Bangladesh Journal of Pharmacology Research Article Anti-inflammatory effect of gallic acid on HaCaT keratinocytes through the inhibition of MAPK-, NF-κB-, and Akt-dependent signaling pathways BJP Introduction Keratinocytes are one of the major cell types in the epi- dermis. In addition to their structural roles in preven- ting pathogens from getting into the body, keratino- cytes play important immune functions by secreting cytokines and chemokines upon stimulation by aller- gens and microbiological agents, resulting in an infla- mmatory response. Gallic acid is a naturally occurring tri-phenolic com- pound found in various plants, with a particularly high abundance in gallnuts, witch hazel, oak bark, tea leaves, areca nut, bearberry, and blackberry. Gallic acid exhi- bits antioxidant and anti-inflammatory properties (Kah- keshani et al., 2019). Because of these properties, its potential application in treating atopic dermatitis, a widely prevalent and chronically relapsing inflamma- tory skin disease, has been studied. Gallic acid has been reported to suppress the expression of intercellular adhesion molecule-1 and the release of chemokines and cytokines in KU812 basophilic cells (Liu et al., 2013). In addition, gallic acid can inhibit the release of the cyto- kine interleukin (IL)-12 and the expression of functional surface markers in monocyte-derived dendritic cells (Chan et al., 2015). Gallic acid also suppressed the release of cytokines and chemokines in an eosinophil- dermal fibroblast co-culture (Tsang et al., 2016). Fur- thermore, in a 4-dinitrochlorobenzene-induced atopic dermatitis-like mouse model, gallic acid alleviated skin inflammation through the immunomodulation of Th17 cells (Hu and Zhou, 2021). Although an anti-inflammatory effect of gallic acid on dermatitis has been proposed, this was previously stu- died in white blood cells, such as basophils, eosino- Abstract The objectives of the present study were to evaluate the antioxidant and anti- inflammatory effects of gallic acid, a naturally occurring triphenolic compound, on HaCaT keratinocytes and study its mechanisms of action. The results showed that gallic acid at concentrations lower than 30 µM was non- toxic to HaCaT cells, reduced the intracellular level of reactive oxygen species, and suppressed the release of chemokines interleukin-8 and monocyte chemoattractant protein-1 in tumor necrosis factor-α- and interferon-γ- stimulated HaCaT keratinocytes. In addition, gallic acid reduced the total protein expression of NF-κB and inhibited the phosphorylation of ERK1/2, p38 MAPK, and Akt in stimulated HaCaT keratinocytes. In conclusion, our study revealed that gallic acid exhibited antioxidant and anti-inflammatory effects on keratinocytes, probably through the inhibition of MAPK-, NF-κB-, and Akt-dependent signaling pathways. Article Info Received: 1 December 2022 Accepted: 6 January 2023 Available Online: 13 January 2023 DOI: 10.3329/bjp.v18i1.62914 Cite this article: Shiu PHT, Zheng C, Rangsinth P, Wang W, Li J, Li R, Leung GPH. Anti- inflammatory effect of gallic acid on HaCaT keratinocytes through the inhibition of MAPK-, NF-kB-, and Akt -dependent signaling pathways. Bangladesh J Pharmacol. 2023; 18: 24- 32. Anti-inflammatory effect of gallic acid on HaCaT keratinocytes through the inhibition of MAPK-, NF-kB-, and Akt-dependent signaling pathways Polly Ho-Ting Shiu1, Chengwen Zheng1, Panthakarn Rangsinth1, Wen Wang1, Jingjing Li2, Renkai Li1 and George Pak-Heng Leung1 1 Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong SAR, China; 2 Department of Rehabilitation Sciences, Faculty of Health and Social Sciences, Hong Kong Polytechnic University, Hong Kong SAR, China. This work is licensed under a Creative Commons Attribution 4.0 License. You are free to copy, distribute and perform the work. You must attribute the work in the manner specified by the author or licensor. A Journal of the Bangladesh Pharmacological Society (BDPS) Bangladesh J Pharmacol 2023; 18: 24-32 Journal homepage: www.banglajol.info; www.bdpsjournal.org Abstracted/indexed in Academic Search Complete, Agroforestry Abstracts, Asia Journals Online, Bangladesh Journals Online, Biological Abstracts, BIOSIS Previews, CAB Abstracts, Current Abstracts, Directory of Open Access Journals, EMBASE/Excerpta Medica, Global Health, Google Scholar, HINARI (WHO), International Pharmaceutical Abstracts, Open J-gate, Science Citation Index Expanded, SCOPUS and Social Sciences Citation Index ISSN: 1991-0088 phils, and monocytes. To our knowledge, the effect of gallic acid on keratinocytes, which comprise 95% of the dermis and are involved in the inflammatory response of the skin, has never been investigated. Therefore, this study aimed to evaluate the antioxidant and anti- inflammatory effects of gallic acid on tumor necrosis factor (TNF)-α/interferon (IFN)γ-stimulated HaCaT keratinocytes. The mechanism of action underlying these effects was also explored. Materials and Methods Chemicals and reagents RPMI 1640 medium, fetal bovine serum, penicillin- streptomycin, 0.25% trypsin, human TNF-α recombi- nant protein, and CM-H2DCFDA were purchased from Invitrogen (USA). RIPA lysis and extraction buffer, Halt™ protease inhibitor cocktail, and bicinchoninic acid protein assay kit were purchased from Thermo Scientific (USA). Gallic acid, thiazolyl blue tetrazolium bromide (MTT), dimethyl sulfoxide, and phenylmethyl- sulfonyl fluoride were purchased from Sigma-Aldrich (USA). The human CXCL8/IL-8 DuoSet, human CCL2/ MCP-1 DuoSet, and human IL-1 beta/IL-1 F2 Duoset Enzyme-Linked Immunosorbent Assay (ELISA) kits and human IFN-γ recombinant protein were purchased from R&D Systems (USA). All antibodies used for western blotting were purchased from Cell Signaling Technology (USA). ECL select western blotting detec- tion reagents were purchased from GE Healthcare Life Sciences (USA). Cell culture and drug treatment HaCaT keratinocytes (Thermo Fisher Scientific) were cultured in RPMI medium supplemented with 8% heat- inactivated fetal bovine serum and 1% penicillin- streptomycin and cultured at 37°C in an incubator with a humidified atmosphere of 5% CO2. HaCaT keratinocytes were treated without (control) and with different concentrations of gallic acid in the presence of 10 ng/mL recombinant human TNF-α and 10 ng/mL IFN-γ for 24 hours. Thereafter, cell viability assay, reactive oxygen species (ROS) measurement, cytokine and chemokine release, and western blotting analysis were carried out as described below. Cell viability assay To study the toxicity of gallic acid in HaCaT keratino- cytes, cell viability was assessed using the MTT assay (Bahuguna et al., 2017 for video). The cells were incubated in 0.4 mg/mL MTT for 4 hours at 37°C. Dimethyl sulfoxide was added to lyse the cells and dissolve the formazan crystals formed in the cells. The absorbance was measured at 560 nm using a microplate reader. ROS measurement The cells were washed with phosphate buffer solution and stained with 2 µM CM-H2DCFDA for 15 min. Unbound dye was removed by washing with PBS. The cells were then detached from the culture plates using 0.25% trypsin. The green fluorescent signal, which is an indicator of ROS, was detected and quantified using a flow cytometer. ELISA The cell suspension was centrifuged at 5,000 x g at 4°C for 10 min to remove cell debris. IL-1β, IL-8, and mono- cyte chemoattractant protein (MCP)-1 in the superna- tants were detected using the human IL-1 beta/IL-1 F2 Duoset ELISA, human CXCL8/IL-8 DuoSet ELISA, and human CCL2/MCP-1 DuoSet ELISA kits, according to the manufacturer’s instructions. Western blotting analysis The total protein from HaCaT keratinocytes was extrac- ted using RIPA lysis buffer containing 1% phenyl- methylsulfonyl fluoride and 1% Halt™ protease inhibi- tor cocktail. The cell lysate was centrifuged at 13,000 rpm for 10 min at 4°C to remove the unbroken cell debris and nuclei. The supernatant was collected, and its protein concentration was measured using the BCA assay according to the manufacturer’s instructions. Protein samples (30 µg) were separated using 10% sodium dodecyl sulfate-polyacrylamide gel for electro- phoresis and then electrotransferred onto phenyl- methylsulfonyl fluoride membranes. The membranes were blocked with 5% non-fat milk for 1 hour at room temperature and then incubated with primary antibody (1:1000 dilution in 5% bovine serum albumin in tris- buffered saline) at 4°C overnight. After washing thrice with tris-buffered saline containing 0.1% tween-20 (TBST), the membrane was incubated with a horse- radish peroxidase-conjugated secondary antibody (1:2500 dilution in 5% bovine serum albumin in tris- buffered saline) for 1 hour at room temperature. The membrane was washed with TBST, and the protein bands were visualized using ECL select western blott- ing detection reagents with a ChemiDoc XRS molecular imager (Bio-Rad Laboratories, USA). Glyceraldehyde-3- phosphate dehydrogenase (GAPDH) protein expression was detected using a monoclonal mouse anti-actin antibody. The intensity of the different bands was normalized to that of the GAPDH bands for semi- quantitative analysis (Lim et al., 2021 for video). Statistical analysis All data are expressed as the mean ± SD of at least three independent experiments. A one-way analysis of vari- ance (ANOVA) followed by Dunnett's multiple compa- risons test was performed using GraphPad Prism 9 software (GraphPad Software Inc., USA) to determine the statistical significance within groups. Statistical significance was set at p<0.05. Bangladesh J Pharmacol 2023; 18: 24-32 25 Results Effect of gallic acid on the viability of HaCaT keratino- cytes The cytotoxic effects of gallic acid were studied by incubating HaCaT keratinocytes with different concen- trations of gallic acid for 24 hours. The results of the MTT assay showed that the viability of HaCaT kerati- nocytes was reduced by 18% at 100 µM but was not affected by lower concentrations (Figure 1). Therefore, gallic acid at concentrations below 30 µM was used in subsequent experiments. Effect of gallic acid on intracellular level of ROS in HaCaT keratinocytes The intracellular ROS levels in HaCaT keratinocytes were detected using the fluorescent probe CM- H2DCFDA. The ROS levels in HaCaT keratinocytes were elevated by 209% upon stimulation with TNF-α/ IFN-γ. The TNF-α/IFN-γ-induced ROS levels were reduced by 17% and 9% by 30 µM and 10 µM gallic acid, respectively (Figure 1). Effects of gallic acid on the release of cytokines and chemokines in HaCaT keratinocytes The effects of gallic acid on the pro-inflammatory cytokine IL-1β and the chemokines IL-8 and MCP-1 were evaluated. TNF-α/IFN-γ increased the levels of IL -1β, IL-8, and MCP-1 released by HaCaT keratinocytes 39.2-, 11.3-, and 85.7-fold, respectively (Figure 2). Gallic acid at 30 µM inhibited TNF–α/IFN-γ-induced IL-8 and MCP-1 release by 29% and 46%, respectively, but did not affect IL-1β release. Lower concentrations of gallic acid did not affect Il-1β, IL-8, or MCP-1 release. A B C Control + - - - - - Gallic acid 1 3 10 30 100 µM A B C Figure 1: Effect of gallic acid on the viability of HaCaT keratinocytes (A) and ROS generation (B,C). HaCaT cells were treated with various concentrations of gallic acid or vehicle (control) for 24 hours. Cell viability was determined using the MTT assay. ROS generation in HaCaT cells was detected by CM-H2DCFDA staining and quantified via flow cytometry. HaCaT cells were treated without (control) and with different concentrations of gallic acid in the presence of 10 ng/mL recombinant human TNF-α and 10 ng/mL IFN-γ (T/I) for 24 hours. Data are presented as a percentage of control group values (mean ± SD of three independent experiments). ap<0.0001 and bp<0.05 indicate a significant difference Figure 2: Effects of gallic acid on cytokine and chemokine release in HaCaT keratinocytes. HaCaT cells were treated without (control) and with different concentrations of gallic acid in the presence of 10 ng/mL recombinant human TNF-α and 10 ng/mL IFN-γ (T/I) for 24 hours. IL-1β, IL-8, and MCP- 1 in the culture media were detected using ELISA. Data are presented as a percentage of control group values (mean ± SD of three to six independent experiments). ap<0.0001, bp<0.001, and cp<0.05 indicate a significant difference 150 100 50 0 CM-H2DCFDA fluorescence intensi- Control Gallic acid T/I Gallic acid 10 µM + T/I Gallic acid 30 µM + T/I 400 300 200 100 0 Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + Control + - - - - Gallic acid - - 3 10 30 µM T/I - + + + + 15 10 5 0 1000 800 600 400 200 0 5000 4000 3000 2000 1000 0 a a a b b a a b b c 26 Bangladesh J Pharmacol 2023; 18: 24-32 Effects of gallic acid on inflammation-related signaling pathways in HaCaT keratinocytes Western blot analysis was performed to study the effects of gallic acid on inflammation-related signaling pathways, including mitogen-activated protein kinase (MAPK), NF-κB, and Akt-dependent pathways. TNF- α/IFN-γ did not affect the expression levels of total MAPK kinase (MEK)1/2 and extracellular signal- regulated kinase (ERK)1/2 but could increase their phosphorylation levels by 4.6- and 3.6-fold, respective- ly. Gallic acid (30 µM) did not affect the total and phosphorylated protein expression of MEK1/2 and ERK1/2 or the TNF-α/IFN-γ-induced phosphorylation of MEK1/2, but it reduced the TNF-α/IFN-γ-induced phosphorylation levels of ERK1/2 by 22% (Figure 3). TNF-α/IFN-γ also did not affect the expression levels of total stress-responsive c-Jun N-terminal kinase (JNK) and p38 MAPK but increased their phosphorylation levels by 1.9- and 11.8-fold, respectively. Gallic acid (30 µM) did not affect the total and phosphorylated JNK Figure 3: Effects of gallic acid on total and phosphorylated protein levels of MEK1/2, ERK1/2, JNK and p38 MAPK in HaCaT keratinocytes. HaCaT cells were treated without (control) and with different concentrations of gallic acid in the presence of 10 ng/ mL recombinant human TNF-a and 10 ng/mL IFN-γ (T/I) for 24 hours. Protein expression levels of MEK1/2, p-MEK1/2, ERK1/2, p-ERK1/2, JNK, p-JNK, p38 MAPK, and p-p38 MAPK in HaCaT cells were determined using western blotting analysis. GAPDH was used as a reference and the amounts of different proteins were normalized to that of GAPDH. Data are presented as a percentage of control group values (mean ± SD of three to six independent experiments). ap<0.0001, bp<0.01, and cp<0.05 indicate a significant difference A B C Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + p-MEK1/2 MEK1/2 p-ERK1/2 ERK1/2 GAPDH Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + D E 150 100 50 0 200 150 100 50 0 800 600 400 200 0 800 600 400 200 0 Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + p-JNK JNK p-p38 P38 GAPDH 150 100 50 0 150 100 50 0 500 400 300 200 100 0 2000 1500 1000 500 0 F G H I J a a c a a c c a a a a c b Bangladesh J Pharmacol 2023; 18: 24-32 27 and p38 MAPK protein levels. At a concentration of 30 µM, gallic acid reduced the TNF-α/IFN-γ-induced phosphorylation levels of p38 MAPK by 20%, but it did not effect the phosphorylation of JNK (Figure 3). TNF-α/IFN-γ increased the expression level of total nuclear factor-kappa B (NF-κB) by 60% but did not affect the expression level of total nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibi- tor alpha (IκBa). TNF-α/IFN-γ increased the phospho- rylation levels of NF-κB and IκBa by 267% and 91%, respectively. Gallic acid (30 µM) alone did not affect the total and phosphorylated protein levels of NF-κB and IκBa and abolished the TNF-α-/IFN-γ-induced expre- ssion of total NF-κB. However, 30 µM gallic acid did not affect the phosphorylation of IκBa or NF-κB (Figure 4). Lastly, TNF-α/IFN-γ did not affect the expression levels of protein kinase B (Akt) and the mammalian target of rapamycin (mTOR) but increased their phos- phorylation levels by 6- and 1.5-fold, respectively. Figure 4: Effects of gallic acid on total and phosphorylated protein levels of IkBa, NF-kB, Akt and mTOR in HaCaT keratinocytes. HaCaT cells were treated without (control) and with different concentrations of gallic acid in the presence of 10 ng/mL recombi- nant human TNF-α and 10 ng/mL IFN-γ (T/I) for 24 hours. Protein expression levels of IκBa, p-IκBa, NFκB, p-NF-κB, Akt, p-Akt, mTOR, and p-mTOR in HaCaT cells were determined using western blotting analysis. GAPDH was used as a reference and the amounts of different proteins were normalized to that of GAPDH. Data are presented as a percentage of control group values (mean ± SD of three to six independent experiments). ap<0.0001 and bp<0.01 indicate a significant difference A p-NF-κB NF-κB p-IκBα IκBα GAPDH Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + B C D E 200 150 100 50 0 150 100 50 0 800 600 400 200 0 250 200 150 100 50 0 Control + - - - - Gallic acid - + - 10 30 µM Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + Control + - - - - Gallic acid - + - 10 30 µM T/I - - + + + p-Akt Akt p-mTOR mTOR GAPDH F G H 150 100 50 0 150 100 50 0 1500 1000 500 0 400 300 200 100 0 I J a a a a a b a a a a a a b b b 28 Bangladesh J Pharmacol 2023; 18: 24-32 Gallic acid (30 µM) alone did not effect total and phos- phorylated protein levels of Akt and mTOR. Gallic acid (30 µM) reduced the TNF-α/IFN-γ-induced phosphory- lation levels of Akt by 34% but did not effect the phos- phorylation of mTOR (Figure 4). Discussion Gallic acid has been reported to suppress inflammatory responses in immune cells, such as monocytes, baso- phils, and eosinophils (Liu et al., 2013; Chan et al., 2015: Tsang et al., 2016). This study was designed to examine whether gallic acid exerts anti-inflammatory effects on keratinocytes. Primary culture of human keratinocytes is sometimes used to study the immunological and inflammatory responses of the skin. However, donor difference, instability between passages, and short culture lifetimes may affect data interpretation. There- fore, HaCaT cells were used in the present study. They are immortalized human keratinocyte lines that can differentiate and are similar to normal keratinocytes in terms of the release of inflammatory mediators in response to TNF-α and INF-γ (Cho et al., 2003; Han et al., 2021). They have been widely used as models to investigate anti-inflammatory pharmacology in skin diseases, including atopic dermatitis. First, the cytotoxicity of gallic acid was examined. The results of the MTT assay showed that 30 µM gallic acid did not affect the viability of HaCaT keratinocytes; however, 100 µM gallic acid was slightly cytotoxic. These values were consistent with those of previous studies in which gallic acid was reported as safe and effective for most cells at lower concentrations and toxic at higher concentrations. For instance, 200 μM gallic acid had no effect on the viability of HepG2 cells (Su et al., 2013), while higher concentration was slightly cytotoxic to B16F10 and RAW 264.7 cells (Cheng et al., Tanaka et al., 2020). Gallic acid concentrations higher than 100 μM were cytotoxic to BV-2 and Nerve-2A cells; however, concentration less than 50 μM was safe to the cells (Kim et al., 2011). Gallic acid also produced signi- ficant cytotoxicity in Caco2, L929, and U937 cells at concentrations above 200 μM (Truzzi et al., 2020). Oxidative stress is a major factor that contributes to inflammatory responses. ROS can activate NF-κB, which in turn regulates the gene expressions of TNF-α, IL-1, IL-6, IL-8, and inducible nitric oxide synthase (Allen and Tresini, 2000; Baeuerle and Henkel, 1994). Moreover, oxidative stress activates protein kinase C (Ricciarelli et al., 1998), which can increase the expre- ssion of TNF-α (Wang and Smart, 1999) and the produc -tion of cytokines (Chabot-Fletcher et al., 1994) in kerati- nocytes. Therefore, antioxidant compounds may attenu- ate skin inflammation (Portugal et al., 2007; Sardana and Sachdeva, 2022). The antioxidant effect of gallic acid is one of the most widely reported bioactivities (Cho et al., 2003; Serrano et al., 1998; Yoshino et al., 2002). The present study showed that gallic acid consis- tently reduced ROS production in TNF-α/IFN-γ-treat- ed HaCaT keratinocytes. Gallic acid possesses compara- ble or even higher antioxidant activity than trolox, ascorbic acid, caffeic acid, sinapic acid, and vitamin E in scavenging DPPH (Badhani et al., 2015; Karamac et al., 2005; Nenadis et al., 2007; Sánchez-Moreno et al., 1998). The para-substituted OH group of gallic acid scavenges radicals through intramolecular hydrogen bonding. The efficient hydrogen donation ability of gallic acid is also due to the presence of an easily ionizable carboxylic group (Al Zahrani et al., 2020). Keratinocytes play a critical role in the initiation and maintenance phases of skin inflammation. Keratino- cytes respond to multiple triggers and release cytokines to stimulate the activation and maturation of myeloid dendritic cells. Once synergistically activated by pro- inflammatory cytokines, keratinocytes can produce chemokines to recruit leukocytes and other inflamma- tory mediators to amplify inflammation (Zhou et al., 2022). Gallic acid can eliminate and regulate inflamma- tory molecules (Tsang et al., 2016; Chao et al., 2020; Fan et al., 2019). It has been reported that gallic acid can suppress the levels of cytokines IL-1 and IL-6, chemo- kines MPC-1 and CCL-7, cyclooxygenase-2, and matrix metalloproteinase-9 in rheumatoid arthritis fibroblast- like synovial cells (Yoon et al., 2013). Gallic acid also decreased IL-4, IL-13, and IL-17 levels in nasal lavage fluid of a mouse model of allergic rhinitis (Fan et al., 2019). Interestingly, oral administration of gallic acid could reduce TNF-α, IL-4, IFN-γ, and IL-17 levels in the lymph nodes of a 4-dinitrochlorobenzene-induced mouse model of skin inflammation (hu and Zhou, 2021). In the same model, gallic acid activated regula- tory T cells to suppress the immune response via the production of IL-10 and TGF-β (Hu and Zhou, 2021). Although the topical effect of gallic acid on skin cells in an in vivo model is not yet known, this systemic effect of gallic acid may shed light on its potential implications in inflammatory skin diseases. The results herein show- ed that gallic acid did not affect the production of cytokine IL-1β but reduced the release of chemokines IL -8 and MCP-1 in TNF-α/IFN-γ-stimulated keratino- cytes. The present findings were different from those in other tissues because gallic acid mainly modulates the action of chemokines but not cytokines (Yoon et al., 2013; Hu and Zhou, 2021). The reason for the lack of an effect of gallic acid on IL-1β release is unknown, but it cannot exclude the possibility that IL-1β release in kera- tinocytes is relatively independent of ROS. TNF-α/IFN-γ triggers the release of cytokines and chemokines in HaCaT cells by activating MAPKs, inclu- ding ERK1/2, JNK, and p38 MAPK (Sung et al., 2012; Takada et al., 2004; Kyriakis and Avruch, 2001). These MAPKs are activated by MEK phosphorylation. For instance, ERK1/2 is activated by MEK1/2. In addition Bangladesh J Pharmacol 2023; 18: 24-32 29 to the MAPK signaling pathway, the NF-κB signaling pathway is also involved in inflammation by regulating the expression of genes, enzymes, and adhesion molecules (Lai et al., 2017). NF-κB is activated by IκBα phosphorylation. It has been reported that gallic acid mitigated the immunoglobulin E-induced systemic or local inflammatory reactions by inhibiting the activation of NF-κB and p38 MAPK-dependent path- ways, resulting in the decreased expression of TNF-α and IL-6 (Dominque et al., 2020). Gallic acid also redu- ced the release of intercellular adhesion molecules, chemokines, and inflammatory factors in KU812 cells via the inhibition of p38 MAPK, JNK, and NF-κB (liu et al., 2013). Similarly, these results showed that gallic acid reduced the total protein expression of NF-κB and inhi- bited the phosphorylation (an indicator of activation) of ERK1/2, p38 MAPK in TNF-α/IFN-γ-stimulated HaCaT keratinocytes. Interestingly, gallic acid also inhibits Akt phosphorylation in HaCaT keratinocytes. There is no direct evidence that the anti-inflammatory effect of gallic acid is due to the inhibition of the Akt/ mTOR-dependent pathway. However, consistent with the present findings, polyphenols extracted from man- goes, which contained mainly gallic acid, reduced the inflammatory response by Akt/mTOR-dependent mechanism, partly through up-regulation of miRNA- 126 expression (Kim et al., 2017). Moreover, the inhibi- tory effect of gallic acid on the Akt/mTOR-depen-dent pathway has been reported in other cell types, such as bone marrow cells, in which the inhibition of the Akt/ mTOR pathway by gallic acid could suppress mito- chondrial respiration and induce apoptosis (Gu et al., 2018). The findings in this study will provide valuable information for the research and development of novel therapeutic agents for inflammatory skin diseases, such as atopic dermatitis. Corticosteroids, commonly used in clinical practice, can cause skin atrophy if applied frequently and for prolonged periods. Gallic acid has few adverse effects. Interestingly, gallic acid could also lower the hydrocortisone concentration required to resolve the inflammatory response (Liu et al., 2013; Chan et al., 2015). Gallic acid not only acts on keratino- cytes but also on other immune cells in the skin. 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