Superparamagnetic iron oxide nanoparticles combined with NGF and quercetin promote neuronal branching morphogenesis of PC12 cells

Introduction

Recovery of nerve function and nerve regeneration have been the most important issues in neuroscience, due to their considerable role in the treatment of injured neurons during a degenerative disease or after an accident.¹

Appropriate cell morphology regulation by intrinsic and extrinsic factors is an important requirement for cell to cell communication during the differentiation process. Neuronal cells undergo remarkable changes in cytoskeletal organization and morphology.² Different factors have been revealed to induce neuritogenesis including different molecular signals such as extracellular matrix (ECM) proteins, growth factors, and mechanical tensile forces.³

Cell cultures of neuronal cell lines or primary neurons are usually used to study compounds controlling plasticity of neuronal processes and differentiation. In particular, PC12 cells (pheochromocytoma cell line) have been extensively used in both neurotoxicological and neurobiological studies as a model of neuronal differentiation.⁴

The nerve growth factor (NGF) as an important growth factor is critical for the neuritogenesis and maintenance of neurons under in vitro and in vivo conditions. NGF-incubated PC12 cells stop proliferation, outspread neurites, and become electrically impulsive. During differentiation with NGF, the tyrosine kinase receptor A is activated and initiates a number of signaling pathways containing phosphatidylinositol 3-kinase pathway, and the extracellular signal-regulated kinase (ERK) cascade, which obstructs proliferation and encourages neurite growth.^4,5

For improving the natural effect of growth factors, nanotechnology has been proposed as a considerable item in therapeutic and diagnostic fields. Especially, magnetic nanoparticles (MNPs) could have different therapeutic applications such as cell-labeling, drug delivery, and medical imaging.^6,7

The superparamagnetic iron oxide nanoparticles (SPIONs) with characteristics such as nano size, modified surfaces, monodispersed shape, enhanced magnetization, colloidal stability, bio-distribution, and cellular uptake are considerably focused for their applications in biomedical applications.^6–8 Furthermore, the surface of SPIONs could be modified by different organic materials, such as polymers and biomolecules.

Biological molecules in different cells may also be bound to the surface of iron oxide nanoparticles. The interactions between biological molecules and iron oxide nanoparticles are studied to determine the cellular response of the MNPs.^7,9,10

It has been shown that metal ions including cobalt, manganese, and iron could modify cell attachment and have an important impact on neuronal differentiation.^9,11,12 These ions are related to adhesion molecules (exactly the RGD-dependent ECM). Cell adhesion molecules modulate cell proliferation, differentiation, survival, and migration by interacting with the ECM.^13,14

So far, the potential cytotoxicity of MNPs due to the formation of reactive oxygen species (ROS) remains an issue of debate.¹⁵ Great efforts have been taken to eliminate the cytotoxic effects of nanoparticles such as coating or combination of iron oxide nanoparticle with different agents.^16–18

Recent research has indicated that a variety of natural flavonoids reduce the toxicity of ROS in neural cells by their antioxidant activity.^19–21 It is important to note that a selected group of flavonoids (such as quercetin and fisetin) have demonstrated neuroprotective activity and play a critical role in the neurite outgrowth and differentiation of neural cells.^20,22

An important natural bioflavonoid is quercetin (3,3′,4′,5′-7-penta-hydroxy flavone, Figure 1). This flavonoid is abundantly found in vegetables, edible fruits, and medicinal plants. It has an extensive range of chemotherapeutic applications for many diseases such as anti-viral, anti-cancer, and anti-oxidant.^23–25 A number of quercetin actions make it an important neuroprotective agent, including interaction with different proteins and protective effects of neuronal cells from oxidative stress.²⁶

Figure 1 The two dimensional chemical structure of quercetin.

In this study, we suggest a new combination of SPIONs and quercetin to enhance the effect of NGF during neural differentiation of cells. In this combination, the role of iron oxide nanoparticles is more prominent. By increasing the attachment of PC12 cells, iron oxide nanoparticles help to preserve viability of cells and increase the effect of NGF and quercetin. Quercetin could bind to NGF and enhance the effect of NGF.^9,27 We used PC12 cells as a model for studying different aspects of developmental cell biology. Based on morphometric assessments, we show that the combination of SPIONs and quercetin promotes neuronal branching morphogenesis of PC12 cells in the presence of NGF.

Materials and methods

Materials

Poly-L-ornithine (PLO), MTT, quercetin (3,3′,4′,5′-7-penta-hydroxy flavone), and PBS were obtained from Sigma-Aldrich Co. (St Louis, MO, USA). Horse serum (HS), T-25, T-75 flasks, 12-well and 96-well plates, and L-glutamine were purchased from Corning Incorporated (Corning, NY, USA). BSA, FBS, penicillin-streptomycin, and RPMI medium were bought from Thermo Fisher Scientific (Waltham, MA, USA). NGF-β (GFM11) obtained from Cell Guidance Systems (St Louis, MO, USA). Iron oxide nanoparticles (Nano-screen MAG-DXS) were purchased from Chemicell GmbH (Berlin, Germany). PC12 cell line (National Center for Biotechnology code: C153) was purchased from Pasteur Institute of Iran (Tehran, Iran).

Cell culture

PC12 cells were cultured in the RPMI medium containing 10% HS, 5% FBS, 1% L-glutamine, and antibiotics. For differentiation, PC12 cells (5,000 cells/cm²) were seeded on PLO/laminin (Sigma-Aldrich Co.)-coated plates and incubated for 24 hours in serum-reduced media (0.5% FBS, 1% HS). Recombinant mouse NGF-β (50 ng/mL) was then added to the medium (every 2 days) to induce the differentiation of PC12 cells. Five treatments were examined: 50 ng/mL (free NGF), 100 ng/mL-NGF, MNPs, NGF-quercetin (10 μM), and NGF + MNPs + quercetin.

Cell viability assay

To examine the cytotoxic effects of quercetin and MNPs on PC12 cells, MTT assay was applied. The cells (30,000/well) were seeded onto the PLO-coated 96-well plates. At 24, 48, and 72 hours after incubation with the MNPs and quercetin at concentrations ranging from 10 to 100 μg/mL for MNPs and 10–50 μg/mL for quercetin, PC12 cells were incubated with 0.5 mg/mL MTT according to the Mosmann method.²⁸ The absorbance at 560 nm was measured using the ELISA reader (Thermo LabSystems Inc., Beverley, MA, USA).

Quantification of nanoparticle intracellular uptake

In order to quantitate the intracellular uptake of nanoparticles by the PC12 cells, following experiments have been performed.

Inductive coupled plasma-atomic emission spectrometer (ICP-AES)

Total MNPs in the cell cytoplasm were measured by evaluating the amount of iron in PC12 cells. PC12 cells were incubated with different concentrations of iron oxide nanoparticles (from 10 to 100 μg/mL). After 24 hours of incubation, the cells were sequestered and lysed with hydrochloric acid. Iron absorption was quantified using an ICP-AES (ICPS-7500; Shimadzu Corp., Kyoto, Japan).²⁹

Flow cytometric analysis

In this study, dextran sulfate-coated MNPs sized 100 nm were used (Nano-screen MAG-DXS). The surface coating of nanoparticles was dextran sulfate with a fluorophore that has an absorbance maximum of 476 nm and an emission maximum of 490 nm. All samples (incubated cells with iron oxide nanoparticles at concentrations ranging from 10 to 100 mg/mL) were analyzed by flow cytometry (FACSCalibur; BD Biosciences, San Jose, CA, USA). Green fluorescence was detected using an FL-1 sensor, a 525 nm band-pass filter. Statistics from 10,000 cells per sample were analyzed and three measurements per sample were recorded.

Prussian blue staining

PC12 cells treated with different concentrations of iron oxide nanoparticles were stained with Prussian blue dye for tracing iron in the cell cytoplasm by dipping the cells in a mixture of equal parts of 10% potassium ferrocyanide solution and 20% hydrochloric acid. In this method, trivalent iron in the PC12 cells interacts with the ferrocyanide and results in the formation of ferric ferrocyanide (the blue pigments).³⁰ A light microscope (Inverted Microscope; Nikon, Tokyo, Japan) was used to acquire images of stained cells.

Cresyl violet staining (Nissl staining)

The cresyl violet method was used to show the Nissl substance as an important characteristic of neurons. In the neural differentiation, the maturation grade of neuronal cells is reflected by formational changes in the neuroplasm. The Nissl bodies are rough endoplasmic reticulum (with ribosomes) and are the site of protein synthesis.³¹ PC12 cells were stained with 0.1% cresyl violet solution for 4–15 minutes and washed three times with PBS to remove excess stain. PC12 cells were photographed by inverted microscopy and scored for the presence of Nissl substance and neurites.

Immunocytochemistry

PC12 cells were immunostained against β3-tubulin (in green) as an important neural specific marker. To stain PC12 cells with antibodies against β3-tubulin, cultures were fixed with 4% for 30 minutes and permeabilized with 0.3% Triton X-100 diluted in PBS. PC12 cells were incubated with the primary antibody (β3-tubulin) for 24 hours and then treated with a fluorescein isothiocyanate-conjugated secondary antibody for 1 hour. The nuclei were marked with DAPI for 15 minutes. Light and fluorescent microscopy (Olympus US SZX12 fluorescent stereo microscope; Olympus Corporation, Tokyo, Japan) identified the temporal relationship between neurites morphogenesis and different treatments.

Neuritogenesis in PC12 cells

Neuritogenesis in PC12 cells was studied in a time-dependent method with different treatments either alone or in combination for 5 days. NGF-β (50 ng/μL) was added to the medium of all treatments because this concentration was optimized. Due to lack of serum in the differentiation medium, NGF should be added to the cell culture every 2 days to maintain the viability of the PC12 cells during differentiation process. NGF blocked the apoptotic death of attached cells.⁹

PC12 cells were incubated with NGF and MNPs with or without quercetin. At different days (from 1 to 5) after incubation, the percentage of neurite outgrowth, number of branching points, and number of neurites originating from soma were quantified (three random images from triplicate tests). Neuritogenesis was measured as described by Kim et al.²⁹ Neurite length was defined as L0 to L4 according to the length of the neurites. L0 was demarcated as cells with no neurites, L1 as cells whose neurite length was shorter than the size of the soma, L2 as cells with neurite length between the original size of the soma and twice the size, and L3 as cells whose neurite length was longer than twice the size of soma.²⁹ Also the number of neurites originating from soma were defined as N1, N2, N3, and N4 (N1, N2, N3, and N4 were defined as one, two, three, and four neurites in the PC12 cells, respectively). Length and number of neurites of 200 cells were measured in three random fields from triplicate experiments.

The effect of different treatments on neuritogenesis

First, the efficiency of free NGF as a differentiating factor was measured. Then, the efficiency of free NGF treatment was compared to other treatments such as quercetin solution and using iron oxide nanoparticles with or without quercetin. The PC12 (2×10³) cells were plated on PLO-coated plates and incubated with five different treatments including free NGF, NGF (50 ng/mL) and quercetin (10 μM), quercetin–NGF–MNPs (20 μg/mL), and NGF–MNPs (20 μg/mL). After incubation in different treatments, PC12 cells were washed and fixed with 4% paraformaldehyde for 30 minutes. Percentage of neurite outgrowth, branching points, and differentiation of PC12 cells under different treatments were measured using the light microscope. Light and fluorescent microscopy was used to evaluate both the terminal branch number and the total branch length of neurites.

Statistical analysis

All values of differentiation rate of PC12 cells are presented as mean ± SD. The analysis method was a one-way ANOVA. When the P-value was <0.05 (P<0.05), differences among the treatments were considered statistically significant.

Results

In this study, uniform fluorescent iron oxide (Fe₃O₄) nanoparticles were used. The surface of the nanoparticles was coated with dextran sulfate with a green fluorophore. The number of particles was ~1.8×10¹⁵/g with a density of 1.25 g/cm³. The size distribution of the dextran sulfate-coated iron oxide nanoparticles was found to be 100 nm (Figure 2A). Figure 2B shows the energy dispersive X-ray pattern of dextran-coated iron oxide nanoparticles (Fe₃O₄), and their sizes were determined by scanning electron microscopy.

Figure 2 SEM (A) and EDX (B) images of iron oxide nanoparticles used for neurite outgrowth. Abbreviations: C, carbon; Fe, iron; O, oxygen; SEM, scanning electron microscope; EDX, energy dispersive X-ray analysis.

The MTT cell viability assay was employed to examine the cytotoxicity of SPIONs and quercetin. PC12 cells were treated with SPIONs at different concentrations from 10 to 100 μg/mL. Figure 3 shows the effects of different treatments on the viability of PC12 cells. Superparamagnetic nanoparticles in the concentration of 100 μg/mL show significant cytotoxicity in comparison with the control and other groups (P<0.01). Quercetin in the range of 60–100 μg/mL was significantly cytotoxic (Figure 3D).

Figure 3 Effect of different treatments on the viability of PC12 cells. Cell viability was determined by MTT assay. PC12 cells were treated with 10, 20, 50, and 100 μg/mL for 24 (A), 48 (B), and 72 hours (C). (D) PC12 cells were treated with 5, 10, 20, 40, 60, 80, and 100 μg/mL for 24 hours. There were significant differences between the viability of PC12 cells from different treatments (P<0.05). Data are presented as the mean ± SD, n=3, *P<0.05, **P<0.01, and ***P<0.001 vs control group.

Total MNPs in the cell cytoplasm were measured by evaluating the amount of iron in the PC12 cells using ICP-AES (Figure 4A). During incubation with different concentrations of MNPs, iron in the cell cytoplasm increased up to the 35 pg per cell.

Figure 4 Internalization of superparamagnetic iron oxide nanoparticles into the PC12 cells. (A) Uptake of iron oxide nanoparticles by PC12 cells 24 hours after exposure to the iron oxide nanoparticles. Iron oxide nanoparticles were added to the media in a dose-dependent manner ranging from 10 to 100 μg/mL. (B) Fluorescent images of incubated cells with the different concentrations of fluorescent iron oxide nanoparticles. (C) Different histograms using Flowing Software (version 2.5.1) were combined: the red curve represents the maximum fluorescence. In this case, PC12 cells were incubated with 100 μg/mL of iron oxide nanoparticles. (D) Prussian blue method: PC12 cells treated with iron oxide nanoparticles were also stained for tracing the iron in the cell cytoplasm. Arrow represents the position of the iron oxide nanoparticles in PC12 cells (dark blue dots). Abbreviation: MNPs, magnetic nanoparticles.

The fluorescent microscopic study of the PC12 cells treated with different concentration of iron oxide nanoparticles exhibited a bright green color emission as shown in Figure 4B. These data show that the majority of superparamagnetic nanoparticles were internalized into the cells.

Also as it is shown in Figure 4C, treatment of PC12 cells with different concentration of iron oxide nanoparticles (10–50 μg/mL) led to an increase in fluorescence up to 89%±0.7% intensity (yellow, violet, and blue curves). Surprisingly, during the use of maximum concentration of MNPs, the fluorescence intensity of about 97% was recorded (red curve).

PC12 cells incubated with iron oxide nanoparticles were also stained for tracing the iron in the PC12 cell cytoplasm (Figure 4D). The red arrow represents the position of the MNPs in PC12 cells (dark blue dots).

Based on the internalization and MTT assay results and considering published articles, a dose of 20 μg/mL for nanoparticle and a dose of 10 μM for quercetin were chosen. Differentiation was studied by observing the morphology of PC12 cells. First, the efficacy of free NGF as a differentiating factor was experienced. As shown in Figure 5, when PC12 cells were treated with free NGF, neurite outgrowth and neurite arborization were observed. While the use of NGF with quercetin led to an increase in neurite outgrowth between 1 and 5 days after differentiation induction (exactly neurite length). As shown in Figure 6A, the Nissl substance was represented dark blue due to the staining of ribosomal RNA. The distribution of the neurite length of PC12 cells 5 days after the induction of differentiation is shown in Figure 6B. Neurite length was significantly affected by the quercetin treatment. The percentage of the PC12 cells with longer neurite (L3 and L4) increased when quercetin was added to the cells (Figure 6C). To examine the effect of MNPs on neuronal differentiation, PC12 cells were incubated with a combination of NGF and iron oxide nanoparticles. The results showed that the number of neurites originating from the soma and branching points of the cells increased when PC12 cells were incubated with iron oxide nanoparticles (Figure 7B).

Figure 5 Typical images of differentiated PC12 cells at 1, 3, and 5 days after treatment with NGF (50 ng/mL) and quercetin (10 μM) and NGF + quercetin. Quercetin induces PC12 cell differentiation (magnification: 200×). Abbreviation: NGF, nerve growth factor.

Figure 6 Neurite outgrowth of PC12 cells. (A) Cresyl violet staining: the Nissl substance (rough endoplasmic reticulum) appeared dark blue due to the staining of ribosomal RNA. Magnification ×400. (B) Distribution of the neurite length of PC12 cells 5 days after the induction of differentiation (L0 refers to the cells without neurites; L1 refers to the cells with neurites whose length is shorter than the size of the cell body; L2 refers to the cells with neurites whose length is between the original and twice the size of the cell body; L3 refers to the cells with neurites whose length is longer than twice the size of the cell body). (C) Neurite length of PC12 cells under different treatments. Cells were scored positive if one or more neurites with length >1 cell body diameter was observed. The results presented are the mean ± SD of 10 independent experiments. *P<0.05, **P<0.01. Abbreviations: NGF, nerve growth factor; Q, quercetin; MNP, magnetic nanoparticle.

Figure 7 Compartment between different treatment effects on neurite morphology. PC12 cells were treated with NGF (A), NGF + MNPs (B), NGF + quercetin (C), and NGF + quercetin + MNPs (D). For each treatment, 100 cells in each of three separate fields were counted. Abbreviations: MNPs, magnetic nanoparticles; NGF, nerve growth factor.

PC12 cells incubated with NGF and MNPs developed more branching points, more neurites per cell, and maximum percentage of cells expressing neurites in comparison with other groups (Figure 7D). Surprisingly, the treatment of PC12 cells with iron oxide nanoparticles together with NGF and quercetin demonstrated considerable enhancement in the neurite lengths and branching points in comparison with those treated with free NGF (Figures 7 and 8). Neural-specific marker (β3-tubulin) was studied immunohistochemically using specific monoclonal antibodies in PC12 cells incubated with NGF and SPIONs (Figure 9).

Figure 8 Effect of different treatments (NGF–MNPs–quercetin) on morphological parameters of neuronal differentiation, comparing between the four treatments: free NGF, non-conjugated MNPs with free NGF, NGF–MNPs + quercetin, and NGF + quercetin (A, B). (C) The number of neurites originating from the soma. Scale bar set at 30 μM. (D) The number of branching points. ANOVA test, *P<0.05, **P<0.01. Abbreviations: MNPs, magnetic nanoparticles; NGF, nerve growth factor; Q, quercetin.

Figure 9 Immunofluorescence images of differentiated PC12 cells 5 days after treatment with iron oxide nanoparticles. (A) Control, (B) cells stained with DAPI, (C) cells stained with β3-tubulin, and (D) the merge of (B) and (C). Green and blue fluorescence represent β3-tubulin and nucleus, respectively. Nuclei marked with DAPI.

Several studies have shown that 1 day after incubation of PC12 cells on the PLO-coated plate, neuritogenesis and neurite arborization have begun as an important neuronal differentiation stage (Figure 5). Figure 7 shows neuritogenesis in PC12 cells cultured for 3 days in NGF + MNP treatment. Neurite outgrowth in PC12 cells treated with NGF + quercetin was considerable, although the neuronal processes have fewer branches than comparable processes in MNP treatment (Figure 7). Measurement of branching points, neurites per cell, and percentage of cells expressing neurites in cells cultured in different treatments show that PC12 cells grown in MNP treatment have significantly more branches than those treated with NGF or quercetin (Figures 7 and 8). The branching frequency on the NGF + MNPs + quercetin was significantly higher than the branching frequency of neurons in NGF + MNP treatment (Figures 7 and 8).

Ethics statement

No animal or human subjects were used in this study.

Discussion

PC12 cells are an important model system by which to study how growth factors and external signals initiate neuronal differentiation. In this study, we have described an important nano-based combination of iron oxide nanoparticles and quercetin to enhance the effect of NGF during neural differentiation of cells. The data from the MTT assay demonstrated that quercetin and dextran sulfate-coated SPIONs possess low cytotoxicity at low concentration. Increasing the concentration of iron oxide nanoparticles leads to cellular dysfunction and the development of neurological diseases.^17,32 Pisanic et al reported that Fe at 1.5 mM concentration is very toxic to PC12 cells.³³ Based on the data presented in this study, when the concentration of iron oxide nanoparticles was <50 μg/mL, there was no significant difference in the viability of PC12 cells. Under our experimental conditions, iron oxide nanoparticle treatment increased the efficacy of NGF compared to those that were incubated with free NGF. Flow cytometry technique, Prussian blue staining, and ICP-AES allowed us to observe and quantify the intracellular MNP content in PC12 cells.

A considerable issue in this study is the significant increase of neurite length and branching point when MNPs and quercetin were applied together. Kim et al demonstrated that MNPs taken up by PC12 cells improved neurite outgrowth, especially the percent of neurite-bearing cells.²⁹ This behavior is observed in a dose-dependent manner. Sagara et al found that a special group of bio-flavonoids could trigger neuritogenesis by an ERK-dependent process.²⁶

Cell adhesion regulates different growth factor signaling in different cell lines. Cell anchorage to the ECM is recognized to have considerable effects on cell proliferation and differentiation.³⁴ The growth factors such as NGF are activated by their receptor tyrosine kinase, but only under the suitable condition of the cell anchorage.^9,13,35

How can iron oxide nanoparticles affect differentiation? Several authors have reported a number of changes in genes related to cell morphology and behavior including receptors of growth factors, ion channels, and the cytoskeleton.^5,29,36

Berry et al demonstrated extensive changes in gene expression of human fibroblasts when treated with MNPs.³⁷ These genes were associated with the receptors of growth factors, ion channels, collagen, laminin, cytoskeleton, and different proteins related to cell movement and cell interactions (Figure 10).³⁸ Kim et al²⁹ proposed a hypothesis to presume the state of Fe ions. In this hypothesis, Fe ions were released from internalized MNPs due to acidic pH inside the internal organelles and promoted neuritogenesis.

Figure 10 Schematic representation of different treatments (NGF plus iron oxide nanoparticle and quercetin) effects on PC12 cell signaling during differentiation. Growth factors such as NGF are optimally activated by their ligands but only under the appropriate condition of cell attachment. MNPs and quercetin as the neuroprotective agents induced neurite outgrowth by an ERK-dependent process. Abbreviations: ERK, extracellular signal-regulated kinase; NGF, nerve growth factor; MNP, magnetic nanoparticle; ECM, extracellular matrix.

How can quercetin affect differentiation? The data presented in our study demonstrated that neurite length was significantly affected by the quercetin treatment. This flavonoid is capable of inducing PC12 cell differentiation and can surprisingly enhance the efficacy of NGF function.²⁷

Tangsaengvit et al demonstrated that quercetin at a very low concentration of 1 nm improved the viability of P19-derived neurons, considerably increased neuritogenesis.³⁹ Ishige et al demonstrated that certain flavonoids can protect different cell lines from oxidative stress. Some of these flavonoids (such as quercetin and fisetin) are also capable of inducing PC12 cell differentiation.¹⁹

The bioflavonoids fisetin and quercetin were reported to have a stimulatory effect on alkaline phosphatase activity through the ERK signaling pathway.^40,41 Quercetin has an additional hydroxyl group at C-5 than fisetin. Therefore, based on quercetin antioxidant properties, this bioflavonoid has the ability to improve differentiation through modulation of signal cascades.^19,26

Sagara et al reported that four-oxo group and 2,3-double bond in the C ring of quercetin play a significant role in quercetin neuroprotective effects.^42,43 They indicated that Ras-ERK cascade is essential for quercetin-induced PC12 cell differentiation. Also, the results of Sagara et al showed that three different mitogen/extracellular signal-related kinase inhibitors block both flavonoid-induced ERK activation and differentiation of PC12 cells.²⁶

In this study, we examined neurite branching morphogenesis in PC12 cells under different treatments. We present in vitro results that demonstrate neuritogenesis and neurite arborization in the presence of extracellular factors. We established that iron oxide nanoparticles can enhance neurite branching and produce more complex branching trees and that quercetin can increase the length of neurites. Combination of MNPs with quercetin leads to considerable enhancement in the neurite lengths and branching points.

How do neurite branches form during the development of PC12 cells? Actin rearrangements are extremely controlled by actin-associated proteins, which have essential roles in neuritogenesis and neurite arborization (Figure 10). A highly dynamic area is found at the tips of growing neurites, where extreme rearrangements of actin filaments and microtubules occur during neurite elongation.⁴⁴ Recent studies have shown the importance of enabled/vasodilator-stimulated phosphoprotein proteins, formins, actin-related protein 2/3, and cordon-bleu in the neurite morphogenesis.^45,46

In the present study, we have described a new effective combination of quercetin and iron oxide nanoparticles with neuroprotective effects that are capable of promoting neuritogenesis at a high level. This combination has great potential for increasing neuronal differentiation and may function as a novel therapeutics in the field of neuronal regeneration and repair.

Conclusion

While it is well recognized that different cells can respond to various external signals during neuritogenesis and neurite arborization, only limited studies have examined the effects of SPIONs and quercetin on neural differentiation parameters. The results of this study suggest that SPIONs and quercetin have considerable effects on neuritogenesis, specifically the neurite arborization. Findings of the present study showed that the combination of iron oxide nanoparticles with a flavonoid can be an appropriate candidate for improving the efficiency of NGF during differentiation.

Data sharing statement

The data sets used and/or analyzed during the present study are available from the corresponding author upon reasonable request.

Acknowledgments

We thank the vice chancellor for research and technology of the University of Isfahan. The authors are grateful to the University of Isfahan for providing support to undertake this work. This work was supported by the grant from the University of Isfahan.

Author contributions

All authors contributed toward data analysis, drafting and revising the paper, gave final approval of the version to be published and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.

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