Intracerebral adult stem cells transplantation increases brain-derived neurotrophic factor levels and protects against phencyclidine-induced social deficit in mice.

Stem cell-based regenerative therapy is considered a promising cellular therapeutic approach for the patients with incurable brain diseases. Mesenchymal stem cells (MSCs) represent an attractive cell source for regenerative medicine strategies for the treatment of the diseased brain. Previous studies have shown that these cells improve behavioral deficits in animal models of neurological disorders such as Parkinson's and Huntington's diseases. In the current study, we examined the capability of intracerebral human MSCs transplantation (medial pre-frontal cortex) to prevent the social impairment displayed by mice after withdrawal from daily phencyclidine (PCP) administration (10 mg kg(-1) daily for 14 days). Our results show that MSCs transplantation significantly prevented the PCP-induced social deficit, as assessed by the social preference test. In contrast, the PCP-induced social impairment was not modified by daily clozapine treatment. Tissue analysis revealed that the human MSCs survived in the mouse brain throughout the course of the experiment (23 days). Significantly increased cortical brain-derived neurotrophic factor levels were observed in the MSCs-treated group as compared with sham-operated controls. Furthermore, western blot analysis revealed that the ratio of phosphorylated Akt to Akt was significantly elevated in the MSCs-treated mice compared with the sham controls. Our results demonstrate that intracerebral transplantation of MSCs is beneficial in attenuating the social deficits induced by sub-chronic PCP administration. We suggest a novel therapeutic approach for the treatment of schizophrenia-like negative symptoms in animal models of the disorder.

Introduction

Stem cells research is a rapidly developing field with implications that can revolutionize medicine, promising remedy to devastating diseases of the brain.[1] Stem cell-based therapy could exploit one of the two strategies: (i) cell replacement, when the administered stem cells substitute the cells lost in a disease. An example for this approach could be transplantation of functional insulin-producing beta-cells for diabetes mellitus or dopamine-secreting cells for Parkinson's disease. (ii) Cell restoration, when the administered cells provide a trophic effect, protect, rescue and minimize ongoing deterioration of the tissue affected in a disease. An example of this approach would be transplanting cells that provide neurotrophic support in neurodegenerative diseases.[2]

Mesenchymal stem cells (MSCs) hold a potential for regenerative therapy in neurological diseases.[1, 3] Previous studies have shown that bone marrow MSCs express genes and proteins associated with the neural lineage, and have been shown to hold neurogenic differentiation potential in vitro.[4, 5, 6] In our lab, we have shown that brain transplantation of MSCs in animal models of Parkinson's disease, Huntington's disease and multiple sclerosis results in engraftment into the brain, migration to lesioned sites and, most importantly, improvement in neuro-behavioral tests.[2, 7, 8, 9, 10, 11, 12] A single report has recently described the efficacy of brain MSCs transplantation, also in a rat model of depression.[13] In the aforementioned studies, though there is no conclusive evidence for the molecular mechanism underlying the behavioral improvement, it was shown to involve, at least in part, an increase in the availability of neurotrophic factors.

The complex pathophysiology underlying schizophrenia (SCZ) has been traditionally related to dysregulation of dopamine neurotransmission.[14] Additional data suggest that SCZ is associated with glutamate NMDA receptor dysfunctions.[15] This hypothesis is based on the experimental finding that agents that block NMDA receptors such as phencyclidine (PCP) and MK801 induce SCZ-like psychosis.[16] Over the past few years, other molecular contributors were implicated in the disease pathophysiology, such as reduced availability of neurotrophic factors, specifically brain-derived neurotrophic factor (BDNF) in specific brain regions,[17, 18] activation of the immune system,[19] impaired neurogenesis,[20] oxidative stress[21] and mitochondrial dysfunctions.[22]

Modeling SCZ in rodents is a challenge due to the complexity, the lack of clarity regarding the molecular processes involved in SCZ and the difficulty to relate distinct behavioral abnormalities in rodents to specific relevant symptoms in patients.[23, 24] However, in recent years studies have shown that specific animal models can be used as tools to investigate distinct endophenotypes of the disease.[25] Sub-chronic PCP administration is considered to establish specific endophenotypes associated with SCZ,[26] especially the negative symptoms. Specifically, social behavior of rodents treated with PCP is impaired while locomotor activity is preserved.[27]

To date, no study has investigated the application of a stem cell-based therapeutic strategy in an animal model of SCZ-like behaviors. A single report has indicated the potential of this approach in an in vitro study, using neural stem cells to protect cultured neurons against insult induced by a specific NMDA receptor antagonist.[28] In the present study, we sought to conduct a proof-of-concept experiment to explore the possible benefit of MSCs transplantation for PCP-induced impaired social behavior. We transplanted MSCs into the prefrontal cortex of mice sub-chronically treated with PCP and hypothesized that the engrafted MSCs will prevent or attenuate the development of PCP-induced impaired social behavior.

Materials and methods

The subacute PCP mouse model

A total of 54 male C57BL/6 mice aged 6 weeks (Harlan, Jerusalem, Israel) were used in this experiment. Mice were placed under 12 h light/12 h dark conditions and grown in individual ventilated cages with ad libitum access to food and water. All experimental protocols were approved by the University Committee of Animal Use for Research and Education. PCP (Sigma-Aldrich, St. Lewis, MO, USA; 10 mg kg−1 dissolved in 0.9% normal saline) was injected subcutaneously daily for 14 days.

Cell culture and Transplantation

Human MSCs were purchased from the Cambrex Bio Science Walkersville (Walkersville, MD, USA), cultured and expanded as previously described.[2] On treatment day, the cells were harvested, washed and prepared for transplantation at a concentration of 40 000 cells ul−1. Under chloral hydrate anesthesia, the mice were placed in a digital stereotactic frame (Stoelting, Wood Dale, IL, USA) and the cells (1 μl per injection site) were injected bilaterally to the following coordinates (relative to the bregma and dura): anterior–posterior +2 mm, medial–lateral ±0.4 mm, dorsal–ventral −3.5 mm at a rate of 1 μl min−1 using a Hamilton 701N syringe (Sigma-Aldrich). The inserted needle was withdrawn from each location after 5 min. Cells viability was assessed at the end of transplantation session using Trypan blue (Sigma-Aldrich). For cell tracking purposes, four animals in each group received injection of cells labeled with the red fluorescent marker PKH-26 (Sigma-Aldrich).

Experimental design

Transplantation took place at the first day of PCP administration. Sham surgery mice underwent identical surgical procedure without cells (saline injection only), clozapine-treated mice received daily clozapine injections (6 mg kg−1 i.p., from the first PCP administration), daily until the day of testing. The following groups were evaluated: controls (saline s.c., n=14), sham surgery PCP treated (n=15), MSCs transplanted PCP treated (n=13), clozapine and PCP treated (n=12). In order to prevent immune response, animals received 15 mg kg−1 s.c. cyclosporine A (Novartis, Basel, Switzerland) for 3 days around transplantation. Thereafter, cyclosporine was added to drinking water (15 mg kg−1 according to expected daily drinking volume per mouse). Behavioral tests included open-field test conducted 1 day after last PCP administration, and social preference test was conducted a week after the last PCP administration. Animals were killed 1 day following the social preference test. The experimental design is depicted in Figure 1.

Figure 1

The study design.

Behavioral tests

Open-field test was conducted by introducing the animals into a 50-cm2 arena and videotaping the spontaneous behavior of the mice for 60 min. The effects of sub-chronic PCP treatment on social behavior were assessed using the social preference test, as previously described.[29] The apparatus was divided into three compartments (one central and two lateral) containing two transparent plastic cups with holes placed on either side of the arena. Before the test day, mice were habituated for two consecutive days for 20 min, during that time the mice were free to explore the middle chamber. On the test day, the test mouse was initially habituated to the arena for 10 min, during that time two black partitions completely covered the sides of the arena containing the cups. Thereafter, the Plexiglas partitions were removed and an unfamiliar male C57BL/6 mouse was placed in one cup (social stimulus). The other cup remained empty (inanimate stimulus). The test mouse was free to explore all the chambers and was videotaped for another 10 min. Videos were analyzed using the Ethovision 7 software (Noldus, Wageningen, The Netheralnds), analysis allowed tracking either the center of the animal or the nose. Parameters analyzed included total time spent in each chamber; total nose pokes to the cups and total time in which the test mouse was in proximity to the cup—as a representation of social exploration. For calculation of the behavioral parameters obtained from the social preference test, we used a preference index, which is calculated as follows: if time in social chamber is S and time in non social chamber is NS, then preference index equals to (S−NS)/(S+NS).

Immunohistochemistry

At the end of the experiment (23 days post transplantation), eight animals of each group (four animals that were transplanted with the pre-labeled MSCs and four other randomly selected animals) were anesthetized with chloral hydrate and transcardially perfused with cold phosphate-buffered saline, followed by 4% paraformaldehyde in phosphate buffer. The brains were then immersed in 4% paraformaldehyde for 24 h at 4 °C followed by cryoprotection in 30% sucrose for an additional 48 h. The brains were frozen in chilled 2-methylbutane (Sigma-Aldrich), stored at −70 °C, and subsequently sectioned to slices measuring 10 μ. For microglial labeling, fluorescein isothiocyanate-conjugated Bandeiraea simplicifolia isolectin B4 (1:50 in phosphate-buffered saline; Sigma-Aldrich) was added for 1 h. Detection of BDNF was conducted following 5 min antigen retrieval in 5% SDS using rabbit anti-BDNF antibody (1:200 in blocking solution, Chemicon/Millipore, Billerica, MA, USA) followed by highly absorbed goat anti-rabbit Alexa 488 (1:500, Molecular Probes/Invitrogen, Carlsbad, CA, USA) diluted in phosphate-buffered saline. Nuclei were counterstained with 4′,6-diamidino-2-phenylindole (Sigma-Aldrich). Sections were mounted with fluorescent mounting solution (Dako, Glostrup, Denmark), covered with a cover slide and sealed. Digital images were obtained with a fluorescence Olympus BX52TF microscope (Olympus, Tokyo, Japan).

Western blot

At the end of the experiment, based on proximity to the average behavioral data, four animals from each group were killed using CO2. Immediately thereafter, crude dissection of the brains was conducted and whole cortex tissues were separated and cryopreserved in −70 °C. Consequently, tissue was thawed and total protein was produced as previously described.[30] Protein concentration was determined using BCA kit (Thermo Scientific, Rockford, IL, USA). Protein samples underwent western blot analysis as described previously.[31] Fifty microgram of protein was loaded in each lane. The following antibodies were employed: rabbit anti-AKT, rabbit anti-phospho-AKT (Cell Signaling Technology, Danvers, MA, USA), anti-ERK (extracellular signal-regulated kinase), anti-phospho-ERK (Santa Cruz Biotechnology, Santa Cruz, CA, USA) and anti actin (Millipore). Visualization and analysis of band intensities were performed using the Odyssey system (LI-COR, Lincoln, NE, USA).

ELISA

Quantification of BDNF levels was conducted using a BDNF specific enzyme-linked immunosorbent assay (ELISA) kit (Millipore) according to the manufacturer's instructions. Protein extracts were loaded on the ELISA plate (in quadruple samples, 25 μg protein in each well). The absorbance at 450 and 570 nm was recorded on a Microplate Reader (Labsystems, Helsinki, Finland). Results were normalized to total amount of protein.

Statistics

Data were analyzed using SPSS 17.0. software (SPSS, Inc., Chicago, IL, USA). Comparisons between groups were performed with the two-tailed analysis of variance, with Tukey post hoc test. The results were considered significant at P<0.05. All results are expressed as mean±s.e.m.

Results

Intra-cortical transplantation of MSCs prevents the impairment of social preference exhibited in PCP-treated mice

A day after the last PCP administration, mice were observed in the open-field test and showed no difference in total locomotor behavior (Supplementary Figure 1). One week later, mice underwent the social preference test. In the first 10 min of the test in which the mouse was limited to explore the central zone, empty of the social/non social stimulus, there was no difference in the total locomotor activity of the mice (as observed by total distance moved, Figure 2a). However, after 10 min, when allowed to explore both the chambers, that is, the chamber harboring the social stimulus and the chamber harboring the non-social stimulus, we found significant differences between the treatment groups in the preference towards the social stimulus.

Figure 2

Social preference test. (a) Total distance moved in the 10 min before the exploration of the lateral compartments harboring the social and inanimate stimuli. (b–d) Preference index calculated in 10 min at which the test mouse was free to explore all the chambers. (b) Preference index of time spent in chamber. (c) Preference index of frequency of nose pokes to the social stimulus. (d) Preference index in social exploration. Results are displayed as mean+s.e.m. Preference index was calculated as follows: if social is S and non-social is NS, then index=(S−NS)/(S+NS). *P<0.05, **P<0.01. MSCs, mesenchymal stem cells; PCP, phencyclidine.

Control saline-injected mice showed significant preference towards the social stimulus. In contrast, PCP-treated mice, which received sham surgery, did not show significant preference for the social stimulus, whereas the PCP-treated mice transplanted with MSCs showed significant preference towards the social stimulus. Daily clozapine administration to the PCP-treated mice did not alter the impaired social preference. Analysis of the social preference indices revealed that the same patterns of preference were registered for the total time spent in chambers (Figure 2b), total number of nose pokes towards the stimuli (Figure 2c) and total time in close proximity to the stimuli (Figure 2d).

The transplanted human MSCs survive in the mouse brain along the experiment without prominent immune reaction

To evaluate the effect of PCP and the insult of intra-cortical injection on global inflammatory state in the brain (regardless of cell transplantation), we stained the sham-treated brains with the fluorescein isothiocyanate-conjugated microglia marker IB4 and did not detect positive staining at the end of the experiment (Figure 3a). Upon analysis of the MSCs-treated mouse brains, we first attempted to locate the transplanted human MSCs. Fluorescent microscopy analysis revealed that the transplanted MSCs, pre-labeled with the red fluorescent dye PKH-26, were detected in the cortex near the site of transplantation (Figure 3b). We did not find any PKH-26-labeled cells in other brain areas such as the subventricular zone or the hippocampus. To assess the possibility of immune rejection in the brains following xenograft transplantation, we stained the sections harboring the transplanted cells. Intact PKH-26-positive cells indicated MSCS survival throughout the experiment. We did detect some microglia staining overlap the transplanted cells staining, suggesting that immune response was present only to some extent (Figures 3c–e).

Figure 3

Immunohistochemistry of cortical brain slices. (a) Green signal is microglia stained with fluorescein isothiocyanate-conjugated IB4 in the brain of mouse treated with PCP who underwent sham transplantation. (b) Red cells are human MSCs pre-labeled with PKH-26. (c–e) Evaluation of rejection using merged photo of PKH-26-labeled MSCs and microglia staining. IB4, Bandeiraea simplicifolia isolectin B4; MSCs, mesenchymal stem cells; PCP, phencyclidine.

Increased levels of BDNF in the cortex following MSC transplantation

Protein lysates of dissected cortical tissues from PCP-treated mice were analyzed by ELISA. We found 20.53% higher BDNF levels in the cortex of MSCs-transplanted mice in comparison with mice injected with saline (P<0.05, Figure 4a). BDNF levels in the MSCs-treated group was 32.25% (P<0.01) higher compared with the clozapine-treated group. Of note, no changes in total BDNF levels were observed in the hippocampal tissues of the mouse groups (data not shown). Immunohistochemistry study using anti-BDNF antibodies in the brain sections revealed that the transplanted MSCs expressed BDNF. However, the majority of the BDNF-positive cells were mouse cells located in the transplanted area (Figures 4b and c).

Figure 4

BDNF levels in the cortex. (a) Quantification of BDNF levels using ELISA, results represent picogram BDNF measured normalized to milligram cortex tissue (*P<0.05, **P<0.01). (b, c) Immunohistochemistry against BDNF in cortical brain slices of mice transplanted with MSCs (red, PKH pre-labeled human cells; green, BDNF signal; yellow, merge). BDNF, brain-derived neurotrophic factor; ELISA, enzyme-linked immunosorbent assay; MSCs, mesenchymal stem cells; PCP, phencyclidine.

MSCs transplantation into the cortex resulted in increased p-AKT/total AKT ratio

To evaluate the possible effect of MSCs transplantation on specific molecular pathways associated with PCP-induced insult, we analyzed phosphorylated AKT and ERK levels by western blot. Analysis of the ratios of phosphorylated ERK to total ERK (Figure 5b) did not reveal significant differences between the groups. In contrast, we found significant difference in the levels of AKT phosphorylation in the examined protein lysates of the cortex (Figure 5a), namely, the percent of phosphorylated-AKT from total AKT was significantly higher in the cortex of the MSCs-treated mice as compared with the PCP sham surgery group (1.85-fold, P<0.05). AKT phosphorylation ratio in MSCs-treated group was also significantly higher compared with the PCP-clozapine group (3.82-fold, P<0.01).

Figure 5

Western blot analysis of phosphorylated AKT (a) and ERK (b) in cortical lysates. Results represent ratio of phosphorylated protein to total protein—each was normalized to actin. The ratio obtained in untreated controls (saline instead of PCP (phencyclidine) and no cell/clozapine treatment) is represented as 100%. *P<0.05, **P<0.01.

Discussion

In this study, we present a novel approach for the treatment of an animal model of SCZ-like social impairment. In the current proof-of-concept study, we specifically show that the social deficit behavior induced by sub-chronic administration of PCP can be prevented by intra-cortical transplantation of MSCs, at variance from clozapine that failed to prevent the social deficit. The notion of applying MSCs-based therapeutic approach to an animal model of SCZ stems from the two complementing details: (1) the frustrating deadlock of antipsychotics in the treatment of negative symptoms of SCZ.[32] (2) The accumulating body of evidence suggesting the benefit of MSCs-based therapeutic strategies for brain diseases.[33, 34]

Current treatments for SCZ are aimed mainly at antagonizing dopamine and other neurotransmitter receptors, and yield relatively limited success in the treatment of SCZ-related negative symptoms and cognitive deficits. Importantly, current antipsychotic medications rely upon the rationale of over-active dopaminergic activity or other dysregulated neurotransmitter systems in the brain. Therefore, antipsychotics are efficient in controlling the positive symptoms, which are strongly associated with post-synaptic monoamine receptors over-activity.[14] Recent studies suggest that the pathophysiology underlying SCZ may also involves processes associated with neurodegeneration.[21, 22, 35, 36, 37] For these aspects of the disease, current antipsychotic therapy offers limited resolution. Intra-brain MSCs transplantation has been shown to influence specific processes relevant to the pathophysiology of neuropsychiatric diseases. Those include the effect of MSCs on the (i) brain immune status,[38] (ii) neurotrophic factor availability[39, 40] and (iii) neurogenesis.[41, 42]

Designing the study, we sought to utilize one of the most established rodent model of SCZ-negative symptoms, namely, the subacute PCP model.[43] We chose the social preference test as it presents a relatively straightforward paradigm of measuring sociability and was recently validated in C57/BL mice.[27] We performed cell transplantation concomitantly with the first dose of PCP, aiming to provide the transplanted cells the optimal chances of protection against the iatrogenic insult. Transplantation was aimed at the anatomical site, which is assumed to be involved in the social insult induced by the PCP, namely, the prefrontal cortex.[44, 45]

We included clozapine-treated mice as a comparator group owing to a report which had shown that clozapine treatment could reverse some of the social deficits induced by sub-chronic PCP treatment.[46] The fact that clozapine did not reverse the social deficits in our study may be explained by the differences in the behavioral test, the mouse strain or the treatment regimen employed in our study.

We chose to transplant human MSCs as they are more readily cultured, better characterized, not tumorogenic and not contaminated by hematopoietic cells in comparison with mouse-derived MSCs.[47] Importantly, our previous experience with transplantation into various models of neurodegenerative diseases has shown that human MSCs survive in the brain and exert some beneficial effects.[2, 8, 10] This choice faced us with the challenge of immune rejection and the need to use cyclosporine. In order to minimize the possible effects of cyclosporine on the social behavior,[48] all the groups, including the control, received identical cyclosporine treatment. Evidently, the intensity of immunosuppression we employed was sufficient to allow the human MSCs to survive in the brain along the whole experiment period, 23 days, with only limited immune rejection.

The behavioral results of the social preference test seemed to confirm our hypothesis that MSCs could act to protect against the social deficit induced by the PCP administration. As it is known that MSCs modulate immune response in the CNS,[38] we first evaluated whether an immune process/inflammation occurred following the PCP insult. To that end, we used the staining for microglia and found that no inflammation was present in the brains following the PCP treatment.

Neurotrophic factor availability, specifically BDNF, is postulated to have a key role in many aspects of brain development, maintenance and function, including the formation of synapses and neural circuits.[49, 50] Several studies have shown that dysregulation of BDNF expression in specific brain regions may be involved in the pathophysiology of various neuropsychiatric disorders, including SCZ.[51, 52] Of note, BDNF has emerged as a key factor in the development and maintenance of social behavior.[53, 54] Importantly, BDNF mRNA levels were recently reported to be downregulated in the prefrontal cortex of female rats sub-chronically treated with PCP.[55] MSCs are known to enhance neurotrophic factor availability, either by direct secretion by the engrafted cells [2] or by enhancement of endogenous levels through in situ interaction with the host brain cells.[40] On the basis of the above mentioned data, we postulated that transplantation of MSCs into the cortex of mice sub-chronically treated with PCP, could increase BDNF levels adjacent to the transplantation site, and counteract some of the negative behavioral effects of the PCP. Notwithstanding, we cannot rule out that other soluble factors that are increased following administration of MSCs could also be involved in the positive behavioral outcome of MSCs intra-cortical transplantation.[56]

Quantitative ELISA analysis of BDNF levels in the cortex extracts of PCP-injected mice indeed demonstrated higher BDNF levels in the MSCs-treated group compared with the sham-operated or clozapine-treated groups. The relatively low number of transplanted cells (only 40 000 cells per cortex) together with the immunohistochemical analysis of BDNF implies that although some BDNF was secreted from the transplanted human MSCs, most BDNF originated from the endogenous mouse brain cells. This explanation is in context with a recent report in a stroke rat model that has shown that MSCs transplantation induces a therapeutic response through the induction of the host astrocytes to upregulate the levels of neurotrophic factors.[40]

Recently it was shown that, in vitro, acute exposure of neurons to PCP results in rapid death through apoptosis.[57] Importantly, this study has demonstrated that the insult induced by PCP could be prevented following the addition of recombinant BDNF. It was suggested that the protective effect of BDNF is associated with the activation of the phosphatidylinositol 3-kinase/AKT and the ERK pathways. Interestingly, the only report to date to examine stem cell protective effect on cultured neurons following NMDA receptor blockade showed that the protection occurs via AKT/ERK signal regulation.[28] Our data show that MSCs transplantation results in higher phosphorylated AKT/total AKT ratio as compared with the sham-operated or clozapine-treated mice. We could not detect significant differences in the phosphorylated ERK ratios or in the total levels of cleaved caspase (data not shown). This could be explained by the fact that we killed the animals 10 days following the last PCP dose, while the in vitro study mentioned above showed that PCP-induced apoptosis occurs within hours after the exposure.[57]

Our study serves as a pioneer proof-of-concept for cell-based therapeutic strategies for SCZ animal models. To our knowledge, this is the first report of stem cell transplantation study in an animal model of SCZ. Evidently, future studies would have to face the challenge of enlarging the battery of behavioral tests representing several SCZ-related endophenotypes/dimensions. We have shown that MSCs transplantation can protect against the PCP insult, however, future studies should be performed in an attempt to explore the possibility of reversing an already established damage (that is, transplant cells after the last PCP dose), or to try and use stem cell-based approaches in relevant transgenic mouse models of SCZ. Another prospect that would have to be explored in the future is the optimal site of transplantation, that is, evaluation of effects of MSCs in other brain sites affected in SCZ and PCP abuse, such as the hippocampus.

To conclude, we showed that intra-cortical MSCs transplantation protected against the social deficit induced by sub-chronic PCP administration. Analysis of the mouse brains showed higher levels of BDNF in the MSCs-treated mouse cortex and elevated ration of p-AKT/AKT compared with the sham-treated controls. Interestingly, BDNF and p-AKT were recently reported to protect neuronal culture against PCP insult in vitro. Our study suggests that MSCs transplantation might be considered, at least at the experimental laboratory level, as a putative strategy for the treatment of some SCZ-related endophenotypes/dimensions, such as negative symptoms and cognitive deficits.