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PET imaging studies show enhanced expression of mGluR5 and inflammatory response during progressive degeneration in ALS mouse model expressing SOD1-G93A gene
Journal of Neuroinflammation volume 12, Article number: 217 (2015)
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative motor neuron disorder. Genetic studies have linked mutation of the gene SOD1 to ALS pathology as well as several other pathological processes including modulation of glutamatergic function and inflammatory processes. Since therapeutic approaches for ALS are focused on glutamatergic function, we investigated modulation of glutamate transport based on its receptor function as well as excitotoxicity-induced inflammatory response.
In vivo positron emission tomography (PET) imaging studies of metabotropic glutamate receptor subtype 5 (mGluR5) using [18F]FPEB ([18F]3-fluoro-5-(2-pyridylethynyl)benzonitrile) and inflammatory response using [11C]PBR28 (peripheral benzodiazepine receptor ligand 28) were done in an early and a late phase of neurodegeneration in four ALS mice expressing SOD1-G93A gene and four control base mice (C57/BL6). Accumulation of [18F]FPEB and [11C]PBR28 were quantitated in several brain areas and spinal cord to determine degeneration-induced modulation. The studies were completed with immunohistochemical analyses of mGluR5 and inflammatory response.
These studies showed enhanced binding potential of [18F]FPEB in several brain areas including striatum, hippocampus, and frontal cortex. In the whole brain, the binding potential increased 49 ± 9 % from base mice to ALS-type mice and further enhanced 23 ± 4 % during disease progression. Also, in the spinal cord 6–22 %, enhanced accumulation of [18F]FPEB was observed during progression of the disease. The accumulation of [11C]PBR28 increased by 110 ± 33 % in the whole brain during progression of the disease indicating significant inflammatory process. [11C]PBR28 accumulation enhanced 89–264 % in the spinal cord and 204 % in the lungs. The end point immunohistochemical analyses verified the enhanced mGluR5 expression and inflammation.
These results confirm the role of glutamate and inflammation in ALS-type pathology. These data also support the hypothesis that excessive glutamate may contribute to inflammation in the chronic neurodegenerative processes in ALS.
Amyotrophic lateral sclerosis (ALS) is a devastating neuromuscular disorder without known cause or curative treatment. The pathological processes linked to ALS are formation of intraneuronal aggregates of neurofilament ; microglia mediated neurotoxicity as a result of enhanced inflammatory response [2–5]; glutamatergic neurotoxicity as a result of deficit in glutamate transporter or receptor function [6–11]; and mitochondrial dysfunction as a result of failure in oxidative metabolism [12, 13] and superoxide dismutase-1 (SOD1) mediated neurotoxicity, which is associated to gene mutation and found in familiar form of ALS [14, 15]. Altogether, ALS is a multimodal disorder and it is not yet known what mechanism ignites the fast progression of the disease.
For the treatment of ALS, the Food and Drug Administration has approved one drug, riluzole, which inhibits glutamate release. Another drug, ceftriaxole, which belongs to penicillin family, increases glutamate transport and is used in clinical trials [16, 17]. Thus, glutamate-related research is an essential part for development of diagnosis and treatment of ALS. It has been shown that ALS patients have enhanced glutamate levels in serum and spinal cord. Extracellular glutamate can induce neurotoxicity by either increasing neuronal sodium and chloride influx during depolarization or increasing calcium influx. Increased calcium influx may lead to activation of several calcium-dependent enzymes with end point damage in DNA and mitochondrial dysfunction [1, 7]. It is noticeable that neurotransmitter glutamate does not cross blood-brain barrier but its function can be investigated based on its receptors.
Metabotropic glutamate receptors (mGluRs) have various physiological functions in the central nervous system by affecting on several intracellular signal transduction mechanisms through G-protein [18, 19]. A large amount of pharmacological agents acting on metabotropic glutamate receptors have appeared in literature. Starting from 1996 , several non-competitive negative, positive, and neutral allosteric modulators have been developed as mGluR ligands [21, 22]. These ligands modulate mGlu receptor activity by binding to allosteric binding sites that are located in the seven strand transmembrane domains. The allosteric binding site is structurally distinct from the classical agonist or antagonist orthosteric binding site .
The glial cells that usually support and nourish neighboring neurons in the nervous system can become overactive in certain conditions. If glia becomes too activated, it can damage the tissue. When glutamate is taken up into glial cell by excitatory amino acid transporters, it is not reused directly but converted to glutamine and stored in vesicles. Subsequently, these vesicles are released from glial cells, and glutamine is transported back into presynaptic neuron and converted back to glutamate . Excitotoxicity, which is mediated by the excessive activation of glutamate receptors, has been implicated in the pathogenesis of ALS. Aronica et al.  demonstrated with immunocytochemical analyses that mGluR5 expression was high in neuronal cell throughout the human spinal cord with the highest expression in ventral horn neurons. Regional differences in immunoreactivity were observed in ALS compared to control studies. Especially, mGluR5 expression was increased in reactive glial cell in both gray (ventral horn) and white matter of ALS spinal cord . Upregulation of mGluRs in reactive astrocytes may represent a critical mechanism for modulation of glial function and changes in glial-neuronal communication in chronic neurodegeneration . Activated microglial cells can play a major role in the neuronal loss after a lesion or an insult, such as neurotoxin exposure . There is increasing evidence that inflammation accompanies the death of motor neurons in ALS .
We have developed several allosteric modulators to image metabotropic glutamate subtype receptors 5 (mGluR5s) [27–29] and characterized their in vivo dynamic biodistribution and functional binding properties in different experimental animal models including ALS mouse model using in vivo microPET imaging studies [30–32]. Here, we report preliminary positron emission tomography (PET)/computerized tomography (CT) imaging studies of modulation of mGluR5 expression and CNS inflammation during progressive degeneration in ALS mouse model carrying SOD1-G93A gene.
In vivo PET imaging studies
All animal studies were approved by the subcommittee on research animals of the Massachusetts General Hospital and Harvard Medical School and carried out by the guidance of the National Institute of Health Guide for the Care and Use of Laboratory Animals.
In vivo PET imaging studies were conducted in four base mice (C57/BL6) and four transgenic mouse model of ALS expressing human gene, SOD1-G93A (superoxide dismutase 1-glycine 93S mutation), to investigate synaptic glutamatergic function and inflammatory response during progression of the disease. The used PET imaging ligand for mGluR5, [18F]FPEB ([18F]3-fluoro-5-(2-pyridylethynyl)benzonitrile)  is developed by our team and it is presently in a routine production. Imaging of inflammatory response was done using [11C]PBR28 (peripheral benzodiazepine receptor ligand 28), an imaging ligand for translocator protein 18kDA (TSPO) which is a biomarker for inflammation and activated microglia.
For imaging studies, animals were anesthetized with isoflurane/nitrous oxide/oxygen (1–1.5 % isoflurane at 1 l/min flow) and placed on the imaging table. Catheterization of tail vein was done for the administration of the radiolabeled ligands. The animal head was secured in a plexiglass custom-made head holder equipped with ear and mouth bars designed to ensure reproducible head positioning. Level of anesthesia and vital signs was monitored throughout the imaging procedures using the physiological monitoring system included to the imaging device (Triumph II, Trifoil Imaging, Inc).
After the animal was adjusted into the imaging position, a computerized tomography (CT) imaging was done before administration of the radioactivity to obtain high-resolution anatomical information and data for attenuation correction. Radiolabeled ligand, [18F]FPEB or [11C]PBR28, (0.1–0.2 mCi, specific activity of 1900 mCi/μmol for [18F]FPEB or 0.2–0.3 mCi of [11C]PBR28) was injected into the tail vein. The radioactivity was diluted into the saline in portion 1 to 10 before the injection to decrease the ethanol concentration that was 10 % after the production of the ligand. Dynamic volumetric imaging data were acquired for 60 min after the administration of the radiolabeled ligand. Imaging data were corrected for uniformity, sensitivity, scatter, attenuation, decay, and acquisition time. PET images were reconstructed using a volumetric maximum likelihood estimation method (three-dimensional maximum likelihood estimation method) with 30 iterations (the software provided by the manufacturer of the scanner). The regions of interest including striatum, frontal cortex, hippocampus, cerebellum, whole brain area, and several areas in spinal cord were drawn on all coronal and axial levels, visualized in the fused PET-CT images. Activity per unit volume, percent activity of injected dose, and the ligand concentration were calculated.
Studies of mGluR5 expression with [18F]FPEB were done at first and followed by studies of inflammation with [11C]PBR 2 days later. To follow the progressive degeneration, the PET imaging studies were repeated 2 weeks later. The experimental studies of neurodegeneration were completed with immunohistological studies (IHS) including expression of mGluR5 and inflammation with IBA1.
Kinetic analysis of [18F]FPEB data obtained from brain was done using the Pmod software package (Pmod Technologies, Zurich, Switzerland) to determine regional values for binding potential [29, 33, 34]. Since rodent cerebellum does not express mGlu5 receptors or the expression is minimal, the input function can be processed from the data obtained from cerebellum in calculating regional maps for binding potential [27, 29]. Concerning [11C]PBR28, cerebellum cannot be used as a reference area, since inflammation is not brain area specific. For that reason, the accumulation of [11C]PBR28 was expressed as percent of the injected dose per cm3 (%id/cm3).
Scoring of the progressive degeneration was determined according to the following criteria: if the hind legs were fully extended away from lateral midline when mouse was suspended by its tail and the mouse could hold this for 2 s when suspended 2–3 times the score was 1 and if two toes curled under at least twice during walking of 12 in. or any part of foot was dragging along cage bottom/table the score was 3. The scoring model was modified from the behavioral model of Knippenberg et al.  in ALS mice.
Statistical analyses between the control and ALS mice as well as during progressive degeneration were done using Student’s t test.
The mice were anesthetized with sodium pentobarbital (60 mg/ml, i.p. (0.1 ml/100 g)) and perfused transcardially with heparinized saline followed by 4 % paraformaldehyde (PFA) in 0.1 M phosphate-buffered saline, pH 7.4. The brain and spinal cord were removed and fixed in 4 % formalin for 5 days. They were processed for immunohistochemical staining by dehydrating through a series of increasing ethanol concentrations (50, 70, to 100 %) followed by immersing in xylaxine to enable paraffin embedding. Paraffin blocks with the brain and spinal cord were prepared and sectioned using a microtome at 8 μm. The sections were air dried overnight before immunostaining. Each slide with three serial sections of the brain and spinal cord was immersed in xylaxine to dewax the sections. The tissues were rehydrated through increasing ethanol concentrations and finally in distilled water before antigen retrieval in citrate buffer for 5 min. The sections were washed and outlined with a PAP pen before blocking for endogenous peroxidase for 1 h. Non-specific antibody was blocked with goat serum for 1 h. One serial section was incubated with antibody for mGluR5 (Abcam) applied at 1:200 dilution, while the adjacent section was incubated with IBA1 antibody (Abcam) at 1:100 dilution. The sections were incubated with the respective antibodies overnight at 4 °C. The negative control did not have the primary antibody. On the following day, the sections were washed before applying biotinylated goat anti-rabbit secondary antibody for 1 h. After that, the slides were incubated in streptavidin-HRP for 30 min. The antibody was detected with the chromogen 3,3′-diaminobenzidine (DAB). The secondary antibodies with developing reagents were purchased from Millipore. The nuclei were stained with hematoxylin. The sections were washed after each step before subsequent application. The stained mGluR5 positive cells and IBA1 positive microglial cells were viewed under a light microscope.
The binding potential (BPND) of [18F]FPEB in the whole brain of the base mice was 2.09 ± 0.36; in ALS mice at stage 1, it was 3.13 ± 0.15 and at stage 3 3.85 ± 0.47 indicating 49 ± 9 % increase from the base mice to ALS-type mice and further enhancement of 23 ± 4 % during disease progression. In the individual brain areas, the highest increase was in the hippocampus being 115 ± 15 % from base mice to ALS mice and further 30 ± 5 % during degeneration. The corresponding values for the binding potential in the striatum were 2.69 ± 0.13 in the base mice, 5.61 ± 0.27 in ALS mice at stage 1, and 7.22 ± 1.31 at stage 3 indicating 108 ± 11 % increase from the base mice to the ALS mice and 29 ± 5 % increase during progression of the disease. Correspondingly, the binding potential in the cortex of the base mice was 1.17 ± 0.12, in the ALS mice at stage 1 2.41 ± 0.13, and 2.88 ± 0.19 at stage 3 indicating 105 ± 11 % increase from the base mice and further increase of 19.5 ± 3 % during disease progression (Figs. 1 and 2). The accumulation of [11C]PBR28 was increased by 110 ± 33 % in the whole brain during progression of the disease indicating significant inflammatory process (Fig. 3). The accumulation of [18F]FPEB was enhanced 6 % in thoracic spinal cord and 22 % in lumbar cord while [11C]PBR28 accumulation was enhanced 89 and 264 %, respectively, in the same areas during progression of the disease. Also, in the lungs, [11C]PBR28 accumulation was increased by 204 % indicating excessive inflammatory process. [18F]FPEB accumulation was enhanced only 6 % in the lungs (Fig. 4). The immunohistological studies verified enhanced mGluR5 expression and inflammatory response in the brain and spinal cord (Fig. 5).
Compared to the base mice, the mGluR5 expression was significantly enhanced in the brain of ALS mouse model especially in the hippocampus, striatum, and cortex as well as in the averaged whole brain enhancing significantly also during progression of the disease in the hippocampus and cortex. Significant enhancement of mGluR5 expression was observed also in the cervical spinal cord during the disease progression. However, [11C]PBR28, which is a marker for TSPO and microglial activation, showed the most significant enhancement in the brain and spinal cord during progression of the disease. The enhancement in the whole brain was 110+/33 %, five times more than averaged enhancement of mGluR5 expression. In the spinal cord, the enhancement was from 89 to 264 % and in the lungs 204 %. The difference between enhancements of mGluR5 expression and inflammatory response might be caused by the excessive glutamate-induced excitotoxicity in the synapses which may contribute to enhanced inflammatory processes in CNS.
Concerning the imaging ligand [11C]PBR28, the accumulation in the lungs might be affected by non-specific binding, which has been reported for [11C]PBR28 in the lungs . In addition, TSPO has polymorphism that effects binding potential in vitro and in vivo in humans . In this experiment, we followed the same animals with the same imaging procedures so even if the non-specific binding or polymorphism effects on absolute values, their effect on the difference between the values is minimal.
Since inflammation can occur in any brain area, reference tissue model cannot be used to analyze [11C]PBR28 data. These data are presented as percent accumulation of the injected radioactivity per tissue volume. The selected regions of the interest are the same as for the studies with [18F]FPEB. During the disease progression from stage 1 to 3, inflammatory response increased five times more than mGluR5 expression in the whole brain providing strong evidence that inflammation can be dependent on enhanced glutamatergic function. Since mGlu5 receptors have primary postsynaptic location, the enhanced binding potential values of mGluR5 may indicate enhanced glutamate content in the synapse.
Cerebellum data cannot be used as a reference tissue in the data analyses of [18F]FPEB in the spinal cord since the transportation of the radioligand is not the same as inside the brain, so expression was determined as a percent of the injected dose in cubic centimeter.
Resolution of the microPET imager is 0.9 mm, which will create errors in absolute values in quantification of data in small brain areas because of the partial volume effect. To minimize this issue, we have conducted longitudinal imaging studies in the same animals to evaluate functional changes and have used the same size for region of interest in consecutive studies. To be noted that the resolution of the CT is 50 μm enabling us to localize very tiny areas even in the spinal cord but when we record the radioactivity in that tiny area, the absolute value will be underestimated.
The obtained values for excessive inflammation support the fast decline of the health status of these mice, and the immunohistological studies verify the end point data of enhanced mGluR5 expression and inflammation in the brain and spinal cord.
Using the powerful imaging technology, we have conducted imaging studies of mGluR5 expression and inflammatory response in SOD1 G93 mice and found enhanced mGluR5 expression in several brain areas and spinal cord with enhancement in 2 weeks follow-up period (Figs. 1 and 2). We found also significantly enhanced accumulation of [11C]PBR28, marker for activated microglia, in hind brain, areas in spinal cord, and the highest accumulation in the lungs (Figs. 3 and 4). The enhanced expression of mGluR5 in the brain of ALS mice support the regional inflammation observed in ALS patients using [11C]PBR28 as an imaging ligand . The regional areas of the brain in these human studies were determined by the simultaneous anatomical MR imaging. These studies also showed that [11C]PBR28 binding was enhanced in all brain areas of ALS patients compared to age-matched controls.
The studies on ALS pathology based on glutamatergic function and inflammatory response using the highly innovative in vivo imaging technology recently developed by our team [27, 30] show significant local pathophysiological changes that can be targeted with therapeutic approaches. The results of these exploratory experiments can be immediately extended to ALS patients to enhance early diagnosis and follow therapeutic response and even to design more effective therapeutic approaches. Imaging ligands of mGluR5 ([18F]FPEB) and inflammatory response ([11C]PBR 28) are already in human use, so the technical aspects for transition are immediate. It is notable that there have been several failed clinical trials in ALS. One contributing matter for this might be that previously, there has been limitation to spatially and temporally record involved pathophysiological mechanisms.
With in vivo PET imaging studies, we have shown that SOD1-G93A gene will significantly enhance mGluR5 expression in the brain and spinal cord in ALS mouse model. In addition, mGluR5 expression increased in the whole brain significantly and moderately in the spinal cord during progression of the disease. Inflammation increased in all brain areas and spinal cord up to fivefold more than mGluR5 expression during progression of the disease indicating the excitatory role of excessive glutamate may contribute or accelerate of inflammation in ALS pathology.
peripheral benzodiazepine receptor ligand 28
three-dimensional-minimum likelihood estimation method
amyotrophic lateral sclerosis
- BPND :
binding potential using reference tissue model
marker for inflammation (calcium binding adaptor molecule)
metabotropic glutamate receptor subtype 5
positron emission tomography
superoxide dismutase 1-glycine 93S mutation (glycine 93 changed to alanine)
translocator protein 18 kDA (kilo Dalton)
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These studies were conducted by support of NIH grants NIBIB-R01EB012864 and NIMH-R01MH91684 to ALB. The following supporting instrument grants (1S10RR029495-01, 1S10RR026666-01, and 1S10RR023452-01) to ALB are also acknowledged.
There are no competing interests.
ALB designed the studies, participated in the experimental work and data analyses, and wrote the manuscript; DK performed the immunohistochemical analyses; KEK synthetized the used radioligands; KJ participated in the imaging and data analyses; PP participated in the data analyses and manuscript writing; AZ participated in the data analyses; and MM performed the behavioral analyses and removed the spinal cords. All authors read and approved the final manuscript.
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Brownell, A., Kuruppu, D., Kil, K. et al. PET imaging studies show enhanced expression of mGluR5 and inflammatory response during progressive degeneration in ALS mouse model expressing SOD1-G93A gene. J Neuroinflammation 12, 217 (2015) doi:10.1186/s12974-015-0439-9