Curcumin could reduce the monomer of TTR with Tyr114Cys mutation via autophagy in cell model of familial amyloid polyneuropathy

Abstract

Transthyretin (TTR) familial amyloid polyneuropathy (FAP) is an autosomal dominant inherited neurodegenerative disorder caused by various mutations in the transthyretin gene. We aimed to identify the mechanisms underlying TTR FAP with Tyr114Cys (Y114C) mutation. Our study showed that TTR Y114C mutation led to an increase in monomeric TTR and impaired autophagy. Treatment with curcumin resulted in a significant decrease of monomeric TTR by recovering autophagy. Our research suggests that impairment of autophagy might be involved in the pathogenesis of TTR FAP with Y114C mutation, and curcumin might be a potential therapeutic approach for TTR FAP.

Keywords:

• curcumin
• familial amyloid polyneuropathy
• transthyretin
• autophagy

Introduction

Transthyretin (TTR) familial amyloid polyneuropathy (FAP) is an autosomal dominant inherited disease, characterized clinically by progressive sensory, motor, and autonomic impairment, which typically lead to death around a decade after diagnosis.¹ Since the first identification of TTR with Val30Met mutation (TTR V30M), the most common gene mutation in FAP patients, more than 100 TTR mutations have been found to cause FAP.² However, the detailed pathogenesis underlying TTR FAP remains undefined. Previous studies of the TTR V30M mutant have shown that misfolding and self-aggregation of TTR are implicated in the pathogenesis of TTR FAP involving abnormal endoplasmic reticulum (ER) stress.³

Corresponding to the various TTR gene mutations and a wide range of geographical distributions, FAP presents diverse characteristics in genotype-phenotype in different regions. We have recently published the first report of a TTR Tyr114Cys (TTR Y114C) mutation in a Chinese family with TTR FAP.⁴ Compared with TTR V30M, the TTR Y114C mutation showed different clinical manifestations, and was also observed in a Japanese family.^5,6 This suggests that the pathogenesis of the TTR Y114C and TTR V30M mutations might be different. Studies focused on monomer generation and tetramer depolymerization have been performed.^1,2 However, the mechanisms underlying the clearing of the abnormally increased monomer are unknown.

Autophagy is the major lysosomal pathway via which cells degrade intracytoplasmic protein. It is widely accepted that autophagy plays a key role in the process of amyloid deposition in certain neurodegenerative diseases, including alpha-synuclein, beta peptides, tau oligomers, and misfolded prion protein.⁷ Therefore, autophagy may be involved in degradation of the TTR monomer in TTR FAP.

Curcumin and its analogs have demonstrated a protective effect in many diseases involving antimicrobial, antitubercular,⁸ and anticancer mechanisms,⁹ and they can also modulate innate immunity.¹⁰ Of note, curcumin has been shown to promote autophagy.¹¹ Therefore, we hypothesized that autophagy might be involved in the pathogenetic mechanism of the TTR Y114C mutation in TTR FAP and curcumin might have potential therapeutic role in this disease. In this study, we aimed to identify the role of autophagy in the pathogenetic mechanism of TTR FAP and to assess the therapeutic effect of curcumin in the disease.

Materials and methods

Plasmid construction, cell culture, and stable cell line generation

Human TTR complementary DNA was amplified from the human fetal brain complementary DNA library (Invitrogen, Carlsbad, CA, USA) and ligated to the pcDNA3.0 vector with a C terminal Myc tag. TTR Y114C and TTR V30M were generated using a site-directed mutagenesis kit (Qiagen, Hilden, Germany). Human embryonic kidney (HEK) 293T cells (American Type Culture Collection, Manassas, VA, USA) were cultured in Dulbecco’s Modified Eagle’s Medium with 10% fetal bovine serum and 100 U/mL penicillin/streptomycin. TTR Y114C and TTR V30M were transfected into HEK293T cells and stable clones were selected with 500 µg/mL G418.

Cell viability assay

The cytotoxic effect of curcumin was determined using the cell proliferation reagent 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT; Sigma-Aldrich). In brief, HEK293T cells were seeded at 2×10⁴ cells/well in 96-well flat-bottomed plates and incubated at 37°C overnight. The cells were then treated with 0, 2.5, 5.0, 7.5, 10, 15, 20, or 25 µM curcumin for 24 hours. Next, they were exposed to 10 µL of the MTT (0.5 mg/mL) reagent for 4 hours at 37°C. Absorbance was measured at 570 nm using a microplate reader. All experiments were performed in triplicate.

Antibodies and reagents

The following antibodies were used: anti-LC3 rabbit (Novus Biologicals, San Diego, CA, USA), Myc-Tag (19C2) mouse monoclonal antibody (Abmart, Shanghai, People’s Republic of China), BiP antibody (Cell Signaling Technology, Danvers, MA, USA), eukaryotic initiation factor 2 alpha (eIF2α) antibody (Cell Signaling Technology), phospho-eIF2α (Ser51) antibody (p-eIF2α) (Cell Signaling Technology), and mouse monoclonal anti-beta-actin antibody (Sigma-Aldrich). Curcumin with purity greater than 95% was obtained from Sigma and dissolved in dimethyl sulfoxide. Fresh stock solutions of curcumin were prepared in dimethyl sulfoxide and diluted to stock concentrations with 10 mM and used immediately. All the curcumin solutions were kept in the dark to avoid exposure to light. 3-Methyladenine (3-MA), a phosphatidylinositol 3-phosphate kinase inhibitor, was purchased from Sigma and dissolved in dimethyl sulfoxide to produce a 300 mM stock solution.

Western blotting

Cells were plated in six-well plates at a density of 2×10⁶ cells per well for 36 hours prior to treatment with 5 µM curcumin or 1 mM 3-MA. Equal amounts of the supernatant from each sample were then mixed with a native sample buffer (0.05 M Tris-HCl at pH 6.8, 10% glycerol) using the method described by Tojo et al.¹² The supernatant was mixed with non-natured buffer (50 mM Tris·HCl pH 7.6, 150 mM NaCl, 1% NP-40, 1% sodium deoxycholate), with protease inhibitor cocktail (Roche Applied Science, Indianapolis, IN, USA) and 1 mM phenylmethylsulfonyl fluoride (Sigma-Aldrich). The cells were lysed in RIPA buffer (50 mM Tris·HCl pH 7.6, 150 mM NaCl, 1% NP-40, 1% sodium deoxycholate, 0.1% sodium dodecyl sulfate) with protease inhibitor cocktail and 1 mM phenylmethylsulfonyl fluoride for 30 minutes on ice. After centrifugation at 14,000× g for 30 minutes, the protein concentration was assayed using a bicinchoninic acid protein assay kit (Thermo Fisher Scientific, Waltham, MA, USA). The samples were detected by immunoblotting. Band intensities were quantified by densitometric analyses using NIH ImageJ software. For all the Western blot results, at least three independent experiments were done and the most representative result was shown.

Immunocytochemistry assay

Cells were seeded on poly-L-lysine-coated glass coverslips, fixed with 4% paraformaldehyde for 20 minutes, permeabilized with 0.2% Triton X-100 for 15 minutes, blocked with 3% bovine serum albumin in phosphate-buffered saline and 0.2% Tween 20 for 1 hour, and then incubated with primary antibodies against LC3-II overnight at 4°C, followed by washing in phosphate-buffered saline and 0.2% Tween 20 three times for 10 minutes each. An Alexa Fluor 488 anti-rabbit immunoglobulin G tagged secondary antibody (Invitrogen) was added. After washing three times using phosphate-buffered saline, anti-fade mounting medium (Vector Laboratories Inc., Burlingame, CA, USA) was added and the stained cells were analyzed using a phase contrast fluorescence microscope (Eclipse E400; Nikon, Tokyo, Japan).

Statistical analysis

The statistical analysis was carried out using Statistical Package for the Social Sciences version 16.0 software (SPSS Inc., Chicago, IL, USA). Quantitative data were expressed as the mean ± standard deviation and compared using one-way analysis of variance. Statistical significance was set at a P-value less than 0.05. All analyses were performed blind to the experimental conditions.

Results

TTR Y114C mutation led to increased monomeric TTR and impaired autophagy in vitro

To investigate the alteration of monomeric TTR with different mutations, we generated HEK293T cell lines with wild-type TTR, TTR Y114C, and stable overexpression of TTR V30M. Wild-type TTR represented the normal control and TTR V30M represented the positive control. Western blotting analysis of the TTR level in the cells when cultured for 24 hours showed that the monomer of TTR Y114C and TTR V30M was increased by approximately 2.3 times and 2.78 times, respectively, compared with wild-type TTR (Figure 1A and B). Mutation of TTR Y114C was related to the increase in monomeric TTR, as well as the mutation of TTR V30M.

Figure 1 Changes in autophagy and endoplasmic reticulum stress related to wild-type TTR, TTR V30M, and TTR Y114C.

Notes: (A) Western blot analysis of tetrameric TTR, monomeric TTR, BiP, eIF2α, p-eIF2α, and LC3 from TTR WT, TTR V30M, and TTR Y114C stable overexpressed HEK293T cell lines, respectively. (B–D) Bar graphs show the statistical analysis of tetrameric TTR, monomeric TTR, BiP, p-eIF2α, eIF2α, and LC3 (mean ± standard deviation), *P<0.05 versus wild-type. (E) Representative immunofluorescence images stained with LC3 in wild-type TTR, TTR V30M, and TTR Y114C (green).
Abbreviations: HEK, human embryonic kidney; NS, no significant difference; p-elF2α, phosphorylated elF2α; TTR, transthyretin; WT, wild-type.

Next we investigated the activation of several markers associated with ER stress, including ER-resident chaperone BiP and p-eIF2α. Our results showed the levels of BiP and p-eIF2α is higher in TTR V30M than those in wild-type TTR. In contrast, BiP and p-eIF2α levels in TTR Y114C were similar to those in wild-type TTR (Figure 1A and C), indicating ER stress might not be the main pathogenetic mechanism for the TTR Y114C mutation. We then investigated whether autophagy plays a role in the mechanism of TTR Y114C mutation. LC3-II is well known to be a robust marker of autophagosomes, and immunofluorescent staining of LC3-II can be used to assay for autophagosome formation. A high ratio of LC3-II to LC3-I would indicate induction of autophagy. Our results revealed that the ratio of LC3-II/I was markedly decreased for TTR Y114C, but less suppressed for TTR V30M (Figure 1A and D). Likewise, a significant decrease in LC3-II immunoreactivity was detected in TTR Y114C (Figure 1E). The results of Western blotting and immunofluorescence indicated that autophagy in TTR Y114C was significantly downregulated. Therefore, impaired autophagy might be responsible for the pathogenesis of TTR Y114C mutation.

Curcumin decreased monomeric TTR by promoting autophagy

The effects of curcumin were investigated in TTR Y114C and wild-type TTR stable overexpressed HEK293T cells. Curcumin did not show toxic effects in the stable overexpressed cell lines at curcumin concentrations below 10 µM (Figure 2A and B). We chose 5 µM as the experimental concentration, because it is the minimal effective concentration of curcumin in these cell lines. Further, we wanted to determine whether curcumin could decrease monomeric TTR by promoting autophagy at the minimal effective concentration. Therefore, we used curcumin (2.5 µM and 5 µM) as a protective agent to assess whether it could decrease monomeric TTR with mutation by promoting autophagy. Quantification of LC3-II and LC3-I indicated markedly higher activation of LC3 in TTR Y114C treated with curcumin 5 µM for 24 hours (Figure 2D). In contrast, treatment with curcumin at different concentrations could not activate LC3 in wild-type TTR (Figure 2C, E). We next examined the ratio of monomers to tetramers in TTR Y114C, which was significantly decreased after 24 hours of treatment with 5 µM curcumin compared with no treatment with curcumin (Figure 2D and F). However, for wild-type TTR, the ratio of monomers to tetramers was unchanged after treatment with curcumin (Figure 2C and E). These results indicate that treatment with curcumin 5 µM for 24 hours was able to decrease the monomer in the TTR Y114C mutation by promoting autophagy.

Figure 2 Curcumin decreased monomeric TTR by promoting autophagy.

Notes: (A, B) Effect of curcumin on the cell viability of TTR WT and TTR Y114C stable cell lines, respectively. (C, D) Western blot analysis of LC3, tetrameric TTR, and monomeric TTR from TTR WT and TTR Y114C. (E, F) Bar graphs show the statistical analysis of LC3, tetrameric TTR, and monomeric TTR from TTR WT and TTR Y114C (mean ± standard deviation). *P<0.05 versus curcumin 0 mM.
Abbreviations: TTR, transthyretin; WT, wild-type; Cur, curcumin.

Protective effect of curcumin on TTR Y114C could be partially blocked by 3-MA

To further validate whether the decrease in monomer by curcumin in our experiments was mediated by autophagy, 3-MA, an inhibitor of autophagosome formation, was implied to negatively regulate autophagy. 3-MA (1 mM) was added to the cell culture medium 2 hours before curcumin and incubated for 24 hours. Analysis of LC3, tetrameric TTR, and monomeric TTR from TTR Y114C revealed that 3-MA partly reversed the LC3 II activation induced by curcumin and increased the monomer of TTR Y114C (Figure 3). These results confirm that curcumin induced the decrease in the TTR Y114C monomer by promoting the autophagy pathway.

Figure 3 Protective effect of curcumin on TTR Y114C could be partially blocked by 3-MA.

Notes: (A) Western blot analysis of LC3, tetrameric TTR, and monomeric TTR from TTR WT and TTR Y114C. (B) Bar graph indicates the statistical analysis of LC3, tetrameric TTR, and monomeric TTR from TTR WT and TTR Y114C (mean ± standard deviation). *P<0.05 versus ctrl.
Abbreviations: ctrl, control; Cur, curcumin; 3-MA, 3-methyladenine; TTR, transthyretin; WT, wild-type.

Discussion

TTR FAP is a severe autosomal dominant inherited disease, for which the treatment options are limited. Liver transplantation performed early in the course of the disease is the only therapeutic strategy known to stabilize this neuropathy.^1,13 More recently, tafamidis meglumine, a potent inhibitor of misfolding and deposition of mutated TTR, has completed an 18-month, placebo-controlled Phase II/III clinical trial for the treatment of FAP.¹⁴ However, in June 2012, the US Food and Drug Administration Peripheral and Central Nervous System Drugs Advisory Committee rejected this drug, stating a lack of convincing data supporting its efficacy.¹⁵ Hence, it is important to identify the pathogenetic mechanism of FAP to find an alternative effective treatment strategy.

Accumulating studies focused on the TTR mutation gene and protein have provided insights into the pathogenesis of TTR FAP, including decreased stability of TTR tetramers, conformational change in the crystal structure of variant TTR, altered kinetics of denaturation, and disturbing endoplasmic ER quality control system.^1,16–18 Previous studies have demonstrated that increased levels of ER stress are correlated with extracellular TTR deposition. Two ER stress markers, BiP and p-eIF2α, have been observed to be present and upregulated in the salivary gland tissue of FAP patients.³ However, the precise molecular mechanisms underlying TTR FAP and its phenotypic heterogeneity are not yet fully understood.

Our current study investigated whether the two mutations, TTR Y114C and TTR V30M, share the same pathogenesis and evaluated the effect of pathogenic mutations on the clearance of the monomer. Our results show that the ratio of LC3-II/I was markedly decreased, while BiP and p-eIF2α levels remained constant in TTR Y114C when compared with wild-type TTR and TTR 30M. The results of our research indicate the impaired autophagy contributed to the TTR Y114C mutation, but not ER stress. This observation indicates that abnormal accumulation of TTR caused by a different mutation might be cleared by different pathways, and more studies are necessary to confirm whether this difference applies to other TTR mutations.

Curcumin is known to have neuroprotective properties through a variety of mechanisms.^8–11 Our research indicates that curcumin decreased the monomeric TTR by promoting autophagy, and without toxic effects. Moreover, this protective effect of curcumin on TTR Y114C could be partially blocked by 3-MA. Pullakhandam et al showed that curcumin binds to wild-type TTR and prevents urea-induced perturbations in the tertiary structure of TTR in vitro.¹⁹ Recently, Ferreira et al reported that dietary curcumin modulated TTR amyloidogenicity.²⁰ Therefore, curcumin might be an effective therapy for FAP involving multiple molecular pathways.

Overall, our findings show that abnormal accumulation of TTR caused by different mutations might be cleared in different ways, and curcumin might be an effective therapy for FAP by promoting autophagy. Further studies are necessary to determine whether this phenomenon exists in other TTR mutations.

Acknowledgments

This study was supported by grants from the National Program of Basic Research of China (2010CB945200, 2011CB504104), The National Natural Science Foundation of China (number 81301081), the Shanghai Key Project of Basic Science Research (10411954500), and the Program for Outstanding Medical Academic Leader (LJ 06003).

Disclosure

The authors report no conflicts of interest in this work.