Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells

Abstract

d-Glucosamine (GlcNH₂) and several of its derivatives are known to possess immunosuppressive activities in various immune cell lines. The novel GlcNH₂-containing oligosaccharide Galα1-6GlcNH₂ (designated melibiosamine; MelNH₂) is expected to be immunosuppressive also. In Jurkat cells (immortalized human T lymphocytes), interleukin 2 (IL-2) production (an index of the T-cell immune response) can be induced by stimulation with a mitogen, such as concanavalin A. Here, we compared the effects of GlcNH₂ and MelNH₂ on concanavalin A-induced IL-2 production (CIIP) in Jurkat cells and found that GlcNH₂ and MelNH₂ at millimolar levels both significantly suppressed CIIP without affecting cell viability. When we examined the effects of GlcNH₂ and MelNH₂ on the activation of the three transcription factors required for CIIP—NFAT (nuclear factor of activated T-cells), NFκB (nuclear factor kappa-light-chain-enhancer of activated B cells), and AP-1 (activator protein 1)—we found that GlcNH₂ and MelNH₂ both suppressed CIIP by inhibiting the activation of NFAT and NFκB, but, unlike GlcNH₂, MelNH₂ also promoted the activation of AP-1. These results suggest that MelNH₂ may be a potentially useful lead compound for development as an immunosuppressive or anti-inflammatory drug.

Highlights

• •Immunosuppressive effects of MelNH₂ (Galα1-6GlcNH₂) were examined in Jurkat cells.
• •Concanavalin A induces IL-2 production in Jurkat cells.
• •MelNH₂ at millimolar levels dose-dependently suppressed ConA-induced IL-2 production.
• •MelNH₂ inhibited the activation of NFAT and NFκB, which control IL-2 expression.

1. Introduction

Interleukin 2 (IL-2) is an immunoregulatory cytokine produced by activated T lymphocytes. IL-2 production is considered an index of immune response in vivo. In Jurkat cells, an immortalized human T lymphocyte cell line, IL-2 production can be induced by stimulation with a mitogen such as concanavalin A (ConA) [[1], [2], [3]]. ConA binds to T-cell receptor, which triggers signaling pathways that lead to the activation of three transcription factors—nuclear factor of activated T cells (NFAT), nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB), and activator protein 1 (AP-1, a complex of c-Fos and c-Jun)—which induce the expression of IL-2 mRNA (Fig. 1) [[4], [5], [6], [7]].

Fig. 1.

(A) Chemical structures of d-glucosamine and melibiosamine. (B) Hypothetical scheme for the signaling cascades leading to the expression of interleukin (IL)-2 mRNA in Jurkat cells and the actions of GlcNH₂ and MelNH₂. The mitogen concanavalin A (ConA) stimulates IL-2 production via T-cell receptor (TCR) and subsequent activation of the calcineurin/nuclear factor of activated T-cells (CN/NFAT), IκB kinase/nuclear factor kappa-light-chain-enhancer of activated B cells (IKK/NFκB), and mitogen-activated protein kinase/activator protein 1 (MAPK/AP-1) pathways. The immunosuppressive drugs cyclosporine A (CsA) and tacrolimus (FK506) inhibit CN via immunophilins. It was assumed that phorbol 12-myristate 13-acetate (PMA) and ionomycin (IM) together mimic the actions of ConA with regard to the induction of IL-2 expression in vitro. MelNH₂ and GlcNH₂ suppress the activation of NFATc1 and NFκB by ConA, whereas MelNH₂, but not GlcNH₂, promotes the activation of AP-1. PM, plasma membrane; PLC, phospholipase C; IP₃, inositol 1,4,5-trisphosphate; DAG, diacylglycerol; PKC, protein kinase C. ‘P-’ indicates phosphate group, and the gray arrow inside the nucleus indicates IL-2 transcription.

In T lymphocytes, the immunosuppressive drugs cyclosporine A (CsA) and tacrolimus (FK506) suppress IL-2 production by inhibiting calcineurin (a Ca²⁺/calmodulin–dependent protein serine/threonine phosphatase) via immunophilins, which suppress the activation of NFAT (Fig. 1) [[8], [9], [10]]. CsA and tacrolimus prevent organ graft rejection and disease progression in patients with rheumatoid arthritis [11]. However, because the clinical use of these and other immunosuppressants (e.g. glucocorticoids) have serious toxicities that affect the renal, nervous, and gastrointestinal systems [[12], [13], [14], [15], [16]], novel immunosuppressants with fewer toxicities are needed.

D-Glucosamine (GlcNH₂) (Fig. 1A), a naturally occurring derivative of glucose, possesses various biological and pharmacological activities, including anti-tumor and anti-inflammatory activities [[17], [18], [19], [20], [21], [22], [23], [24], [25]]. Recently, a novel GlcNH₂-containing oligosaccharide, Galα1-6GlcNH₂ (designated melibiosamine; MelNH₂) (Fig. 1A), was found to exhibit anti-proliferative effects in human leukemia and breast cancer cells in vitro [26,27]. However, the potential biological and pharmacological activities of MelNH₂ are yet to be fully elucidated.

Here, to assess the potential pharmacological activity and toxicity of MelNH₂ on the immune system, we compared the effects of GlcNH₂ and MelNH₂ on ConA-induced IL-2 production (CIIP) in Jurkat cells. We found that MelNH₂ suppressed CIIP via a mechanism that is, at least in part, different from that through which GlcNH₂ suppresses CIIP, suggesting that MelNH₂ may be a useful lead compound for the development of novel immunosuppressive or anti-inflammatory drugs.

2. Materials and methods

2.1. Cell line and reagents

Jurkat cells were maintained at 37 °C (5% CO₂) in tissue-culture dishes containing RPMI 1640 growth medium supplemented with 10% (v/v) fetal bovine serum, 25 μg/mL penicillin, and 50 μg/mL streptomycin. MelNH₂ was synthesized as described previously [26], and GlcNH₂ was purchased from Sigma (St. Louis, MO); these compounds were each dissolved in phosphate-buffered saline (pH 7.4) as 0.1 M solutions, sterilized through a 0.45-μm filter, and stored at −20 °C until use. Phorbol 12-myristate 13-acetate (PMA) and ionomycin (IM) were obtained from Sigma, and CsA was purchased from Calbiochem (San Diego, CA), and these compounds were stored as 1, 0.5, and 0.5 mM stock solutions, respectively, in dimethyl sulfoxide (DMSO).

2.2. Assay of cell number and viability

Jurkat cells were pre-incubated at 37 °C (5% CO₂) for 30 min in 0.5 mL RPMI 1640 (1 × 10⁶ cells/mL) in a 24-well plate in the presence of 5–20 mM MelNH₂ or GlcNH₂. Then, ConA was added to each well at a final concentration of 50 μg/mL, and the cells were further incubated at 37 °C (5% CO₂) for 12 h. After the addition of 0.5 mL trypan blue solution to each well, living and dead cells were counted under a microscope by using a hemocytometer.

2.3. Assay of IL-2 production by Jurkat cells

IL-2 production was assessed as described previously with some minor changes [2,28,29]. Jurkat cells were pre-incubated at 37 °C (5% CO₂) for 30 min in 1 mL RPMI 1640 (1 × 10⁶ cells/mL) in a 12-well plate in the presence of the indicated concentrations of MelNH₂ or GlcNH₂ or 1 μM CsA. After the addition of ConA (final concentration, 50 μg/mL) or the combination of PMA (1 μM) and IM (0.5 μM), the cells were further incubated at 37 °C (5% CO₂) for 12 h. Aliquots of the culture media were collected, and the concentration of IL-2 was determined by using a Quantikine Human IL-2 ELISA Kit (R&D Systems, Minneapolis, MN). Briefly, 50-μL aliquots (in duplicate) of the culture media or IL-2 standard from the kit were added to the wells of 96-well plates pre-coated with anti-human IL-2 antibody. After incubation (at 37 °C) with biotinylated antibodies against human IL-2 and then with streptavidin–horseradish peroxidase conjugate, color was developed and the level of IL-2 was quantified by measuring absorbance at 450 nm (reference at 570 nm).

2.4. Semi-quantitative reverse transcription–polymerase chain reaction assay

Jurkat cells were pre-incubated at 37 °C (5% CO₂) for 30 min in 1 mL RPMI 1640 (1 × 10⁶ cells/mL) in a 12-well plate in the presence or absence of 15 mM GlcNH₂ or MelNH₂ or 5 μM CsA. After the addition of ConA (50 μg/mL), the cells were further incubated at 37 °C (5% CO₂) for 3 h. Cells were collected by centrifugation (400×g, 5 min), and total RNA was prepared from the cells by using an RNeasy Mini Kit (Qiagen, Hilden, Germany). One microgram of total RNA was reverse transcribed into complementary DNA by using a ReverTra Ace qPCR Kit (Toyobo Co. Ltd., Osaka, Japan), and polymerase chain reaction amplification for IL-2 and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) complementary DNA was performed as previously described [2,29]. The following primer pairs were used: IL-2, forward-5′-CAACTCCTGTCTTGCATTGCACTAA-3′, reverse-5′-AATGTGAGCATCCTGGTGAGTTTG-3′; GAPDH, forward-5′-GCACCGTCAAGGCTGAGAAC-3′, reverse-5′-ATGGTGGTGAAGACGCCAGT-3′.

2.5. Preparation of nuclear extracts and transcription factor assay

Jurkat cells were pre-incubated at 37 °C (5% CO₂) for 30 min in a 10-cm dish in the presence or absence of 5–20 mM GlcNH₂ or MelNH₂. After the addition of PMA (1 μM) and IM (0.5 μM), or 0.2% DMSO (vehicle), the cells were further incubated at 37 °C (5% CO₂) for 3 h. After incubation, the cells were collected by centrifugation (200×g, 2 min), lysed with a lysis buffer (in the kit below), and nuclear extracts were prepared by using a Nuclear Extract kit (Active Motif, Carlsbad, CA). After measurement of protein concentrations with a RC-DC Protein Assay Kit (Bio-Rad Laboratories, Hercules, CA), the nuclear extracts were aliquoted and stored at −80 °C until use.

We measured the activation (the contents in nuclear extracts) of NFAT cytoplasmic 1 (NFATc1), NFκB, and phospho-c-Jun by using enzyme-linked immunosorbent assay-based TransAM NFATc1, TransAM NFκB, and TransAM AP-1 c-Jun kits (Active Motif Corp.), respectively. Briefly, nuclear extracts from control and GlcNH₂- or MelNH₂-treated cells were incubated in a 96-well plate containing immobilized oligonucleotides (consensus sequences) specific for the particular transcription factor, and bound transcription factor was quantified by enzyme-linked immunosorbent assay.

3. Results and discussion

3.1. Effects of MelNH₂ on IL-2 production and cell viability in Jurkat cells

To assess the potential immunological activity and toxicity of MelNH₂, we compared the effects of GlcNH₂ and MelNH₂ on CIIP and cell viability in Jurkat cells. As expected from previous reports, the immunosuppressive drug CsA at 1 μM strongly suppressed CIIP [28,29], and GlcNH₂ at 2.5–20 mM suppressed CIIP in a dose-dependent manner (Fig. 2A) [21,23]. Similarly, MelNH₂ at 2.5–10 mM suppressed CIIP in a dose-dependent manner (Fig. 2A). In addition, neither GlcNH₂ nor MelNH₂ at 20 mM or less had any effect on cell number and viability (Fig. 2C and D), suggesting that these compounds are not toxic to Jurkat cells.

Fig. 2.

Effects of GlcNH₂ and MelNH₂ on IL-2 production and cell number (viability) in Jurkat cells. Cells were pre-incubated for 30 min in the absence or presence of the indicated concentrations of GlcNH₂ or MelNH₂ (A–D), or 1 μM CsA (A, B). After the addition of ConA (A, C, D) or the combination of PMA (1 μM) and IM (0.5 μM) (B), cells were further incubated for 12 h and assayed for IL-2 protein production (A, B), living cell number (C), and cell viability (D). *P < 0.05, **P < 0.01, ***P < 0.001; unpaired t-test (2-tailed), as compared with control.

When administered together to Jurkat cells, PMA and IM mimic the effects of ConA by activating protein kinase C and raising cellular calcium levels, respectively (Fig. 1B) [2,3]. As expected [28,29], CsA at 1 μM strongly suppressed PMA/IM-induced IL-2 production (PIIP), and GlcNH₂ at 2.5–20 mM suppressed PIIP in a dose-dependent manner. In addition, MelNH₂ at 5–10 mM suppressed PIIP (Fig. 2B).

Next, we examined the effects of GlcNH₂ and MelNH₂ on ConA-induced IL-2 mRNA expression in Jurkat cells (Fig. 3). As expected, CsA at 1 μM strongly suppressed ConA-induced IL-2 mRNA expression; GlcNH₂ and MelNH₂ at 15 mM also significantly (P < 0.01) suppressed ConA-induced IL-2 mRNA expression.

Fig. 3.

Effects of GlcNH₂ and MelNH₂ on ConA-induced IL-2 mRNA expression in Jurkat cells. Cells were pre-incubated for 30 min in the absence or presence of 15 mM GlcNH₂ or MelNH₂, or 1 μM CsA. After the addition of ConA, cells were further incubated for 3 h and assayed for IL-2 mRNA expression. **P < 0.01; unpaired t-test (2-tailed), as compared with control.

Together, these results suggest that GlcNH₂ and MelNH₂ both suppress CIIP and PIIP by disrupting the signaling cascade downstream from where PMA and IM exert their actions but upstream of the three transcription factors that regulate IL-2 mRNA expression (Fig. 1B).

3.2. Effects of MelNH₂ on the activation of NFAT, NFκB, and AP-1 in Jurkat cells

To elucidate the mechanisms underlying the immunosuppressive activities of GlcNH₂ and MelNH₂, we examined the effects of these compounds on the cytosol-to-nucleus translocation (i.e. the activation) of the three transcription factors that regulate IL-2 expression—NFATc1 (NFAT cytoplasmic 1), NFκB, and AP-1 (Fig. 1B). GlcNH₂ and MelNH₂ at 5–20 mM both dose-dependently attenuated the activation of NFATc1 and NFκB by PMA/IM (Fig. 4A–D). However, unlike GlcNH₂, MelNH₂ at 5–20 dose-dependently promoted the activation of AP-1 by PMA/IM (Fig. 4E and F).

Fig. 4.

Effects of GlcNH₂ and MelNH₂ on PMA/IM-induced activation of NFATc1, NFκB, and AP-1 in Jurkat cells. Cells were pre-incubated for 30 min in the presence of the indicated concentrations of GlcNH₂ (A, C, E) and MelNH₂ (B, D, F). After the addition of DMSO (0.2%) (vehicle: veh) or the combination of PMA (1 μM) and IM (0.5 μM), cells were further incubated for 3 h and assayed for the activation of NFATc1 (A, B), NFκB (C, D), and AP-1 (E, F). Data are the mean and standard deviation (bars) of three independent experiments. *P < 0.05, **P < 0.01, ***P < 0.001; unpaired t-test (2-tailed), as compared with control.

These results suggest that MelNH₂ and GlcNH₂ both suppress PIIP (and thus CIIP) by inhibiting the activation of NFATc1 and NFκB.

3.3. Comparison of the actions of GlcNH₂ and MelNH₂

We previously reported that GlcNH₂ at 5 mM significantly (P < 0.01) suppressed the growth of human K562 leukemia cells and human HUC-F2 (non-transformed) cells, whereas MelNH₂ at 5 mM significantly (P < 0.01) suppressed the cell growth of K562 cells but not of HUC-F2 cells, as assessed at day 3 after exposure [26]. This suggests that GlcNH₂ is toxic to both tumor cells and non-transformed cells, whereas MelNH₂ is toxic to tumor cells but not to non-transformed cells. In the present study, we found that GlcNH₂ and MelNH₂ at up to 20 mM had no effect on cell number and viability in Jurkat cells, as assessed at hour 12 after exposure (Fig. 2C and D), suggesting that the two saccharides are not toxic to mammalian cells, at least within that period of exposure.

The present observation that GlcNH₂ suppressed CIIP (Fig. 2, Fig. 3) by, at least in part, inhibiting the activation of NFATc1 and NFκB (Fig. 4A–D) is consistent with a previous observation that GlcNH₂ reduces IL-2 production in mitogen-activated Jurkat cells by inhibiting the NFAT pathway [30]. Interestingly, MelNH₂, but not GlcNH₂, promoted the activation of AP-1 by PMA/IM (Fig. 1, Fig. 4E and F). Although the biological significance of this promotion of AP-1 activation by MelNH₂ is currently unknown, this result suggests that GlcNH₂ and MelNH₂ suppress IL-2 production through different mechanisms; that is, MelNH₂ has two target molecules, one of which is also the target molecule of GlcNH₂ and leads to the inhibition of NFAT and NFκB activation, whereas the other stimulates AP-1 activation. In the near future, we intend to elucidate the target molecule(s) of MelNH₂ in Jurkat cells, which the present results indicate reside downstream from where PMA and IM exert their actions but upstream of the three transcription factors that regulate IL-2 mRNA expression.

4. Conclusions

The present results suggest that, like GlcNH₂, MelNH₂ may be a promising lead compound for development as a novel immunosuppressive drug with an improved adverse effect profile compared with those of currently available immunosuppressive drugs.

Conflicts of interest

The authors declare no competing interests.