Figures
Abstract
Background
As pharmacological therapies have largely failed so far, stem cell therapy has recently come into the focus of ALS research. Neuroprotective potential was shown for several types of stem and progenitor cells, mainly due to release of trophic factors. In the present study, we assessed the effects of intracerebroventricular injection of glucagon-like peptide 1 (GLP-1) releasing mesenchymal stromal cells (MSC) in mutant SOD1 (G93A) transgenic mice.
Methodology/Principal Findings
To improve the neuroprotective effects of native MSC, they had been transfected with a plasmid vector encoding a GLP-1 fusion gene prior to the injection, as GLP-1 was shown to exhibit neuroprotective properties before. Cells were encapsulated and therefore protected against rejection. After intracerebroventricular injection of these GLP-1 MSC capsules in presymptomatic SOD1 (G93A) mice, we assessed possible protective effects by survival analysis, measurement of body weight, daily monitoring and evaluation of motor performance by rotarod and footprint analyses. Motor neuron numbers in the spinal cord as well as the amount of astrocytosis, microglial activation, heat shock response and neuronal nitric oxide synthase (nNOS) expression were analyzed by immunohistological methods. Treatment with GLP-1 producing MSC capsules significantly prolonged survival by 13 days, delayed symptom onset by 15 days and weight loss by 14 days and led to significant improvements in motor performance tests compared to vehicle treated controls. Histological data are mainly in favour of anti-inflammatory effects of GLP-1 producing MSC capsules with reduced detection of inflammatory markers and a significant heat shock protein increase.
Citation: Knippenberg S, Thau N, Dengler R, Brinker T, Petri S (2012) Intracerebroventricular Injection of Encapsulated Human Mesenchymal Cells Producing Glucagon-Like Peptide 1 Prolongs Survival in a Mouse Model of ALS. PLoS ONE 7(6): e36857. https://doi.org/10.1371/journal.pone.0036857
Editor: R. Lee Mosley, University of Nebraska Medical Center, United States of America
Received: December 8, 2011; Accepted: April 15, 2012; Published: June 20, 2012
Copyright: © 2012 Knippenberg 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 study was supported by a grant from Deutsche Gesellschaft für Muskelkranke to SP and by a grant from Deutsche Forschungsgemeinschaft (Pe 924/2-2) to SP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No additional external funding was received for this study.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder which causes death of motor neurons in the cortex, brain stem and spinal cord. Patients develop rapidly progressive paralysis and muscle wasting and ultimately die due to respiratory insufficiency within 3–5 years after diagnosis [1]. Aproximately 10% of ALS cases are familial (fALS). About 20% of these fALS cases are linked to mutations in the gene coding for superoxide dismutase 1 (SOD1) [2]. In a transgenic mouse model expressing a mutant form of SOD1 carrying the Gly93 → Ala substitution, progressive death of motor neurons occurs in the ventral horn region of the lumbar spinal cord and the mice develop a phenotype similar to ALS [3].
So far, only the glutamate antagonist riluzole has shown marginal neuroprotective potential in the treatment of amyotrophic lateral sclerosis (ALS) [4]. Therefore, current efforts focus on experimental therapies. Recent studies have demonstrated that stem cell transplantation presents a novel therapeutic approach for a variety of neurological diseases (for review see [5]). Current attempts to establish cell therapy in ALS mainly focus on the generation of a more protective environment for degenerating motor neurons rather than on cell replacement. Genetic modification of transplanted cells aiming to increase the production of trophic factors is feasible and enhances the benefit of native cells [6]–[8]. The use of a single drug targeting only one out of many interacting pathomechanisms in ALS has proven to be of little or no effect in a large number of previous studies. Therapeutic approaches which combine several mechanisms of action appear more promising.
In this context, glucagon-like peptide 1 (GLP-1) is an interesting candidate for the treatment of neurodegenerative disorders. GLP-1 is an intestinal peptide, stimulating glucose-dependent insulin secretion after food intake and thereby leading to reduction of blood glucose levels [9], [10]. GLP-1 and its receptor can be found in pancreatic β cells, intestinal cells but also in the brain [11], [12]. Besides its insulinotropic effects, GLP-1 exhibits anti-oxidant capacities [13] and is neuroprotective against excitotoxicity in vitro and in vivo [14], [15]. While GLP-1 penetrates the blood brain barrier, its short half life prevents systemic administration [16], [17]. This led to the development of GLP-1 analogues with increased half life such as exendin 4 or liraglutide [18]–[20] for subcutaneous injection. Several studies showed therapeutic potential of these GLP-1 agonists in animal models of neurodegenerative diseases such as Alzheimer’s disease [21], Parkinson’s disease [22], Huntington’s disease [23] and also after experimental traumatic brain injury [24]. In a study in SOD1 (G93A) mice, exendin 4 did not prolong survival or slow down disease progression of the mice, but led to amelioration of motor neuron [25].
One major advantage of intracerebroventricular implantation of a vehicle releasing GLP-1–as opposed to daily injections of GLP-1 analogues is that it warrants continuous release of the neurotrophic factor. Another method to assure continuous growth factor delivery would be the use of osmotic minipumps which must be replaced every few weeks. Encapsulated cells instead of mini pumps allow the abandonment of catheters which reduces the risk of complications and requires only one surgical procedure that was shown several times to be feasible in humans before [26], [27].
Encapsulated cell biodelivery has been suggested as a novel approach in cellular therapy to deliver therapeutic substances like GLP-1 in a sustainable fashion. Encapsulation in a biopolymer material allows the use of non-autologous cells as it prevents any host versus graft reaction [28].
In our study, we investigated an encapsulated mesenchymal stromal cell (MSC) line, which has been modified to produce GLP-1. Neuroprotective effects of these GLP-1 producing MSC capsules have already been shown in experimental traumatic brain injury and in a transgenic Alzheimer’s disease model [21], [24]. The rationale to use these genetically modified MSC was to combine the genuine neuroprotective potential of adult stem cells together with their ability to serve as a vehicle for continuous release of a trophic factor. In a mouse model of Alzheimer’s’ disease, is has already been established that the neurotrophic effects of native mesenchymal cells can be potentiated by increased GLP-1 production [8].
We administered GLP-1 MSC capsules to transgenic SOD1 (G93A) mice via intracerebroventricular injection before disease onset (day 40). By monitoring of survival, motor function, weight and general condition and by additional histological analyses, we could provide evidence for their neuroprotective potential in the ALS mouse model.
Results
Survival Study
General condition.
Disease onset was defined by daily assessment of the general condition of the mice. Animals treated with GLP-1 MSC showed a slighter deterioration compared to vehicle controls (figure 1B). The shift in symptom onset was 15 days on average. Differences to controls were significant between day 110 and 120 (Two-way ANOVA, p<0.01 and p<0.001).
Survival.
Survival times of animals treated with GLP-1 MSC were significantly prolonged as compared to vehicle-treated mice (figure 1A) (Gehan-Breslow-Wilcoxon test, p<0.05). On average, GLP-1 MSC- treated animals lived 13 days longer than the controls (130d vs. 117d).
Presymptomatic GLP-1 treatment (GLP-1 MSC) prolonged survival (A) and improved general condition (B) compared to vehicle controls (vehicle). GLP-1 treated animals gained weight for a longer period than vehicle controls (C). Data are mean ± SEM of 8 (5♀/3♂) (control) and 10 (6♀/4♂) (GLP-1) treated animals. (A) Kaplan-Meyer Curve, followed by Gehan-Breslow-Wilcoxon test. (B & C) two-way ANOVA, followed by Bonferroni post-test. (**) p<0.01; (***) p<0.001.
Weight.
Treatment with GLP-1 MSC led to a significant delay of weight loss (figure 1C). While vehicle treated controls started to lose weight already at week 14, GLP-1 MSC- treated animals gained weight until week 15. Significant differences to controls were measured for two weeks (week 16 & 17, two-way ANOVA, p<0.05 & p<0.01).
Rotarod.
Rotarod performance of vehicle treated controls started to decrease at week 13, while performance of GLP-1 MSC- treated animals was not altered before week 16 (figure 2A). For two weeks the deterioration of motor performance was significantly less in the GLP-1 MSC group (week 16 & 17, two-way ANOVA, p<0.001).
Presymptomatic GLP-1 treatment (GLP-1 MSC) improved rotarod performance (A), step length (B) and runtime (C) compared to vehicle controls (vehicle). Data are mean ± SEM of 8 (5♀/3♂) (control) and 10 (6♀/4♂) (GLP-1) treated animals. Two-way ANOVA, followed by Bonferroni post-test. (*) p<0.05; (**) p<0.01; (***) p<0.001.
Footprint analyses – step length.
First decrease in step length occurred at week 14 in vehicle treated controls; therefore 3 weeks earlier than in GLP-1 MSC- treated mice (figure 2B). Differences between both groups were significant from week 16 to week 18 (Two-way ANOVA, p<0.001).
Footprint analyses – runtime.
While runtime along the footprint track started to increase not before week 18 in the GLP-1 MSC- treated group, vehicle treated controls already showed an increase at week 15 (figure 2C). From week 17 to week 18 these differences became significant (Two-way ANOVA, p<0.01 & p<0.001).
Histological Analyses
Brain sections of 6 vehicle and 6 GLP-1 MSC- treated mice were studied by GFAP staining. We found a glial scar above the right ventricle in five of 12 animals (figure 3). Capsules within the ventricles or in surrounding tissue were not detectable as most likely the capsules remained in the ventricles and were washed out during perfusion of animals prior to paraffin embedding. Enlarged ventricles were not observed.
In 5 of 12 animals there was a glial scar visible above the right ventricle as it was shown by GFAP staining. Rectangle in the left picture is showed enlarged on the right side. Scale bar 500 µm.
Motor neuron numbers were not significantly altered between vehicle- and GLP-1 MSC- treated groups as shown by cresyl violet staining (figure 4A). Treatment with GLP-1 MSC led to a reduction of astrocytosis as detected by GFAP (glial fibrillary acidic protein) staining in lumbar spinal cord sections compared to vehicle treated controls even though quantitative analysis was not statistically significant (figure 4B). Similarly, microgliosis as measured by Iba1 (ionized calcium binding adaptor molecule 1) immunostaining was reduced in GLP-1 MSC- treated animals (figure 4C). Staining for anti-HSP70 (heat shock protein 70) revealed a significantly increased heat shock response in GLP-1 MSC- treated mice compared to controls (unpaired t-test, p<0.05) (figure 4D). nNOS (neuronal nitric oxide synthase) immunolabelling was slightly decreased in the GLP-1 MSC- treated animals (figure 4E).
(A) Motor neuron loss was not ameliorated by GLP-1 treatment (GLP-1 MSC) compared to vehicle treated controls (vehicle). (B) Astrocytosis (C) and microglial activation were marginally less in GLP-1 treated animals compared to controls. (D) Heat shock response was significantly increased by GLP-1 treatment and nNOS (E) was reduced slightly in these animals. Unpaired t-test. (*) p<0.05. Scale bar 100 µm.
Even though counting of motor neuron cell bodies in cresyl violet stained spinal cord sections did not result in apparent differences between GLP-1 MSC and vehicle-treated animals, staining for mictrotubule-associated protein 2 (MAP2) as a neuronal marker shower more intense labelling, namely of neuronal processes in spinal cord sections of GLP-1 MSC- treated animals (figure 5).
Staining against microtubule associated protein 2 was stronger in animals treated with GLP-1 (GLP-1 MSC) compared to vehicle treated controls (vehicle). Scale bar 100 µm.
(A) Encapsulation with alginate leads to GLP-1 MSC capsules with a mean diameter of 161 µm. (B) GLP-1, oxygen and nutrients are able to pass the alginate barrier, but the cells are protected against the hosts’ immune system.
Discussion
Cellular therapy is currently being investigated as a novel therapeutic option for the treatment of ALS, mainly with the aim to provide a neuroprotective environment and trophic support for degenerating motor neurons. Mesenchymal stem cells (MSC) present good candidates for this approach as they are easily available, highly proliferative and barely immunogenic [29]. A previous study assessed the effect of intraspinal injection of MSC in an ALS rodent model: the authors showed moderate improvements in motor function and survival which were attributed to anti-inflammatory and neurotrophic effects of MSC [30]. One reason for the limited efficacy of intraspinal injection of cells in ALS could be that motor neuron degeneration is widespread along the spinal cord, brain and brainstem [1]. As cells do barely migrate following injection into brain or spinal cord parenchyma, local administration may therefore not be sufficient to delay disease progression over a long period. Other studies have evaluated the benefit of intravenous administration of mesenchymal cells in ALS mouse models and could show that cells migrated some distance away from blood vessels to the gray and white matter of brain and spinal cord [31], [32]. But intravenous administration holds the risk of cell loss during circulation due to settling of infused cells in many peripheral tissues, such as lung, liver or spleen [32], [33], and moreover requires high numbers of cells.
As opposed to local intraspinal or intravenous administration, intracerebroventricular injection has the advantage that neuroprotective factors released by the cells can directly reach the whole spinal cord and brain via the cerebrospinal fluid (CSF), reducing the risk of adverse effects and the number of cells required. This is a major advantage for future translation into clinical trials. It is not necessary to make the cells enter the spinal cord directly because trophic factors can be distributed via the CSF. This assumption is confirmed by a study of Zhang et al. who showed limited migration of intrathecally administered human MSC in the spinal cord parenchyma of ALS mice but nevertheless significant neuroprotection [34].
There is evidence that MSC cause direct trophic effects without further differentiation into new phenotypes, probably due to release of trophic factors such as VEGF and BDNF [35], [36]. To further enhance the effects of native stem cells, they can be genetically engineered to produce neuroprotective proteins. This approach was tested before in studies using genetically modified GDNF-releasing MSC in a rat model of ALS: The protective effects of native MSC on motor neuron survival, preservation of motor endplates and survival and motor function of animals were improved by GDNF producing MSC [7]. Encapsulation is a promising approach to reduce the risks and complications associated with cellular therapies in the central nervous system: In a first phase I clinical trial in ALS to assess safety and tolerability of encapsulated genetically engineered baby hamster kidney (BHK) cells releasing human ciliary neurotrophic factor (CNTF), therapeutic levels of the secreted peptide could be detected for several weeks without limiting side effects [37]. A phase I/II clinical trial confirmed the safety and tolerability of intrathecal implants of these cell capsules, with signs of only a very mild humoral immune response [38]. Studies in experimental animal models using the same cell capsules as in the present study showed complete prevention of any immune response by microencapsulation of cells prior to transplantation [21], [24]. Use of encapsulated cells may further be considered as a safety measure against tissue damage which occurred in a study assessing intraspinal transplantation of non-encapsulated cells in a model of focal spinal cord demyelination: MSC migrated into the tissue and caused collagen depositions and subsequent local tissue damage [39]. Our post mortem analysis of brain sections after intracerebroventricular injection of encapsulated MSC showed only minor glial scars along the injection channel in part of the animals but no further abnormalities such as enlargement of the ventricles. This indicates safety and tolerability of the implantation technique. In the present study, the intestinal peptide GLP-1 was used to increase the therapeutic capacity of MSC, based on several studies showing neuroprotective effects of a stimulation of GLP-1 receptors which are present in the mammalian brain [14], [21], [24], [40]. While analogues of GLP-1, like exendin 4 or liraglutide, showed neuroprotective potential in models of Alzheimer’s [20] and Parkinson’s disease [19], [41], the effect in ALS mice so far has been insufficient. Exendin 4 treatment via subcutaneous pumps protected motor neurons and reduced GFAP and caspase 3 amount in spinal cord tissue of SOD1 mice, but disease progression and survival of the animals were not affected [25].
We decided to use GLP-1 releasing MSC to combine the protective effects of adult stem cells and continuous growth factor delivery into the CSF. The commercial availability of well characterized GMP manufactured GLP-1 producing MSC allows fast translation to clinical trials in case of a positive outcome in preclinical studies. Previous studies with GLP-1 releasing CellBeads®, have confirmed steady GLP-1 production at a rate of 2.85–3.68 fmol/capsule/h after intracerebroventricular injection. Further it was shown that GLP-1 reaches the affected regions by circulation within the CSF after intracerebroventricular injection in cats [40] and rats [24] by measurement of the CSF concentrations of GLP-1. These studies have also proven steady GLP-1-release of CellBeads® after explantation and a cell viability of at least 95%, independent from the time interval between cell implantation and analysis [24]. Based on these results, we conclude that the beneficial effects of intracerebroventricular injection of GLP-1 producing MSC capsules in SOD1 (G93A) mice resulted at least in parts from increased GLP-1 concentrations in the CSF. Treatment with GLP-1 releasing MSC significantly increased lifespan and improved motor function of SOD1 (G93A) mice. Even though motor neuron loss as assessed by cresyl violet staining and counting of motor neuron cell bodies was not significantly different between vehicle- and GLP-1 MSC-treated groups, we found a stronger signal of MAP2 staining after GLP-1 treatment. One of the earliest events in mutant SOD1 mice is impaired axonal transport [42], [43]. Increased staining for could indicate preservation of neuronal processes, resulting in increased functional capacity of remaining motor neurons due to preserved integrity of microtubules and axonal transport. Further experiments should include analysis of neuromuscular end plates to clarify whether GLP-1 MSC have an effect on terminal motor axons. Besides a direct effect on motor neurons, positive effects on the disease course may be explained by an anti-inflammatory mechanism of action of GLP-1-releasing MSC. Increased astrocytosis and microglial activation are hallmarks of the disease [44] and is now well recognized that SOD1 (G93A) glial cells contribute to motor neuron death in ALS [45], [46]. Intracerebroventricular injection of GLP-1 releasing MSC led to a (not significant) reduction of astrocytosis and to a significant increase of the heat shock response, suggesting less functional impairment of remaining astrocytes. Increased levels of HSP were already shown to be neuroprotective [47] and the HSP-inducing drug arimoclomol slowed down disease progression and increased survival in ALS mice [48]. This is in line with the reduced microglial activation and nNOS immunostaining after GLP-1 MSC injection. Similar to astrocytes, unaffected microglia provide trophic support but activation leads to increased release of neurotoxic factors such as nitric oxide [49], [50]. Reduced microglial activation therefore may lead to reduced levels of nitric oxide and therefore have contributed to the better outcome of GLP-1 MSC-treated mice.
In our pilot study we could demonstrate the feasibility of intracerebroventricular injection of encapsulated GLP-1 producing MSC in ALS mice. Our results regarding motor performance and survival of the animals as well as the observed effects on inflammatory markers in the spinal cord strongly suggest further evaluation of the potential of encapsulated MSC therapy for treatment of ALS.
Material and Methods
Ethics Statement
All experiments were carried out in strict accordance with the internationally accepted principles in the care and use of experimental animals and were approved by the Institutional Animal Care and Research Advisory Committee at Hanover Medical School and permitted by the Lower Saxonian State Office for Consumer Protection and Food Safety regional (Permit Number: AZ 07/1324).
Animals
G93A transgenic familial ALS mice (high copy number; B6SJLTg (SOD1-G93A)1Gur/J) [3] were obtained from The Jackson Laboratory (Bar Harbor, ME, USA). These mice over-express the human mutant SOD1 allele containing the Gly93 → Ala (G93A) substitution. We maintained the transgenic G93A hemizygotes by mating transgenic males with B6SJLF1/J hybrid females. Transgenic offspring was genotyped by PCR assay of DNA obtained from tail tissue. Mice were housed under controlled conditions (12∶12 light:dark cycle) with free access to food and water. Animals of the same sex were kept in groups of up to five animals in Makrolon cages type II (UNO, Zevenaar, Netherlands). Males were kept solitary in the same cage type only when they were also used for breeding.
Alginate Microcapsules
A human, bone marrow-derived, single cell derived mesenchymal stromal cell line provided by CellMed AG, Alzenau, Germany as previously described [21] was used in this study. It was immortalized by transduction with the human Telomerase Reverse Transcriptase (hTERT) gene [51]. After transfection with a plasmid vector encoding a GLP-1 fusion gene, the cells produced an 8.7 kDa dimeric GLP-1 molecule. The cells are embedded in a spherical shaped alginate matrix (about 160 µm in diameter, figure 6). The alginate matrix is generated by cross-linking alginate with barium ions. Each capsule (trademark CellBeads®) contained about 94 cells. Until use, the cell capsules were stored in liquid nitrogen.
Preoperative Procedure
For surgery animals were anesthetized by a combination of ketamine (0.1 ml/100 g, 100mg/kg), xylazine (0.01 ml/100g, 2 mg/kg) and midazolame (0.05 ml/100 g, 0.5 mg/kg), prepared under sterile conditions with 0.9% sodium chloride. Appropriate to the body weight (0.1 ml/10 g) anaesthesia was administered intraperitoneally. Duration of anaesthesia was up to 60 minutes, which was sufficient for the surgery. Depth of anaesthesia was controlled by the toe-and eyelid- reflex.
Cerebroventricular Injection
The heads of the animals were shaved and disinfected. Eye ointment protected the eyes against dehydration. The head was fixed with ear bars in a stereotactic frame and the skin was disclosed longitudinally. Bregma was visualized by 30% hydrogen peroxide and coordinates of bregma were recorded. From bregma injection coordinates (1 mm lateral, 0.5 mm anterior) were adjusted before the cranial bone was enclosed under visual control with a drill head of 1.4 mm diameter. Following the preparation of injection position, 100 µl of the cell solution was dropped on a glass dish and up to 30 GLP-1 MSC capsules were taken with a 10 µl Hamilton syringe under visual control. Thy syringe filled with GLP-1 MSC capsules was kept upright until usage so the beads were concentrated in the top of the tip. After adjustment of injection coordinates, the syringe was inserted 5 mm into the brain, and then withdrawn 1 mm so the cells were injected 4 mm distal from the cranial bone. 1 µl cell solution was injected all at once. After a waiting period of 3 minutes the syringe was withdrawn slowly and washed with 0.9% sodium chloride under visual control. Remaining cell capsules were counted and recorded in the surgery protocol.
Postoperative Procedure
Following wound closure animals received a single dose of carprofene (5 mg/kg subcutaneously) and metamizole via drinking water (200 mg/kg/day) for 3 postoperative days for analgesia.
Treatment Groups
Mice were treated with either GLP-1 producing MSC capsules or empty alginate capsules as vehicle control (control: n = 10 (6♀/4♂); GLP-1 MSC: n = 8 (5♀/3♂) for assessment of survival and motor performance; control: n = 6 (5♀/1♂); GLP-1 MSC: n = 6 (5♀/1♂) for histological analyses). An increase in the therapeutic effect of encapsulated GLP-1 producing MSC capsules as compared to native encapsulated MSC has already been proven before [24]. To reduce the total number of animals in the study, we therefore did not include a second control group of mice injected with alginate beads filled with native MSC. Animals of each litter were randomly attributed to either the GLP-1 MSC group or the control group and were monitored until they reached disease end stage. The cerebroventricular injection of either GLP-1 producing or empty capsules was administered once at a presymptomatic disease stage (d40). After surgery, experimenters were blinded to treatment groups so that animals were objectively monitored throughout the whole period of behavioural assessment.
Behavioural Assessment
General condition.
For weekly assessment of general condition from week 14 we used a behavioural score system as previously described [52], [53], based on the score developed by Vercelli et al. [30] from 1 to 5 defined as follows:
- healthy without any symptoms of paralysis,
- slight signs of destabilized gait and paralysis of the hind limbs,
- obvious paralysis and destabilized gait
- fully developed paralysis of the hind limbs, animals only crawl on the forelimbs
- fully developed paralysis of the hind limbs, animals predominantly lie on the side and/or are not able to straighten up after turning them on the back or lost more than 20% of their starting weight.
When animals reached a score of 2, macerated food was given daily for easy access to food and hydration. Reaching a score of 1, the animals were euthanized.
Evaluation of onset and survival.
Day of onset was set as the first day the animals reached a score of 4 in the daily behavioural assessment. Animals were killed when they reached a score of 1 and this age (in days) was recorded as survival time.
Weight.
We recorded the weight of the animals weekly, beginning at 10 weeks of age, using a normal digital balance ranging up to 800 g in 0.1 g steps.
Rotarod.
Beginning at 11 weeks of age, we analyzed motor function using a rotarod apparatus from IITC (IITC Life Science Inc. California). After an adaptation period of 5 days the test was performed weekly. Mice had to remain on the rotating cylinders for up to 180 s with an increasing speed up to 18 rpm. Rotarod test was performed as previously described [52].
Footprint analyses.
Footprint analyses for step length and runtime were performed weekly starting the same week as rotarod tests performance [52]. The hind feet were dipped into black finger print and animals were placed on a gangway covered with conventional masking tape. Footprints were analyzed with respect to the step length using the FOOTPRINTS software (Version 1.22 by K. Klapdor and B. Dulfer [54]). In addition, the time animals needed to run along the track (50 cm) was measured.
2.4 Histological Evaluation
At d110, six vehicle and six GLP-1 MSC-treated animals (5♀/1♂) were sacrificed by an overdose of anesthetic (ketamine (0.1 ml/100 g, 100 mg/kg), rompune (0.01 ml/100 g, 2 mg/kg) and midazolame (0.05 ml/100 g, 0.5 mg/kg)). After transcardial perfusion with 25 ml 4% paraformaldehyde (PFA) in phosphate buffer (PBS), the brain and lumbar part of the spinal cord was removed. Postfixation for 1 day in 4% PFA was followed by storage in 70% ethanol until dehydration by progressively more concentrated ethanol baths and xylene (Mallinckrodt Baker B.V., Deventer, Netherlands) and embedding in paraffin blocks. Sections of 7 µm were cut on a microtome and 5–6 sections were transferred to one object slide, respectively.
2.4.1 Motor neuron survival.
One slide per animal (i.e. 5–6 spinal cord sections) was rehydrated in xylene and graded ethanol, stained with 0.2% Thionin, dehydrated in graded ethanol and xylene and coverslipped with Eukitt quick hardening mounting medium (Sigma-Aldrich, Steinheim, Germany). At 20x magnification in an Olympus B×61 microscope, cells in the ventral horn region with a diameter >200 µm2 were defined as motor neurons, according to Chen et al., who determined α- motor neurons as cells with cell body areas ranging from 200 to 1100 µm2 [55]. Motor neurons were counted, using cell* software (Olympus, Hamburg, Germany). Only intact ventral horn regions were used for counting so that, depending on the quality of the section, 5 to 12 ventral horn regions were counted for motor neuron numbers and the mean was used for statistical evaluation.
2.4.2 Immunohistochemistry.
For immunohistochemical staining, slides were rehydrated in xylene, graded ethanol and PBS. For antigen retrieval, slides were boiled for 5–10 min in citrate buffer and cooled for 15 minutes at 4°C. After immersion in PBS, slides were blocked for 5 min with peroxidase block (DakoCytomation, Glostrup, Denmark) and antibody diluent (DakoCytomation, Glostrup, Denmark) for 1 h followed by overnight incubation at 4°C with primary antibodies specific for GFAP (1∶600; polyclonal rabbit anti glial fibrillary acidic protein; DakoCytomation, Glostrup, Denmark), Iba1 (1∶250; polyclonal rabbit anti ionized calcium binding adaptor molecule 1; WAKO Chemicals GmbH, Neuss, Germany), HSP70 (1∶250; monoclonal mouse anti heat shock protein; Acris antibodies, Herford, Germany) or nNOS (1∶250; polyclonal rabbit anti neuronal nitric oxide synthase; Millipore, Bedford, USA) diluted in antibody diluent. Secondary HRP antibody anti-rabbit or anti-mouse respectively (EnVision+System-HRP (AEC+); DakoCytomation, Glostrup, Denmark) was added for 30 min, followed by 20–25 min incubation in chromogene substrate (EnVision+System-HRP (AEC); Dako-Cytomation, Glostrup, Denmark). Slides were covered with Kaiser’s glycerol gelatin (Merck, Darmstadt, Germany).
For quantitative analyses of astrocytosis, microglial activation, heat shock response and nNOS staining, the percentage of stained area of the ventral horn was determined using the phase analysis tool of cell* software in pictures taken at 20x magnification by an Olympus Bx61 microscope.
For MAP2 staining, slides were blocked with 5% goat serum in PBS with 0.3% Triton X-100 (Sigma-Aldrich, Steinheim, Germany) for 1 h followed by overnight incubation at 4°C with primary antibodies specific for MAP2 (1∶250; polyclonal rabbit anti microtubule-associated protein 2; Millipore, Bedford, USA) diluted in 5% goat serum in PBS with 0.3% Triton X-100. Secondary anti-rabbit or Alexa Fluor 488 antibody (1∶500; anti-IgG (H+L); Invitrogen, Darmstadt, Germany) was added for 45 min. Slides were then counterstained with the fluorescent DNA dye DAPI (10 mg/ml; Invitrogen, Darmstadt, Germany).
Statistics.
Data were analyzed by two-way ANOVA in order to evaluate time evolution of the different parameters. In case of significant parameter interaction (p<0.05), comparison with a Bonferroni posthoc test was performed. All data are presented as mean ± SD and significance level was set as p<0.05. Survival was analyzed by the Gehan- Breslow- Wilcoxon test with a significance level of p<0.05.
Acknowledgments
We thank C. Kassebaum for help with the surgeries, C. Hotopp-Hergesell for genotyping of the mice and A. Niesel for technical support. Further we acknowledge the support of C. Wallrapp (CellMed AG, Alzenau), who provided the cell capsules and M Kassem who provided the hTERT immortalized mesenchymal stem cell line to CellMed.
Author Contributions
Conceived and designed the experiments: SK RD TB SP. Performed the experiments: SK NT SP. Analyzed the data: SK NT SP. Contributed reagents/materials/analysis tools: RD TB SP. Wrote the paper: SK NT RD TB SP.
References
- 1. Kunst CB (2004) Complex genetics of amyotrophic lateral sclerosis. Am J Hum Genet 75: 933–947.
- 2. Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, et al. (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362: 59–62.
- 3. Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, et al. (1994) Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science 264: 1772–1775.
- 4. Bensimon G, Lacomblez L, Meininger V (1994) A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. N Engl J Med 330: 585–591.
- 5. Hedlund E, Hefferan MP, Marsala M, Isacson O (2007) Cell therapy and stem cells in animal models of motor neuron disorders. Eur J Neurosci 26: 1721–1737.
- 6.
Lu Z, Hu X, Zhu C, Wang D, Zheng X, et al. (2008) Overexpression of CNTF in Mesenchymal Stem Cells reduces demyelination and induces clinical recovery in experimental autoimmune encephalomyelitis mice. J Neuroimmunol.
- 7. Suzuki M, McHugh J, Tork C, Shelley B, Hayes A, et al. (2008) Direct muscle delivery of GDNF with human mesenchymal stem cells improves motor neuron survival and function in a rat model of familial ALS. Mol Ther 16: 2002–2010.
- 8. Klinge PM, Harmening K, Miller MC, Heile A, Wallrapp C, et al. (2011) Encapsulated native and glucagon-like peptide-1 transfected human mesenchymal stem cells in a transgenic mouse model of Alzheimer's disease. Neurosci Lett 497: 6–10.
- 9. Mojsov S, Heinrich G, Wilson IB, Ravazzola M, Orci L, et al. (1986) Preproglucagon gene expression in pancreas and intestine diversifies at the level of post-translational processing. J Biol Chem 261: 11880–11889.
- 10. Nathan DM (1992) The rationale for glucose control in diabetes mellitus. Endocrinol Metab Clin North Am 21: 221–235.
- 11. Jin SL, Han VK, Simmons JG, Towle AC, Lauder JM, et al. (1988) Distribution of glucagonlike peptide I (GLP-I), glucagon, and glicentin in the rat brain: an immunocytochemical study. J Comp Neurol 271: 519–532.
- 12. Alvarez E, Roncero I, Chowen JA, Thorens B, Blazquez E (1996) Expression of the glucagon-like peptide-1 receptor gene in rat brain. J Neurochem 66: 920–927.
- 13. Perry T, Lahiri DK, Sambamurti K, Chen D, Mattson MP, et al. (2003) Glucagon-like peptide-1 decreases endogenous amyloid-beta peptide (Abeta) levels and protects hippocampal neurons from death induced by Abeta and iron. J Neurosci Res 72: 603–612.
- 14. Perry T, Haughey NJ, Mattson MP, Egan JM, Greig NH (2002) Protection and reversal of excitotoxic neuronal damage by glucagon-like peptide-1 and exendin-4. J Pharmacol Exp Ther 302: 881–888.
- 15. During MJ, Cao L, Zuzga DS, Francis JS, Fitzsimons HL, et al. (2003) Glucagon-like peptide-1 receptor is involved in learning and neuroprotection. Nat Med 9: 1173–1179.
- 16. Kastin AJ, Akerstrom V, Pan W (2002) Interactions of glucagon-like peptide-1 (GLP-1) with the blood-brain barrier. J Mol Neurosci 18: 7–14.
- 17. Banks WA, During MJ, Niehoff ML (2004) Brain uptake of the glucagon-like peptide-1 antagonist exendin(9–39) after intranasal administration. J Pharmacol Exp Ther 309: 469–475.
- 18. Lee J, Hong SW, Chae SW, Kim DH, Choi JH, et al. (2012) Exendin-4 Improves Steatohepatitis by Increasing Sirt1 Expression in High-Fat Diet-Induced Obese C57BL/6J Mice. PLoS ONE 7: e31394.
- 19. Bertilsson G, Patrone C, Zachrisson O, Andersson A, Dannaeus K, et al. (2008) Peptide hormone exendin-4 stimulates subventricular zone neurogenesis in the adult rodent brain and induces recovery in an animal model of Parkinson's disease. J Neurosci Res 86: 326–338.
- 20. McClean PL, Parthsarathy V, Faivre E, Holscher C (2011) The diabetes drug liraglutide prevents degenerative processes in a mouse model of Alzheimer's disease. J Neurosci 31: 6587–6594.
- 21.
Klinge PM, Harmening K, Miller MC, Heile A, Wallrapp C, et al. (2011) Encapsulated native and glucagon-like peptide-1 transfected human mesenchymal stem cells in a transgenic mouse model of Alzheimer's disease. Neurosci Lett.
- 22. Kim S, Moon M, Park S (2009) Exendin-4 protects dopaminergic neurons by inhibition of microglial activation and matrix metalloproteinase-3 expression in an animal model of Parkinson's disease. J Endocrinol 202: 431–439.
- 23. Martin B, Golden E, Carlson OD, Pistell P, Zhou J, et al. (2009) Exendin-4 improves glycemic control, ameliorates brain and pancreatic pathologies, and extends survival in a mouse model of Huntington's disease. Diabetes 58: 318–328.
- 24. Heile AM, Wallrapp C, Klinge PM, Samii A, Kassem M, et al. (2009) Cerebral transplantation of encapsulated mesenchymal stem cells improves cellular pathology after experimental traumatic brain injury. Neurosci Lett 463: 176–181.
- 25. Li Y, Chigurupati S, Holloway HW, Mughal M, Tweedie D, et al. (2012) Exendin-4 ameliorates motor neuron degeneration in cellular and animal models of amyotrophic lateral sclerosis. PLoS ONE 7: e32008.
- 26. Svennerholm L, Brane G, Karlsson I, Lekman A, Ramstrom I, et al. (2002) Alzheimer disease - effect of continuous intracerebroventricular treatment with GM1 ganglioside and a systematic activation programme. Dement Geriatr Cogn Disord 14: 128–136.
- 27. Nutt JG, Burchiel KJ, Comella CL, Jankovic J, Lang AE, et al. (2003) Randomized, double-blind trial of glial cell line-derived neurotrophic factor (GDNF) in PD. Neurology 60: 69–73.
- 28. Lindvall O, Wahlberg LU (2008) Encapsulated cell biodelivery of GDNF: a novel clinical strategy for neuroprotection and neuroregeneration in Parkinson's disease? Exp Neurol 209: 82–88.
- 29. Jiang Y, Jahagirdar BN, Reinhardt RL, Schwartz RE, Keene CD, et al. (2002) Pluripotency of mesenchymal stem cells derived from adult marrow. Nature 418: 41–49.
- 30. Vercelli A, Mereuta OM, Garbossa D, Muraca G, Mareschi K, et al. (2008) Human mesenchymal stem cell transplantation extends survival, improves motor performance and decreases neuroinflammation in mouse model of amyotrophic lateral sclerosis. Neurobiol Dis 31: 395–405.
- 31. Garbuzova-Davis S, Sanberg CD, Kuzmin-Nichols N, Willing AE, Gemma C, et al. (2008) Human umbilical cord blood treatment in a mouse model of ALS: optimization of cell dose. PLoS ONE 3: e2494.
- 32. Zhao CP, Zhang C, Zhou SN, Xie YM, Wang YH, et al. (2007) Human mesenchymal stromal cells ameliorate the phenotype of SOD1-G93A ALS mice. Cytotherapy 9: 414–426.
- 33. Garbuzova-Davis S, Willing AE, Zigova T, Saporta S, Justen EB, et al. (2003) Intravenous administration of human umbilical cord blood cells in a mouse model of amyotrophic lateral sclerosis: distribution, migration, and differentiation. J Hematother Stem Cell Res 12: 255–270.
- 34. Zhang C, Zhou C, Teng JJ, Zhao RL, Song YQ (2009) Multiple administrations of human marrow stromal cells through cerebrospinal fluid prolong survival in a transgenic mouse model of amyotrophic lateral sclerosis. Cytotherapy 11: 299–306.
- 35. Caplan AI, Dennis JE (2006) Mesenchymal stem cells as trophic mediators. J Cell Biochem 98: 1076–1084.
- 36. Crigler L, Robey RC, Asawachaicharn A, Gaupp D, Phinney DG (2006) Human mesenchymal stem cell subpopulations express a variety of neuro-regulatory molecules and promote neuronal cell survival and neuritogenesis. Exp Neurol 198: 54–64.
- 37. Aebischer P, Schluep M, Deglon N, Joseph JM, Hirt L, et al. (1996) Intrathecal delivery of CNTF using encapsulated genetically modified xenogeneic cells in amyotrophic lateral sclerosis patients. Nat Med 2: 696–699.
- 38. Zurn AD, Henry H, Schluep M, Aubert V, Winkel L, et al. (2000) Evaluation of an intrathecal immune response in amyotrophic lateral sclerosis patients implanted with encapsulated genetically engineered xenogeneic cells. Cell Transplant 9: 471–484.
- 39. Hunt DP, Irvine KA, Webber DJ, Compston DA, Blakemore WF, et al. (2008) Effects of direct transplantation of multipotent mesenchymal stromal/stem cells into the demyelinated spinal cord. Cell Transplant 17: 865–873.
- 40. Glage S, Klinge PM, Miller MC, Wallrapp C, Geigle P, et al. (2011) Therapeutic concentrations of glucagon-like peptide-1 in cerebrospinal fluid following cell-based delivery into the cerebral ventricles of cats. Fluids Barriers CNS 8: 18.
- 41. Li Y, Perry T, Kindy MS, Harvey BK, Tweedie D, et al. (2009) GLP-1 receptor stimulation preserves primary cortical and dopaminergic neurons in cellular and rodent models of stroke and Parkinsonism. Proc Natl Acad Sci U S A 106: 1285–1290.
- 42. Williamson TL, Cleveland DW (1999) Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons. Nat Neurosci 2: 50–56.
- 43. Zhang B, Tu P, Abtahian F, Trojanowski JQ, Lee VM (1997) Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation. J Cell Biol 139: 1307–1315.
- 44. Hall ED, Oostveen JA, Gurney ME (1998) Relationship of microglial and astrocytic activation to disease onset and progression in a transgenic model of familial ALS. Glia 23: 249–256.
- 45. Clement AM, Nguyen MD, Roberts EA, Garcia ML, Boillee S, et al. (2003) Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice. Science 302: 113–117.
- 46. Nagai M, Re DB, Nagata T, Chalazonitis A, Jessell TM, et al. (2007) Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons. Nat Neurosci 10: 615–622.
- 47. Hargitai J, Lewis H, Boros I, Racz T, Fiser A, et al. (2003) Bimoclomol, a heat shock protein co-inducer, acts by the prolonged activation of heat shock factor-1. Biochem Biophys Res Commun 307: 689–695.
- 48. Kieran D, Kalmar B, Dick JR, Riddoch-Contreras J, Burnstock G, et al. (2004) Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice. Nat Med 10: 402–405.
- 49. Frankola KA, Greig NH, Luo W, Tweedie D (2011) Targeting TNF-alpha to elucidate and ameliorate neuroinflammation in neurodegenerative diseases. CNS Neurol Disord Drug Targets 10: 391–403.
- 50. Appel SH, Zhao W, Beers DR, Henkel JS (2011) The microglial-motoneuron dialogue in ALS. Acta Myol 30: 4–8.
- 51. Simonsen JL, Rosada C, Serakinci N, Justesen J, Stenderup K, et al. (2002) Telomerase expression extends the proliferative life-span and maintains the osteogenic potential of human bone marrow stromal cells. NatBiotechnol 20: 592–596.
- 52. Knippenberg S, Thau N, Dengler R, Petri S (2010) Significance of behavioural tests in a transgenic mouse model of amyotrophic lateral sclerosis (ALS). Behav Brain Res 213: 82–87.
- 53.
Knippenberg S, Thau N, Schwabe K, Dengler R, Schambach A, et al. (2011) Intraspinal Injection of Human Umbilical Cord Blood-Derived Cells Is Neuroprotective in a Transgenic Mouse Model of Amyotrophic Lateral Sclerosis. Neurodegener Dis. 2011/11/30 ed.
- 54. Klapdor K, Dulfer BG, Hammann A, Van der Staay FJ (1997) A low-cost method to analyse footprint patterns. J Neurosci Methods 75: 49–54.
- 55. Chen L, Lund PK, Burgess SB, Rudisch BE, McIlwain DL (1997) Growth hormone, insulin-like growth factor I, and motoneuron size. J Neurobiol 32: 202–212.