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Abstract
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the selective loss of motor neurons. Recent studies have implicated that chronic hypoxia and insufficient vascular endothelial growth factor (VEGF)-dependent neuroprotection may lead to the degeneration of motor neurons in ALS. Expression of apelin, an endogenous ligand for the G protein-coupled receptor APJ, is regulated by hypoxia. In addition, recent reports suggest that apelin protects neurons against glutamate-induced excitotoxicity. Here, we examined whether apelin is an endogenous neuroprotective factor using SOD1G93A mouse model of ALS. In mouse CNS tissues, the highest expressions of both apelin and APJ mRNAs were detected in spinal cord. APJ immunoreactivity was observed in neuronal cell bodies located in gray matter of spinal cord. Although apelin mRNA expression in the spinal cord of wild-type mice was not changed from 4 to 18 weeks age, that of SOD1G93A mice was reduced along with the paralytic phenotype. In addition, double mutant apelin-deficient and SOD1G93A displayed the disease phenotypes earlier than SOD1G93A littermates. Immunohistochemical observation revealed that the number of motor neurons was decreased and microglia were activated in the spinal cord of the double mutant mice, indicating that apelin deficiency pathologically accelerated the progression of ALS. Furthermore, we showed that apelin enhanced the protective effect of VEGF on H2O2-induced neuronal death in primary neurons. These results suggest that apelin/APJ system in the spinal cord has a neuroprotective effect against the pathogenesis of ALS.
Citation: Kasai A, Kinjo T, Ishihara R, Sakai I, Ishimaru Y, Yoshioka Y, et al. (2011) Apelin Deficiency Accelerates the Progression of Amyotrophic Lateral Sclerosis. PLoS ONE 6(8): e23968. https://doi.org/10.1371/journal.pone.0023968
Editor: Melissa Coleman, Claremont Colleges, United States of America
Received: June 3, 2011; Accepted: July 28, 2011; Published: August 24, 2011
Copyright: © 2011 Kasai et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported in part by Grant-in-Aid for Scientific Research (C) 21590110 (to S.M.) (http://www.jsps.go.jp/english/e-grants/grants.html), the Naito Foundation 2008-116 (to A.K.) (http://www.naito-f.or.jp/grant), and the Sasagawa Scientific Research Grant 21-404 from The Japan Science Society (to A.K.) (https://www.jss.or.jp/sasagawa). The funding organizations had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Amyotrophic lateral sclerosis (ALS), the most common adult-onset motor neuron disease, is caused by a selective loss of motor neurons leading to progressive paralysis of muscles and ultimately death [1]. Approximately 10% of ALS cases is familial, of which 20% are associated with dominant mutations in the gene encoding the human Cu2+/Zn2+ superoxide dismutase-1 (SOD1) [2]. Transgenic animals overexpressing mutant SOD1 develop progressive motor neuron disease that resembles the clinical and pathological features of human familial ALS [3]. Although the precise pathogenesis of ALS remains unclear, studies using these animal models have proposed several hypotheses to explain motor neuron degeneration, including glutamate-induced excitotoxicity [4] and oxidative damage [1].
Recently, chronic hypoxia and insufficient vascular endothelial growth factor (VEGF)-dependent neuroprotection has been linked to the degeneration of motor neurons in ALS. Mice with deletion of the hypoxia-response element in the VEGF promoter region (VEGFδ/δ) develop spinal hypoperfusion and adult-onset progressive motor neuron degeneration [5]. Prior to motor neuron degeneration, SOD1 mutants exhibit disruption of the blood-spinal cord barrier, endothelial damage, and hypoperfusion [6]. Furthermore, Crossbreeding SOD1G93A mutant mice with mice overexpressing VEGF in neurons produces a phenotype characterized by delayed motoneuron loss and motor impairment, and prolonged survival compared with mice carrying the SOD1G93A gene alone [7]. In addition, the cerebrospinal fluid VEGF levels are significantly increased in patients with long duration of ALS [8]. These findings suggest that chronic hypoxia have been implicated in the pathology of ALS.
The human apj gene encodes a G protein-coupled receptor (GPCR) [9]. Apelin was identified as an endogenous ligand for the orphan GPCR APJ [10]. Apelin expression is high in human spinal cord [11], and regulated by hypoxia [12], [13]. Recent studies suggest that apelin protects neurons against glutamate-induced excitotoxicity [14], [15]. Furthermore, we previously showed that the apelin/APJ system cooperates with VEGF to regulate vascular development in the retina [16]. Kidoya et al. also demonstrated that apelin in combination with VEGF induced proliferation and assembly of endothelial cells [17]. Therefore, the apelin/APJ system alone or in combination with VEGF may play a neuroprotective role in the pathogenesis of ALS. Here, to examine whether apelin is an endogenous neuroprotective factor using the SOD1G93A mouse model of ALS, we have established apelin deficient mice carrying the SOD1 mutation. In the present study, we demonstrated that the apelin receptor APJ was detected in neuronal cell bodies located in spinal cord, that apelin expression in spinal cord of SOD1G93A mice was reduced along with the paralytic phenotype, and that apelin deficiency accelerated the progression of ALS. In addition to in vivo studies using transgenic mice, our in vitro studies showed that apelin enhanced the protective effect of VEGF on oxidative stress-induced neuronal death. Our findings suggest that apelin/APJ system plays a protective role in the pathogenesis of ALS.
Results
Apelin and APJ expressions in mouse CNS tissues
We analyzed the precise distribution of apelin and APJ mRNA in mouse CNS tissues by real-time RT-PCR method. As shown in Fig. 1, the highest expression of apelin was observed in the spinal cord (4-fold higher than olfactory bulb, Fig. 1A). APJ receptor expression was also highest in the spinal cord (Fig. 1B).
Expression of apelin (A) and APJ (B) in wild type mice were examined by real-time PCR (n = 3–4). Data are expressed as arbitrary units normalized to β-actin, and represent mean ± SEM.
To identify the target cells for apelin/APJ system in spinal cord, we examined APJ expression in the spinal cord by immunohistochemical staining. In the spinal cord from wild-type mice at 14 weeks of age, APJ-positive cells were located in the ventral horn and around the central canal, which were colocalized with NeuN, a neuronal marker, -positive cells throughout the spinal cord gray matter (Fig. 2A–C). In contrast, APJ was expressed in neither glial fibrillary acidic protein (GFAP)-positive glial cells Fig. 2D–F) nor IbaI-positive microglia (data not shown) in spinal cord. In addition that the APJ-positive cells were in the large neurons of ventral horn, we addressed APJ was expressed in the choline acetyltansferase (ChAT)-positive cells by immunostaining in adjacent sections (data not shown). These data indicated that APJ was expressed in the motor neurons.
Representative pictures of ventral horn show double immunostaining for APJ and NeuN (A–C) or GFAP (D–F) in the lumbar spinal cord. Scale bar = 200 µm (upper panels), 100 µm (lower panels).
Apelin mRNA expression is downregulated in spinal cords of SOD1G93A mice
The first clinical signs of motor neuron disease in SOD1G93A mice were fine hind limb tremors. The SOD1G93A mice began to display hind limb tremors around 10 weeks, gait abnormalities around 14 weeks, and dragging of at least one hind limb around 18 weeks, whereas the control mice never showed signs of motor dysfunction (Fig. 3A). Contrasted with the progressive weight gain of the control group, body weight loss in SOD1G93A mice became evident around 10 weeks of age (Fig. 3B). Furthermore, we investigated the number of motor neuron in the lumbar spinal cord sections from 4-week-old to adult mice by ChAT immunostaining. Compared with control group, SOD1G93A mice began to show prominent depletion of anterior horn motor neurons around 14 weeks age (Fig. 3C).
(A) Motor signs (hind limb tremors) were measured with the clinical scoring system (see methods). (B) Body weight was monitored twice a week. (C) The number of ChAT-positive cell bodies was decreased at end-stage disease for SOD1G93A mice. **p<0.01 vs. wild-type mice. Data represent mean ± SEM.
We next compared the expressions of apelin and APJ mRNA in lumbar spinal cord of SOD1G93A mice with those of control mice using real-time RT-PCR. In SOD1G93A mice, apelin expression in the spinal cord was significantly decreased at the 14 and 18 weeks age (Fig. 4A). In contrast to spinal cord, apelin expression in the lung of SOD1G93A mice was similar to that of control mice at the 18 weeks age (Control: 1.00±0.11, TG: 1.00±0.12). On the other hand, there was not a significant difference in APJ expression in lumbar spinal cord of between control and SOD1G93A mice (Fig. 4B).
Temporal expression patterns of apelin (A) and APJ (B) in the lumbar spinal cord of wild-type (open column) and SOD1G93A (closed column) mice were examined by real-time RT-PCR (n = 3–6). Data are mean ± SEM. **p<0.01 vs. wild-type mice.
Apelin deficiency accelerates the progression of the disease in SOD1G93A mice
To evaluate the effects of apelin deficiency on the SOD1G93A neurodegenerative phenotype, we compared double mutant apelin-KO and SOD1G93A (KO-SOD1G93A) mice with their SOD1G93A littermates in motor performance. We previously reported that apelin-KO mice exhibited normal behavioral phenotype other than ocular abnormality [16]. We also performed the rotarod and footprint tests recording locomotion which displayed comprised motor functions and gait disturbance of mice. Consistent with our previous data [16], we could not detect the abnormality of the motor performance in apelin-KO mice with intact SOD1 (Fig. 5). On the other hand, KO-SOD1G93A mice displayed hindlimb tremors earlier than SOD1G93A littermates (Fig. 6A). In the rotarod test, SOD1G93A littermates had a learning phase showing improvement until 11 weeks of age, sustained their maximal performance level, and began to decline steadily at 14 weeks of age. In contrast to SOD1G93A littermates, KO-SOD1G93A mice had a learning phase until 9 weeks of age and subsequently performed significantly less well than SOD1G93A littermates (Fig. 6B). Moreover, we investigated the number of motor neurons in lumbar spinal cord of KO-SOD1G93A mice and SOD1G93A littermates at 14 weeks of age by ChAT immunostaining. The number of ChAT-positive neurons in KO-SOD1G93A mice was significantly decreased compared with SOD1G93A littermates (Fig. 6C).
(A) Rotarod test. The average for time spend on the rotarod across five test trials for wild-type (open circles, n = 22) and apelin-KO (closed circles, n = 22) mice. (B) Footprint analysis of wild-type (open column, n = 12) and apelin-KO (closed column, n = 14). The base of support was determined by measuring the distance between the central pads of the hind paws (DBF). The stride lengths of the hind paws (SL) were measured in two consecutive prints. Data are mean ± SEM.
(A) Motor signs (hind limb tremors) were measured as in Fig. 3B. (B) Rotarod performance of SOD1G93A littermates (open circles) and KO-SOD1G93A (closed circles) mice was measured as described in the methods for 180 s. (C) The number of motorneurons was decreased in the lumbar spinal cord of KO-SOD1 G93A mice at 14 weeks-old (n = 3). Data represent mean ± SEM. *p<0.05 vs. SOD1 G93A mice.
Microglial activation contributes to the oxidative stress and damage involved in the ALS process, and parallels the disease progression [18]. Also, the expression of mutant SOD1 in microglia contributes to the progression motor neuron degeneration [19], [20]. In fact, we detected that the microglia of SOD1G93A mice in lumber spinal cord were significantly activated at 18 weeks of age (WT: 2.64±0.22%, SOD1G93A: 6.75±2.16%). Therefore, to evaluate the disease progression, we next examined the microglia activation in lumbar spinal cord of KO-SOD1G93A mice and SOD1G93A littermates at 14 weeks of age. The Iba1+ microglial cell population in the lumbar spinal cord of KO-SOD1G93A mice was significantly increased two-fold compared with SOD1G93A littermates (Fig. 7). These data suggest that apelin deficiency promotes the disease progression of SOD1G93A mice.
Representative pictures show that Iba1-positive microglia in the lumbar spinal cord of SOD1 G93A (A) and KO-SOD1G93A (B) mice. (C) The Iba1-positive area was increased in the lumbar spinal cord of KO-SOD1G93A mice at 14 weeks-old (n = 3). Scale bar = 50 µm. *p<0.05 vs. SOD1G93A. Data represent mean ± SEM.
Neuroprotective effect of apelin on cell death induced by hydrogen peroxide in primary neurons
We next examined whether apelin protects neurons against cell death. Consistent with previous report [14], we detected the robustly expressed APJ in rat primary hippocampus neurons, not cerebral cortex neurons, by RT-PCR (Fig. 8A). The cultured hippocampal neurons were exposed to 10 µM hydrogen peroxide, which is known to induce apoptosis for 24 hours, and then cell death was measured 24 h later by 3- (4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazoilium bromide (MTT) assay. Apelin alone did not affect on cell viability in the absence of hydrogen peroxide (Fig. 8B). Moreover, Apelin alone (1–100 µM) did not protect hydrogen peroxide-induced cell death (Fig. 8C). However, 100 µM apelin co-applied with VEGF (50 ng/ml) showed significant neuroprotection (Fig. 8D).
(A) Representative picture shows the expression of APJ and apelin mRNA in primary cortical and hippocampal neuronal cultures (representatively, C and H). Culture medium was replaced with neurobasal media without B27 supplement for 24 hours. (B) Cell viability of hippocampal neuronal cultures treated with indicated concentration of apelin for 24 hours. The cultures were treated with the indicated concentration of apelin (C) or with VEGF (50 ng/ml) and apelin (indicated concentration) (D) for 15 min prior to exposure to H2O2 (10 µM) for 24 hours. Cell viability was assessed by MTT assay (n = 4). *p<0.05 vs. control. Data represent mean ± SEM.
Discussion
SOD1 mutants such as G93A lead to the blood-spinal cord barrier breakdown and subsequent reduction in blood flow through lumbar spinal cord [6], [21]. In VEGFδ/δ mice exhibiting ALS like phenotype, baseline neural blood flow was also lower than that of control mice [5]. Chronic hypoxia has been linked to motor neuronal death in ALS [1], [22]. In addition, apelin expression was upregulated by hypoxia in astrocyte (data not shown) as well as other cell types [12], [13]. Therefore, we predicted that apelin expression would be upregulated in the spinal cord of SOD1G93A mice. Unexpectedly, we found that apelin expression in spinal cord was declined along with the progression of ALS. Mutant SOD1 including G93A disrupts the RNA stabilization, possibly by altering the ribonucleoprotein complex, and downregulates VEGF expression [23]. This dysregulation is mediated through the adenylate/uridylate-rich elements (AREs) in the VEGF 3′-untranslated region (UTR), where an aberrant ribonucleoprotein complex is formed in the presence of mutant SOD1. In silico analysis, we found that the apelin 3′-UTR also have five AREs (unpublished). Accordingly, the decline of apelin expression in spinal cord may be due to the disruption of RNA stabilization by mutant SOD1.
The APJ expression was not changed in spite of a decrease in ChAT neurons in the ALS mouse spinal cord, although the APJ expressed in ChAT-positive neurons in the spinal cord. APJ is expressed in not only ChAT-positive motor neurons but also interneurons in the gray matter of the spinal cord (Fig. 2). Therefore, the reason why we could not detect the decrease of APJ expression may result from APJ abundantly expressed in other neurons such as interneurons with the exception of motor neurons. On the other words, apelin/APJ system may have not only the neuroprotective effect, as suggested here, but also other roles such as the regulation of reflex or nerve conduction. In fact, we detected that the latency to lick the hind paw of apelin-KO mice was significantly decreased that of wild-type mice using 55°C hot plate test (wild-type: 26.3±1.31 s, apelin-KO: 22.1±1.56 s).
The distribution profiles were different from each other between mRNA expression of apelin and APJ in murine brains, although the highest expressions of apelin and APJ were observed in the spinal cord (Fig. 1). One possibility is that apelin could additionally act on receptors other than APJ in both the pons/medulla and the midbrain with enrichment of white matter. Alternatively, APJ could play a role other than apelin receptors in the cerebellum with a lower expression of apelin.
Apelin which activates the PI3K/AKT signaling pathway enhances angiogenesis induced by VEGF which also has a neuroprotective effect through VEGFR-2/AKT signaling pathway [16], [17]. Therefore, we examined whether apelin significantly enhances the neuroprotective effect of VEGF (Fig. 8). Apelin expectedly had a neuroprotective effect combined with VEGF, although further study on the relation between the apelin/APJ system and VEGF signaling is required. Meanwhile, a previous report also shows that a low dose of apelin (1–5 nM) significantly protects quinolinic acid-induced neuronal apoptosis in mouse cortical neurons [15]. In this study, we could not detect the neuroprotective effect of apelin alone (1–100 µM) against hydrogen peroxide-induced neuronal death in rat hippocampal neurons, and that was unexpected. The difference of neuroprotective effect could be explained on the basis of experimental conditions used such as treatment or species difference, or high doses of apelin (1 µM). This induces not only the activation of cell survival signaling such as ERK1/2 and AKT activation [24], [25], but also AMP-activated protein kinase (AMPK) activation [26]. Therefore, we cannot deny the possibility that the neuroprotective effect of apelin could be masked by activating other signaling pathways.
Currently, existing treatment for ALS provides only marginal benefit [27]. Insulin like growth factor-1 (IGF-1) is one of the most promising factors as neurotrophic factors against ALS-related neuronal death [28]. However, intramuscular- or intrathecal administration of IGF-1 had no significant effect on disease progression of SOD1G93A mice [29], and subcutaneous IGF-1 has not shown benefit in 2-year ALS trial [30]. Furthermore, several factors, including lithium and BDNF, also delay the disease progression, but not completely protect the neuronal death in ALS [31], [32]. These results indicate that it is difficult for single factor to improve disease progression or survival of ALS. Our data that apelin enhanced the neuroprotective effect of VEGF on oxidative stress-induced neuronal death suggest a new cocktail therapy for ALS.
In conclusion, this is the first experimental study addressing the involvement of an endogenous apelin in the pathogenesis of ALS by using SOD1G93A mouse model, familial ALS model. Oxidized species of wild-type SOD1 acquired 3′-UTR binding and toxic properties of ALS-linked mutant SOD1, implying that wild-type SOD1 may be a contributor of pathogenesis in sporadic ALS [33]. Although further studies are required to determine the mechanisms of apelin/APJ system in pathogenesis of ALS, impairment of posttranscriptional processing of apelin RNA by mutant or oxidized SOD1 may block an important neuroprotective pathway and accelerates motor neuron degeneration.
Materials and Methods
Animals
Ethics Statement.
The animal experiments were performed in accordance with the guidelines of the Japanese Society for Pharmacology and were approved by the Committee for the Ethical Use of Experimental Animals at Setsunan University (approval ID: K08-13/08.04.14.2.S.017). All efforts were made to minimize animal suffering, reduce the number of animals used, and utilize alternatives to in vivo techniques.
C57BL/6 mice with targeted disruption of the apelin gene (apelin-KO) were generated as described previously [17]. Male mice expressing SOD1G93A (Jackson Laboratory #002726) was backcrossed to C57BL/6 for at least 6 generations before the start of the experimentation with the apelin-KO mice. We crossbred male SOD1G93A with female apelin+/− to assess the effect of endogenous apelin deficient on motor performance in SOD1G93A mice. Apelin gene is located in chromosome X. Hence, all analyses were performed with male littermates. Genotyping analysis was performed in accordance with the Jackson Laboratory protocols for SOD1G93A mice and as previously described for apelin gene [17]. These mice were housed in metallic breeding cages in a room with a 12 h/12 h light/dark cycle. The humidity was 55%, temperature was 23°C, and mice had free access to food and water.
Quantitative PCR to measure transcription levels
Mice were euthanized and lumbar spinal cords were removed. Total RNA extraction from lumbar spinal cord and reverse transcription of total RNAs (1 µg) were performed as described previously [34]. For gene expression analysis in cell culture, total RNA extraction from primary neurons, and reverse transcription of total RNAs (1 µg) were performed. Quantification of all gene transcripts was conducted using quantitative real-time RT-PCR with ABI Prism 7900-HT (Applied Biosystems; Foster City, CA). Real-time RT-PCR was performed using SYBR premix Ex Taq II (Takara, Ohtsu, Japan) with the use of primer pairs as previously described [34].
Immunohistochemistry
Perfusion-fixed spinal cords were embedded in paraffin, and serial transverse sections (3 µm) through the lumbar spinal cord (L2–L4) were cut. Immunostaining for APJ, NeuN, GFAP, activated microglia (IbaI), and ChAT was performed using rabbit polyclonal anti-APJ as previously described [32], mouse monoclonal anti-neuronal nuclei (1∶300, Millipore), mouse monoclonal anti-GFAP (Progen), rabbit polyclonal anti-Iba1 (WAKO), and rabbit polyclonal anti-ChAT (1∶350, Millipore). Secondary antibodies were Alexa 568-conjugated anti-rabbit IgG (Molecular Probes), biotin-labeled anti-mouse IgG (1∶200, Dako) and FITC-conjugated streptavidin (1∶200, BD Bioscience), or peroxidase-conjugated anti-rabbit IgG (Nichirei) and Immpact DAB (Vector Laboratories). Immunostained sections were photographed using a fluorescence microscope (AZ-100M, Nikon, Japan). Preimmunized rabbit immunoglobulins were used as a negative control to confirm specific staining.
For the number of motor neurons, we counted the total number of the ChAT-positive cell bodies in 8 sections of lumber spinal cord (L2–4) selected every 100 µm. For quantification of microglial activation, we measured the percentage of the area of IbaI positive cells in the gray matter of lumber spinal cord (L2–L4).
Behavioral test
Beginning at 7.5 weeks, all animals (n = 10/genotype) were weighed and evaluated for signs of motor deficit with the following 4 point scoring system twice a week (clinical score). 4 points if normal, 3 points if hind limb tremors are evident when suspended by the tail, 2 points if gait abnormalities are present, 1 point for dragging of at least one hind limb, 0 points for inability to right itself within 30 s.
For the rotarod test of evaluating the paralysis phenotype, the time for which an animal could remain on the rotating cylinder of a rotarod apparatus (Ugo Basile) at a constant speed of 12 rpm was measured. Each animal was given three tries and the longest latency to fall was recorded. 180 s was chosen as the arbitrary cut-off time. For phenotype analysis of the apelin-KO mice with intact SOD1, an accelerated rotarod was used. The apparatus has an initially speed of 2 rpm and gradually accelerated at a rate of 0.11 rpm/s. Each animal was given five trials; interval time was 30 min; 300 s was chosen as a arbitrary cut-off time.
The footprint test was used to qualitatively compare the gait of wild-type and apelin-KO mice. Footprint tests were performed at 8–12 weeks age of mice. To obtain footprints, the hind and forefeet of the mice were coated with black nontoxic paints. The animals were then allowed to walk along a 40-cm-long, 5-cm-wild runway coated with a white paper. Each mouse had three trials.
Cell culture
Primary rat hippocampal cultures were prepared from embryonic day 17 Wister rat pups as previously described [35]. Cells were plated at a density of 5×105 cells/ml on culture dish pre-coated with polyethylenimine and maintained in neurobasal media with B27 supplement (Invitrogen) at 37°C/5% CO2 air, as previously described [36]. After 8 days, the percentage of neurons was assessed by counting the Microtubule-associated protein-2 (MAP-2) positive neurons, and then we could detect more than 95% neurons in primary neuronal culture.
Assessment of cell viability
Culture medium was replaced with neurobasal media without the B27 supplement for 24 h. The cultures were treated with apelin (Peptide institute Inc.) or with VEGF (Peprotech) and apelin for 15 min prior to exposure to H2O2 for 24 h. Cell viability was determined by the colorimetric MTT assay. After exposure to H2O2, 0.5 mg/ml MTT was added and incubation carried out for an additional 1 h. Then, 100 µl of dimethyl sulfoxide was added to dissolve the formazan particles. Finally, absorbance at 570 nm was measured with a microplate reader.
Acknowledgments
We appreciate the helpful comments and proofreading of Prof. James A. Waschek at UCLA.
Author Contributions
Conceived and designed the experiments: AK SM. Performed the experiments: AK TK RI IS YI. Analyzed the data: AK YY AY. Contributed reagents/materials/analysis tools: KI YI. Wrote the paper: AK.
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