PiT-1 (encoded by SLC20A1) and PiT-2 (encoded by SLC20A2) are type-III sodium-dependent phosphate cotransporters (NaPiTs). Recently, SLC20A2 mutations have been found in patients with idiopathic basal ganglia calcification (IBGC), and were predicted to bring about an inability to transport Pi from the extracellular environment. Here we investigated the effect of low Pi loading on the human neuroblastoma SH-SY5Y and the human glioblastoma A172 cell lines. The results show a different sensitivity to low Pi loading and differential regulation of type-III NaPiTs in these cells. We also examined whether 5-aminolevulinic acid (5-ALA) inhibited low Pi loading-induced neurotoxicity in SH-SY5Y cells. Concomitant application of 5-ALA with low Pi loading markedly attenuated low Pi-induced cell death and mitochondrial dysfunction via the induction of HO-1 by p38 MAPK. The findings provide us with novel viewpoints to understand the pathophysiology of IBGC, and give a new insight into the clinical prevention and treatment of IBGC.
Inorganic phosphate (Pi) is an essential nutrient for a variety of biological functions, such as cell signaling, nucleic acid synthesis, energy metabolism, membrane function, as well as bone mineralization. Pi is required for optimal cellular growth, and homeostatic mechanisms exist to maintain extra- and intracellular Pi content within the physiologic range through the regulatory actions of sodium-dependent phosphate cotransporters (NaPiTs). There are three families of NaPiTs: type-I (the SLC17 family), type-II (the SLC34 family), and type-III (the SLC20 family)1. Among them, PiT-1 (encoded by SLC20A1) and PiT-2 (encoded by SLC20A2) are type-III NaPiTs. Type-III NaPiTs have a broad tissue distribution, suggesting they play a housekeeping role for Pi homeostasis in mammalian cells2,3,4. The contribution of Pi to the regulation of mitochondrial respiratory control and mitochondrial substrate oxidation has also been reported in previous studies5, 6. Pesta et al. suggested that Pi is an important determinant of mitochondrial adenosine 5′-triphosphate (ATP) synthesis via mitochondrial phosphorylation activity7. The enzyme responsible for ATP synthesis is associated with the Pi carrier and ADP carrier in a large protein complex called ATP synthasome. ATP synthase then combines Pi and ADP to form ATP8. Therefore, an increase in intracellular Pi content is likely to activate ATP synthesis, and conversely, a decrease in intracellular Pi content may lower ATP synthesis and subsequently lead to mitochondrial dysfunction and cell damage.
Familial idiopathic basal ganglia calcification (IBGC) is a rare genetic condition characterized by symmetric calcification in the basal ganglia and other brain regions, and a wide spectrum of neuropsychiatric symptoms9. In 2012, the first causative gene was determined to be SLC20A2, which was linked to IBGC by the identification of seven families with IBGC that had mutations in this gene10. In addition, several groups, including our own research team, have reported novel mutations in SLC20A2 11,12,13,14,15. Mutations of SLC20A2 associated with IBGC were shown or were predicted to result in an inability to transport Pi from the extracellular environment10,11,12,13,14,15. For instance, Wang et al. showed that the six mutations of SLC20A2 in IBGC patients (encoding S601W, S601L, T595M, E575M, G498R, and V42del) brought about impaired Pi uptake using 32Pi transport assays in Xenopus oocytes 10. Yamada et al. showed that in silico analysis using PolyPhen-2 of the missense mutations of SLC20A2 (encoding T115M and S637R) predicted that all were likely to be damaging to the function of SLC20A2 12. Therefore, at least, mutations in SLC20A2 lead to insufficient Pi uptake capability. These results suggest that the mutations in SLC20A2 may induce depletion of intracellular Pi.
5-Aminolevulinic acid (5-ALA), a natural amino acid, is synthesized through the condensation of glycine and succinyl-CoA by the catalytic effect of 5-ALA synthase. In the cytosol, 5-ALA is converted into coproporphyrinogen III by sequential biosynthetic pathways via several intermediates (beginning with 5-ALA, and through porphobilinogen, hydroxymethylbilane, and uroporphyrinogen III, before being finally converted to coproporphyrinogen III). Coproporphyrinogen III is transported to the mitochondria and it undergoes further biosynthesis, being converted to protoporphyrin IX via the intermediate, protoporphyrinogen IX. Iron is inserted into protoporphyrin IX via a ferrochelatase-catalyzed reaction to eventually generate heme16,17,18. Heme oxygenase-1 (HO-1) is a key enzyme for heme metabolism. HO-1 metabolizes excess heme, which can cause cell toxicity, and protects cells from oxidative stress19. Recent studies have reported that 5-ALA induces the upregulation of HO-116,17,18. In addition, 5-ALA has been implicated in the treatment of inflammatory disease, autoimmune disease and transplantation due to the anti-inflammatory and immunoregulatory actions that are associated with the expression of HO-1 via mitogen-activated protein kinase (MAPK) activation16,17,18.
Recently, we have detected type-III NaPiTs immunopositivity in neurons, astrocytes, and vascular endothelial cells20, 21. The results suggest that Pi homeostasis may be controlled by different mechanisms underlying activation of PiT-1 and PiT-2 in each cell type, and also, that the degree of cellular dysfunction and/or cytotoxicity is different even in the CNS cells in which both PiT-1 and PiT-2 are expressed20, 21. In addition, mutations of SLC20A2 associated with IBGC were predicted to induce depletion of intracellular Pi10,11,12,13,14,15. However, the role of type-III NaPiTs in CNS cells is still unclear. Here, we investigated the effect of low Pi loading on the human neuroblastoma cell line SH-SY5Y and the human glioblastoma cell line A172. In addition, we examined whether 5-ALA inhibited low Pi loading-induced neurotoxicity via the induction of HO-1 by MAPK activation in SH-SY5Y cells.
Effects of low Pi loading on cytotoxicity
At 24 h after low Pi loading, SH-SY5Y cells treated with 0 mM Pi exhibited cell death, but those treated with 0.5 and 1 mM Pi did not (Fig. 1A left lane). On the other hand, A172 cells treated with 0, 0.5 and 1 mM Pi did not exhibit cell death at 24 h after low Pi loading (Fig. 1A right lane). Treatment with 0 mM Pi for 48 h completely caused cell death in SH-SY5Y cells (Fig. 1B). Long-term treatment with 0.5 mM Pi (for 24, 48, and 72 h) increased death of SH-SY5Y cells in a time-dependent manner (Fig. 1B). However, in A172 cells, significant cell death was observed only at 72 h after 0 mM Pi loading, and no other low Pi loading treatment-induced cell death during our experimental period (Fig. 1C).
Effects of low Pi loading on mRNA expression of type-III NaPiTs
Previous studies have shown that changes in extracellular Pi content modified the expression of NaPiTs mRNA including that of SLC20A1 and SLC20A2 2, 22, 23. Therefore, we postulated that low Pi loading could change mRNA expressions of SLC20A1 and SLC20A2 in neurons and glial cells, and we determined which NaPiTs are expressed in SH-SY5Y and A172 cells (Fig. 2A). Reverse transcription polymerase chain reaction (RT-PCR) analysis showed that SLC20A1 and SLC20A2 mRNAs were clearly expressed in both SH-SY5Y and A172 cells. The mRNA of other NaPiTs including SLC17A1, SLC17A3, SLC34A1, SLC34A2, and SLC34A3 was barely detected in these cells in our experimental conditions (Fig. 2A). Quantitative RT-PCR (qRT-PCR) analysis showed that the expression level of SLC20A1 mRNA was higher than the expression level of SLC20A2 mRNA in both SH-SY5Y and A172 cells (Fig. 2B). In addition, phosphonoformic acid (PFA), an inhibitor of PiT-1 and PiT-2, induced cell death in a concentration-dependent manner, suggesting that PiT-1 and PiT-2 play a functional role in cell viability in SH-SY5Y and A172 cells (Fig. 2C).
In SH-SY5Y cells, mRNA expressions of SLC20A1 and SLC20A2 were not affected by low Pi loading for 24 h (Fig. 2D). On the other hand, SLC20A1 mRNA expression in A172 cells was significantly increased by treatment with 0 mM Pi for 24 h, although SLC20A2 mRNA expression did not change (Fig. 2E). To confirm the compensatory role of PiT-1 and PiT-2, we also performed a knockdown experiment using siRNA against SLC20A1 and SLC20A2 in SH-SY5Y cells and A172 cells. We found that in SH-SY5Y cells, SLC20A1 mRNA expression was not changed by the suppression of SLC20A2 expression, compared with non-targeted siRNA controls (NC) (Fig. 2F). In A172 cells, SLC20A1 mRNA expression was significantly elevated in SLC20A2-suppressed cells (Fig. 2G). On the other hand, SLC20A2 mRNA expression was not changed by the suppression of SLC20A1 mRNA expression in either SH-SY5Y cells or A172 cells (Fig. 2F and G).
In SH-SY5Y cells, Pi uptake was significantly decreased by the suppression of either SLC20A1 or SLC20A2 expression, compared with NC (Fig. 2H). However, although Pi uptake was significantly decreased by the suppression of SLC20A1 expression in A172 cells, Pi uptake was significantly increased by the suppression of SLC20A2 expression (Fig. 2I).
Effects of 5-ALA on cytotoxicity induced by low Pi loading
In order to examine whether 5-ALA could inhibit low Pi-induced cell death in SH-SY5Y cells, we performed a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay. Concomitant application of 5-ALA (25–75 µM) with low Pi loading markedly attenuated low Pi-induced cell death (Fig. 3A). Similarly, treatment with 50 µM 5-ALA significantly attenuated PFA-induced cell death (Fig. 3B).
We also examined the involvement of mRNA expressions of SLC20A1 and SLC20A2 in 5-ALA-induced neuronal protection. 5-ALA had no effect on mRNA expressions of SLC20A1 and SLC20A2 (Supplementary Fig. S1).
Effects of 5-ALA on mitochondrial dysfunction and oxidative stress induced by low Pi loading
The contribution of Pi to the regulation of mitochondrial respiratory control and mitochondrial substrate oxidation has been reported previously5, 6. An earlier study showed that mitochondrial dysfunction caused by high Pi levels induced the production of reactive oxygen species (ROS) in bovine aortic smooth muscle cells24. Thus, we examined whether low Pi levels could affect the regulation of the mitochondrial membrane potential (MP) and the production of ROS. Representative images show that the ratio of mitochondrial JC-1 aggregates (red) to cytosolic JC-1 monomers (green) was reduced 24 h after low Pi loading, compared with the control condition (Fig. 4A and B). In addition, low Pi loading reduced ATP synthesis (Fig. 4C). To investigate whether low Pi loading could increase ROS production in SH-SY5Y cells, all control and treatment groups were examined using the CellROX dye, where changes in fluorescence intensity act as an indicator of ROS production. As shown in Fig. 4D and E, low Pi loading significantly enhanced ROS production. As the main source of cellular ROS production is mitochondrial dysfunction, we further measured mitochondrial O2 − using the MitoSOX dye. Low Pi loading significantly increased MitoSOX fluorescence intensity (Fig. 4F and G).
We also investigated whether 5-ALA could prevent mitochondrial dysfunction and ROS production caused by low Pi loading. 5-ALA improved the reduction in the red/green fluorescence intensity ratio of JC-1 after low Pi loading (Fig. 4A and B) and recovered ATP synthesis (Fig. 4C). Moreover, 5-ALA significantly decreased the low Pi loading-induced enhancement of mitochondrial O2 − levels, and the subsequent heightened oxidative stress was significantly alleviated (Fig. 4D–G).
5-ALA increases HO-1 up-regulation via p38 MAPK
We examined the involvement of MAPK cascades leading to the activation of ERK and p38, as 5-ALA has been shown to activate ERK and p3816. As shown in Fig. 5A–C, treatment with 5-ALA for 1 h activated ERK and p38. Concomitant application of SB203580 (SB), a p38 inhibitor, with low Pi loading for 48 h attenuated the protective effect of 5-ALA on low Pi loading-induced cell death in SH-SY5Y cells (Fig. 5D). On the other hand, concomitant application of PD98059 (PD), an ERK inhibitor, did not have an effect (Fig. 5D).
In a previous study 5-ALA was shown to induce activation of nuclear factor erythroid 2-related factor 2 (Nrf2) via MAPK16. Nrf2 induces the expression of antioxidant and phase II enzymes by binding to the antioxidant response element (ARE) region of the gene promoter. To examine whether the actions of 5-ALA contribute to the Nrf2 antioxidant pathway, we carried out an ARE reporter assay (Fig. 6A). 5-ALA induced luciferase activity, suggesting that it contributes to the Nrf2 antioxidant response pathway. Nrf2 regulates the expression of antioxidative and phase II detoxifying enzymes including HO-1, NAD(P)H:quinone oxidoreductase 1 (NQO1), γ-glutamyl cysteine synthetase modifier subunit (GCLM), and γ-glutamyl cysteine synthetase catalytic subunit (GCLC). qRT-PCR analysis showed that HO-1 mRNA was increased at 12 h by 5-ALA (Fig. 6B). However, other enzymes were not affected (Fig. 6C–E). Western blot analysis also demonstrated that levels of the HO-1 protein were increased at 24 h after 5-ALA treatment (Fig. 6F). Moreover, concomitant application of SB with low Pi loading attenuated 5-ALA-induced HO-1 expression (Fig. 6G).
We have found that SH-SY5Y cells are more vulnerable upon exposure to low Pi levels compared with A172 cells. In SH-SY5Y cells, mRNA expressions of SLC20A1 and SLC20A2 were not affected by low Pi loading. Similarly, expressions of these mRNA were not affected by siRNA transfection of SLC20A2 or SLC20A1. In A172 cells, SLC20A1 expression was significantly elevated both in low Pi loading and in the suppression of SLC20A2. On the other hand, SLC20A2 expression did not change in low Pi loading-treated cells or in response to the suppression of SLC20A1. In SH-SY5Y cells, Pi uptake was significantly decreased by the suppression of either SLC20A1 or SLC20A2. In A172 cells, Pi uptake was significantly elevated by the suppression of SLC20A2. In contrast, Pi uptake was significantly decreased by the suppression of SLC20A1. These results suggest that A172 cells have a mechanism to maintain intracellular Pi content in the physiologic range mainly through regulation by PiT-1, and that the difference in the mechanism between SH-SY5Y cells and A172 cells underlies the differential vulnerability to low Pi.
A previous study that used northern blot analysis showed a time-dependent increase in the expression of PiT-1 in response to BMP-2 in MC3T3-E1 cells, an osteogenic cell line, although the expression level of PiT-2 was not affected by BMP-225. Similar findings have been demonstrated in ATDC5 chondrogenic cells, or other osteogenic cell lines, stimulated with TGF-β26. Another previous study showed that PiT-2 could mediate Pi uptake and calcification of cultured human vascular smooth muscle cells (VSMCs) in the absence of PiT-1, and that PiT-1 and PiT-2 could serve redundant roles in Pi-induced calcification of VSMCs27. In the present study, SLC20A1 mRNA expression was significantly elevated in SLC20A2-suppressed A172 cells, while SLC20A1 mRNA expression was not changed in SLC20A2-suppressed SH-SY5Y cells. These results indicate that Pi homeostasis may be controlled by different mechanisms with respect to the activation of PiT-1 and PiT-2, depending on the cell type, and that the degree of cellular dysfunction and/or cytotoxicity is also different even in CNS cells which express both PiT-1 and PiT-2.
Pi is one of the substrates for ATP synthesis and also plays an important role in regulating mitochondrial MP and ROS production in isolated mitochondria28. Therefore, the disruption of intracellular Pi homeostasis causes mitochondrial dysfunction and increased oxidative stress. Indeed, in the present study, low Pi loading lowered the mitochondrial MP and increased oxidative stress. Therefore, we investigated the effects of 5-ALA, which is thought to activate mitochondrial functioning in response to low Pi-induced cytotoxicity29. In the present study, 5-ALA prevented mitochondrial dysfunction and ROS production caused by low Pi loading and had no effect on mRNA expressions of SLC20A1 and SLC20A2. Therefore, NaPiTs expression may not be involved in the protective effects of 5-ALA against low Pi. Our study also showed that 5-ALA suppressed cytotoxicity associated with low Pi loading via p38 MAPK. 5-ALA is the starting point for heme synthesis in mitochondria, and 5-ALA synthase is the rate-limiting enzyme for the production of heme. These results suggest that 5-ALA may have helped to recover mitochondrial activity in our experiment, although much research has been carried out on the detailed actions of 5-ALA in the mitochondria with respect to cellular mechanisms16,17,18.
A previous study demonstrated that 5-ALA induced expression of HO-116. In mammals, HO is present in at least two isozymes, that is, an inducible type (HO-1) and a constitutive type (HO-2). HO-1 is induced by a number of stimuli such as heme, nitric oxide, heavy metals, growth factors, cytokines, modified lipids, among others19. HO-1 is a rate-limiting enzyme for the degradation of heme into biliverdin, carbon monoxide (CO), and free iron30, 31. HO-1 and its reaction products protect against various injuries32. HO-1 knockdown in mice results in substantially increased susceptibility to numerous toxic chemical and disease conditions associated with oxidative pathology31. In contrast, enhancing HO-1 activity by genetic tools or certain antioxidants has beneficial effects on cell survival. Our study demonstrated that HO-1 protein was increased by 5-ALA via p-38 MAPK. These results suggest that HO-1 was involved in the protective effect of 5-ALA against low Pi loading.
In IBGC, SLC20A2 mutation is believed to reduce intracellular Pi uptake and disrupt intracellular Pi homeostasis. Low levels of intracellular Pi affect various functions such as the production of ATP, intracellular signaling and mitochondrial function. Patients with IBGC show various clinical manifestations, including psychological disorders and mental deterioration. This indicates that intracellular dysfunction such as oxidative stress occurs in the neurons vulnerable to low Pi levels in the brain. In autopsy findings, calcification is rarely seen within neurons33, and neuronal cell damage does not seem to be associated with calcification. From our investigation, mitochondrial dysfunction in neurons is thought to represent a crucial pathophysiological pathway in the progression of neuronal damage in patients with IBGC, although the morphological and functional abnormalities associated with this have not yet been clarified. From this viewpoint, mitochondrial dysfunction may be a therapeutic target in IBGC and 5-ALA considered a novel therapeutic candidate for neuronal protection, but not for the prevention of calcification, in IBGC.
In conclusion, our results suggest that neuronal and glial cells may exhibit different sensitivity to low Pi loading and different regulation between PiT-1 and PiT-2. These findings provide us with novel viewpoints to understand the pathophysiology in neurons and astrocytes in cases of IBGC. In addition, the activation of mitochondrial functioning may provide a new avenue with respect to clinical improvement in patients with IBGC, especially with SLC20A2 mutation.
Cell culture and low Pi loading experiment
The human neuroblastoma cell line SH-SY5Y and the human glioblastoma cell line A172 were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% (v/v) fetal bovine serum (FBS) and kept at 37 °C in humidified 5% CO2/95% air. For the low Pi experiment, these cells were seeded on a 96-well plate and cultured in DMEM containing 10% FBS for 24 h. Subsequently, the medium (DMEM containing 10% FBS) was replaced with FBS-free/Pi-free DMEM (Thermo Fisher Scientific) and appropriate amounts of sodium phosphate buffer (0.1 M Na2HPO4/NaH2PO4, pH 7.4) were immediately added to produce final Pi concentrations of 0, 0.5, and 1 mM, as indicated in the figure legends. Treatment with 1 mM Pi with FBS-free DMEM was used as a control in this study.
For cytotoxicity assays, the LIVE/DEAD Cell Imaging Kit (Thermo Fisher Scientific) and Cell Count Reagent SF (Nacalai Tesque) were used, in accordance with the manufacturer’s instructions. Briefly, reagent was added to wells and the plate was incubated at 37 °C for 4 h. The optical density of formazan was detected at 450 nm by the GloMax-Multi Detection system (Promega) to calculate cell viability. A wavelength of 600 nm was used as a reference.
For the SLC20A1 and SLC20A2 knockdown experiments, SH-SY5Y cells and A172 cells were transfected with a siGENOME pool targeted against human SLC20A1 (SLC20A1-siRNA; L-007432-01, Dharmacon Research), SLC20A2 (SLC20A2-siRNA; L-007433-02, Dharmacon Research) or siCONTROL non-targeting siRNA (NC, Dharmacon Research), using Lipofectamine RNAiMAX reagent (Life Technologies Japan), and incubated for 24 h in accordance with the manufacturer’s instructions (Thermo Fisher Scientific).
Determination of mitochondrial membrane potential (JC-1 Staining) by fluorescence microscopy
5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolylcarbocyanine iodide (JC-1; Thermo Fisher Scientific) is a cationic dye that exhibits potential-dependent accumulation in mitochondria, indicated by a fluorescence emission shift from green (~525 nm) to red (~590 nm). Consequently, mitochondrial depolarization is indicated by an increase in the green/red fluorescence intensity ratio and can be quantified using fluorescence microscopy. Briefly, SH-SY5Y cells were incubated in a medium containing JC-1 at a final concentration of 50 µg/mL for 30 min at 37 °C, and were washed with PBS in accordance with the manufacturer’s instructions (Thermo Fisher Scientific). Samples were observed using a fluorescence microscopy system (Zeiss LSM 700, Carl Zeiss). The stock solution of JC-1 was dissolved in 100% DMSO, and the final concentration of DMSO used was <0.1%.
Intracellular ATP was measured using a luciferin–luciferase bioluminescence assay and the ‘Cell’ ATP assay reagent (Toyo Ink), in accordance with the manufacturer’s instructions. The SH-SY5Y cells were seeded on a 96-well tissue culture plate, and incubated in a CO2 incubator at 37 °C. The plate was incubated at room temperature for 30 min, and 100 µL ATP reagent was then added to each well. The plate was stirred for 1 min followed by incubation in a luminometer (GloMax-Multi Detection system, Promega) for 10 min at 25 °C. The relative light intensity was then measured.
Cell culture and ROS production
To detect low Pi loading-induced intracellular ROS production, we used the redox-sensitive dyes, CellROX Green (Thermo Fisher Scientific) and MitoSOX Red (Thermo Fisher Scientific). After SH-SY5Y cells were prepared in uncoated glass-bottomed microwells, CellROX Green and MitoSOX Red were added to the cell culture to give a final concentration of 5 μM and the cells were incubated for 30 min at 37 °C, in accordance with the manufacturer’s instructions (Thermo Fisher Scientific). Samples were observed using a confocal imaging system (Zeiss LSM 700, Carl Zeiss).
The treated cells were lysed by adding lysis buffer (150 mM NaCl, 10 mM Tris–HCl, 1% NP-40, 1 mM EDTA, 10 µg/mL aprotinin, 10 µg/mL leupeptin, 1% phosphatase inhibitor, 0.1 mM PMSF) and centrifuged under the conditions of 14,000 g at 4 °C for 30 min. The supernatant was collected as protein samples. The concentration of protein was determined using the Pierce BCA protein assay kit (Thermo Fisher Scientific). Samples underwent SDS-PAGE in order to separate proteins on the basis of molecular weight. SDS-PAGE was performed under constant voltage at 200 V at room temperature for 60 min. The separated proteins in polyacrylamide gel were transferred to a PVDF membrane in transfer buffer (0.3% Tris, 1.44% glycine, 20% methanol) under constant voltage at 100 V at 4 °C for 60 min. The transferred membrane was incubated in 5% skim milk (Nakarai Tesque) or 5% BSA (Wako) at room temperature for 60 min. After a blocking reaction, the membrane was incubated with primary antibodies: the mouse monoclonal antibody, β-actin (1:1000, Santa Cruz Biotechnology); rabbit polyclonal antibodies: HO-1 (1:1000, Enzo Life Sciences), p44/42 MAPK (1:1000, Cell Signaling Technology), phospho-p44/42 MAPK (1:1000, Cell Signaling Technology), p38 MAPK (1:1000, Cell Signaling Technology), and phospho-p38 MAPK (1:1000, Cell Signaling Technology), dissolved in 5% skim milk or 5% BSA at 4 °C overnight. After the primary antibody reaction, the membrane was incubated with the secondary antibody: goat anti-rabbit antibody conjugated with HRP (1:2000, Santa Cruz Biotechnology), and goat anti-mouse antibody conjugated with HRP (1:2000, Santa Cruz Biotechnology) dissolved in 3% skim milk or 3% BSA for 30 min. The membrane was incubated in ECL Prime (GE Healthcare, Buckinghamshire, UK) to generate the chemiluminescence from HRP antibodies. The chemiluminescence was detected using the LAS3000 Mini (Fujifilm). The band density was measured by ImageJ software.
RNA preparation and qRT-PCR
Reverse transcription was performed using the SuperScript® VILO cDNA Synthesis Kit (Invitrogen). The cDNA samples were used as templates for RT-PCR and qRT-PCR. The sequences of primer sets for RT-PCR are shown in Table 1. qRT-PCR was performed using the TaqMan probes (SLC20A1, Hs00965587; SLC20A2, Hs00198840; ribosome 18 RNA; Life Technologies) and gene-specific primers for SYBR Green on a StepOne Real-Time PCR System, in accordance with the manufacturer’s instructions (Life Technologies). The sequences of primer sets are shown in Table 2. The expression levels of mRNA were normalized to the expression levels of ribosome 18 RNA and GAPDH mRNA.
A cell suspension with Opti-MEM (Invitrogen) at the concentration of 5.0 × 105 cells/mL was co-transfected with pGL4.37[luc2/ARE/Hygro] (Promega) and pAcGFP-C1 (Clontech) vectors by using the NEPA21 Super Electroporator (Nepa Gene). The transfected cells were seeded on multi-well plates of 24 wells. The medium was replaced with 1 mM Pi medium, and transfected cells were treated with 5-ALA for 30, 60, 180, and 360 min. Treated cells were lysed by adding 1× Passive Lysis Buffer (Promega) and incubated for 15 min at 4 °C. The supernatant was collected. Twenty µL of supernatant was used in the luciferase assay and 50 μL of supernatant was used to measure GFP fluorescence. For the luciferase assay, luciferin reagent (0.5 mM luciferin, 20 mM tricine, 1.1 mM MgCO2, 2.7 mM MgSO4, 33.3 mM DTT, 0.2 mg/mL coenzyme A, 0.53 mM ATP, 0.1 mM EDTA) was added to 100 μL of supernatant and samples were incubated for 10 min. The level of luminescence and GFP fluorescence was measured using the GloMax-Multi Detection system. Luciferase activity was normalized using GFP fluorescence levels.
32Pi transport assays
A Pi uptake assay was carried out on SLC20A1- and SLC20A2-suppressed cells grown to confluency in 24-well plastic plates as previously described34. The transport rate was expressed as nmol Pi per minute per mg protein.
Data are given as the mean ± standard error of the mean (SEM). The significance of differences was determined by an analysis of variance (ANOVA). Further statistical analysis for post-hoc comparisons was performed using the Bonferroni/Dunn test (SigmaPlot 11, Systat Software).
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This work was supported by a grant from Gifu Pharmaceutical University and grants from JSPS KAKENHI Grant Number 17H04198 (IH).
The authors declare that they have no competing interests.
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