Regulatory T cells (Treg) play a critical role to control immune responses and to prevent autoimmunity, thus selective increase of Treg cells in vivo has broad therapeutic implications for autoimmune and inflammatory diseases. Licorice is a well-known herbal medicine used worldwide for over thousands of years, and accumulating evidence has shown its immunomodulatory potential. However, it is not clear whether licorice could regulate the induction and function of Treg cells. Here we found licorice extract could promote Treg cell induction, and then we used a rational approach to isolate its functional fractions and constituents. The results showed that two constituents, isoliquiritigenin and naringenin, promoted Treg cell induction both in vitro and in vivo. The effective fractions and two constituents of licorice also enhanced immune suppression of Treg cells, and they further reduced severity of DSS-induced colitis in mice. This study suggested that promotion of regulatory T cell induction could be an underlying mechanism of the historically and widely used herbal medicine licorice, providing its two effective molecules against autoimmune and inflammatory diseases.
Regulatory T (Treg) cells are a developmentally and functionally distinct CD4+ T cell subpopulation that is essential for maintaining immune tolerance and moderate inflammation induced by pathogens and environmental insults1,2. Treg cells comprise approximately 10% of peripheral CD4+ T cells and generate in the thymus3,4. However, peripheral naive CD4+ T cells can differentiate into induced Foxp3+ Treg cells in certain microenvironments, such as the gut5,6,7. Because of its pivotal role in modulating immune response and inflammation, there has been more interest in therapeutic manipulation of Treg cells to prevent autoimmune and limit chronic inflammatory diseases, such as inflammatory bowel disease (IBD)8,9. Forkhead box P3 (Foxp3) is a master regulator of Treg cell development and function. Foxp3 deficiency leads to systemic autoimmunity1,10,11,12. Other investigations showed activation of TGFβ-SMAD pathway is required for Treg cell generation from naive mouse CD4+ T cells13. However, a growing data has revealed that other pathways contribute to the regulation of Treg cell differentiation, including the downstream signaling of T cell receptor (TCR)14,15. Notably, inhibition of AKT and mTOR signaling, lead to Foxp3 expression upon TCR stimulation and promote Treg cells differentiation15,16,17,18.
Licorice, the root of Glycyrrhiza species, is one of the oldest and most popular herbal medicines used in many Asian and European countries for over 4000 years19. It is known as a well-recognized medicine against peptic ulcer disease, constipation, cough and viral infection7,8. Glycyrrhizin and flavonoids such as liquiritin, isoliquiritin, and their aglycones have been reported as the major constituents of licorice20. Licorice and its constituent, isoliquiritigenin, were reported to inhibit LPS-induced NF-kB activation and NLRP3 inflammasomes activation21,22,23. Glycyrrhizin inhibits tissue inflammation by reducing reactive oxygen species (ROS) generation by neutrophils24. In another study, licorice was believed to be involved in COX-2 inhibition and reducing prostaglandin (PGE2) which play a role in repression of inflammation23,25. Those investigations show that licorice has a significant anti-inflammatory properties in vitro and in vivo through multiple mechanisms. But whether licorice and its constituents could regulate the Treg cells generation and function is not clear.
Here, we explored the activity of licorice in Treg cell differentiation and function. By fractionation and tracing the Treg cell-inducing activity, we found isoliquiritigenin and naringenin, two constituents of licorice, increase Treg cell differentiation.
Licorice extract promote regulatory T cells differentiation in vitro
The in vitro T cell differentiation assay was carried out to examine whether the tested traditional Chinese medicine extracts could increase the generation of Foxp3+ regulatory T cells. Indeed, we found that extract of licorice, an immunomodulatory traditional Chinese medicine, potentiated induction of Foxp3 after stimulation of purified naive (CD4+CD25−) T cells by CD3 and CD28 antibodies and transforming growth factor-beta (TGFβ)(Fig. 1a and Supplementary Fig. 1). The effect was dose dependent and an optimum of Treg cell induction was achieved by adding 1 mg/ml licorice extract in the presence of Treg-inducing cytokines. We also examined the effects of licorice extract on Th17 and Th1 cell differentiation in vitro, the percent of IL-17-and IFN-γ-expressing cells were not changed in Th17-or Th1-incuction conditions (Supplementary Fig. 2). These results indicated that licorice extract specific promote Foxp3+ Treg cell induction, but not Th1 or Th17 cell induction.
Licorice fractions promote regulatory T cell differentiation and function in vitro
To identify the active ingredient in licorice, the extract of licorice was fractionated into four fractions and tested for the activity on the induction of Treg cells in vitro. Naive CD4+ T cells were treated with these licorice fractions in Treg-inducing condition, and CD4+CD25+Foxp3+ Treg cells were monitored. We found Gly1 fraction significantly increased the numbers of Treg cells in purified naive CD4+ T cells stimulated by CD3 and CD28 antibody and TGFβ. This effect was also dose dependent and an optimum of Treg cell induction was achieved by adding 0.03 mg/ml Gly1 (Fig. 1b). In our experiment, the Gly4 fraction also exhibited potential in promoting the induction of Foxp3+ Treg cells, although the effect was weaker than the Gly1 fraction (Fig. 1b). We analyzed the composition of Gly4 fraction, and found glycyrrhizic acid was abundant in it. As reported, glycyrrhizic acid has a potential to enhance Treg cells in lung of ovalbumin-sensitized mice26. Changes of Th1 and Th17 cells were not observed in their inducing conditions with licorice fractions (Supplementary Fig. 2). We also analyzed the Th1 and Th17 cytokines expression on CD4+ T cells with licorice and Gly1 fraction treatment. The result showed that most Th1 and Th17 cytokines, including IFNγ, TNF-α, IL17A, IL-17F, IL-21 and IL-22, expression was not changed (Supplementary Fig. 4). But we found IL-2, which was produced by Th1 cells and promoting T cells proliferation and survival, was reduced with licorice or Gly1 treatment. It indicated that licorice might suppress inflammation by reducing the expression of IL-2.
In addition to increasing the number of Treg cells, we found that Treg cells generated in the presence of licorice fraction Gly1 in vitro expressed higher amounts of Foxp3 protein on a per-cell basis than those from licorice extract-free cultures (Fig. 1c). It has been reported Foxp3 was a key regulatory factor in not only Treg cell differentiation, but also Treg cell function to suppress immune response10. The high level of Foxp3 expression indicated Treg cells induced by licorice extract and its active fraction might have an enhanced function. To verify whether the licorice active fraction Gly1 improved Treg cell function, Treg cells treated with or without Gly1 fraction were co-cultured with conventional T cells (Tconv) and antigen present cells. Proliferation of Tconv cells were analyzed after 4 days by FACS. Compared with Treg cells without treatment, Treg cells treated with Gly1 fraction displayed enhanced suppressive function toward Tconv cells proliferation (Fig. 1d,e). Thus, licorice extract and its active fraction Gly1 both promote Treg cells induction and function in vitro.
Licorice and its fraction promote regulatory T cell induction in vivo
To corroborate the role of licorice extract in Treg cell induction in vivo, specific pathogen-free (SPF) C57BL/6 mice were orally administered with licorice extract and monitored the Foxp3+ population of Treg cells in the peripheral blood every three days, and we detected an increased Treg cell percentage in the peripheral blood (Fig. 2a,b). Then we monitored the Treg cells in spleen, lymph node and colonic lamina propria after two weeks treated with licorice extract. Although we detected only very modest changes in the splenic and lymph node Treg cell subsets, provision of licorice extract to mice resulted in a robust increase in colonic lamina propria Treg cells in vivo (Fig. 2c,e). Consistent with the result in vitro, Th1 and Th17 cells were not changed in vivo, which suggested licorice and its fraction specifically promote Treg cell induction (Supplementary Fig. 3). To determine whether the Gly1 fraction could increase Treg cells induction in vivo like total licorice extract, we orally administrated Gly1 fraction to C57BL/6 mice and monitored the Treg cells in spleen, lymph node and colonic lamina propria. Consistent with the total extract of licorice, colonic Treg cells were significantly augmented with Gly1 fraction administrated, whereas it was slightly in spleen and lymph node (Fig. 2d,f).
As we known, Regulatory T cells are critical in the prevention of inflammatory diseases. Selective increase of Treg cells in vivo could control inflammatory responses and have broad therapeutic implications8,27,28. As licorice extract and Gly1 fraction generated Treg cells more significant in colon, we sought to investigate the possibility that Gly1 would be efficacious for colitis, potentiating its application as a treatment for inflammatory colitis. Animals were induced for DSS induced inflammatory bowel disease (IBD), and groups were treated with water or Gly1 fraction by oral administration. Water-treated DSS induced animals lost a significant amount of weight by day 8, whereas Gly1 treatment significantly reduced the symptoms of DSS-induced IBD, such as weight loss and colon shortening were significantly suppressed in Gly1 treated groups (Fig. 2g,h).
Isoliquiritigenin and naringenin are two active constituents of licorice to promote Treg cell induction and function
To identify the active constituents with Treg cell-inducing activity, we fractionated the Gly1 fraction into four sub-fractions and tracing the Treg cell-inducing activity of those sub-fractions on in vitro Treg cell differentiation assay. As a result, only the Gly18 and Gly19, two sub-fraction of Gly1, had the ability to promote Treg cell induction and function (Supplementary Fig. 5). Then the chemical composition of Gly18 and Gly19 sub-fraction was analyzed by thin layer chromatography (TLC) and NMR (Supplementary Fig. 6 and Supplementary Fig. 7). Four constituents, liquiritigenin, isoliquiritigenin, naringenin and licoricidin were found in these fractions (Fig. 3a)29,30. Recent study reported that naringenin could affect Treg cells induction in vitro, but the Treg cells inducing capability of other three chemicals were still unexplored31. We wanted to know whether other three chemicals could also increase Treg cell generation. So we examined Treg cell induction by these four chemicals in vitro. Indeed, isoliquiritigenin and naringenin were found to increase Treg cells differentiation in Treg cell inducing condition in vitro, and the other two chemicals didn’t exhibit the activity of promoting Treg cells (Fig. 3b).
Next, we examined whether isoliquiritigenin and naringenin could enhance Treg cell function. CD4+ naive T cells were isolated from spleen of wild type C57BL/6 mice and labeled with CFSE, then co-cultured with Treg cells treated with or without isoliquiritigenin and naringenin. Finally, we found that Tconv cells co-cultured with Treg cells treated with these two chemicals showed lower proliferation than which co-cultured with Treg cells without treatment (Fig. 3c,d). These results showed isoliquiritigenin and naringenin not only promote Treg cells differentiation, but also enhanced Treg cells function to suppress effector T cells proliferation.
Isoliquiritigenin and naringenin promote Treg cells in vivo and attenuate DSS induced colitis
To confirm that isoliquiritigenin and naringenin promote Treg cells in vivo, wild type C57BL/6 mice were orally administrated with isoliquiritigenin, naringenin, or water. As expected, increased Treg cells were observed in peripheral blood and colonic lamina propria after two weeks of treatment, but the Th1 and Th17 cell change were not observed (Fig. 3e–g and Supplementary Fig. 9). Then we tested these two chemicals in DSS-induced mouse model of IBD. Animals were induced by 2.5% DSS in drinking water and isoliquiritigenin, naringenin or water were oral administrated every day. Compared with water-treated group, the symptoms of colitis, such as weight loss and rectal bleeding, colon shortening were significantly suppressed in isoliquiritigenin or naringenin treated groups (Fig. 4a–d). And an increase of Treg cells was observed in colonic lamina propria of isoliquiritigenin or naringenin treated groups (Fig. 4e). Interestingly a reduced number of Th1 cells was also observed in isoliquiritigenin treated group (Fig. 4e). These results suggested isoliquiritigenin and naringenin had therapeutic potential for inflammatory bowel disease.
Isoliquiritigenin and naringenin promote Treg cells by affect TCR-Akt-mTOR and AhR signaling
The aforementioned findings suggested that isoliquiritigenin and naringenin were agents effective in regulating Treg cell induction and function to suppress the immune response. We sought to further understand the molecular mechanism underlying those effects on Treg cells. The aryl hydrocarbon receptor (AHR), a transcription factor mediating xenobiotic detoxification, plays an important role in controlling Treg cells generation32, and recent study reported that naringenin promote Treg cells as an AHR agonist31. So we wanted to know whether licorice, its active fraction and its constituent, isoliquiritigenin promote Treg cells also by AHR signaling. We cultured the naive CD4+ T cells in presence of licorice, Gly1 fraction, isoliquiritigenin or naringenin for 24 hr and AHR indicator gene Cyp1a was detected by real-time PCR. Naive CD4 T cells cultured with naringenin, licorice extract or Gly1 fraction were found an increased expression of CYP1A as expected (Fig. 5e). But different with naringenin, the increased expression of CYP1A was not obvious in naive CD4 T cells cultured with isoliquiritigenin (Fig. 5e). That result suggested isoliquiritigenin might control Treg cells generation in a different way from naringenin.
The mTOR pathway is important in regulating Th cells and Treg cells differentiation11,16,33. Inhibition of the mTOR pathway leads to enhanced Treg cells generation, an observation similar to isoliquiritigenin-mediated effect. We thus hypothesized that isoliquiritigenin affected the mTOR signaling in T cells to control Treg cells generation. Indeed, by assessing the phosphorylation of P70S6K, an indicator for the activation of the mTOR signaling, we found that isoliquiritigenin treatment reduced mTOR signaling activity in response to TCR activation (Fig. 5a). Notably, the mRNA expression of Treg-related mTOR downstream genes, such as hypoxia-inducible factor 1 (Hif1α) and glucose transporter 1 (Slc2a1) was also lower in CD4 T cells treated with isoliquiritigenin (Fig. 5b)34. This decrease was also observed in T cells treated with Licorice extract or Gly1 fraction (Fig. 5b).
The reduction in p70S6K phosphorylation in response to TCR by isoliquiritigenin suggested that isoliquiritigenin interfered TCR- and mTOR-mediated pathway. One of the major molecules in that pathways downstream of TCR is the AKT. Previous research has reported TCR controlling Foxp3 expression and Treg generation via Akt15,16, and isoliquiritigenin was reported as an inhibitor of Akt in cancer cells35. To evaluating whether Akt activation on response to TCR activation was affected by isoliquiritigenin, we measuring the phosphorylation of Akt upon CD3 and CD28 antibody stimulation in the presence or absence of isoliquiritigenin. The significantly reduced Akt phosphorylation was observed in isoliquiritigenin treated CD4 T cells, whereas the phosphorylation change of ERK was not observed (Fig. 5c). Consistent with isoliquiritigenin, licorice and its active fraction Gly1 also reduced the Akt activation upon TCR stimulation (Fig. 5d). These results suggest licorice, its active fraction Gly1 and active constituent isoliquiritigenin could attenuate TCR-Akt-mTOR axis and promote Treg cell generation.
Our data presented in this study demonstrate that licorice, an old and widely used herbal medicine, could increase the induction of Treg cells in vitro and in vivo. These findings suggested that promotion of regulatory T cell induction could be an underlying mechanism of licorice to modulate immune response. So far, more than 400 compounds have been isolated from licorice20,36. Triterpene saponins and flavonoids are believed to be responsible for the bioactivities of licorice20,37. It has been believed glycyrrhizic acid and its aglycone glycyrrhetic acid are the only pharmacological active constituent of licorice for a long time37. In recent years, licorice flavonoid are more and more popular because of their significant bio-activity in antimicrobial, antioxidative, and anti-inflammatory function. Isoliquiritigenin and naringenin are two important flavonoids in licorice. The concentration of isoliquiritigenin is about 9 mg/g in licorice extract, and naringenin in licorice is much less than isoliquiritigenin38. In our study, we found isoliquiritigenin and naringenin showed a notable capacity for promoting Treg cell induction. Compared with glycyrrhizic acid which was reported increasing Treg cells in lung26, these two flavonoid inducing more Treg cells at a lower dose than glycyrrhizic acid. Licorice fractions contain these two flavonoids shown a significant potential to promote Treg cell induction and function, but the fractions without these two constituents didn’t show similar activities. These results suggested that isoliquiritigenin and naringenin could be the major constituents in licorice to promote Treg cell induction and enhance its function. Because isoliquiritigenin promoted Treg cells to almost maximum level in vivo, we couldn’t detect any additive Treg promoting effects with both isoliquiritigenin and naringenin treatment in vivo.
Though the licorice has been widely used as a drug to treat peptic ulcer, asthma, colitis and other inflammatory diseases for a long time, the molecular mechanism of licorice is not well understood. Recent study reported naringenin promote Treg cells as an AhR agonist31. Our study confirmed it and found licorice and its active fractions also could activate AhR signaling like naringenin, but isoliquiritigenin could not. These data indicated isoliquiritigenin might promote Treg cells by a different mechanism to naringenin. AKT-mTOR signaling has been found to suppress the induction of FOXP3 expression in vitro and in vivo. Manipulation of AKT-mTOR signaling activity by pharmacological compounds such as rapamycin and everolimus (Afinitor; Novartis) has been approved for clinical use in autoimmune and inflammatory diseases, such as inflammatory colitis8. In our study, the inhibition of AKT/mTOR signaling was observed in CD4+ T cells treated with isoliquiritigenin in Treg cell-inducing conditions, which was not detectable in CD4+ T cells treated with naringenin. Licorice extract and it active fraction was also found reducing activity of AKT, suggesting inhibition of AKT-mTOR signaling was another mechanism for licorice promoting Treg cells and suppressing inflammation.
The pivotal role of Treg cells in immune regulation has been widely appreciated. Transfer of Treg cells or increasing Treg cells induction have been proved to be an efficient therapeutic methods for autoimmune and inflammatory diseases in variety animal models. Oral administration of isoliquiritigenin, naringenin or Gly1 fraction ameliorated pathological symptoms of DSS-induced colitis. Our preliminary results suggest that isoliquiritigenin, naringenin and Gly1 fraction might serve as a potential therapeutic drug for inflammatory colitis or other autoimmune and inflammatory diseases, including inflammatory bowel disease, rheumatoid arthritis and multiple sclerosis.
C57BL/6 mice were obtained from the Shanghai Laboratory Animal Center (Chinese Academy of Sciences). Foxp3-IRES-GFP (Foxp3egfp) mice, which contain the enhanced green fluorescence protein (egfp) gene under the control of an internal ribosomal entry site (IRES) inserted downstream of the foxp3 coding region as described elsewhere, were provided by Dr honglin Wang (Shanghai Jiaotong University). All mice were maintained in pathogen-free conditions. Animal care and use were in accordance with the guidelines of the Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences. All animal experimental procedures were approved and overseen by the Animal Care and Use Committee of the Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences.
FITC-conjugated anti-mouse CD4 (GK1.5; 11-0041), PE-Cy7-conjugated anti-mouse IFN-γ (XMG1.2; 25-7311), APC-conjugated anti-mouse Foxp3 (FJK-16s; 17-5773) were from eBioscience. APC-conjugated anti-mouse IL17A (TC11-18H10; 559502) were from BD Biosicence. Collagenase D (11088866001) was from Roche Diagnostics GmbH. Dispase (17105-041, GIBCO) was from Invitrogen Corporation. DNase I was from Worthington. Dextran Sulfate Sodium Salt (M.W. = 36,000–50,000, 160110) was purchased from MP Biomedicals, LLC.
Primary CD4 T-cell purification, culture and in vitro differentiation
Naive CD4+ CD25− T cells from the spleen of 8- to 12-week-old mice were purified by selection using magnetic cell sorting. For in vitro T helper (Th) cell differentiation assay, sorted cells were activated with anti-CD3e (2 ug/ml; 145-2C11, soluble; BD Pharmingen) and anti-CD28 (2 ug/ml; 37.51, soluble; BD Pharmingen) and were induced to differentiate into Th1 cells by supplementation with IL-12 (10 ng/ml; Peprotech) plus anti-IFN-γ (5 ug/ml, XMG1.2; BD Pharmingen); or into Th17 cells with transforming growth factor-β1 (TGF-b1; 3 ng/ml, Peprotech), IL-6 (30 ng/ml; eBioscience) and anti-IFN-γ. For inducing the differentiation of naive CD4+CD25− T cells into Treg cells, cells were activated by plate-coating anti-CD3e (1 ug/ml) plus soluble anti-CD28 (1 ug/ml) and treated with TGF-β1 (1 ng/ml) and anti-IFN-γ. Cells stimulated in ‘neutral’ conditions (anti-IL-4, anti-IFN-γ but without additional cytokines) were considered to be ‘Th0’ cells.
For intracellular cytokine staining, cells were stimulated for 4 hr. with phorbol 12-myristate 13-acetate (50 ng/ml; P8139; Sigma) and ionomycin (1 μM; I3909; Sigma) in the presence of Brefeldin A (3 μg/ml; 00–4506; eBioscience). Then, cells were stained for surface molecules, fixed and made permeable with Fixation/Permeabilization Solution Kit (554714; BD Bioscience), and stained with fluorescence labeled antibodies. For analysis of intracellular Foxp3, cells were stained for surface markers, fixed and made permeable with Foxp3 Staining Buffer Set (00–5523; eBioscience), and stained with fluorescence labeled antibodies. Samples were run with FACSCalibur (BD Bioscience) and analyzed using FLOWJO software (Treestar Inc, Ashland, OR).
In vitro suppression assay
Cells were isolated from the spleen of 8- to 12-week-old mice. Regulatory T cells were isolated by the CD4+CD25+Regulatory T Cell Isolation Kit (130-091-041, Miltenyi Biotec). CD4+CD25− T cells were used as T conventional cells. T conventional cells were labelled with 1 μM CFSE (C34554, life technologies). Magnetically sorted Treg cells were cultured with T conventional cells (5 × 104 cells) at different ratios in 96-well round bottom plates together with irradiated T-cell-depleted splenocytes (5 × 104 cells) as antigen-presenting-cells and anti-CD3 (1 μg/ml). 96 hr. later, the suppression was assayed by FACS analysis for dilution of CFSE in gated conventional T cells.
Colonic lamina propria lymphocyte isolation
To isolate lamina propria (LP) lymphocytes, colons were collected and opened longitudinally, and shaken with HBSS containing 5 mM EDTA at 37 °C with gentle shaking for 30 minutes to remove epithelial cells. Then the colons were cut into small pieces and incubated with PRMI 1640 containing 0.5 mg/ml collagenase D and 0.5 mg/ml Dispase and 40 mg/ml DNase I for 1 hr. at 37 °C with gentle shaking. The digested tissues were collected by filtering through a 40-μm cell strainer and washed with RPMI 1640 containing 2 mM EDTA. LP lymphocytes (LPLs) were resuspended in 5 ml of 40% Percoll and layered on top of 2.5 ml of 80% Percoll. LPLs were collected from the interface of the 40% and 80% gradient after centrifugation.
Preparation and fractionation of extracts from licorice
The water extract of licorice from Inner Mongolia Autonomous Region in China (purchased from Jiangyin Tianjiang Pharmaceutical Co., Ltd) was dissolved in water and extracted by ethyl acetate for four times. The organic solvents were removed by vacuum evaporation and named Gly1. The water soluble fraction was chromatographed on silica gel with CHCl3-MeOH-H2O (9:1:0.1 to 0:1:0) and get the fraction Gly2, Gly3 and Gly4. The Gly1 fraction was chromatographed on silica gel with Petroleum ether-acetone (10:0 to 8:2), and get the fraction Gly17, Gly18, Gly19 and Gly20. The Gly18 fraction was chromatographed on silica gel for several times and get two chemicals, Gly27 and Gly28. Gly19 fraction was chromatographed and get two chemicals, Gly29 and Gly30. The Gly27 (liquiricidin), Gly28 (liquiritigenin), Gly29 (naringenin), Gly30 (isoliquiritigenin) was analyzed by NMR.
C57BL/6 mice were given 2.5% (w/v) DSS in drinking water for 6 days. Licorice extracts, fractions or chemicals were dissolved in water and orally administrated every day, starting 7 days prior to the DSS treatment and continued to the end of the experiment. After induction of colitis, body weight and stool condition were analyzed on a daily basis. The disease severity was measured by percent weight loss, intestinal bleeding (no blood, occult blood, or gross blood), stool consistency (normal, loose stool or diarrhea) and colon length.
Reverse transcription and quantitative real-time PCR
Total RNA was extracted with TRI Reagent (T9424; Sigma) according to the manufacturer’s instructions. Random hexamer primer and M-MLV Reverse Transcriptase (M5301; Promega) were used for reverse transcription. Real-time PCR was performed using JumpStart Taq ReadyMix (D7440; Sigma) supplemented with EvaGreen Dye (31000; Biotium) on a Stratagene Mx3000P (Agilent Technologies). Primers used to quantify HIF1α mRNA were 5′-ACCTTCATCGGAAACTCCAAAG-3′(forward) and 5′-CTGTTAGGCTGGGAAAAGTTAGG-3′(reverse); SLC2A1 mRNA were 5′-CAGTTCGGCTATAACACTGGTG-3′(forward) and 5′-GCCCCCGACAGAGAAGATG-3′(reverse); CYP1A1 mRNA were 5′-GACCCTTACAAGTATTTGGTCGT-3′(forward) and 5′-GGTATCCAGAGCCAGTAACCT-3′(reverse).
CD4+CD25− T cells were stimulated under conditions as described. Cells were collected and lysed for SDS-PAGE. Proteins were blotted onto nitrocellulose membrane (GE Healthcare). Blots were probed with the following antibodies: phosphor-Akt (Ser473) (4060, Cell Signaling), Akt (pan) (4691, Cell signaling), phosphor-Erk1/2 (9101, Cell Signaling), Erk1/2 (sc-94, Santa Cruz), phosphor-P70 S6 kinase (Thr389) (9234, Cell Signaling), P70 S6 kinase (2708, Cell Signaling), phosphor-S6 Ribosomal (Ser240/242) (4858, Cell, Signaling). The IRDye800CW-conjugated secondary antibody (Rockland) was then added. Data were assessed by the Odyssey Infrared Imaging System (Li-COR Bioscience, Lincoln, NE).
Thin layer chromatograph and NMR
1D NMR were recorded on AVANCE III-600 spectrometers (Bruker, Bremerhaven, Germany). Silica gel (200–300 mesh) for column chromatography was purchased from Qingdao Makall Chemical Company (Makall, Qingdao, China). Sephadex LH-20 (20–50 μm) for chromatography was obtained from Pharmacia Fine Chemical Co., Ltd. (Pharmacia, Uppsala, Sweden). Fractions were monitored by thin layer chromatography (TLC) (GF254, Qingdao Haiyang, Qingdao, China), and spots were visualized by heating silica gel plates sprayed with 10% H2SO4 in EtOH.
The compounds Gly29 and Gly30 were identified as naringenin29 and isoliquiritigenin30 by comparing their NMR data with literatures.
In addition, the structures were also confirmed by the thin layer chromatography (TLC) method. The TLC was performed on plates coated with silica gel F254 and developed with ethyl acetate-chloroform (2:8, v/v) and acetone-petroleum ether (3:7, v/v), respectively. Both compounds Gly29, Gly30 and corresponding standard compounds (naringenin and isoliquiritigenin) had the identical Rf values on TLC from two mobile phases mentioned above.
Therefore, the structure of compounds Gly29 and Gly30 were established as naringenin and isoliquiritigenin, respectively.
Data are presented as means ± SEM. Differences between data sets were analyzed by Mann-Whitney U tests, or one-way ANOVA followed by Bonferroni’s test. The two-way ANOVA and Mann-Whitney U test were used to assess the differences in the DSS-induced colitis mice between groups. P-value < 0.05 was considered statistically significant. Graphs were created in GraphPad Prism software.
How to cite this article: Guo, A. et al. Promotion of regulatory T cell induction by immunomodulatory herbal medicine licorice and its two constituents. Sci. Rep. 5, 14046; doi: 10.1038/srep14046 (2015).
This research was supported by grants from National Natural Science Foundation of China(31371419), National Science and Technology Support Program (2012BAI10B03), and Shanghai Municipal Commission for Science and Technology (14DZ1900402). We are grateful to Dr Honglin Wang (Shanghai Jiaotong University) for the Foxp3egfpmice. We thank Longfei Gao, Shunmei Xin, Xianglu Zeng, Yin Yun for technical assistance. We also thank all laboratory members for advices.