Proliferation and committed differentiation into dopamine neurons of neural stem cells induced by the active ingredients of radix astragali.

Neural stem cells (NSCs) are important cellular sources of transplantation therapies for Parkinson's disease. This study aimed to determine the effects of extracts of radix astragali on the proliferation and differentiation into dopamine (DA) neurons in NSCs. NSCs were dealt with astragaloside IV (ASI), astragalus polysaccharide (APS), and astraisoflavan (ASF), the main active ingredients of radix astragali. First, the results from cell-count kit-8 (CCK-8) assay showed that ASI, ASF, and APS had positive effects on the proliferation of NSCs. Next, we also confirmed the effects of ASI, APS, and ASF on BrdU and nestin by immunocytochemistry. Moreover, results from quantitative RT-PCR showed ASI, APS, and ASF could promote the expressions of tyrosine hydroxylase and dopamine transporter mRNA, which are specifically expressed in DA neurons. Simultaneously, sonic hedgehog (Shh), orphan nuclear hormone 1 (Nurr1), and pituitary homeobox 3 (Ptx3) are considered to motivate the formation of DA neurons. Our result showed ASI, APS, and ASF can also promote the expressions of Shh, Nurr1, and Ptx3 mRNAs. In conclusion, our study verifies that the active ingredients of radix astragali can promote the proliferation of NSCs and induce NSC differentiation toward DA neurons in vitro. These phenomena may occur through upregulation of Shh, Nurr1, and Ptx3 in the process of drug treatment.

Introduction

Parkinson’s disease (PD) is one of the most common neurodegenerative diseases characterized by the progressive loss of midbrain dopamine (DA) neurons in the substantia nigra. Although L-DOPA replacement therapy is currently the main method to treat PD, it cannot increase DA neurons and effect a radical cure. Currently, neural stem cells (NSCs) transplantation is thought to be a promising method to cure PD. NSCs are able to self-renew, migrate, and differentiate into the essential cells, such as neurons, astrocytes, and oligodendrocytes 1,2. However, how to induce NSCs to differentiate into DA neurons is indeed a challenge.

Chinese medicinal herbs have been shown to have a variety of effects on proliferation and differentiation of NSCs 3,4. Radix astragali (Astragalus menbranaceus Fisch; Huangqi), a Chinese medicinal herb, has been widely used in the therapies for PD in China. Previous studies have confirmed that radix astragali has an effect on the proliferation and differentiation of NSCs into neurons and astrocytes 5–8. The main active components of radix astragali are astragaloside IV (ASI), astragalus polysaccharide (APS), and astraisoflavan (ASF). Therefore, we hypothesized that ASI, APS, and ASF might also induce differentiation of NSCs to DA neurons, which had not been reported in any studies.

In this study, we further investigated the effects of the main active components of radix astragali on the proliferation and differentiation of NSCs in vitro. Cell-count kit-8 (CCK-8) assay and BrdU staining were used to detect the proliferation of NSCs, and qRT-PCR was used to detect the mRNA levels of differentiation factors, tyrosine hydroxylase (TH), dopamine transporter (DAT), sonic hedgehog (Shh), orphan nuclear hormone (Nurr1), and pituitary homeobox 3 (Ptx3), after drug treatment. These findings would be helpful to find a new method for the adjuvant treatment of PD after NSC transplantation.

Materials and methods

Prepare for ASI, ASF, APS, and complete DMEM/F12 medium

ASI (assay standard, No.: B20564), ASF (assay standard, No.: B20563), and APS (assay standard, No.: B20562) were purchased from Yuanye Biotechnology Company (Shanghai, China), and they were dissolved in complete DMEM/F12 medium (Gibco, New York City, New York, USA), containing 10 ng/ml of basic fibroblast growth factor (Gibco), 20 ng/ml of epidermal growth factor (PeproTech, Rocky Hill, Connecticut, USA), 2% B-27 supplement without vitamin A (Gibco), 1% N2 (Invitrogen, New York City, New York, USA), and penicillin (100 U/ml)/streptomycin (100 ug/ml) (Boster, Wuhan, China).

NSCs culture and identification

NSCs derived from the mesencephalons of Sprague-Dawley rat embryos at embryonic day 16 were grown in complete DMEM/F12 medium in cell culture flasks in a 37°C incubator with 5% CO2. The method was as described in the study by Huang et al. 9. In brief, the cells were plated at a density of 1×105/ml cells in the medium. Half of the medium was replaced every other day, and passaging was performed every 7 days. For identification in vitro, the formed neurospheres were placed in 24-well plates coated with 0.1 mg/ml poly-l-lysine (Sigma, Missouri, USA) and incubated for 24 h, and then fixed with 4% paraformaldehyde for 30 min. The expression of nestin protein, a specific biomarker of NSCs, was determined by immunocytochemistry as described in the study by Huang et al. 9. Anti-nestin antibody produced in rabbit (1 : 100, ab5968; Abcam, Cambridge, UK) was used as primary antibodies, as well as anti-rabbit IgG-Cy3 antibody (1 : 70, No.: BA1032; Boster, Wuhan, China) was used as secondary antibody. DAPI (Boster, Wuhan, China) was applied to label nuclei.

Cell-count kit-8 assays

The cell viability was determined using cell-count kit-8 (CCK-8) (Dojindo, Tokyo, Japan). NSCs were plated into 96-well culture plates coated with poly-l-lysine at an optimal density of 1×105 cells/well. Following this, the cells were treated with different concentrations of ASI (including 0, 1, 2, 5, 10, 20, and 50 μg/ml), APS (including 0, 0.005, 0.01, 0.02, 0.05, 0.1, 0.2, 0.5, 1, and 2 μg/ml), and ASF (including 0, 10, 20, 50, 100, 200, 500, and 1000 μg/ml). After 7 days, the medium was gently aspirated, and 5 μl of CCK-8 reagent was added to each well and incubated at 37°C for 2 h. The optical density of each sample was immediately measured in a multiwell spectrophotometer at 450 nm.

Immunocytochemical analysis

The cells were cultured with the corresponding optimum concentrations of ASI, APS, and ASF as determined from CCK-8 method, and then bromodeoxyuridine (BrdU) staining was applied to detect the proliferation of NSCs on days 7 and 14. The cells were pretreatment with 10 μM BrdU (No.: B5002; Sigma) for 5 days. The method was as described in the study by Huang et al. 9 and Liu et al. 10. Anti-nestin antibody produced in rabbit and anti-BrdU antibody produced in mouse (1 : 100, No.: B8434; Sigma) were used as primary antibodies, as well as anti-rabbit IgG-Cy3 antibody (1 : 70, No.: BA1032) and anti-mouse IgG-FITC antibody (1 : 50, No.: BA1101) (Boster, Wuhan, China) were used as secondary antibodies. DAPI was applied to label nuclei. Flouorescent images were obtained under a Leica confocal microscope with LAS AF Lite software (QS00IW; Leica, Wetzlar, Germany), and the number of BrdU-positive cells was counted by Image pro plus 6.0 (Media Cybernetics, Maryland, USA).

The differentiation and the mechanism were detected by fluorescence quantitative PCR

To compare the alteration in DA neuronal marker and relative factors of differentiation into DA neurons, total RNA of cells was isolated using Trizol reagent (Invitrogen) and reverse-transcribed to synthesize cDNA with a RevertAidTM First Strand cDNA Synthesis Kit (Fermentas, Vilnius, Lithuania). The LA PCR Kit (Takara, DaLian, China) was used to detect the expression of TH, DAT, Nurr1, Ptx3, and Shh mRNAs. The primer sequences are listed in Table 1.

Table 1

Oligonucleotide sequences of primers used for qPCR

Statistical analysis

All quantitative data are expressed as mean±SD. Differences between each group were assessed by one-way analysis of variance. P value less than 0.05 was considered statistically significant. All data were analyzed using SPSS 21.0 (SPSS Inc., Chicago, USA).

Results

Primary culture and identification of NSCs

The isolated cells formed floating neurospheres after culturing for 3 days (Fig. 1a1), and when adhered for 24 h, the branches were noted (Fig. 1a2). The result from immunocytochemistry showed positive immunoreactivity to nestin, a marker of NSCs (Fig. 1a3), and Tuj-1, a marker of neurons (Fig. 1a4), which indicated the cells were NSCs and expressed genes to promote differentiation into neurons.

Fig. 1

(a) The primary neural stem cells (NSCs) cultured for 3 days (a1); The NSCs branched after adhering for 24 h (a2); Immunostaining of NSCs with nestin (a3); and Tuj-1 (a4). Scale bar: (a1–a3) 200 μm, (a4) 100 μm. (b) The optical density of NSCs treated with differentiation of ASI, APS, and ASF as measured by CCK-8 assay. (c) Expression of BrdU and nestin after treating with ASI, APS, and ASF; DAPI was used to counterstain nuclei. Scale bar: 200 μm. (d) Quantitative analysis of relative BrdU+ cells (d1) and Nestin+ cells (d2). Data was as mean±SEM; N=3–4/group. *P<0.05. APS, astragalus polysaccharide; ASF, astraisoflavan; ASI, astragaloside IV.

ASI, APS, and ASF promoted the proliferation of NSCs

The results from CCK-8 showed that the cell viability of ASI group in 20 μg/ml (424±108%) and 5 μg/ml (391±71%), APS group in 0.02 μg/ml (198±36%) and 0.05 μg/ml (188±45%), and ASF group in 10 μg/ml (145±7%), 20 μg/ml (167±14%), and 50 μg/ml (155±11%) was increased compared with the control (P<0.05) (Fig. 1b), suggesting ASI, APS, and ASF were able to promote proliferation of NSCs.

Next, NSCs were treated with 2 μg/ml of ASI, 0.02 μg/ml of APS, and 20 μg/ml of ASF, and then BrdU and nestin staining were used to detect the proliferation viability of NSCs after drug treatment. On days 7 and 14, the ratios of BrdU-positive cells in the ASI (82.4±6.1 and 84.0±3.4%), APS (75.8±7.2% and 80.6±3.4%), and ASF (85.0±6.4 and 96.2±2.3%) groups were all increased compared with the control (61.8±9.2 and 65.6±5.6%) (P<0.05), especially in ASF group on day 14 (P<0.05) (Fig. 1d1), which suggests NSCs might have a high sensitivity to ASF. The expression of nestin was significantly decreased on the seventh day (60.5±10%) compared with the control (77.9±6%) (P<0.05), whereas other groups had no obviously difference compared with the control group (P>0.05) (Fig. 1d2).

ASI, APS, and ASF promoted the differentiation of NSCs to DA by up-regulating the expressions of TH, DAT, Nurr1, Shh, and Ptx3

TH and DAT are markers of DA neurons. In our study, the expressions of TH and DAT mRNA were measured by qPCR. On the seventh day, the expressions of TH and DAT mRNA were significantly increased after treating with ASI (33.5±0.4 and 34.6±0.4%, respectively) and ASF (34.8±0.1 and 34.7±0.1%, respectively) compared with the control group (28.5±0.3 and 28.7±0.2%, respectively) (P<0.05). Moreover, DAT mRNA was increased after treating with APS (30.5±0.5%) (P<0.05). On the 14th day, the expression of TH mRNA was obviously increased after treating with ASI (32.2±0.1%), APS (32.5±0.1%), and ASF (31.2±0.1%) compared with the control group (29.6±0.2%) (P<0.05), whereas the expression of DAT mRNA was significant increased after treating with ASI (35.2±0.1%), APS (34.9±0.1%), and ASF (34.7±0.1%) compared with the control group (28.6±0.4%) (P<0.05) (Fig. 2a and b). These results suggested ASI, APS, and ASF might be able to induce differentiation of NSCs to DA neurons.

Fig. 2

The expression of relative mRNA by quantitative RT-PCR. The mRNA levels were semiquantified, and normalized with RN18s as internal control. Data were represented with GraphPad Prism 5.02 (GraphPad Software Inc., California, USA). Data were as mean±SEM; N=3/group. *P<0.05 compared with the control group. APS, astragalus polysaccharide; ASF, astraisoflavan; ASI, astragaloside IV; DAT, dopamine transporter; Nurr1, orphan nuclear hormone 1; Ptx3, pituitary homeobox 3; Shh, sonic hedgehog; TH, tyrosine hydroxylase.

Moreover, we found that the expressions of Nurr1, Ptx3, and Shh mRNA were also increased in ASI, APS, and ASF groups on days 7 and 14 (P<0.05). However, there was no difference in the expression of Shh between the ASF group and control on the seventh day (P>0.05). The genes had no apparent change over time in our study (Fig. 2c–e and Table 2). In summary, these results revealed that ASI, APS, and ASF might be able to induce differentiation of NSCs to DA by up-regulating the expression of Nurr1, Ptx3, and Shh.

Table 2

The expression of Nurr1, Ptx3, and Shh mRNAs (%)

Discussion

To cure PD, an increasing number of studies focus on the drugs that can influence the survival, regeneration, and differentiation of NSCs, and the traditional Chinese medicine is a valuable candidate. Radix astragali has been widely used to postpone the development of PD in clinical treatment 11,12. Therefore, we hypothesized that radix astragali might induce the neurogenesis of DA neurons. Related studies have reported that R. astragali could promote the proliferation and differentiation of NSCs; however, the potential to differentiate into DA has not been reported.

In this study, we first confirmed that ASI, ASF, and APS had significant effects on proliferation of NSCs in vitro. In ASI and ASF groups, with increasing concentration, proliferation gradually increased and then decreased. Next, we also found that BrdU-positive cells were increased after drug intervention, indicating ASI, ASF, and APS were able to promote NSCs proliferation, especially ASF on the 14th day. Meanwhile, ASI could reduce the expression of nestin, which might be related to the increased differentiation in the process of cells culture.

Moreover, our study showed ASI, ASF, and APS could promote the expression of TH and DAT at the mRNA level. TH, produced by DA neurons in central nervous system, is the enzyme responsible for catalyzing the conversion of the amino acid l-tyrosine to l-3,4-dihyroxyphenylalanine, which is a precursor for dopamine. Then TH is transmitted to the synaptic destinations by the axons and produce dopamine 13,14. DAT is a membrane-spanning protein that pumps the neurotransmitter dopamine out of the synaptic cleft back into cytosol, and is highly expressed in the substantia nigra pars compacta and located in cell bodies, axonal, and dendritic plasma membranes 15,16.

Nonetheless, how do these drugs regulate the differentiation of NSCs? Nurr1 plays a key role in the maintenance of the DA system of the brain 17, and the mutation in this gene leads to disorders of DA dysfunction, including PD. Nurr1 induces DA gene expression in NPCs, and some co-activators, such as Ptx3, can potentiate Nurr1-induced DA gene transcription 18. Ptx3 gene, a transcription factor belonging to the RIEG/PITX homeobox family, can regulate terminal differentiation of mesencephalic DA neurons in the substantia nigra compacta of brain 19. It has been reported that overexpression of Nurr1 and Ptx3 genes could promote the differentiation of NSCs into DA neurons and induce the expression of TH in the brains of PD models 20. Additionally, Shh, which has an important role in the generation of a neural model, is a mitogenic signal that induces differentiation of various cells, as well as the proliferation and differentiation of NPCs in the embryonic and postnatal periods 21,22. To further verify the mechanisms of NSCs differentiation induced by ASI, ASF, and APS, we tested the expression of Nurr1, Ptx3, and Shh in mRNA levels. We found that Shh, Nurr1, and Ptx3 mRNAs were significantly enhanced after treatment of ASI, ASF, and APS, except Shh mRNA in ASF group on the seventh day. This may suggest that ASF might affect the differentiation into DA neurons by up-regulating Nurr1 and Ptx3. Additionally, in the APS group, the expressions of Nurr1, Ptx3, and Shh mRNA were all elevated on day 7. Our study suggested that ASI, ASF, and APS have the abilities to enhance NSCs to differentiate to DA neurons partially by up-regulating the expression of Nurr1, Ptx3, and Shh.

Conclusion

Our study confirmed the components of radix astragali had significant effects on proliferation and differentiation of NSCs. Notably, we found the active ingredients of radix astragali could induce the differentiation of NSCs to DA neurons possibly though upregulation of Shh, Nurr1, and Ptx3.