Neuroprotective effect of rapamycin on spinal cord injury via activation of the Wnt/β-catenin signaling pathway

Abstract

The Wnt/β-catenin signaling pathway plays a crucial role in neural development, axonal guidance, neuropathic pain remission and neuronal survival. In this study, we initially examined the effect of rapamycin on the Wnt/β-catenin signaling pathway after spinal cord injury, by intraperitoneally injecting spinal cord injured rats with rapamycin over 2 days. Western blot analysis and immunofluorescence staining were used to detect the expression levels of β-catenin protein, ca-spase-3 protein and brain-derived neurotrophic factor protein, components of the Wnt/β-catenin signaling pathway. Rapamycin increased the levels of β-catenin and brain-derived neurotrophic factor in the injured spinal cord, improved the pathological morphology at the injury site, reduced the loss of motor neurons, and promoted motor functional recovery in rats after spinal cord injury. Our experimental findings suggest that the neuroprotective effect of rapamycin intervention is mediated through activation of the Wnt/β-catenin signaling pathway after spinal cord injury.

Introduction

Rapamycin, an antifungal agent, is clinically utilized as an efficient immunosuppressant after solid organ transplantation (Chen et al., 2013; Li et al., 2013). Recent evidence of pleiotropic effects of rapamycin has aroused much concern; for example, rapamycin inhibits the growth of abdominal aortic aneurysms, restrains glioblastoma cancer stem cells and alleviates brain edema (Guo et al., 2014; Mendiburu-Eliçabe et al., 2014; Rouer et al., 2014). Some reports have claimed that rapamycin can induce autophagy, reduce neural tissue damage and improve the recovery of locomotor function after spinal cord injury (SCI) (Sekiguchi et al., 2012; Wang et al., 2014). However, the specific molecular mechanism of action of rapamycin after SCI has not been elucidated.

Wnts are a family of glycoproteins (Cao, 2013). The Wnt/β-catenin signaling pathway, a canonical Wnt signaling pathway, plays a significant role in neural development, axonal guidance, neuropathic pain remission and neuronal survival (Suh et al., 2011; Zhang et al., 2013). Thus, studies investigating the roles of the Wnt/β-catenin signaling pathway may provide a novel molecular mechanism and therapeutic target for treating SCI.

In the present study, we hypothesized that rapamycin would have an impact on the Wnt/β-catenin signaling pathway after SCI, and aimed to explore the expected neuroprotective mechanism of action of rapamycin in the treatment of SCI.

Materials and Methods

Animals

Seventy-two adult male Sprague-Dawley rats (of specific pathogen-free grade, aged 8-12 weeks, weighing 250-300 g) were purchased from the Laboratory Animal Centre of Liaoning Medical University (Jinzhou, Liaoning Province, China; license No. SCXK (Liao) 2003-0011). Rats were raised in the SPF Laboratory Animal Center, which maintained the environment at 23 ± 0.5°C with an alternating 12-hour light/dark cycle. The experimental procedure had full ethical approval from the Animal Ethics Committee of Liaoning Medical University in China. The rats were randomly divided into three groups: a rapamycin group (n = 24), a saline group (n = 24) and a sham group (n = 24).

Establishment of SCI model in rats

SCI models were established using the modified Allen technique (Yacoub et al., 2014). Briefly, the rats in the rapamycin and saline groups were anesthetized with 10% chloral hydrate (0.33 mL/kg) via intraperitoneal injection, the backsides of rats were disinfected and incised, and the spinal cords were clearly exposed after spinous T 9/10 was removed. Then, a striker (weight: 10 g, diameter: 2 mm) was dropped from a height of 25 mm.The injury was rapidly induced and both lower extremities of rats also quickly withdrew and trembled, while gatism was also observed. Rats were not selected for the study until the SCI model was successfully established. However, the sham-operated animals (sham group) underwent laminectomy alone after being anesthetized. Then, rats were injected with antibiotics for 3 successive days and the bladder was massaged three times daily to accelerate the recovery of automatic micturition function.

Drug administration

Rapamycin (Life Technologies, Carlsbad, CA, USA) was dissolved in DMSO at a concentration of 25 mg/mL, and diluted to a final concentration of 1 mg/mL with saline before being injected. Then, rapamycin (0.5 mg/kg) and saline (0.5 mL/kg) were administered to rats in the rapamycin and saline groups via intraperitoneal injection at 1 hour after SCI and then once daily for 2 days (Chen et al., 2013).

Functional analysis

The Basso, Beattie & Bresnahan (BBB) open-field locomotor rating scale was utilized to evaluate the recovery of motor function in rats after SCI (Basso et al., 1995). Briefly, three independent examiners were blinded to assess BBB scores before operation and at 1, 3, 7, 14, 21 and 28 days after SCI. The BBB scores ranged from 0 to 21 points. The minimum score (0) indicated complete paralysis, and the maximum score implied normal function. The average scores were calculated according to the progression of locomotion recovery after SCI.

Western blot analysis

The rats were severally narcotized with 10% chloral hydrate (0.33 mL/kg) via intraperitoneal injection at 3 and 5 days post-surgery, and the T 8-11 spinal cord (2 mm cephalad and caudally from the epicenter) was dissected out. The tissues were homogenized in RIPA lysis buffer (50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1% NP-40, 0.25% Na-deoxycholate, 1 mM EDTA). Then, the concentrations of proteins were assessed using the bicinchoninic acid kit, adjusted to 2 μg/μL, and 40 μg of protein was resolved on 12% Tris-glycine SDS-PAGE gels. Then, the proteins were transferred to polyvinylidene fluoride membranes and incubated with primary antibodies (rabbit anti-β-catenin polyclonal antibody, 1:1,000, Abcam, Cambridge, UK; rabbit anti-caspase-3 polyclonal antibody, 1:1,000, Abcam; mouse anti-β-actin polyclonal antibody, 1:1,000, Abcam) at 4°C overnight after being sealed. On the following day, the membranes were washed three times with Tris-buffered saline (TBS; 150 mM NaCl, 100 mM Tris-HCl, pH 7.4) containing 0.1% Tween-20, and then incubated with goat anti-rabbit/mouse IgG (1:3,000, Abcam) at room temperature for 2 hours. Finally, the membranes were developed using a ChemiDoc-It™ TS2 Imager (UVP, LLC, Upland, CA, USA) and relative optical density was measured using ImageJ2x software (National Institutes of Health, Bethesda, MD, USA).

Immunofluorescence analysis

At 7 days after the operation, rats were anesthetized with 10% chloral hydrate (0.33 mL/kg) and then perfused with 4% paraformaldehyde. In brief, spinal cord tissues (T 8/9 ) 3 mm rostral to the epicenter were harvested from the rats and fixed in 4% paraformaldehyde. Tissues were immersed in 30% sucrose overnight and sliced into cross-sections at a thickness of 5 μm. Sections were placed into a box with 0.01 M citric acid for antigen retrieval. Then, the sections were blocked using blocking buffer (5% normal goat serum and 0.1% Triton-X100 in PBS) at 4°C for 1 hour and incubated with primary antibodies (rabbit anti-β-catenin polyclonal antibody,1:400, Abcam; rabbit anti-BDNF polyclonal antibody, 1:500, Novus Biologicals, Littleton, CO, USA) at 4°C overnight. Next, the tissues were incubated with FITC-goat anti-rabbit IgG (1:400, Abcam) and the nuclei were stained with DAPI (1:1,000) solution. All slides were observed under a fluorescence microscope (Leica, Heidelberger, Germany) after being mounted with Permount TM Mounting Medium (Sigma-Aldrich, St. Louis, MO, USA). The optical density of fluorescence was analyzed using ImageJ2x software.

Nissl staining

To observe the morphology and number of neurons in different groups, spinal cord tissues (T 8/9 , 3 mm rostral to the epicenter) were captured from the rats at 7 days after SCI. Cross-sections at 20 μm thickness were dried at room temperature and placed into miscible liquids (alcohol/chloroform = 1:1) overnight. Then, the slices were dehydrated through 100% alcohol, 95% alcohol and distilled water. The slices were stained in 0.1% cresyl violet (Sigma-Aldrich) solution at 40°C for 10 minutes and rinsed quickly in distilled water. Subsequently, the slices were differentiated in 95% ethyl alcohol for 5 minutes, dehydrated in 100% alcohol and cleared in xylene for 5 minutes. The slices were mounted and observed under a light microscope (Leica). The average quantities of Nissl bodies were counted by randomly selecting four Nissl-stained sections at the same site from each animal.

Statistical analysis

All data are expressed as the mean ± SD and were analyzed using the Graph Prism Program, Version 5.0 (GraphPad Software, Inc., La Jolla, CA, USA). Comparisons between the two groups were performed using the unpaired Student′s t-test; discrepancies among multiple groups were tested using one-way analysis of variance, and the BBB scores were analyzed using the Mann-Whitney U test. P-values less than 0.05 were considered statistically significant.

Results

Rapamycin treatment improved locomotion function of SCI rats

As shown in [Figure 1], the BBB scores of rats were 21 points before the operation in all three groups and decreased to 0 point at 1 day after SCI. However, the tendency of BBB scores of rats showed no significant difference from 1 to 14 days after SCI in the rapamycin and saline groups (P > 0.05). At 14, 21, and 28 days post-operation, the BBB scores of rats in the rapamycin group were obviously higher than those of rats in the saline group (P < 0.05). These results indicate that the rats′ locomotion function was improved by rapamycin intervention after SCI.{Figure 1}

Rapamycin treatment improved pathologic morphology of spinal neurons in SCI rats

Nissl staining showed that the quantities of Nissl bodies in the spinal cord were obviously lower in the saline group than in the sham group after SCI. On the contrary, compared with the saline group, SCI was distinctly improved and the damaged tissue was also clearly reduced by rapamycin. At the same time, the quantities of motor neurons in the anterior horns were elevated (P < 0.01) and the morphology of neurons from rats in the rapamycin group was perfected compared with that of neurons from rats in the saline group ([Figure 2]).{Figure 2}

The Wnt/β-catenin signaling pathway was activated by rapamycin in the spinal cords of SCI rats

The β-catenin protein, the hallmark protein of the canonical Wnt signaling pathway (Reya and Clevers, 2005), was detected by western blot analysis ([Figure 3]A) and immunofluorescence staining ([Figure 4]A). The expression level of β-catenin protein in the spinal cords of rats was significantly increased at 3 and 5 days after SCI in the presence of rapamycin, compared with the levels in the absence of rapamycin (saline group) (P < 0.05 or P < 0.01; [Figure 3]B). In addition, the intensity of fluorescence for β-catenin in the spinal cords of rats was stronger in the rapamycin group than in the other groups (P < 0.05 or P < 0.01; [Figure 4]B). These findings suggest that the Wnt/β-catenin signaling pathway was significantly enhanced by rapamycin in the spinal cords of SCI rats.{Figure 3}{Figure 4}

Rapamycin inhibited apoptosis in the spinal cords of SCI rats

The expression level of caspase-3 protein in the spinal cords of SCI rats was assessed at 3 and 5 days after SCI by western blot analysis ([Figure 3]A). Compared with the sham group, the level of caspase-3 expression in the spinal cords of rats was increased in the saline group; compared with the saline group, the level of caspase-3 expression in the spinal cord of rats was reduced in the rapamycin group ([Figure 3]C, day 3: P < 0.05, day 5: P < 0.01). These results implied that rapamycin treatment inhibited apoptosis after SCI.

Rapamycin increased BDNF expression in the spinal cord of SCI rats

At day 7 after injury, immunofluorescence analysis was utilized to detect BDNF expression in the three groups of rats ([Figure 5]A). The relative intensity of BDNF fluorescence in the spinal cord of rats was stronger in the rapamycin group than in the other two groups ([Figure 5]B, P < 0.05 or P < 0.01). The level of BDNF fluorescence in the spinal cord of rats was dramatically boosted by rapamycin, which provided a beneficial environment for functional recovery after SCI.{Figure 5}

Discussion

In the present study, the expression of β-catenin protein was increased by rapamycin intervention after SCI, implying that the Wnt/β-catenin signaling pathway was activated by rapamycin after SCI. In addition, the expression level of BDNF protein was enhanced by rapamycin; on the contrary, rapamycin treatment inhibited caspase-3 expression after SCI. Furthermore, the BBB scores and Nissl staining indicated that rapamycin treatment decreased the loss of motor neurons and improved the recovery of locomotor function after SCI. Collectively, these findings suggest that the neuroprotective effect of rapamycin on SCI is mediated through activation of the Wnt/β-catenin signaling pathway.

Secondary injury plays an important part in the process of SCI, which offers a potential clinical therapeutic target for SCI (Xie et al., 2014). Secondary injury is induced by various factors: apoptosis, oxidative stress, immunodeficiency and inflammation (Hayashi et al., 2000; Profyris et al., 2004). Unfortunately, the effect of methylprednisolone, a first-line drug for treating SCI, has been questioned (Hall and Springer, 2004; Wilson and Fehlings, 2011; Fehlings et al., 2014). Hence, our study aimed to identify an alternative effective drug and illuminate the specific molecular mechanism of action of the drug.

Rapamycin is a lipophilic macrolide antibiotic produced by Streptomyces hygroscopicus, which is developed as an immunosuppressive agent in the clinic (Raught et al., 2001; Wang et al., 2014). There is growing evidence that rapamycin can inhibit tumor proliferation and has a cytostatic effect against human cancers (Vignot et al., 2005; Rouer et al., 2014; Weng et al., 2014). Interestingly, an increasing number of effects of rapamycin on SCI has attracted the attention of researchers worldwide; these include anti-inflammation, immunoregulation, autophagy promotion and neuroprotective effects (Kanno et al., 2012; Sekiguchi et al., 2012; Sontag et al., 2013). In the current study, the recovery of locomotor function was reflected in the BBB scores of rats, and the results revealed that rapamycin obviously improved locomotor neurological function at 14 days post-injury. Nissl staining indicated that rapamycin also reduced the loss of motor neurons and accelerated the recovery from injury after SCI. These results have shown that locomotor function is improved by rapamycin after SCI; however, the molecular mechanism of this effect of rapamycin on SCI has not been elucidated.

Wnts are a well-characterized family of glycoproteins, which include at least three different signaling pathways: the canonical Wnt/β-catenin pathway, the noncanonical planar cell polarity pathway, and the Wnt-Ca 2+ pathway (Fernández-Martos et al., 2011; Wang et al., 2013). The Wnt/β-catenin signaling pathway plays a significant role in SCI. Briefly, β-catenin receives a signal from membrane receptors and then transmits this signal to the nucleus, where it binds Lef/Tcf transcription factors, ultimately activating target genes (Rao and Kühl, 2010). The β-catenin protein is the central player, and it promotes the regeneration of axons, inhibits apoptosis and improves functional recovery after SCI (Suh et al., 2011; Hollis ER 2 nd and Zou, 2012; Sun et al., 2013; González-Fernández et al., 2014). Studies of the Wnt/β-catenin pathway may offer an original mechanism for treating SCI. Therefore, a hypothesis that the neuroprotective effect of rapamycin on SCI is mediated through influencing the Wnt/β-catenin signaling pathway was initially put forward. In the present study, the expression of β-catenin protein was detected by western blot analysis and immunofluorescence staining. Western blot analysis results suggested that the expression level of β-catenin was significantly increased by rapamycin treatment after SCI. Analogously, immunofluorescence analysis showed that β-catenin was also markedly increased in the presence of rapamycin. These phenomena clearly show that the Wnt/β-catenin signaling pathway is activated by rapamycin and suggests an underlying mechanism for the action of rapamycin following clinical application.

To further verify the neuroprotective effect of rapamycin on SCI, apoptosis and neurotrophic factors were observed in our experiment. Some researchers have reported that apoptosis is activated after SCI, which increases the loss of neurons and retards neural functional recovery. During apoptosis, the expression of Apaf-1 protein, Bcl-2 protein and caspase family members is altered; in other words, the expression of caspase-3, a vital member of the caspase family, is elevated after apoptosis (Korsmeyer, 1999; Yuan and Yankner, 2000). A decrease in the expression level of caspase-3 protein suggests that apoptosis has been inhibited, and the number of neurons should be preserved and function improved (Fernandes-Alnemri et al., 1994; Sakurai et al., 2003). In addition, recent evidence indicates that the increase in BNDF expression establishes an environment for nerves to recover, reducing the loss of nerves and apoptosis, and accelerating functional recovery after SCI (Kamei et al., 2007; Sasaki et al., 2009). In our current study, western blot analysis demonstrated that the expression level of caspase-3 was evidently lowered by rapamycin; conversely, the expression of BDNF was visibly enhanced by rapamycin in our immunofluorescence analysis.

Our findings jointly indicate that rapamycin treatment inhibited the apoptosis of neurons, increased the number of neurons, improved recovery after injury and increased the expression of BDNF, ultimately exerting a significant neuroprotective effect on SCI, via activation of the Wnt/β-catenin signaling pathway. This significant discovery demonstrates the molecular mechanism underlying the neuroprotective effect of rapamycin treatment after SCI, which could promote clinical application of rapamycin for treating SCI. Nevertheless, the effect of rapamycin has been studied only on neurons in our study, and it will be necessary to further study the effects of rapamycin on astrocytes/microglia after SCI. In addition, ours are only preliminary findings regarding the effect of rapamycin on the Wnt/β-catenin signaling pathway after SCI; further studies are needed to verify the various effects of rapamycin on the Wnt signaling pathway at different time points in rats after SCI. Simultaneously, the in-depth molecular mechanism underlying its effects requires further validation in different neural cells through both in vitro and in vivo experiments, to provide evidence supporting the clinical application of rapamycin.

Acknowledgments: We thank Jing Bi and Dong-he Han from Department of Neurobiology and Key Laboratory of Neurodegenerative Diseases of Liaoning Province, Liaoning Medical University, Jinzhou, China, for providing valuable technical assistance in this work.[36]