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Introduction

Liver cirrhosis is a consequence of diverse mechanisms of liver injury that lead to a wound-healing reponse characterized by necroinflammation and fibrogenesis (1,2). Hepatic stellate cells (HSCs) play a critical role in the transition from chronic liver injury to cirrhosis (3). Upon liver injury, HSCs transdifferentiate from quiescent cells to activated, myofibroblast-like cells, resulting in proliferation, excessive production and secretion of extracelluar matrix (4,5). Thus, the suppression of activated HSCs has been recognized as an effective pathway through which to attenuate liver fibrosis.

Autophagy is a degradation pathway by which the cell self-digests its own components by forming autophagosomes and autolysosomes (4). This self-digestion process occurs in all types of cells at a low basal level, serving a homeostatic function to recycle proteins and organelles. When the cell is going to rid itself of starvation, damaged organelles and superfluous or misfolded proteins, autophagy is rapidly upregulated (6). Moreover, recent studies have revealed that autophagy could be instigated by the upregulation of endoplasmic reticulum (ER) stress (7,8).

ER is a type of flattened sac or tube-like organelle in eukaryotic cells, serving many essential functions, such as correctly folding newly made protein molecules and a Ca2+ reservoir (9,10). Increased protein synthesis load and accumulation of unfolded or misfolded proteins in ER may disturb ER homeostasis, thereby imposing ER stress and the unfolded protein response (UPR) (11,12). The UPR, initially, compensates for the damage caused by ER stress and maintains celluar homeostasis via enhancing the protein-folding ability of the ER and facilitating proteasomal degradation of unfolded or misfolded proteins. However, if ER stress is excessive or prolonged that transcends the protective ability of UPR, the high-intensitive UPR eventually results in cell apoptosis (13–15).

Caffeine, the major compound in coffee, has been identified to have a potential beneficial effect against liver fibrosis (16,17). Recent findings have revealed that caffeine-mediated attenuation of liver fibrosis is probably associated with HSC apoptosis (18). Another study found that caffeine induced apoptosis of SH-SY5Y, PC12D and HeLa cells by stimulating autophagic flux by inhibiting the PI3K/AKT/mTOR pathway (19). However, little is known concerning the mechanism by which caffeine regulates the apoptosis of HSCs.

Here, we report that caffeine-enhanced autophagic flux in HSCs was stimulated by ER stress through the IRE1-α pathway. Furthermore, enhanced autophagy attenuated the expression of α-SMA by instigating HSC apoptosis. Therefore, our results provide new insight into the mechanism of caffeine's anti-fibrotic effects.

Materials and methods

Cell culture and compounds

LX-2 cells, a type of immortalized human HSC line, was purchased from the Cell Center of Xiangya School of Medicine, Central South University (Hunan, China), cultured in Dulbecco's modified Eagle's medium (DMEM) and supplemented with 10% fetal bovine serum (FBS) (both from Gibco, Grand Island, NY, USA), 100 IU/ml penicillin and 100 µg/ml streptomycin at 37° C in 5% CO2. To measure the autophagic flux of LX-2 cells after being treated with caffeine, LX-2 cells were transfected with RFR-GFR-hLC3 lentivirus as previously described elsewhere (20). Caffeine (Sigma-Aldrich, St. Louis, MO, USA) was dissolved and diluted with DMEM to the desired concentrations which we selected according to other articles (16,18,19). 3-Methyladenine (MA) (Sigma-Aldrich) was dissolved in phosphate-buffered saline (PBS) and diluted with DMEM to the concentration of 5 mM.

Western blotting

LX-2 cells were lysed in RIPA (Solarbio, Beijing, China) supplemented with protease inhibitor cocktail (Sigma-Aldrich) and the protein samples were centrifuged for 30 min at 10,000 × g (4°C). The supernatants were collected and the BCA protein assay kit (Pierce, Rockford, IL, USA) was applied to detect the protein concentration. The protein samples were separated by 12.5% SDS-PAGE and subsequently electrotransferred onto PVDF membranes. The membranes were blocked with 5% defatted milk for 1.5 to 2 h and incubated with the primary antibody overnight at 4°C. The primary antibodies were LC3 (4108; Cell Signaling Technology, Inc., Danvers, MA, USA), SQSTM1 (ab109012; Abcam, Cambridge, UK), α-SMA (A7249; ABclonal, Cambridge, MA, USA), Gpr78 (ab21685) and IRE1-α (ab124945) (both from Abcam) and CHOP (2895; Cell Signaling Technology, Inc., Danvers, MA, USA). Afterwards, the membranes were incubated with the HRP-conjugated secondary antibodies (SA00001-1 and SA00001-2; Proteintech Group, Inc., Rosemont, IL, USA) at room temperature for 1.5 h. Finally the results were visualized by enhanced chemiluminescence.

Flow cytometry assay

Annexin V-FITC Apoptosis Detection kit (BD Pharmingen, Franklin Lakes, NJ, USA) was used to detect the apoptosis of cells. In brief, both floating and adherent cells were collected. After being washed and resuspended with PBS twice, the cells were stained with 3 µl Annexin V-FITC and 5 µl PI for 20 min in the dark at room temperature. Then 150 µl binding buffer was added to each sample of cells, after which the cells were analyzed by flow cytometry.

RNA interference

In order to reduce the expression of Atg7 and IRE1-α in LX-2 cells, small interfering RNAs (siRNAs) targeted against human Atg7 and IRE1-α were synthesized by GenePharma (Shanghai, China).

The sequence of Atg7-siRNA was 5′-GCCGUGGAAUUGAUGGUAUTT-3′. The sequence of IRE1-α was 5′-CTACTGGATGATAAATTTGCTTCA-3′. The negative control siRNA sequence was 5′-UUCUUCGAACGUGUCACGUTT-3′. Then LX-2 cells were transfected with Atg7-siRNA, IRE1-α-siRNA or nC-siRNA, respectively, using Lipofectamine 2000 (Thermo Fisher Scientific, Inc., Waltham, MA, USA) according to the production's instruction manual.

Cell viability assay

The effects of caffeine on the viability of LX-2 cells were evaluated by Cell Counting Kit-8 (CCK-8) assay (Dojindo Laboratories, Kumamoto, Japan), as previously described in another article (21).

Intracellular Ca2+ detection

The levels of intracellular Ca2+ were detected using Fluo-3 AM (Beyotime Institute of Biotechnology, Shanghai, China). In brief, LX-2 cells were treated with different concentrations of caffeine (0, 10 and 30 mM) for 24 h, and the cells were harvested and washed twice using Ca2+-free PBS. Subsequently, the cells were resuspended in 5 µm Fluo-3 AM for 30 min in the dark at 37°C, after which the cells were washed twice using Ca2+-free PBS. To ensure that the Fluo-3 AM was completely transformed into Fluo-3 within the cells and to enable the Fluo-3 to more closely combine with Ca2+, the cells were placed quietly for 30 min in the dark at room temperature. Finally, the fluorescence intensities of Fluo-3 combined with Ca2+ were detected by flow cytometery.

Electron microscopy

Transmission electron microscopy was used to identify the ultrastructure of autophagosomes/autolysosomes as previously described elsewhere (22).

Statistical analysis

All data are presented as means ± SD from at least triplicate parallel experiments. The Student's t-test was used to analyze the differences between two groups by SPSS version 23.0 (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered as statistically significant.

Results

Caffeine inhibits the viability of LX-2 cells and induces cell apoptosis

To evaluate the direct effects of caffeine on HSCs in vitro, the LX-2 cell line, a type of immortal human HSCs, was applied in our study. After incubation with various concentrations of caffeine (0, 2.5, 5, 10, 20 and 30 mM) for 48 h or 20 mM caffeine for the indicated times (0, 6, 12, 24, 36 and 48 h), western blotting was used to detect the expression of α-smooth muscle actin (α-SMA), a marker of activated HSCs. We found that the level of α-SMA was inversely proportional to the caffeine concentration and to the duration of exposure. Particularly, caffeine decreased the α-SMA/GAPDH ratio at concentrations as low as 5 mM (Fig. 1A) and at times as early as 6 h (Fig. 1B) in LX-2 cells. Furthermore, the results of the CCK-8 assay showed that the cell viability of the LX-2 cells was markedly reduced in a dose-dependent and time-dependent manner after treatment with caffeine (Fig. 1C). To investigate whether the caffeine-inhibited viability of LX-2 cells is associated with apoptosis, we examined the effects of caffeine on the apoptotic activity of cells by flow cytometry. The percentage of apoptotic cells which is the sum of early apoptotic cells (the low right region) and late apoptotic cells (the upper right region) was significantly increased in both a dose-dependent (Fig. 1D) and time-dependent manner (Fig. 1E) by incubation with caffeine.

Figure 1 Caffeine inhibits the cell viability of LX-2 cells. (A and B) The expression of α-smooth muscle actin (α-SMA) was analyzed by western blotting in LX-2 cells exposed to various concentrations of caffeine for 48 h (A) or (B) 20 mM caffeine for the indicated times. Densitometric analysis of α-SMA levels relative to GAPDH is shown for three respectively individual experiments. **P<0.01. (C) Impacts of caffeine on the viability of LX-2 cells by CCK-8 assay. (D) LX-2 cells were treated with 0, 2.5, 5, 10, 20 and 30 mM caffeine for 48 h or (E) 20 mM caffeine for 0, 24 and 48 h, and the apoptosis of the cells was assessed by flow cytometry (the lower right region represents early apoptotic cells, the upper right region represents late apoptosis cells). Bars are the total percentages of early and late apoptotic cells which represent the means ± SD of triplicate experiments. **P<0.01.

Caffeine induces ER stress in the LX-2 cell line

Here we further investigated whether caffeine-induced HSC apoptosis is mediated by increasing ER stress. From the images taken by transmission electron microscopy, we identified many dilated cytoplasmic vacuoles in the LX-2 cells after caffeine (20 mM) treatment for 48 h. However, there were few dilated cytoplasmic vacuoles in the LX-2 cells cultured with DMEM not containing caffeine (Fig. 2A). These dilated cytoplasmic vacuoles can be recognized as dilated ER lumens as previously described (23), which indicates an increase in ER stress. Furthermore, we detected the expression of GRP78/BiP, IRE1-α and CHOP which all are markers of UPR. Notably, the ratio of GRP78/GAPDH, IRE1-α/GAPDH and CHOP/GAPDH were parallel to the increase in caffeine concentration (Fig. 2B and C) and the duration of exposure (Fig. 2D and E). In addition, Fluo-3 AM was used to label cytoplasmic calcium in the LX-2 cells since calcium disturbance is another agent that induces ER stress. The results showed that caffeine significantly elevated the levels of cytoplasmic calcium in the LX-2 cells (Fig. 2F). Collectively, all these data demonstrated that caffeine induced ER stress in LX-2 cells.

Figure 2 Endoplasmic reticulum (ER) stress induced by caffeine in the LX-2 cell line. (A) Electron microscopy (×8,000) shows dilated ER cavities in LX-2 cells in the presence of caffeine (20 mM/48 h). (a) Control cells and (b) caffeine-incubated cells are shown. →, indicates normal ER; *, represents dilated ER cavity; N, indicates the nucleus. (B) Western blotting and (C) densitometric analysis show a dose response of inositol requiring enzyme 1 (IRE1)-α, GRP78/BiP, and CHOP accumulation in LX-2 cells incubated with various concentrations of caffeine (0, 2.5, 5, 10, 20 and 30 mM) for 48 h. Bars represent the means ± SD of three independent experiments. **P<0.01, ***P<0.001. (D) Western blotting and (E) densitometric analysis show time-dependent changes in the expression of IRE1-α, GRP78/BiP and CHOP in LX-2 cells incubated with 20 mM caffeine for the indicated times. Bars represent the means ± SD of three independent experiments. **P<0.01, ***P<0.001. (F) LX-2 cells were treated with various concentrations of caffeine (0, 10, 30 mM) for 48 h, after which cells were loaded with Fluo-3 AM for 30 min. Flow cytometry was used to detect the changes in cytosolic calcium in LX-2 cells.

Autophagic flux in the LX-2 cell line is increased after caffeine treatment

Four different methods were applied to explore autophagic flux. Firstly, we detected the expression of LC3II, a good indicator for autophagosome formation, in LX-2 cells after caffeine treatment. Our results showed that the expression of LC3II was parallel to the increase in caffeine concentration (Fig. 3A and B) or the duration of exposure to caffeine (Fig. 3C and D). Secondly, we measured the accumulation of p62. p62 is a marker of autophagic flux whose level increases when autophagy is inhibited and decreases when autophagic flux is triggered. Interestingly, we found that caffeine-incubated LX-2 cells exhibited significant reduction in the level of p62 in a dose- and time-dependent manner. The results indicated that autophagy in LX-2 cells was induced by caffeine. Thirdly, autophagy is a dynamic process. The increase in LC3II level can be due to an increased autophagy presence or a result of the accumulation of autophagosomes caused by late autophagy inhibition. For the purpose of distinguishing autophagy induction from autophagy inhibition, a type of lentivirus encoding the RFP-GFP-LC3 fusion gene was used to our study. In this study, the autophagosomes are labeled with yellow dots (the overlay of green and red fluorescence), while autolysosomes are labeled with red dots only. If autophagic flux is upregulated, yellow and red dots are both increased, while only yellow dots are increased if the process of autophagosomes fusing with lysosomes is inhibited. It is the different numbers of red dots that represent changes in autophagic flux. To evaluate whether autophagic flux is upregulated by caffeine in LX-2 cells, we incubated GFP-RFP-hLC3 lentivirus-transfected LX-2 cells with various concentrations of caffeine (0, 10 and 30 mM). At 48 h points, fluorescence images were captured and quantification of the number of yellow and red dots was carried out. As shown in the fluorescence images, the number of yellow dots and red dots alone were both increased (Fig. 3E and F). Finally, electron microscopic evaluation showed an increased amount of autophagosomes/autolysosomes in the cells treated with caffeine (Fig. 3G). Taken together, these findings strongly demonstrated that autophagic flux in LX-2 cells was induced by caffeine.

Figure 3 Autophagy flux is stimulated by caffeine in the LX-2 cell line. (A) Western blotting and (B) densitometric analysis show the dose response of p62 and LC3II accumulation in LX-2 cells incubated with various concentrations of caffeine (0, 2.5, 5, 10, 20 and 30 mM) for 48 h. Bars represent the means ± SD of three independent experiments. **P<0.01, ***P<0.001. (C) Western blotting and (D) densitometric analysis show time-dependent changes in the expression of p62 and LC3II in LX-2 cells incubated with 20 mM caffeine for the indicated times. Bars represent the means ± SD of three independent experiments. **P<0.01, ***P<0.001. (E and F) Representative images and quantification of early-autophagosomes (yellow dots generated from overlapping GFP and RFP puncta) shown as yellow bars and late autolysosomes (red dots generated from RFP puncta) shown as red bars after 48 h of 10 and 30 mM caffeine treatment vs. the controls (treated with 0 mM caffeine) in LX-2 cells transfected with the RFP-GFP-hLC3 lentivirus. Error bar, standard deviation (n=30, from a total of independent three experiments), ***P<0.001. (G) Electron microscopy shows increased autophagosomes/autolysosomes in LX-2 cells incubated with 20 mM caffeine for 48 h (b and d) vs. the control cells (a and c). Arrows indicate autophagosome or autolysosome structures; n, indicates the nucleus. Magnification (×2,000 and ×8,000).

The IRE1-α signaling pathway is required for activation of caffeine-induced autophagy in the LX-2 cell line

It has been reported that autophagy can be triggered by ER stress via the IRE1-α signaling pathway (19,24). Herein, we found that caffeine contributed to autophagy and ER stress, as well as increased the expression levels of IRE1-α and CHOP in LX-2 cells. These findings prompted us to explore whether UPR acts as an upstream event of autophagy and the crucial role of IRE1-α in caffeine-treated LX-2 cells. To confirm the hypothesis, specific siRNAs directly against IRE1-α were used in the RFP-GFP-hLC3-transfected LX-2 cells. In these co-transfected cells, we observed that the numbers of yellow or red dots alone in the negative siRNA-transfected cells were both higher than those in the IRE1-α siRNA-transfected cells (Fig. 4A and B). We also found that the level of p62 accumulation in the IRE1-α siRNA-transfected cells was higher than that in the negative siRNA-transfected cells. Similarly, the accumulation of LC3II was decreased in the IRE1-α siRNA-transfected cells compared with the negative siRNA-transfected cells after caffeine treatment (Fig. 4C and D). All these data indicated that the IRE1-α pathway was an upstream event of caffeine-induced autophagy in the LX-2 cell line.

Figure 4 Autophagy in the LX-2 cell line treated with caffeine was stimulated by endoplasmic reticulum (ER) stress through the inositol-requiring enzyme 1 (IRE1)-α pathway. (A and B) Representative images and quantification of early autophagosomes (yellow dots generated from overlapping GFP and RFP puncta) shown as yellow bars and late autolysosomes (red dots generated from RFP puncta) shown as red bars after 48 h of 20 mM caffeine treatment in LX-2 cells co-transfected with the RFP-GFP-hLC3 lentivirus and IRE1-α-siRNAs vs. the control cells co-transfected with the RFP-GFP-hLC3 lentivirus and negative siRNAs. Error bar, standard deviation (n=30, from a total of independent three experiments), **P<0.001. (C) The expression of IRE1-α, p62 and LC3 in LX-2 cells transfected with IRE1-α-siRNAs or cells transfected with negative siRNAs after treatment with 0/20 mM caffeine for 48 h. (D) Densitometric analysis of IRE1-α, p62 and LC3II levels relative to GAPDH is representative of three parallel experiments. ***P<0.001.

Autophagy triggered by caffeine inhibits cell viability, induces apoptosis and suppresses activation of LX-2 cells

To investigate the roles of autophagy on cell viability in caffeine-treated LX-2 cells, we used Atg7-siRNAs to block autophagosome formation and 3-MA to inhibit the activation of autophagic flux in LX-2 cells. As expected, Atg7-knockdown reduced LC3II accumulation and increased the expression level of p62, which significantly increased the cell viability of the LX-2 cells after caffeine treatment (Fig. 5A). These findings strongly suggest the involvement of autophagy in caffeine-inhibited viability of LX-2 cells. Furthermore, Atg7-knockdown also strongly decreased the extent of apoptotic death of the LX-2 cells after caffeine incubation (Fig. 5C), suggesting that autophagy is essential for caffeine-induced apoptosis of LX-2 cells. Additionally, Atg7-knockdown rescued the expression of α-SMA, indicating a direct link between autophagy and LX-2 activation. Similar results were also found in 3-MA and caffeine co-treated LX-2 cells (Fig. 5B, D and F). All these results indicated that autophagy induced apoptosis, inhibited cell viability and suppressed cell activation in caffeine-treated LX-2 cells.

Figure 5 Effects of autophagy in LX-2 cells incubated with caffeine. (A) The viability of LX-2 cells transfected with Atg7-siRNAs or the cells transfected with negative siRNAs after 20 mM caffeine treatment at the indicated times was detected by CCK-8 assay. (B) The viability of LX-2 cells treated with 3-MA (5 mM), caffeine (20 mM) and caffeine (20 mM) together with 3-MA (5 mM) was detected by CCK-8 assay. (C) The percentage of apoptosis of LX-2 cells transfected with Atg7-siRNAs or the cells transfected with negative siRNAs after 20 mM caffeine treatment for 48 h was detected by flow cytometry. Bars represent the means ± SD of triplicate experiments. **P<0.01. (D) The percentage of apoptotic LX-2 cells treated with 3-MA (5 mM), caffeine (20 mM) and caffeine (20 mM) together with 3-MA (5 mM) was detected by flow cytometry. Bars represent the means ± SD of triplicate experiments. *P<0.05. (E) Western blotting and densitometric analysis show the expression of p62, α-SMA and LC3II in LX-2 cells transfected with Atg7-siRNAs or the cells transfected with negative siRNAs after treatment with 0/20 mM caffeine for 48 h. Bars represent the means ±SD of three independent experiments. **P<0.01. (F) Western blotting and densitometric analysis show the expression of p62, α-SMA and LC3II in LX-2 cells treated with 3-MA (5 mM), caffeine (20 mM), caffeine (20 mM) together with 3-MA (5 mM) and none. Bars represent the means ± SD of three independent experiments. **P<0.01.

Discussion

Recently, many studies have demonstrated that the long-term consumption of caffeine is associated with lower risks for chronic liver diseases, such as nonalcoholic fatty disease and liver fibrosis (25–27). Moreover, other studies have reported that caffeine attenuates liver fibrosis by directly inducing apoptosis of HSCs (18). However, a better understanding of the pathways implicated in this process remains to be characterized. In the present study, our findings established autophagy mediated by ER stress as a novel pathway implicated in caffeine-induced HSC apoptosis.

To the best of our knowledge, liver fibrosis is triggered by hepatocyte apoptosis, while induction of activated HSC apoptosis can reverse the progression of liver fibrosis (28–30). Importantly, our study showed that caffeine markedly reduced the cell viability of activated HSCs and downregulated the expression of α-SMA in vitro, suggesting caffeine as a suppressor of HSC activation. Furthermore, in agreement with other studies, we established the role of caffeine as an important driver of stellate cell apoptosis. The results above correspond to the principle that augmentation of HSC apoptosis is a potential approach through which to promote the resolution of liver fibrosis (31), therefore, epitomizing an anti-fibrotic function of caffeine.

Morphological analysis found that caffeine induced an increase in vacuoles which were recognized as enlarged ERs in HSCs. One reasonable explanation for these enlarged vacuoles is induction of the UPR, a self-protective process initially occurring after ER stress (22,24). Moreover, treatment with caffeine caused upregulated expression of GRP78/BiP. GRP78/BiP is an ER chaperone that normally binds with three transmembrane proteins, IRE1-α, activating transcription factor (ATF)-6α and RNA-activated protein kinase-like ER kinase (PERK) (32,33). Upon ER stress, GRP78/BiP dissociates with the three transmembrane proteins described above, causing the activation of PERK and IRE1-α by trans-autophosphorylation as well as ATF6α via proteolytic processing (34,35). The IRE1-α/CHOP pathway is the most conserved branch of the UPR among the three (7). Notably, our study showed that the accumulation of IRE1-α and CHOP in HSCs was rapidly increased after caffeine treatment. Collectively, these events strongly demonstrated that the ER stress-dependent UPR signaling pathway is triggered in caffeine-treated HSCs.

Although the UPR is an adaptive process that compensates for the damage caused by ER stress, prolonged and massive ER stress that cannot be alleviated by UPR will induce cell apoptosis (12,36). In the present study, we revealed that caffeine inhibited the cell viability of HSCs by inducing apoptosis; meanwhile, ER stress was stimulated after caffeine treatment in HSCs. These results can be explained by the principle that treatment with caffeine induces prolonged and sustained ER stress in HSCs and the ER stress-related damage cannot be eliminated by UPR, eventually, resulting in apoptotic death (22,37). Additionally, we also found that the level of cytosolic calcium was increased after caffeine incubation in HSCs. To date, perturbations in ER calcium have been demonstrated to have a close associate with apoptosis effectors (38). In certain cell lines, ER stress inducers promote calcium to be released from the ER accompanied by some related apoptosis effectors released from mitochondria (33,39). Although the exact functional role of calcium mobilization in caffeine-mediated ER stress remains unclear, the possibility that the calcium released from the ER triggers ER stress and apoptosis seems reasonable.

Recent research of the mechanisms by which caffeine ameliorates the severity of NAFLD has revealed that caffeine markedly decreased intracellular lipids via upregulating autophagic flux in hepatocytes (27). Analogously, in the present research, we demonstrated that the biochemical hallmarks of autophagic flux in HSCs were induced, for example, LC3II accumulation and GFP-RFP-LC3 redistribution in early and late autophagosomes. Furthermore, many double-membrane vacuolar structures, the morphological pattern of autophagosomes, were found in caffeine-treated HSCs, while few were observed in the controls. Notably, we also showed that GFP-RFP-LC3 redistribution in early and late autophagosomes and LC3II accumulation were rapidly decreased after knockdown of IRE1-α. In addition, accumulation of p62 was significantly compromised in the IRE1-α siRNA-transfected HSCs. These data not only demonstrated that caffeine induced the activation of autophagy in HSCs, but also established the role of ER stress as an important driver of autophagic flux induced by caffeine in HSCs.

The primary role of autophagy in cells is complicated, sometimes paradoxical. Whether autophagy protects cells from death or promotes cell death depends on the cellular context, the duration and strength of stimuli (40,41). Previously, one study revealed that caffeine induced apoptosis in SH-SY5Y, PC12D and HeLa cells by enhancement of autophagy (19). Similarly, the data presented here showed that both of the genetic and chemical autophagy inhibitors, Atg7-siRNAs and 3-MA, alleviated caffeine-induced apoptosis. Coincident with the alleviation of cell death by autophagy, the cell viability was increased in the Atg7-knockdown and 3-MA-pretreated HSCs after caffeine treatment. These data strongly demonstrate that autophagy induced by caffeine promoted apoptotic cell death rather than cell survival in the HSCs. To date, many studies have reported that autophagy removes superabundant proteins when the accumulation of unfolded or misfolded proteins surpasses the ability of the degradation system mediated by the proteasome (42,43). The protective function of autophagy was contradictory with our results. One plausible explanation is that the outcome of ER stress-mediated autophagy depends on the type of stimulants and the cellular context. Notably, our findings rightly identify with the anti-fibrosis mechanism of caffeine. In brief, caffeine suppresses activation of HSCs by induction of autophagy via the IRE1-α pathway. And once the activated HSCs are eliminated, the progression of liver fibrosis can be attenuated and reversed. Viewed this way, our finding is consistent with previous studies on the induction of apoptotic cell death by caffeine and provides novel insight into the mechanism involved in the anti-fibrotic function of caffeine.

Additionally, it is worth noting that in our study the concentrations of caffeine that induced apoptosis of HSCs were in a high range. The results disclosed that only a high concentration of caffeine attenuated liver fibrosis, which is in accordance with previous research that individuals who consume a large amount of caffeine every day have the lowest risk of liver disease (44).

In conclusion, our data highlight the importance of autophagy mediated by ER stress in caffeine-treated HSCs as a main driver of apoptosis, extending the mechanisms of the attenuation of liver fibrosis by caffeine. We speculate that moderate to high caffeine intake can be useful in the treatment of liver fibrosis.

Acknowledgments

This study was supported by the National Natural Science Foundation of China (no. 81070358), (http://www.nsfc.gov.cn) to JQY.

References