Regulation of immune response by S−1-propenylcysteine through autophagy-mediated protein degradation

Abstract

Autophagy is a key event in cellular recycling processes due to its involvement in the intracellular degradation of proteins. It has been demonstrated that S−1-propenylcysteine (S1PC), a characteristic sulfur compound in aged garlic extract, induces the activation of autophagy. S1PC degrades the adaptor protein myeloid differentiation response protein 88 (MyD88) of downstream of Toll-like receptor (TLR) by activating autophagy in vitro and in vivo. The degradation of MyD88 inhibits the TLR signaling pathway, including the phosphorylation of interleukin 1 receptor associated kinase 4 (IRAK4) and nuclear factor (NF)-κB p65 in vitro, and eventually leads to the inhibition of interleukin (IL)-6 production in vitro and C-C motif chemokine ligand 2 (Ccl2) mRNA expression in vivo. S1PC also increases the level of intestinal immunoglobulin A (IgA) and the number of IgA-producing cells in Peyer's patches in vivo. In addition, S1PC triggers the mRNA expression of X-box binding protein 1 (Xbp1), an inducer of IgA-producing cell differentiation via the phosphorylation of extracellular signal-regulated kinase (ERK)1/2 and the degradation of paired box protein 5 (Pax5), a suppressor of Xbp1 mRNA expression. The present review summarizes the mechanisms through which the activation of autophagy by S1PC modulates the immune response.

1. Introduction

Aged garlic extract (AGE) is produced by extracting and aging garlic slices in an aqueous ethanol solution for >10 months and has been shown to modulate several immune functions, such as decreasing inflammatory cytokines and chemokines in animal models (1–4). In addition, the supplementation of AGE was previously shown to increase the numbers of γδ-T and natural killer (NK) cells, and to reduce the levels of inflammatory cytokines, such as interleukin (IL)-6 and tumor necrosis factor (TNF)-α, in a clinical study (5). AGE has been shown to exert immuno-enhancing and anti-inflammatory effects (1–5). S−1-propenylcysteine (S1PC), a major characteristic sulfur compound in AGE, which exhibits good oral bioavailability in rats and canines (6), has been shown to exert several beneficial effects, such as immunoregulatory, anti-hypertensive and blood flow-promoting effects (7–10). Moreover, in our previous recent studies, it was indicated that S1PC promoted intestinal immunoglobulin A (IgA) production and inhibited lipopolysaccharide (LPS)-induced IL-6 production (7,10).

Autophagy is a major degradation system of cellular components, including abnormal proteins, protein aggregates and damaged organelles (11–13). In addition, autophagy maintains cellular homeostasis and regulates various cellular events, such as signal transduction, cell growth, apoptosis and differentiation. Autophagy has been shown to regulate the immune response and immune cell differentiation (14–18). The inhibition of autophagy prevents monocyte-to-macrophage differentiation as it contributes to the transition from apoptosis to differentiation (19). In addition, the regulatory T (Treg) cell-specific deletion of autophagy-related gene (Atg) 7 triggers the loss of Treg cells by inducing apoptosis and promotes the development of inflammatory disorders (20). Thus, autophagy plays an important role in the regulation of immune developments and functions. The aim of the present review is to provide a summary and discussion of the mechanisms responsible for the immunoregulatory effects of S1PC which are mediated via the activation of autophagy.

2. S1PC induces the activation of autophagy

Autophagy is activated by several stress conditions, such as nutrient starvation, unfolded proteins and infection (11–13). Autophagy-mediated proteolysis occurs through different steps, which include the elongation of the phagophore and delivery to lysosomes. These processes are regulated by several signaling molecules (21,22). S1PC has been shown to promote the phosphorylation of AMP-activated protein kinase (AMPK), which is a cellular energy sensor and regulates the initial steps of autophagy activation (10). AMPK triggers the phosphorylation of unc-51-like kinase 1/2 (Ulk1/2) and inhibits the phosphorylation of mammalian target of rapamycin (mTOR), a repressor of autophagy. These steps initiate the elongation of the phagophore by phosphorylating the complex of Beclin1/vesicular sorting protein 34 (VPS34) (21–23). Following the formation of the autophagosome membrane, microtubule-associated protein 1 light chain 3 (LC3-I) conjugates with phosphatidylethanolamine by ubiquitin-like enzymes, such as Atg7, Atg3 and the Atg16L:Atg5-Atg12 complex, and is converted to lipidated LC3 (LC3-II). LC3-II interacts with target proteins via adaptor protein p62 on the autophagosome membrane. The LC3-II/LC3-I ratio usually increases upon the activation of autophagy (24,25), whereas S1PC has been shown to increase the levels of both LC3-I and LC3-II. Accordingly, S1PC can not only promote the conversion of LC3-I to LC3-II, but can also increase the production of LC3-I. Subsequently, the autophagosome fuses with the lysosome and then target proteins are degraded with LC3-II and p62 (10). S1PC has been shown to induce the degradation of target proteins and p62 (10). In addition, both 3-methyladenine (3-MA), an autophagy inhibitor and compound C, an AMPK inhibitor, have been shown to block the S1PC-induced activation of autophagy (10). A schematic diagram of the mechanisms through which S1PC induces autophagy is presented in Fig. 1. It is thus suggested that S1PC triggers the activation of autophagy by inducing AMPK phosphorylation.

Figure 1.

S1PC induces the activation of autophagy. S1PC induces the activation of the AMPK-ULK axis and triggers the elongation of phagophore. The Atg7 and Atg16L complex then catalyze the formation of PE-conjugated LC3 (LC3-II). LC3-II interacts with ubiquitinated target protein via adaptor protein p62. Finally, target protein is degraded by autophagy-lysosome degradation system. S1PC, S−1-propenylcysteine; AMPK, AMP-activated protein kinase; ULK, unc-51-like kinase; PE, phosphatidylethanolamine; LC3, light chain 3.

3. Anti-inflammatory effects of S1PC

Chronic inflammation is associated with the onset of several human conditions and diseases, including aging, allergies, autoimmune diseases, atherosclerosis, cancer, chronic wounds, cystic fibrosis, metabolic syndrome and obesity (26,27). The pattern recognition receptors (PRRs) play an important role in innate immunity and host defense by recognizing pathogen-associated molecular patterns (PAMPs). However, PRRs trigger chronic inflammation by consecutively interacting with danger-associated molecular patterns (DAMPs) released from dying cells (28–30). Toll-like receptors (TLRs), which are important members of the PRR family, recognize microbial components and cellular debris (28–30). Therefore, PRRs recognize not only pathogens, but also cellular components. The activation of TLRs recruits myeloid differentiation response protein 88 (MyD88), a common adaptor protein of TLRs, apart from TLR3, and IL-1 receptor-associated kinase 4 (IRAK4) to the plasma membrane (30–32). TLR signaling induces the production of the inflammatory cytokines, IL-6 and TNF-α, and the chemokines, C-C motif chemokine ligand 2 (CCL2) and C-X-C motif chemokine ligand 8 (CXCL8) via the activation of nuclear factor (NF)-κB (34,35). S1PC has been shown to inhibit IL-6 production by suppressing the TLR signaling pathway via the degradation of MyD88 (10). In addition, S1PC blocks the mRNA expression of Ccl2 in the livers of spontaneously hypertensive rats (SHRs) (10). A schematic diagram of the mechanisms through which S1PC induces the degradation of MyD88 and paired box protein 5 (Pax5) by activating autophagy is presented in Fig. 2. The constituents of fresh garlic and AGE have been reported to inhibit the TLR signaling pathway. Alliin, a constituent of fresh garlic, decreases the LPS-induced phosphorylation of extracellular signal-regulated kinase (ERK)1/2 in adipocytes (36). S-allylcysteine (SAC), a constituent of AGE, has been shown to reduce the production of inflammatory cytokines by inhibiting NF-κB phosphorylation (37). The inhibitory effects of S1PC could be considered to be different from those of other garlic constituents. S1PC has been shown to degrade MyD88 by activating autophagy (see schematic diagram in Fig. 2) (10). However, the activation of autophagy alone cannot degrade MyD88 due to the inability of SAC to induce the degradation of MyD88, although SAC also activates autophagy (10). S1PC has been shown to have another distinct feature that directly denatures and aggregates MyD88, whereas SAC is unable to denature MyD88 (10). Aggregated MyD88 is modified with both acetylation and ubiquitination, and forms the histone deacetylase 6 (HDAC6)-dependent aggresome. Subsequently, ubiquitin of the aggresome interacts with p62 and is degraded by the autophagy-lysosome system (10). Thus, as discussed above, it has been suggested by both in vitro and in vivo studies that the anti-inflammatory mechanisms of S1PC involve the degradation of MyD88 by triggering the denaturation of MyD88 and the activation of autophagy.

Figure 2.

S1PC induces the degradation of MyD88 and Pax5 by activating autophagy. S1PC directly denatures MyD88 and then induces the formation of protein aggregates by the lysine acetylation and ubiquitination. S1PC triggers the degradation of MyD88 by inducing AMPK-mediated autophagy activation. Consequently, the degradation of MyD88 inhibits TLR signaling pathway (left part of diagram). S1PC induces the phosphorylation of ERK1/2 and triggers AMPK-induced autophagy activation. Pax5 is phosphorylated by ERK1/2 and then is degraded by autophagy. Therefore, the degradation of Pax5 induces the expression of Xbp1 mRNA and triggered the differentiation of B cells into IgA-producing cells (right part of diagram). S1PC, S−1-propenylcysteine; MyD88, myeloid differentiation response protein 88; AMPK, AMP-activated protein kinase; TLR, Toll-like receptor; ERK1/2, extracellular-regulated kinase 1/2; Pax5, paired box protein 5; Xbp1, X-box binding protein 1; IRAK4, interleukin 1 receptor associated kinase 4.

4. Immuno-enhancing effects of S1PC

The intestine is the largest tissue of the immune system and is the first defense line of the body against foreign antigens, such as infectious pathogens, toxins and food allergens (38,39). IgA is the most abundant secreted antibody involved in protecting intestinal epithelial cells (40). Immunoglobulin class switching from IgM to IgA is induced by the action of both cell-cell contact and cytokines in Peyer's patches (PPs) and becomes rapidly plasmablasts. The oral administration of S1PC has been shown to increase the intestinal IgA level and IgA-producing cells in PPs (7). In addition, S1PC has been found to act on B cells and increase IgA production by promoting the differentiation of B cells into IgA-producing B cells in vitro. Therefore, S1PC is more likely to promote the expression of transcription factors related to immunoglobulin class switching. Several transcription factors, including X-box binding protein 1 (Xbp1), and B cell-induced maturation protein-1 (Blimp1) regulate immunoglobulin class switching (41). S1PC increases the expression of Xbp1 mRNA in vitro and in vivo, whereas the mRNA expression of Blimp1 is not affected. Xbp1 requires the formation of pre-plasmablasts, the early process of plasma cell differentiation that is independent of Blimp1 function. It is possible that S1PC induces the early process of plasma cell differentiation. The mRNA expression of Xbp1 is repressed by Pax5. It is known that ERK1/2 triggers the degradation of Pax5 by inducing its phosphorylation (41). S1PC has been found to induce the degradation of Pax5 by enhancing ERK1/2 phosphorylation (see schematic diagram in Fig. 2) (7). Therefore, on the whole, it is suggested that S1PC induces the degradation of Pax5 by activating both ERK1/2 and autophagy, and then triggers the differentiation of B cells into IgA-producing cells by increasing the mRNA expression of Xbp1.

5. Conclusions and future perspectives

S1PC, a major characteristic sulfur compound in AGE, induces the activation of autophagy via the phosphorylation of AMPK. The activation of autophagy regulates the immune response through the degradation of key molecules. S1PC has been shown not only to induce the activation of autophagy, but also to trigger the post-translational modification of target proteins. Thus, it is suggested that S1PC selectively induces the degradation of proteins. In addition, it is suggested that S1PC exerts immuno-enhancing and anti-inflammatory effects, and may contribute to the maintenance of immune homeostasis by regulating autophagy.

Funding

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Authors' contributions

JIS and YK conceived this review. JIS, SM and MU analyzed the relevant literature. JIS wrote the first draft of the manuscript and produced the figures. JIS, SM, MU and YK critically revised the manuscript. All authors have reviewed and approved the final manuscript.

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Competing interests

The authors declare that they have no competing interests.