1α-Syn, pdat-1GFP], Ex[pdat-1α-Syn, pdat-1GCamP2.0], pmr-1(tm1840)X;Ex[pdat-1α-Syn, pdat-1GCamP2.0] and pmr-1(tm1840)X;Ex[pdat-1α-Syn, pdat-1GFP]. The BZ555 and UA44 strains were generously provided by Guy Caldwell (Department of Biological Sciences, The University of Alabama).
Seven-day-old animals were used for αSyn-induced neurodegeneration quantification. The four CEP dopaminergic neurons in the worm of the head were scored as described previously.59 Experiments were repeated four times, and statistical analyses were performed using the GraphPad Prism software package (GraphPad Software, San Diego, USA). Analysis of variance (ANOVA) was used for comparisons of multiple groups of values (in both approaches of neurodegeneration analysis), followed by Bonferroni multiple-group comparison tests.
For intracellular Ca2+ monitoring experiments, transgenic animals expressing the Ca2+ reporter GCaMP2.045 in dopaminergic neurons were examined under a Zeiss AxioImager Z2 epifluorescence microscope (Zeiss, Thessaloniki, Greece). The four CEP dopaminergic neurons in the worm of the head were imaged. Only neurons of very initial stages of degeneration (based on morphological features using DIC microscopy) were used for analysis, as the expression of GCaMP2.0 ceases during later stages of neurodegeneration. The emission intensity of GCaMP2.0 was calculated by using the ImageJ software (http://rsb.info.nih.gov/ij/).
The line UAS-αSyn was obtained from the Bloomington Stock Centre (Indiana University, USA). The UAS-CG32451RNAi (SPoCk, the Drosophila homologue of PMR1) line (transformant 110379) was obtained from the Vienna Drosophila RNAi Centre (Vienna, Austria). Lines overexpressing αSyn were crossed with the RNAi line to create the following stable stocks of flies: UAS-CG32451RNAi/ UAS-CG32451RNAi; UAS-αSyn/UAS-αSyn. A chromosome III-linked elav-GAL4 enhancer trap line was used to drive expression. To determine survival upon challenge with manganese, 1–3-day-old flies (both sexes, kept separately) were incubated at 29 °C for 24 h and transferred into fresh vials with filter papers soaked with solution containing 10% sucrose and 20 mM MnCl2. Filters were kept wet at all times and numbers of dead flies were recorded at indicated time points. Each experiment was performed with 35–40 flies and repeated 12–20 times (as indicated in the respective figure legend).
To determine climbing ability upon supplementation of food with 20 mM Mn2+ ions for 24 h, eight female flies were placed into a vertical plastic tube with a diameter of 1.5 cm and gently tapped to the bottom. Flies reaching a specific mark (10 cm) within 10 sec were counted. Experiments were conducted in the dark (red light). Six trials of climbing were performed for each set of eight flies to determine the mean climbing activity per experiment, and at least six independent experiments were performed for each genotype.
Immunostaining was essentially performed as described before.60 Brains were dissected in HL3 on ice, fixed in cold 4% PBS for 20 min and washed four times for 15 min in 0.3% PBT. After 1 h in PBT with 10% NGS at RT, brains were incubated for 2 days in PBT with 5% NGS containing primary antibodies against tyrosine hydroxylase (Millipore, Schwalbach, Germany) to detect dopaminergic neurons and against Bruchpilot (BRPNc82) to visualize brain structure and then washed in PBT four times for 20 min. Subsequently, brains were incubated in PBT with 5% NGS, and the respective secondary antibodies labelled with FITC or Cy3 (Invitrogen, Darmstadt, Germany) for 1 day. Finally, brains were washed four times in PBT and transferred onto slides in Vectashield (Vector laboratories, Lörrach, Germany). Image acquisition was performed with a confocal microscope (TCS SP5, Leica Microsystems, Wetzlar, Germany) using the LCS AF software (Leica Microsystems). For immunoblot analysis, 20–30 fly heads were homogenized on ice in 50 μl 2% SDS with protease inhibitor cocktail (Roche Diagnostics, Mannheim, Germany). Equal volume of 2 × Lämmli was added, samples were incubated at 95 °C for 5 min and then kept at RT for 5 min before centrifugation for 5 min at 13 000 × g and subsequent SDS-PAGE analysis. Blots were probed with primary antibodies against α-tubulin (Abcam) and αSyn (Sigma) and respective secondary antibodies.
Supplementary Information accompanies the paper on Cell Death and Differentiation website (http://www.nature.com/cdd)
Edited by N Bazan
This work was supported by the Austrian Science Fund FWF (Grants T414-B09 and V235-B09 to SB, Grant S-9304-B05 to FM and DC-G, P23490-B12 to FM and WNR, P24381-B20 to FM and TE, LIPOTOX to FM and DR and DK-MCD to FM and LH), the European Research Council (ERC to NT), the European Commission (Apo-Sys to FM and TE), the Scientific Research Flanders (Grant G.0498.09 to GC), the University of Leuven (to JW and Grant OT/07/069 to GC), the Herculus funding (Grant HER/08/066 to GC) and the FWO-Vlaanderen and IWT-Vlaanderen (SBO-NeuroTarget to JW).
|PMR1||plasma membrane-related Ca2+-ATPase 1|
|GFP||green fluorescent protein|
|MES||2-(N-morpholino) ethanesulphonic acid|
|ROS||reactive oxygen species|
The authors declare no conflict of interest.
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Keywords: Parkinson's disease models, α-synuclein, Ca2+ homeostasis, yeast cell death, PMR1, dopaminergic neuron loss.
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