Titrated extract of Centella asiatica provides a UVB protective effect by altering microRNA expression profiles in human dermal fibroblasts

  • Authors:
    • In-Sook An
    • Sungkwan An
    • Sang-Mo Kang
    • Tae-Boo Choe
    • Sung Nae Lee
    • Hyun Hee Jang
    • Seunghee Bae
  • View Affiliations

  • Published online on: September 4, 2012     https://doi.org/10.3892/ijmm.2012.1117
  • Pages: 1194-1202
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

The titrated extract of Centella asiatica (TECA) is a reconstituted mixture comprising of asiatic acid, madecassic acid, asiaticoside and madecassoside, and is used as a therapeutic agent in wound healing and also as an anti-microbial, anticancer and anti-aging agent. Although these properties and the associated cell signaling pathways have been elucidated, the cellular mechanism of anti-photoaging upon ultraviolet (UV) exposure in normal human dermal fibroblasts (NHDFs) remains unknown. In this study, we investigated the photoprotective role of TECA via microRNA (miRNA) expression profiling analysis. Low dose of TECA did not exhibit toxicity and showed a protective effect against UVB irradiation in NDHFs. miRNA microarray experiments revealed that specific miRNAs were altered by TECA stimulation in UVB-irradiated NHDFs. Functional bioinformatic analysis showed that the putative target genes of the altered miRNAs were associated with the positive regulation of cell proliferation, anti-apoptosis, small GTPase- and Ras-mediated signal transduction and activation of MAPKK. Therefore, these results suggest that TECA may serve as a potential natural chemoprotective agent against UVB-mediated damage in NHDFs through changes in the expression of specific miRNAs.

Introduction

Centella asiatica (L.) Urb. (Apiaceae), also known as pegaga and gotu kola, has been used as a medicine in tropical regions. This plant contains pharmacologically active compounds including various pentacyclic triterpene derivatives, such as centelloids (13). The Centella asiatica (C. asiatica) extract contains four major triterpenoids, namely asiatic acid, madecassic acid, asiaticoside and madecassoside, and this mixture is commercially marketed as a titrated extract of Centella asiatica (TECA). The C. asiatica extract is used as an anti-microbial, anti-oxidative and anticancer agent, as well as a therapeutic agent in the various processes of wound healing, such as coagulation, inflammation, cell migration and proliferation as well as scar formation and remodeling (49). Following reports of the wound-healing properties of C. asiatica in various studies, it has been used in skin cell development and therapy. The major components of the skin are collagen types I and III, which play a key role in wound healing and are directly related to skin aging (10). Indeed, the C. asiatica extract can promote an increase in both fibronectin and collagen synthesis by 20–35% in skin fibroblasts (7,1012). Furthermore, the C. asiatica extract plays an important role in the process of anti-oxidation by reducing the activity of reactive oxygen species (ROS), and thus prevents hydrogen peroxide (H2O2)-induced senescence in normal human dermal fibroblasts (NHDFs) (1315).

Similar to ROS, ultraviolet (UV) radiation targets the skin and continues to induce skin aging and cancer. Among the three types of UV light (UVA, UVB and UVC), the UVB light only penetrates into the epidermis and, therefore, UVB radiation at a high dose can elicit severe skin damage. UV radiation stimulates several biological processes in the skin, which include adaptive, inflammatory and immunological reactions. Following UV irradiation, adaptive responses are induced in the form of stratum corneum thickening, pigmentation and epidermal hyperplasia (16,17). UV exposure mediates an inflammatory response, which is manifested as erythema and redness, and is followed by the induction of apoptosis in keratinocytes (16,18). Therefore, chronic UV irradiation results in skin photoaging, which is characterized by irregular pigmentation, dryness of the skin, wrinkling and elastosis (18,19). Also, UV radiation activates multiple signaling cascades, such as p38 mitogen-activated protein kinase (MAPK), Jun N-terminal kinase (JNK), extracellular signal-regulated kinase 1/2 (ERK1/2) and the NFκB pathways in skin cells (19).

A preliminary study suggested that the C. asiatica extract can serve as a potential natural protectant against UVB damage in NHDFs (20). However, the cellular mechanisms underlying the photoprotective effect of TECA against UV irradiation have yet to be studied. This is the first report to elucidate the cellular mechanisms of TECA-mediated photoprotection against UV through the investigation of microRNA (miRNA) expression profiling changes in NHDFs.

Materials and methods

Cell culture

The NHDF cells were purchased from Lonza (Basel, Switzerland) and grown in DMEM media (Gibco-Invitrogen Life Technologies, Carlsbad, CA, USA) containing 10% fetal bovine serum (FBS; Sigma-Aldrich, St. Louis, MO, USA) with penicillin/streptomycin in a humidified chamber at 37°C under 5% CO2. Cells (4×103) were seeded into 96-well plates a day before UVB exposure and treatment with the C. asiatica extract. For RNA purification, 7×105 cells were seeded into 60-mm dishes.

UVB irradiation and TECA treatment

Prior to UVB irradiation, cells were pre-treated with control dimethylsulfoxide (DMSO; Sigma-Aldrich) or TECA (Bayer HealthCare, Berlin, Germany) for 4 h. Cells were washed with PBS twice and then exposed to 100 mJ/cm2 UVB without covering the 96-well plates or 60-mm dishes, so that the UVB light was not filtered. Following irradiation, the cells were cultured for 24 h in DMEM media containing 10% FBS with DMSO or TECA.

RNA purification and qualification

NHDF cells exposed to UVB with or without TECA were collected, and then total-RNA, including mRNAs, small RNAs and miRNAs, was extracted and purified from each cell pellet using TRIzol reagent (Invitrogen Life Technologies) according to the manufacturer’s protocol. The integrity of each RNA sample was verified using an Agilent 2100 Bioanalyzer® (Agilent Technologies, Santa Clara, CA, USA). The quality and concentration of each RNA sample were determined using MaestroNano®, a micro-volume spectrophotometer (Maestrogen, Las Vegas, NV, USA). RNA quality parameters for the miRNA microarray analysis were: A260/280 and A260/A230 values >1.8 and an RNA integrity number (RIN) >8.0.

Microarray analysis of miRNA expression

The miRNA profiling analysis was performed using the SurePrint G3 Human v16 miRNA 8×60K (Agilent Technologies) that contained probes for 1,205 and 144 human viral miRNAs. The qualified RNA samples (100 ng) were first dephosphorylated using calf intestinal alkaline phosphatase (CIP) at 37°C for 30 min. Next, DMSO was added to each sample, and the samples were incubated at 100°C for 10 min and immediately transferred to an ice-water bath. The dephosphorylated RNA samples were labeled with cyanine 3-pCp using T4 RNA ligase by incubation at 16°C for 2 h. After the labeling reaction, the samples were completely dried using a vacuum concentrator at 55°C for 4 h. The dried samples were treated with GE Blocking Agent (Agilent Technologies) and hybridized to the probes on the microarray at 55°C with a constant rotation at 20 rpm in the Agilent Microarray Hybridization Chamber (Agilent Technologies) for 20 h. The microarray slide was washed and scanned using the Agilent scanner to obtain the microarray image. The numerical data for the miRNA profiles were extracted from the image using the Feature Extraction program (Agilent Technologies). These data were analyzed with the aid of the GeneSpring GX software version 7.3 (Agilent Technologies).

Classification of miRNAs

Among the total miRNAs probed on the microarray, 866 human miRNAs were selected for further analysis. The miRNAs whose flags were present in at least one sample were filtered and applied to the fold-change analysis. The fold-change analysis was conducted to select miRNAs whose expression changed by a factor of 1.2-fold or more between the following two groups: UVB-exposed and DMSO-treated NHDF control cells and UVB-exposed and 50 μg/ml TECA-treated NHDFs.

Bioinformatic analysis of miRNAs

Changes in miRNA expression of 1.2-fold and more between the two groups were selected, and their putative cellular target genes were determined using MicroCosm Target version 5 (www.ebi.ac.uk/enright-srv/microcosm/thdoc/targets/v5/). Using a gene ontology (GO) analysis tool, AmiGO (amigo.geneontology.org/cgi-bin/amigo/browse.cgi), the target genes were categorized into the following four groups: aging, apoptosis, cell proliferation and skin development. Further GO analysis for miRNA target genes that were also identified by cross-linking and Argonaute (Ago) immunoprecipitation coupled with high-throughput sequencing (CLIP-Seq) data was performed using starBase web-based bioinformatics tools (starBase.sysu.edu.cn) (21).

Results

TECA treatment inhibits the decrease in cell viability caused by UVB irradiation in NHDFs

We first screened for the dose range of TECA that is cytotoxic to NHDF cells. NHDF cells were treated with a series of four concentrations of TECA (25, 50, 100 and 200 μg/ml) for 24 h, and the WST-1-based cellular toxicity assay was used to determine the level of cell viability. As shown in Fig. 1A, low doses (up to 50 μg/ml) of TECA increased cell viability slightly; however, relatively high doses (100 and 200 μg/ml) of TECA decreased cell viability. In particular, although 100 μg/ml of TECA exhibited a low toxicity on NHDF cells, 200 μg/ml of TECA largely decreased cell viability. Therefore, TECA concentrations of 25, 50 and 100 μg/ml were chosen for further experiments. Next, we investigated the protective effect of TECA treatment against UVB-mediated damage of NHDFs. A day before UVB irradiation, NHDF cells were seeded and incubated in 96-well plates. The cells were then pre-treated with TECA, at the indicated concentration, for 4 h. The cells were then washed with PBS and exposed to 100 mJ/cm2 of UVB without putting any protective covers on the microplates. Following UVB irradiation, the cells were incubated with TECA, at the indicated concentration, for 24 h. Cell viability was determined using the WST-1 assay, which revealed that treatment with TECA, in the range of 25 and 50 μg/ml, markedly restored the UVB-mediated loss of cell viability in NHDFs to the normal status in a dose-dependent manner (Fig. 2B). Treatment with 100 μg/ml of TECA did not increase cell viability more than the 50 μg/ml of TECA, which can be attributed to the cytotoxic effect of 100 μg/ml TECA on NHDF cells. Therefore, TECA displayed a protective effect against UVB-mediated loss of cell survival observed in NHDF cells.

The protective role of TECA in UVB-induced NHDF damage is reflected as miRNA expression profiling changes

Since miRNA is an important small non-coding RNA molecule that regulates development, differentiation, proliferation and apoptosis (2225), we determined the protective effect of TECA against UVB-induced cell damage through a miRNA expression profiling analysis. Total-RNAs were purified from UVB-irradiated NHDF control cells and from 50 μg/ml of TECA-stimulated and UVB-irradiated NHDF cells, after which miRNA microarrays were performed using the Agilent SurePrint G3 Human v16 miRNA 8×60K, as described in Materials and methods. A total of 1,205 human miRNAs, including 144 human viral miRNAs, were selected to analyze the miRNA profiles. The human miRNAs whose flags were present in at least one sample were continuously filtered to obtain more defined data using the Agilent GeneSpring software. As shown in Fig. 2A, a total of 40 human miRNAs were differentially expressed following stimulation with TECA in UVB-irradiated NHDF cells compared to cells exposed to UVB alone. Upregulated miRNAs are shown in the left panel and downregulated miRNAs are shown in the right panel of Fig. 2A. The color bar displaying altered fluorescence intensity corresponds to miRNAs that were either upregulated (red colors) or downregulated (blue color) by TECA stimulation. The full list of the 40 miRNAs whose expression was altered by TECA is listed in Table I. The asterisk following the name indicates non-functional miRNA or passenger strand that is released from the miRNA duplex (26). Recent studies suggest that miRNA* may offer potential opportunities for contributing to the regulation network (27). As shown in Fig. 2B, 19 miRNAs were upregulated and 21 miRNAs were downregulated under the experimental conditions. Although the majority of miRNAs did not show significant changes in expression, treatment with TECA did affect certain miRNA expression levels in NHDFs. These differentially expressed miRNAs may be involved in specific mechanisms of TECA-mediated cellular responses during the inhibition of UVB-induced cell damage in NHDFs.

Table I.

miRNAs altered by TECA in UVB-exposed NHDF cells.

Table I.

miRNAs altered by TECA in UVB-exposed NHDF cells.

Upregulated
Downregulated
miR nameFCChromosomemiR nameFCChromosome
hsa-miR-1011.24Chr1ebv-miR-BART121.47-
hsa-miR-12461.21Chr2 ebv-miR-BHRF1-11.24-
hsa-miR-12901.20Chr1hsa-miR-12711.39Chr5
hsa-miR-145*1.27Chr5hsa-miR-181d1.34Chr19
hsa-miR-14712.08Chr2hsa-miR-1971.20Chr1
hsa-miR-19731.25Chr4hsa-miR-2121.67Chr17
hsa-miR-211.21Chr17hsa-miR-31411.21Chr5
hsa-miR-301a1.21Chr17hsa-miR-423-3p2.01Chr17
hsa-miR-322.65Chr9hsa-miR-42712.38Chr3
hsa-miR-36591.28Chr1hsa-miR-4321.35Chr14
hsa-miR-42861.24Chr8hsa-miR-43271.22Chr21
hsa-miR-43131.27Chr15hsa-miR-455-5p1.35Chr9
hsa-miR-450a1.29ChrXhsa-miR-483-5p1.71Chr11
hsa-miR-4521.23ChrX hsa-miR-513a-5p1.81ChrX
hsa-miR-4541.29Chr17hsa-miR-574-3p1.20Chr4
hsa-miR-542-3p1.25ChrXhsa-miR-654-5p1.79Chr14
hsa-miR-6361.83Chr17hsa-miR-7581.25Chr14
hsa-miR-71.20Chr9hsa-miR-7651.75Chr1
hsv1-miR-H151.39-hsa-miR-8871.24Chgr5
hsv1-miR-H1*2.35-
kshv-miR-K12-10b1.51-

{ label (or @symbol) needed for fn[@id='tfn1-ijmm-30-05-1194'] } The list was selected to show miRNAs representing >1.2-fold change in expression after flag sorting.

* Non-functional miRNA or passenger strand that is released from the miRNA duplex.

Bioinformatic analysis of TECA-specific miRNAs and their putative target genes in UVB-induced damage in NHDF cells

miRNA expression profiling suggested a protective role of TECA against UVB-induced damage that may be dependent on the regulation of TECA-specific miRNA expression. These results further highlight the significance of the altered miRNA expression in light of the photoprotective property of TECA in UVB-induced damage of NHDFs. Since the cellular functions of miRNAs are mediated by controlling their target gene expression (28), we analyzed the cellular meaning of the TECA-dependent miRNA expression changes by sorting them according to three independent criteria (Fig. 3): i) the putative target genes of the differentially expressed miRNAs; ii) the cellular functions of the target genes; and iii) the target genes involved in TECA-mediated protective properties. First, using the miRBase Target Database tool, Microcosm, we identified approximately 2,758 potential targets for all miRNA, excluding human viral miRNAs. A total of 1,479 genes were identified as potential target genes for the upregulated miRNAs and 1,279 genes were identified as potential target genes for the downregulated miRNAs. Next, we identified the potential target genes involved in TECA-mediated protective properties against UVB damage, such as aging, apoptosis, cell proliferation and skin development. Using a GO web-based tool, AmiGO, we arranged the gene information in four classes: a total of 388 genes in aging, 3,824 genes in apoptosis, 3,148 genes in cell proliferation and 399 genes in skin development were identified (data not shown). We then compared these genes with the putative target genes (1,479 genes corresponding to upregulated miRNAs and 1,279 genes corresponding to downregulated miRNAs), and the overlapping genes in the two groups are listed in Tables II and III. Some of the miRNAs were potentially targeted by more than one miRNA, since a single miRNA may target a number of mRNAs, and, conversely, a single mRNA target may be modulated by several miRNAs (29).

Table II.

Predicted targets of miRNAs exhibiting an upregulation in response to TECA in UVB-exposed NHDF cells.

Table II.

Predicted targets of miRNAs exhibiting an upregulation in response to TECA in UVB-exposed NHDF cells.

Function of target genes
miRNA nameAgingApoptosisCell proliferationSkin development
hsa-miR-21TBX2, PTEN, LRP2, MSH2, PDCD4ARHGEF12, BCL7, CCR7, FASLG, KRIT1, LRP2, MAP3K1, NTF3, PDCD4, PTEN, RHOB, SKI, TIAM1, UBE2D3, SATB1, ACVR1CDDX11, FGF1, GATAD2B, IL12A, JAG1, KRIT1, LRP6, PBRM1, PELI1, PITX2, SKI, SPRY1, TBX2, TGFB1-
hsa-miR-32HCN2, NOX4, PER2, TWIST1, ADRB1ACTC1, ARHGEF17, BCL2L11, BTG2, GATA6, HAND2, HIPK3, ITGA6, ITGAV, KIF1B, LYST, MAP2K4, RAD21, SGK3, TRAF3, TRIO, TWIST1, UBE2Z, ADRB1, CDK5R1, GP1, JMY, NR4A3, SNF1LKBTG2, CDC27, CDCA7L, CDKN1C, FOSL2, GATA2, MS4A2, NKX2-3, NOX4, PAX3, PCAF, PTPRK, TACC2, TGIF1, TOB2, RAP1B, SOX11, BMPR2, TSC1, ZEB2BCL11B, COL1A2
hsa-miR-101FOS, TIAM2, ADRB1, LRP2ARHGEF3, DUSP1, JAK2, MSX1, PHLDA1, PROK2, RAC1, SCN2A, SGK1, TGFBR1, USP47, UBE2D3, ADRB1, CDKR1, GPI, DDIT4, MITF, PRKCE, TCF7L2, ROBO2, GJA1, NEUROD1, PRKAA1,CDH5, CEBPA, DLG5, ELF5, EMP1, GNB1, HRB, JAK2, NDFIP1, PDS5B, PTGS2, RXRB, SOX9, TAL1, TGFA, TGFBR1, UBE2A, RAP1B, SOX11, FZD6, LRP2, PTCH1-
hsa-miR-7-AMBRA1, COL2A1, CTSB, FNDC4, GLI3, HELLS, OGT, PRMT2, PSME3, RAF1, RB1, SNCA, SORT1, VDAC1, SATB1, DDIT4, JMY, NR4A3, PHF17CONT8, CUL5, EGFR, IRS1, PAX6, UHRF1, SATB1, IRS2COL2A1
hsa-miR-301aTP63, WNT1, LRRK2, LRP2DLC1, TP63, WNT1, TP63, APPL1, FXR1, SOX4, ROBO2DLEC1, ESR1, BMPR2, TSC1, USP28, ZEB2, EREG, FOSL1, HOXA3, IMPDH1, INSIG1, IRF1, JARID2, LRRK2, NR3C2, PPARG, TBC1D8, WNT28, FZD6, LRP2TP63, WNT10A, EDA
hsa-miR-452IGF2BP2, TIMP3ERBB4, VEGFA, IGF1BMI1, CDKN1B, EPS8, ERBB4, IGF2BP2, LAMC1, MAB21L2, MAPRE1, MXD1, NPPC, PURA, RPA1, TIMP2, VEGFA, PTPRJ, IRS2-
hsa-miR-636SOCS3ARF6, GRIK2, ITSN1, PCGF2, PKN2, PROC, RPS6KA2, RTN3, SENP1, SFRP2, SOCS3, MITF, PRKCE, TCF7L2, SNF1LK, TGFBR2, ZAKBCAT1, EMX2, LIFR, SSR1, TRAF5, MITF, TOB1-
hsa-miR-454LRRK2, LRP2NELL1, APPL1, FXR1, SOX4, ROBO2, SIX4, ARHGEF4, BTG1, PAK6, POU4F1, PRKAA2, RASA1, RNF216, RNF41, RNUX3, SLTM, SOS2, SPHK2, TP53INP1, TRIM2, GJA1, NEUROD1, PRKAA1, SYNGAP1, IGF1, ZAKNRP1, TNF, BMPR2, TSC1, USP28, ZEB2, BTG1, EREG, FOSL1, HOXA3, IMPDH1, INSIG1, IRF1, JARID2, LRRK2, NR3C2, PPARG, RUNX3, TBC1D8, WNT2B, FZD6, LRP2EDA

Table III.

Predicted targets of miRNAs exhibiting a downregulation in response to TECA in UVB-exposed NHDF cells.

Table III.

Predicted targets of miRNAs exhibiting a downregulation in response to TECA in UVB-exposed NHDF cells.

Function of target genes
miRNA nameAgingApoptosisCell proliferationSkin development
hsa-miR-197-CECR2, CTNNA1, CYLD, TNFRSF21, RASA1, HIPK2, GP1FZD3, IGFBP3, TAL1, FBXW7, HIPK2, PDGFRA-
hsa-miR-212CTGFARHGEF11, CTGF, DYRK2, EP300, FOXA1, FOXO3, GDF5, ISL1, KCNMA1, MAPK3, MAPT, RASA1, SGK3, RASA1CTGF, EGR1, HHIP, ISL1, RB1, SALL1, SPRY1, ZEB2, HBEGF, SOX11-
hsa-miR-432DLD, MNTADAR, CHAC1, DAB2IP, HOXA5, IL7, MNT, PAX8, PLK3, SORT1, HIPK2CCDC88A, E2F3, IL7, MNT, FBXW7, HIPK2-
hsa-miR-181dADRBK1, PRKCD, PAI, SIRT1, TIMP3ANKRD13C, ATM, BAG4, BCL2L11, BIRC6, CARD11, CBX4, DEPDC6, GATA6, HEY2, HSP90B1, IL1A, INSL3, ITSN1, NOCTCH, PAWR, PDCD6IP, PHLDA1, PRKCD, RAD21, RNF34, RPS6KA3, SIRT1, TGFBR1, TNF, TNFAIP1, UBE2B, TRIM2, USP47, CCNG1ATM, BIRC6, CARD11, CDON, GATA6, HEY2, IGF2BP2, IL1A, ING5, INSL3, IRS2, LRRC32, MCC, NR6A1, PAWR, PDAP1, PLAU, PRDM4, PROX1, RBBP7, SERPINE1, SPRK2, TNF, S1PR1, KRAS, TNS3-
hsa-miR-513a-5pCDK6, CHEK2, GRB2, HMGCR, SERP1BNIP3L, CHEK2, ECE1, EYA1, MAPK7, NOD2, PHLDB3, PPARGC1A, RAG1, XIAP, TRIM2, USP47ASH2L, ATF3, CDK6, DDX11, EHF, EPS8, EYA1, MAGI2, NOD2, PCAF, PDS5B, PURA, SMAD2, TBX19, VSX2, S1PR1, KRAS-
hsa-miR-455-5pLRP2, SOCS3ETS1, FZD5, GABRB2, KPNA1, SOCS3, TJP1, GP1CDC2L5, FZD5, IRF2, KDR, LRP2, NCK2, PTPRJ, PDGFRA, SOX11-
hsa-miR-574-3p-CUL2, RXRACUL2, RXRA-
hsa-miR-654-5pBBC3, DBHARAF, BBC3, WNT11, KPNB1DBH, EFNB1, ELLN, TIMP2, WNT11, IRS1, MTSS1-
hsa-miR-758JUNBCL11B, BMP7, RABEP1BCL11B, BMP7, IGF1, JUN, STAT5BBCL11B
hsa-miR-765LMNA, TIMP3EGLN2, LMNA, OSMCDK2, CSF1R, OSM, TXLNA, GPC3-
hsa-miR-1271CASP2, DDIT3, EDNRA, MAP2K1ALK, AHR, DDIT3, DOCK1, EDNRA, EPHA3, FOXO1, FOXQ1, MBD4, OGT, PLAGL1, PRKCE, PROK2, PSME4, RALB, STK17A, TNFSF13B, TRIB3, TXNDC1, CCNG1, SORT1, KPNB1AHR, CD164, DIXDC1, EDNRA, FRAP1, FRS2, FYN, HOOK3, LAMC1, LIPG, MAB21L2, MAP2K1, MED1, MYO16, NEUROD4, PGGT1B, TACC1, TNFSF13B, TXNDC1, TNS3, HBEGF, KRAS, IRS1, MTSS1, GPC3-

The GO terms in Tables II and III cover a relatively wide range of cellular processes. For example, the GO term of apoptosis encompasses all the genes involved in apoptosis-promoting and apoptosis-inhibiting processes. Therefore, for a more accurate analysis, we rearranged the results shown in Tables II and III into a subset of GO terms, such as positive or negative regulation of the cell cycle, cell division, cell proliferation, cell growth and apoptosis, GTPase-, Ras-, MAPKK-mediated signal transduction and DNA-dependent transcription. As shown in Fig. 4, the target genes of the upregulated miRNAs are involved in promoting processes of cell proliferation; however, the target genes of the downregulated miRNAs are involved in inhibiting processes of apoptosis. Therefore, these findings suggest that TECA-mediated protective effects against UVB-induced damage in NHDFs is related to the changes in expression of specific miRNAs involved in cell proliferation and apoptosis.

Discussion

The present study demonstrated that TECA exhibits a protective effect against UVB-mediated damage in NHDF cells via regulation of miRNA expression. The cytotoxicity and viability assay revealed that a low dose of TECA (25 and 50 μg/ml) is not toxic to NHDF cells, and UVB-mediated loss of cell viability is recovered by stimulation with low doses of TECA. Also, TECA stimulation of NHDF cells changes their miRNA expression profiles, and the differentially expressed miRNAs may have potential anti-apoptotic properties, as revealed by a bioinformatic analysis of their putative target genes and GO analysis of the target genes. Therefore, TECA-mediated changes in miRNA expression may regulate the anti-proliferative effect of UVB irradiation on NHDF cells.

The bioinformatic analysis shown in Fig. 4 may represent the paradoxical roles of TECA in NHDF cell proliferation, since some of the target genes of the upregulated miRNAs were functionally associated with positive regulation of the cell cycle and cell division and with negative regulation of cell growth, thus suggesting that the TECA-mediated upregulation of miRNAs can inhibit cell proliferation. However, these results may be due to the residual cytotoxicity of UVB irradiation in the system used. The fact that treatment with 50 μg/ml TECA did not completely restore the UVB-induced loss of cell viability to the normal status indicates that the anti-proliferative effect of UVB remained, although at a low level, in the experiments shown in Fig. 1B. Of note, the target genes of the miRNAs that were downregulated by TECA were functionally related to anti-apoptosis, negative regulation of cell growth, cell cycle and cell division. These results demonstrate that the downregulated miRNAs can functionally induce pathways of anti-apoptosis and cell proliferation.

Additionally, the target genes of the miRNAs upregulated by TECA were shown to be involved in small GTPase-mediated signal transduction and Ras protein signal transduction. These results indicate that the TECA-mediated anti-apoptotic effect against UVB-mediated NHDF damage can be mediated by inhibiting the small GTPase- and Ras-mediated signaling pathways via upregulation of miRNAs that target the genes involved in the above mechanisms. Rac1 is a small Rho GTPase, which is a key transducer of proliferation and apoptosis in various cells, including NHDFs (3032). Rac1 has primarily been found to induce NHDF proliferation via phosphorylation of the oncogene c-myc (32). However, the pro-apoptotic roles of Rac1 have been reported in previous studies. Rac1 induces apoptosis via JNK in epithelial cells (33). Also, Rac1 stimulates apoptosis through the activation of trivalent chromium in human dermal fibroblasts (34). Furthermore, Rac1 is necessary for the apoptotic process induced by UV irradiation in Rat-2 fibroblasts, suggesting a stimulatory role of Rac1 in apoptosis caused by perturbation of homeostasis (35). Although Ras proteins are known as oncogenes, their pro-apoptotic function has also been reported. UV irradiation induces apoptosis via the activation of Ha-ras and via increasing the phosphorylation of Raf-1 and subsequently activating c-Jun and other AP-1 proteins (36). The R-Ras protein promotes apoptosis that is caused by growth factor deprivation in Rat-1 fibroblasts. Furthermore, in response to stress, the GTP-bound Ras activates MEKKSEK-SARK-c-JUN and induces apoptosis (3739). Therefore, there is a strong possibility that the protective effect of TECA treatment in UVB-irradiated NHDFs can be induced by upregulation of specific miRNAs that inhibit the signal transduction mediated by small GTPases and Ras.

We also showed that the majority of the target genes of the miRNAs upregulated by TECA were involved in the activation of MAPKK activity. MAPKK is a kinase that phosphorylates a MAPK, such as p38, JNK and ERK1/2. UV irradiation of skin cells including keratinocytes, melanocytes and dermal fibroblasts can regulate cell fate via the activation of MAPK-mediated signaling pathways. UV-activated p38 MAPK and JNK in skin cells have been shown to be involved in both cell survival and cell death pathways (4043). However, the ERK1/2 pathway has been implicated in generating anti-apoptotic signals in skin cells (44). Also, UV irradiation did not increase p38 and JNK protein synthesis in the cells, but rather increased the level of phosphorylated p38 activity (45,46). These results indicate that UV irradiation causes phosphorylation-mediated activation of p38 MAPK, JNK and ERK1/2 in skin cells; however, its effects on cells can be observed in both apoptosis and cell survival. Therefore, the reason that the target genes of upregulated miRNAs are highly involved in the activation of MAPKK activity is the possibility that the UVB-protective properties of TECA can be mediated through the regulation of biphasic MAPK responses.

In conclusion, we determined for the first time that TECA treatment of UVB-exposed NHDF cells causes a photoprotective effect via a change in miRNA expression. The cellular mechanisms underlying the photoprotective effect of TECA against UV irradiation remain unknown; however, our study provides substantial evidence of the role of TECA as a chemoprotective agent against UVB-mediated damage in human dermal fibroblasts. Although further studies must be performed to verify the predicted miRNA targets identified in this study, our results suggest that characterization of TECA-specific miRNA changes may provide a useful approach to understanding cellular responses to TECA in UVB-induced NHDF damage.

Acknowledgements

We thank all the members of our research group for their support and advice during this study. This study was supported by the Ministry of Education, Science and Technology (grant 20110028646 to S.A.) of the Republic of Korea.

References

1. 

CD ColdrenP HashimJM AliSK OhAJ SinskeyC RhaGene expression changes in the human fibroblast induced by Centella asiatica triterpenoidsPlanta Med69725732200310.1055/s-2003-4279114531023

2. 

B BrinkhausM LindnerD SchuppanEG HahnChemical, pharmacological and clinical profile of the East Asian medical plant Centella asiaticaPhytomedicine7427448200010.1016/S0944-7113(00)80065-311081995

3. 

JT JamesIA DuberyPentacyclic triterpenoids from the medicinal herb, Centella asiatica (L.) UrbanMolecules1439223941200910.3390/molecules1410392219924039

4. 

G JayashreeG Kurup MuraleedharaS SudarslalVB JacobAnti-oxidant activity of Centella asiatica on lymphoma-bearing miceFitoterapia744314342003

5. 

TD BabuG KuttanJ PadikkalaCytotoxic and anti-tumour properties of certain taxa of Umbelliferae with special reference to Centella asiatica (L.) UrbanJ Ethnopharmacol485357199510.1016/0378-8741(95)01284-K8569247

6. 

FX MaquartF ChastangA SimeonP BirembautP GilleryY WegrowskiTriterpenes from Centella asiatica stimulate extracellular matrix accumulation in rat experimental woundsEur J Dermatol92892961999

7. 

F BonteM DumasC ChaudagneA MeybeckInfluence of asiatic acid, madecassic acid, and asiaticoside on human collagen I synthesisPlanta Med60133135199410.1055/s-2006-9594348202564

8. 

MR CesaroneG BelcaroMT De SanctisEffects of the total triterpenic fraction of Centella asiatica in venous hypertensive microangiopathy: a prospective, placebo-controlled, randomized trialAngiology52Suppl 215182001

9. 

L IncandelaMR CesaroneM CacchioTotal triterpenic fraction of Centella asiatica in chronic venous insufficiency and in high-perfusion microangiopathyAngiology52Suppl 29132001

10. 

F BonteM DumasC ChaudagneA MeybeckComparative activity of asiaticoside and madecassoside on type I and III collagen synthesis by cultured human fibroblastsAnn Pharm Fr5338421995(In French).

11. 

R TenniG ZanaboniMP De AgostiniA RossiC BendottiG CettaEffect of the triterpenoid fraction of Centella asiatica on macromolecules of the connective matrix in human skin fibroblast culturesItal J Biochem3769771988

12. 

FX MaquartG BellonP GilleryY WegrowskiJP BorelStimulation of collagen synthesis in fibroblast cultures by a triterpene extracted from Centella asiaticaConnect Tissue Res24107120199010.3109/030082090091524272354631

13. 

T OttE FritzA PolleA SchutzendubelCharacterisation of antioxidative systems in the ectomycorrhiza-building basidiomycete Paxillus involutus (Bartsch) Fr. and its reaction to cadmiumFEMS Microbiol Ecol42359366200210.1111/j.1574-6941.2002.tb01025.x19709295

14. 

RA MustafaA Abdul HamidS MohamedFA BakarTotal phenolic compounds, flavonoids, and radical scavenging activity of 21 selected tropical plantsJ Food Sci75C28C35201010.1111/j.1750-3841.2009.01401.x20492146

15. 

YJ KimHJ ChaKH NamY YoonH LeeS AnCentella asiatica extracts modulate hydrogen peroxide-induced senescence in human dermal fibroblastsExp Dermatol209981003201110.1111/j.1600-0625.2011.01388.x

16. 

GJ ClydesdaleGW DandieHK MullerUltraviolet light induced injury: immunological and inflammatory effectsImmunol Cell Biol79547568200110.1046/j.1440-1711.2001.01047.x11903614

17. 

A HennessyC OhJ ReesB DiffeyThe photoadaptive response to ultraviolet exposure in human skin using ultraviolet spectrophotometryPhotodermatol Photoimmunol Photomed21229233200510.1111/j.1600-0781.2005.00170.x16149934

18. 

Y MatsumuraHN AnanthaswamyToxic effects of ultraviolet radiation on the skinToxicol Appl Pharmacol195298308200410.1016/j.taap.2003.08.01915020192

19. 

V MuthusamyTJ PivaThe UV response of the skin: a review of the MAPK, NFkappaB and TNFalpha signal transduction pathwaysArch Dermatol Res302517201010.1007/s00403-009-0994-y19756672

20. 

P HashimH SidekMH HelanA SaberyUD PalanisamyM IlhamTriterpene composition and bioactivities of Centella asiaticaMolecules1613101322201110.3390/molecules1602131021278681

21. 

JH YangJH LiP ShaoH ZhouYQ ChenLH QustarBase: a database for exploring microRNA-mRNA interaction maps from Argonaute CLIP-Seq and Degradome-Seq dataNucleic Acids Res39D202D209201110.1093/nar/gkq105621037263

22. 

V AmbrosRC LeeIdentification of microRNAs and other tiny noncoding RNAs by cDNA cloningMethods Mol Biol265131158200415103073

23. 

AM ChengMW ByromJ SheltonLP FordAntisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosisNucleic Acids Res3312901297200510.1093/nar/gki20015741182

24. 

JF ChenEM MandelJM ThomsonThe role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiationNat Genet38228233200610.1038/ng172516380711

25. 

WJ ChoJM ShinJS KimmiR-372 regulates cell cycle and apoptosis of ags human gastric cancer cell line through direct regulation of LATS2Mol Cells28521527200910.1007/s10059-009-0158-019937137

26. 

AS O’TooleS MillerN HainesMC ZinkMJ SerraComprehensive thermodynamic analysis of 3’ double-nucleotide overhangs neighboring Watson-Crick terminal base pairsNucleic Acids Res34333833442006

27. 

L GuoZ LuThe fate of miRNA* strand through evolutionary analysis: implication for degradation as merely carrier strand or potential regulatory molecule?PLoS One5e11387201020613982

28. 

RS PillaiSN BhattacharyyaW FilipowiczRepression of protein synthesis by miRNAs: how many mechanisms?Trends Cell Biol17118126200710.1016/j.tcb.2006.12.00717197185

29. 

B JohnAJ EnrightA AravinT TuschlC SanderDS MarksHuman MicroRNA targetsPLoS Biol2e363200410.1371/journal.pbio.0020363

30. 

AB JaffeA HallRho GTPases: biochemistry and biologyAnnu Rev Cell Dev Biol21247269200510.1146/annurev.cellbio.21.020604.15072116212495

31. 

L WangY ZhengCell type-specific functions of Rho GTPases revealed by gene targeting in miceTrends Cell Biol175864200710.1016/j.tcb.2006.11.00917161947

32. 

E NikolovaV MitevN ZhelevCF DeroanneY PoumayThe small Rho GTPase Rac1 controls normal human dermal fibroblasts proliferation with phosphorylation of the oncoprotein c-mycBiochem Biophys Res Commun359834839200710.1016/j.bbrc.2007.05.21417568564

33. 

S JinRM RayLR JohnsonRac1 mediates intestinal epithelial cell apoptosis via JNKAm J Physiol Gastrointest Liver Physiol291G1137G1147200610.1152/ajpgi.00031.200616798728

34. 

E RudolfM CervinkaTrivalent chromium activates Rac-1 and Src and induces switch in the cell death mode in human dermal fibroblastsToxicol Lett188236242200910.1016/j.toxlet.2009.04.01919406221

35. 

YW EomMH YooCH WooImplication of the small GTPase Rac1 in the apoptosis induced by UV in Rat-2 fibroblastsBiochem Biophys Res Commun285825829200110.1006/bbrc.2001.523311453667

36. 

Y DevaryRA GottliebT SmealM KarinThe mammalian ultraviolet response is triggered by activation of Src tyrosine kinasesCell7110811091199210.1016/S0092-8674(05)80058-31473146

37. 

MT RamirezVP SahXL ZhaoJJ HunterKR ChienJH BrownThe MEKK-JNK pathway is stimulated by alpha1-adrenergic receptor and ras activation and is associated with in vitro and in vivo cardiac hypertrophyJ Biol Chem2721405714061199710.1074/jbc.272.22.140579162028

38. 

I SanchezRT HughesBJ MayerRole of SAPK/ERK kinase-1 in the stress-activated pathway regulating transcription factor c-JunNature372794798199410.1038/372794a07997269

39. 

M YanT DaiJC DeakActivation of stress-activated protein kinase by MEKK1 phosphorylation of its activator SEK1Nature372798800199410.1038/372798a07997270

40. 

N ChouinardK ValerieM RouabhiaJ HuotUVB-mediated activation of p38 mitogen-activated protein kinase enhances resistance of normal human keratinocytes to apoptosis by stabilizing cytoplasmic p53Biochem J365133145200210.1042/BJ2002007212071847

41. 

J HildesheimRT AwwadAJ Fornace Jrp38 Mitogen-activated protein kinase inhibitor protects the epidermis against the acute damaging effects of ultraviolet irradiation by blocking apoptosis and inflammatory responsesJ Invest Dermatol122497502200410.1111/j.1523-1747.2004.22229.x

42. 

YR ChenX WangD TempletonRJ DavisTH TanThe role of c-Jun N-terminal kinase (JNK) in apoptosis induced by ultraviolet C and gamma radiation. Duration of JNK activation may determine cell death and proliferationJ Biol Chem2713192931936199610.1074/jbc.271.50.319298943238

43. 

R WisdomRS JohnsonC Moorec-Jun regulates cell cycle progression and apoptosis by distinct mechanismsEMBO J18188197199910.1093/emboj/18.1.1889878062

44. 

YY HeJL HuangCF ChignellDelayed and sustained activation of extracellular signal-regulated kinase in human keratinocytes by UVA: implications in carcinogenesisJ Biol Chem2795386753874200410.1074/jbc.M40578120015471881

45. 

JW ChoK ParkGR KweonCurcumin inhibits the expression of COX-2 in UVB-irradiated human keratinocytes (HaCaT) by inhibiting activation of AP-1: p38 MAP kinase and JNK as potential upstream targetsExp Mol Med37186192200510.1038/emm.2005.2516000872

46. 

AL KimJM LabasiY ZhuRole of p38 MAPK in UVB-induced inflammatory responses in the skin of SKH-1 hairless miceJ Invest Dermatol12413181325200510.1111/j.0022-202X.2005.23747.x15955110

Related Articles

Journal Cover

November 2012
Volume 30 Issue 5

Print ISSN: 1107-3756
Online ISSN:1791-244X

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
An I, An S, Kang S, Choe T, Lee SN, Jang HH and Bae S: Titrated extract of Centella asiatica provides a UVB protective effect by altering microRNA expression profiles in human dermal fibroblasts. Int J Mol Med 30: 1194-1202, 2012
APA
An, I., An, S., Kang, S., Choe, T., Lee, S.N., Jang, H.H., & Bae, S. (2012). Titrated extract of Centella asiatica provides a UVB protective effect by altering microRNA expression profiles in human dermal fibroblasts. International Journal of Molecular Medicine, 30, 1194-1202. https://doi.org/10.3892/ijmm.2012.1117
MLA
An, I., An, S., Kang, S., Choe, T., Lee, S. N., Jang, H. H., Bae, S."Titrated extract of Centella asiatica provides a UVB protective effect by altering microRNA expression profiles in human dermal fibroblasts". International Journal of Molecular Medicine 30.5 (2012): 1194-1202.
Chicago
An, I., An, S., Kang, S., Choe, T., Lee, S. N., Jang, H. H., Bae, S."Titrated extract of Centella asiatica provides a UVB protective effect by altering microRNA expression profiles in human dermal fibroblasts". International Journal of Molecular Medicine 30, no. 5 (2012): 1194-1202. https://doi.org/10.3892/ijmm.2012.1117