Schwann cells genetically modified to express S100A4 increases GAP43 expression in spiral ganglion neurons in vitro

ABSTRACT

Schwann cells (SCs) have been reported as a possible source of neurotrophic support for spiral ganglion neurons (SGNs). This study was aimed to investigate whether S100A4 was contributed in the functional effects of SCs on SGNs. SCs were transfected with S100A4 vector or small interfering RNA (siRNA) against S100A4, and the transfection efficiency was verified by quantitative PCR (qPCR) and Western blot. The migration of transfected SCs was determined by Transwell assay, and the expression levels of vascular endothelial growth factor precursor (VEGF) and matrix metallopeptidase 9 (MMP-9) were measured by Western blot. Co-culture of either S100A4 overexpressed or suppressed SCs with SGNs, and the growth associated protein 43 (GAP43) expression in SGNs was detected by immunofluorescence (IF), qPCR and Western blot. The migration of SCs was significantly enhanced by S100A4 overexpression (P < 0.001), while was suppressed by S100A4 knockdown (P < 0.01). Further, the expressions of VEGF and MMP-9 were notably up-regulated by S100A4 overexpression, while were down-regulated by S100A4 knockdown. Moreover, co-culture with the S100A4 overexpressed SCs significantly increased the expression of GAP43 in SGNs (P < 0.01). As expected, co-culture with S100A4 knockdown SCs decreased GAP43 level (P < 0.05). S100A4 enhanced the migratory ability of SCs. SCs genetically modified to overexpress the S100A4 could up-regulate the GAP43 expression in SGNs.

KEYWORDS:

• GAP43
• migration
• S100A4
• schwann cells (SCs)
• spiral ganglion neurons (SGNs)

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Corrigendum

Introduction

Schwann cells (SCs) originate from the neural crest are the predominant cell type constituting the structure of peripheral nerves.¹ SCs are implicated in many important aspects of peripheral nerve biology, including the conduction of nervous impulses, production of the nerve extracellular matrix, modulation of neuromuscular synaptic activity, and presentation of antigens to T-lymphocytes.^2-5 Besides, SCs can produce and secrete neurotrophic factors, especially brain-derived neurotrophic factor (BDNF) which supports and influences the growth and regenerative capacity of neurons.⁶ Spiral ganglion neurons (SGNs) are located in Rosenthal's canal within the modiolus of the cochlea.⁷ Maintenance of a robust SGNs population may improve the efficacy of the electrode-neural interface and enhance cochlear implant performance.⁸ Previous studies have shown that BDNF secreted from SCs can improve SGNs survival and prevent degeneration in models of deafness.^9,10 In a word, SCs have an intimate relationship with SGNs.

S100A4, also known as mts1, a member of S100 family of transcription factors, locates in the 1q21 human chromosome region.¹¹ S100A4 has been reported as a vital regulator in modulating cell cycle, proliferation, apoptosis, migration of various types of cells through different mechanisms.^11,12 S100A4 is widely expressed in the nervous system, and it appears to be involved in the regulation of neuron survival plasticity, and responses to injury or disease.¹³ Later studies have identified S100A4 as a neuroprotectant in peripheral nervous system.^14,15 However, little was known about the neuroprotective effects of S100A4 on SCs and SGNs.

In this study, rat SCs line RT4-D6P2T were employed and transfected with S100A4 vector or small interfering RNA (siRNA) against S100A4, to obtain S100A4 overexpressed or suppressed SCs. Further, the migratory ability of transfected cells was determined to reveal the effects of S100A4 on SCs migration. Next, SGNs were co-cultured either with S00A4 overexpressed or suppressed SCs, and the expression level of growth associated protein 43 (GAP43) in SGNs was detected, to investigate the role of S100A4 dysregulated SCs in SGNs. This study might add data on the molecular correlation of SCs with SGNs.

Materials and methods

SCs and primary SGNs culture

Rat SCs line RT4-D6P2T was purchased from the American Type Culture Collection (ATCC; Manassas, VA). Cells were cultured in Dulbecco's modified Eagle's medium (DMEM) high glucose (Life Technologies, Carlsbad), supplemented with 10% fetal bovine serum (FBS; Hyclone, Logan, UT) and were incubated at 37°C in a humidified atmosphere containing 5% CO₂.¹⁶

A total of 12 Sprague-Dawley rats (postnatal day 3–5) were provided by the Animal Center of the Academy of Military Science of the Chinese PLA. Cochleae were isolated after rats were decapitated, and SGNs were dissociated as previous described.¹⁷ The SGNs were cultivated in DMEM high glucose (Life Technologies), 25 mM HEPES (Life Technologies), 30 U/mL penicillin (Grünenthal GmbH, Aachen), 3 μL/mL N2 supplement (Life Technologies) and 5 μg/mL insulin (Sigma-Aldrich, St. Louis).¹⁸ SGNs were incubated in a humidified atmosphere with 5% CO₂ at 37°C. The mere killing of rats for tissue analyses was approved by our local ethics committee. All procedures were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. Precautions were taken to minimize suffering and the number of animals used in each experiment.

Cell transfection

SCs were seeded in 6-well plates at a density of 2 × 10⁵. After culture for 24 h, cells were divided into 3 groups, namely control, pc S100A4 and si S100A4. A S100A4 expression vector, i.e., pc S100A4, was constructed by sub-cloning the full-length S100A4 coding sequence into pcDNA3.1 (Sangon Biotech, Shanghai, China), and the vector was transfected into cells in pc S100A4 group. Cells in si S100A4 group were transfected with siRNA against S100A4 (RiboBio, Guangzhou, China). All transfections were performed by using Lipofectamine 2000 reagent (Invitrogen) following the manufacturer's protocol. At 48 h after transfection, the cells were prepared for further analyses.

Real-time quantitative PCR (qPCR)

After transfection, cells were collected and total RNA in cells were extracted by using TRIzol (Invitrogen). DNaseI (Invitrogen) was used for removing the DNA contamination. Afterward, 1 μg RNAs of each sample were used for cDNA synthesis by using Transcriptor First Strand cDNA Synthesis Kit (Roche, USA), according to the manufacturer's instructions. qPCR was carried out for a total of 20 μL reaction mixtures on an ABI Prism 7000 Sequence Detection System (Applied Biosystems, Foster City, CA, USA) using FastSTART Universal SYBR Green Master (ROX) (Roche, USA).¹⁸ Data were analyzed according to 2^−ΔΔCt method and were normalized to GAPDH expression in each sample. All primers were synthesized by GenePharma (Shanghai, China).

Western blotting

After transfection, cells were collected and cellular protein was extracted by RIPA lysis buffer (Beyotime Biotechnology, Shanghai, China). Protein concentration was quantified using BCA™ Protein Assay Kit (Pierce, Appleton, WI, USA), according to the manufacturer's recommendations. Equal amounts of proteins were separated on a sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and blotted onto polyvinylidene fluoride (PVDF) membranes. The membranes were blocked with 5% skim milk for 1 h, and then probed with primary antibodies: S100A4 (sc-292281), vascular endothelial growth factor precursor (VEGF; sc-7269), matrix metallopeptidase 9 (MMP-9; sc-21733), GAP43 (sc-17790) or GAPDH (sc-365062; Santa Cruz Biotechnology, Santa Cruz, CA) at 4°C, overnight. Afterward, the membranes were incubated with the appropriate horseradish peroxidase-conjugated secondary antibodies. The bands were visualized by the ECL Plus Western Blotting Substrate (Thermo Scientific).¹⁹

Cell migration assay

Cell migration was evaluated by Transwell assay using the 8 μm-pore Transwell migration chambers (Corning, USA). Briefly, transfected cells were seeded in the upper portion of a chamber with serum-free medium. Complete medium filled in the lower chamber as an attractant. At 48 h after incubation, the non-migrated cells in the upper chamber were removed by cotton swabs. The migrated cells were stained with 0.1% crystal violet (Beyotime, Nantong, China) for 30 min, and then photographed and counted under optical microscope (Olympus, Tokyo, Japan).¹⁹

Immunofluorescence (IF)

SGN and SCs were co-cultured as previous described.⁸ Briefly, SGN were plated onto 8-well chamber slides (Nalge Nunc International, Rochester, NY, USA) at a density of 2 × 10⁴ cells/well. The transfected SCs were collected and added to the SGN at 2 × 10⁴ cells/well. After 24 h of incubation in DMEM high glucose with 10% FBS, cells were washed with phosphate-buffered saline (PBS) 3 times and fixed with 4% formaldehyde for 20 min on ice. Cells were then permeabilized with 1% Triton X-100 for 25 min, and blocked in 10% goat serum (Beyotime) for 30 min at 37°C. The cells were incubated with the primary antibody GAP43 (sc-17790, Santa Cruz Biotechnology) overnight at 4°C, and followed by incubation with fluorescent secondary antibody for 1 h at room temperature. Cell nuclei were stain for 5 min by using 4′, 6-diamidino-2-phenylindole (DAPI; Beyotime). The fluorescent images were obtained using an automated upright microscope system (Leica, DM4000B Leica Microsystems, Wetzlar, Germany).²⁰

Statistical analysis

Data in histograms were from 3 independent experiments in triplicate and were presented as the mean ± standard deviation (SD). All other data were displayed from one assaying only. Statistical analyses were performed using GraphPad Prism 5 software (GraphPad, San Diego, CA), and statistical significance between different groups was analyzed by Student's t tests. A P-value of < 0.05 was considered as statistical significance.

Results

Effects of transfection on SCs

SCs were transfected with pc S100A4 or si S100A4, and then the transfection efficiency was verified in vitro. The morphology of transfected SCs observed from a light-microscope shown that (Fig. 1A), there was no notable difference between the control group and transfection group. Subsequently, the protein and mRNA level expression of S100A4 in cells were detected by qPCR and Western blot analysis. As results showed in Fig. 1B and 1C, both the protein and mRNA levels of S100A4 were elevated by pc S100A4 (P < 0.01), while were suppressed by si S100A4 (P < 0.01). Thus, the overexpressed and suppressed S100A4 SCs were successfully obtained, and were used for the forthcoming analyses.

Figure 1. Effects of transfection on SCs. SCs were transfected with S100A4 vector or siRNA against S100A4. (A) The morphology of the transfected SCs was observed and photographed under a light-microscope. (B) The mRNA level expression of S100A4 in transfected SCs was determined by qPCR. (C) The protein level of S100A4 was detected by Western blotting. SCs, Schwann cells; siRNA, small interfering RNA; qPCR, quantitative PCR; **, P < 0.01.

Effects of S100A4 on SCs migration

To explore the functional effects of S100A4 on SCs, the migration of transfected SCs was measured by Transwell assay. Results in Fig. 2A and 2B showed that, cell migration was significantly enhanced by S100A4 overexpression (P < 0.001), while was inhibited by S100A4 suppression (P < 0.01). Furthermore, the protein expressions of VEGF and MMP-9 in transfected SCs were detected by Western blotting, to reveal the underling mechanism of S100A4 on SCs migration. We found that, both VEGF and MMP-9 were upregulated by S100A4 overexpression, whereas were downregulated by S100A4 suppression. Taken together, we inferred that S100A4 improved SCs migration might be via regulating VEGF and MMP-9.

Figure 2. Effects S100A4 on SCs migration. SCs were transfected with S100A4 vector or siRNA against S100A4. (A) SCs migration was measured by Tranwell assay, and the migrated SCs were stained with crystal violet and photographed under a light-microscope. (B) Quantification of migrated SCs. (C) Protein expressions of VEGF and MMP-9 in transfected SCs were measured by Western blot. SCs, Schwann cells; siRNA, small interfering RNA; VEGF, vascular endothelial growth factor precursor; MMP-9, matrix metallopeptidase 9; **, P < 0.01; ***, P < 0.001.

Effects of dysregulated S100A4 SCs on the expression of GAP43 in SGNs

To explore the effects of the dysregulated S100A4 SCs on SGNs, SCs were firstly transfected with pc S100A4 or si S100A4, and co-cultured with SGNs. GAP43 in SGNs was probed by IF and its expression was determined by qPCR and Western blot analysis. As results showed in Fig. 3A, the expression of GAP43 in SGNs was remarkably elevated by S100A4 overexpressed SCs, while was decreased by S100A4 suppressed SCs. In line with the results in Fig. 3A, Fig. 3B and 3C showed that, both the protein and mRNA levels of GAP43 were up-regulated by S100A4 overexpressed SCs (P < 0.01), whereas were down-regulated by S100A4 suppressed SCs (P < 0.05). These data suggested that, the expression of S100A4 in SCs might play a pivotal role in GAP43 expression in SGNs.

Figure 3. Effects of dysregulated S100A4 SCs on the expression of GAP43 in SGNs. SGNs were co-cultured either with S100A4 overexpressed or suppressed SCs. (A) GAP43 in SGNs was probed by IF and observe under an automated upright microscope system. (B) The mRNA level expression of GAP43 in SGNs was detected by qPCR. (C) The protein expression of GAP43 was detected by Western blot. SCs, Schwann cells; SGNs, spiral ganglion neurons; GAP43, growth associated protein 43; IF, immunofluorescence; qPCR, quantitative PCR; *, P < 0.05; **, P < 0.01.

Discussion

SCs have an intimate relationship with SGNs with a number of important functions. S100A4 is widely expressed in the nervous system, and it appears to be involved in the regulation of neuron survival plasticity. However, few investigations have focus on the role of S100A4 in SCs and SGNs. In this study, SCs were genetically modified to overexpress or suppress S100A4. We found that S100A4 overexpression enhanced the migratory ability of SCs, while S100A4 suppression reduced SCs migration. Additionally, the expression levels of VEGF and MMP-9 proteins were upregulated by S100A4 overexpression, while were downregulated by S100A4 suppression. More important, co-culture of S100A4 overexpressed SCs with SGNs remarkably up-regulated the expression of GAP43 in SGNs. However, the level of GAP43 was down-regulated after SGNs were co-cultured with S100A4 suppressed SCs.

SCs migration is a pivotal step preceding myelination and remyelination in the peripheral nervous system.²¹ Biochemical reports also demonstrated that SCs could gradually migrate to the peripheral nerve injured site and provide supportive effects to proximal axons which promotes successive neuro-regeneration by expressing a variety of trophic factors.²² Nowadays, studies have illuminated that multiple factors, such as concentrated growth factor (CGF), NMDA receptors and Netrin-1, have the capacity of improving SCs migration.^23-25 However, our study provided the first evidence that S100A4 could enhance SCs migration. VEGF is a potent soluble growth factor, which plays a key role in regulating angiogenesis.²⁶ Accordingly, an increasing number of studies evidenced VEGF could modify the migration of neurons and glia.²⁷ MMP-9 is an intriguing MMP family member found in adult nerve only after injury and predominantly in SCs.²⁸ MMP-9 was also reported as a pivotal regulator in SCs migration.²⁹ In the current study, both VEGF and MMP-9 were upregulated by S100A4 overexpression in SCs, implying that S100A4 enhanced SCs migration at least partly via modulation these 2 factors.

GAP43, a protein kinase C substrate, is a member of the calmodulin-binding protein family and concentrates in the presynaptic membrane and growth cones.³⁰ GAP43 is enriched in neuronal growth cone and seems to play an important role in neurotransmitter vesicle fusion and recycling, long-term potentiation, spatial memory formation and learning.³¹ Moreover, GAP43 is involved in the damage repair and regeneration of SGNs. In the rat, loss of spiral ganglion caused a substantial re-emergence of GAP43 immunoreactivity in varicose fibers of the ipsilateral ventral cochlear nucleus and cell bodies of the lateral superior olive.³² Up-regulation of GAP43 in SGNs might indicate neuronal regeneration and plasticity.⁷ Interestingly, in the present study, the expression of GAP43 in SGNs was elevated by co-culturing with S100A4 overexpressed SCs, indicating that S100A4 was implicated in the role of SCs in SGNs regeneration.

In summary, this study demonstrated that SCs genetically modified to overexpress the S100A4 could up-regulate the expression of GAP43 in SGNs in vitro. Transplantation of S100A4 overexpressed SCs into the cochlea may provide a clinically relevant means of preventing SGNs degeneration. Nevertheless, further research is still needed to fully confirming this hypothesis.

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Funding

The work is supported by a grant from Surface Project of Beijing Natural Science Foundation (7132109).