Effect of Pentacyclic Triterpenoids-Rich Callus Extract of Chaenomeles japonica (Thunb.) Lindl. ex Spach on Viability, Morphology, and Proliferation of Normal Human Skin Fibroblasts

The effect of the well-characterized callus extract of Chaenomeles japonica on viability, morphology, and proliferation of normal human skin fibroblasts was investigated. The phytochemical analysis was performed using the ultra-high performance liquid chromatography method. The total phenolic, phenolic acid, and flavonoid contents were determined spectrophotometrically. The antioxidant activity was investigated using the DPPH (1,1-Diphenyl-1-picrylhydrazyl Radical Scavenging), FRAP (Ferric Reducing Antioxidant Power), and CUPRAC (CUPric Reducing Antioxidant Capacity) assays. The callus growth index during passages was high as well as the content of pentacyclic triterpenoids. The microscopic observations of the fibroblast viability, morphology and the evaluation of the proliferation ratio (xCELLigence system) proved that the influence of callus extract on the fibroblasts was dose-dependent. The evaluated level of fibroblasts proliferation rate after 72 h of incubation with callus extract at concentration 12.5 µg L−1 was the highest compared to all the analyzed ligands. Moreover, callus extract administrated for 72 h caused a significant increase in the proliferation rate in comparison with the control group (5.7 ± 0.1 vs. 4.4 ± 0.9; p < 0.01). The preliminary studies carried out may suggest that the callus extract rich in triterpenoids may be a potential source of cosmetic ingredients with a beneficial effect on human skin.

On these selected growing media, the biomass of the studied lines of callus intensively increased, reaching high rates of cell proliferation during the latest passages. The callus growth index depended on the line tested and ranged from 844.98 ± 28.62% to 893.90 ± 21.68% (Table 1, Figure 1). Although the A2 line callus was characterized by the lowest concentration of polyphenols, mainly phenolic acids (the sum of chlorogenic acid, dicaffeoylquinic acid, hexoside quercetin and epicatechin was 0.21 mg g −1 d.w., the total content of phenolic acids was 1.67 ± 0.03 mg CA g −1 ) and a negligible level of flavonoids (the total content of flavonoids was 0.47 ± 0.01 mg QE g −1 ), and thus the lowest antioxidant activity (the CUPric Reducing Antioxidant Capacity assay-CUPRAC: IC0.5 187.70 µg mL −1 , the Ferric Reducing Antioxidant Power assay-FRAP: IC0.5 168.08 µg mL −1 , the1,1-diphenyl- On these selected growing media, the biomass of the studied lines of callus intensively increased, reaching high rates of cell proliferation during the latest passages. The callus growth index depended on the line tested and ranged from 844.98 ± 28.62% to 893.90 ± 21.68% (Table 1, Figure 1). Although the A2 line callus was characterized by the lowest concentration of polyphenols, mainly phenolic acids (the sum of chlorogenic acid, dicaffeoylquinic acid, hexoside quercetin and epicatechin was 0.21 mg g −1 d.w., the total content of phenolic acids was 1.67 ± 0.03 mg CA g −1 ) and a negligible level of flavonoids (the total content of flavonoids was 0.47 ± 0.01 mg QE g −1 ), and thus the lowest antioxidant activity (the CUPric Reducing Antioxidant Capacity assay-CUPRAC: Molecules 2018, 23, 3009 4 of 14 IC 0.5 187.70 µg mL −1 , the Ferric Reducing Antioxidant Power assay-FRAP: IC 0.5 168.08 µg mL −1 , the1,1-diphenyl-1-picrylhydrazyl Radical Scavenging assay-DPPH: IC 50 516.88 µg mL −1 ). It, however, had the highest content of pentacyclic triterpenoids (the sum of ursolic acid, oleanolic acid and betulinic acid −9.81 ± 0.89 mg g −1 d.w.) (Tables 2-5; Figure 2) and on this basis, was selected for further research of biological activities on fibroblasts.          It can be seen that non-stimulated cells and fibroblasts treated with a callus extract at a lower concentration (12.5 µg mL −1 ) were characterized by a correct, elongated shape. The cells contained centrally located large and round nuclei that revealed chromatin with a granular structure. The morphology of the fibroblasts treated with 100 µg mL −1 extract was characterized by an incorrect morphology with narrow projections. Many dead cells were observed among these fibroblasts.
As a result of the microscopic observations of the fibroblast morphology ( Figure 3) and the evaluation of the proliferation ratio ( Figure 4), it can be noticed that the influence of C. japonica callus extract on the fibroblasts was dose-dependent. It can be seen that non-stimulated cells and fibroblasts treated with a callus extract at a lower concentration (12.5 µg mL −1 ) were characterized by a correct, elongated shape. The cells contained centrally located large and round nuclei that revealed chromatin with a granular structure. The morphology of the fibroblasts treated with 100 µg mL −1 extract was characterized by an incorrect morphology with narrow projections. Many dead cells were observed among these fibroblasts.
As a result of the microscopic observations of the fibroblast morphology ( Figure 3) and the evaluation of the proliferation ratio ( Figure 4), it can be noticed that the influence of C. japonica callus extract on the fibroblasts was dose-dependent.
Molecules 2018, 23, x 6 of 14 Figure 3 shows the morphology of the control fibroblasts and those treated with C. japonica extract from the callus A2 line in the selected concentrations and time intervals. It can be seen that non-stimulated cells and fibroblasts treated with a callus extract at a lower concentration (12.5 µg mL −1 ) were characterized by a correct, elongated shape. The cells contained centrally located large and round nuclei that revealed chromatin with a granular structure. The morphology of the fibroblasts treated with 100 µg mL −1 extract was characterized by an incorrect morphology with narrow projections. Many dead cells were observed among these fibroblasts.
As a result of the microscopic observations of the fibroblast morphology ( Figure 3) and the evaluation of the proliferation ratio ( Figure 4), it can be noticed that the influence of C. japonica callus extract on the fibroblasts was dose-dependent. Cell proliferation assays were performed using the xCELLigence system (ACEA Biosciences Inc., San Diego, CA, USA). After seeding CRL-2522 cells into the wells, the mean impedance change (n = 5) was measured. No significant differences in the proliferation rate among all analyzed groups were observed before stimulation (p > 0.05). Impedance was monitored every 15 min. Only four post stimulation points were analyzed: at 12, 24, 48, and 72 h to improve the clarity of the results presentation. The control cells showed a significant cell index increase, which, 12 h after stimulation, attained 1.4 ± 0.4 and increased to 4.4 ±1.2 after 72 h of incubation (p < 0.001).
RTCA DP software (Version 1.2.1, ACEA Biosciences Inc., San Diego, CA, USA) analysis performed after 12, 24, 48, or 72 h incubation showed a significant decrease of the cell index (CI) in case of cells stimulated with callus extract at final concentrations 100 or 50 µg L −1 in comparison to control. However, the rate of CI in CRL-2522 cells stimulated with callus extract of 12.5 µg L −1 was higher in comparison to the control cells in all time intervals (Table 6).
Cell index value was monitored using the xCELLigance system. Results are from five repeats. P-value calculated from one-way analysis of the variance; * p < 0.01 vs. control; ** p < 0.001 vs. control.
The representative graph, comparing the rate of CI in callus extracts stimulated CRL-2522 cells, was presented in Figure 4. The evaluated level of the fibroblast proliferation rate after 72 h of incubation with 12.5 µg L −1 callus extract was the highest compared to all analyzed ligands. Moreover, the callus extract administrated for 72 h caused a significant increase in the proliferation rate in comparison with the control group (5.7 ± 0.1 vs. 4.4 ± 0.9; p < 0.01).
Kinetin (N6-furfuryladenine), known from the literature as a small-molecule plant compound that acts as a growth factor, has been selected as a reference substance. It is one of the cytokinin compounds, where anti-aging effects on cultured human skin cells have been reported [20,21]. However, in our study after kinetin stimulation, no difference between the proliferation rate of CRL-2522 fibroblasts and the control cells was observed.

Discussion
The beneficial effect of the C. japonica callus extract on fibroblasts may be related to the compounds present in the biomass, in which pentacyclic triterpenoids and phenolic compounds predominate. The preliminary studies carried out may suggest that the callus extract rich in triterpenoids may be a potential source of cosmetic ingredients with a beneficial effect on human skin.
As it is known from the literature, ursolic and oleanolic acids (those compounds present in extracts from the callus and fruits of C. japonica), have demonstrated activity on human fibroblasts [22]. Oleanolic acid with less cytotoxicity than ursolic acid can be used as a complementary ingredient in products intended for dermal use [22]. However, the liposome-encapsulated ursolic acid increased the collagen synthesis of dermal fibroblasts and it is a promising agent with a wide variety of applications, for example, in anti-aging skin care products [23]. Moreover, the extract of Manilkara bidentate, with a beneficial effect on collagen and fibronectin synthesis and the extract of birch (Betula sp.) bark, both rich in pentacyclic triterpenes, have been considered as anti-aging ingredients for the cosmetic industry [24,25]. Asiaticoside, an active compound belonging to pentacyclic terpenoids from Centella asiatica, has enhanced the number of normal human dermal fibroblasts in the in vitro system [26]. The Terminalia chebula fruit extract is rich in phenolic acids and flavonol glycosides. Fibroblasts treated with extracts of this species at concentrations of 10-100 µg mL −1 survived and were divided even up to day 21 of culture. The cytoprotective effect of the extracts of this plant has been demonstrated in combination with high antioxidant activity. Treated fibroblasts were characterized by a normal morphology and good parameters of growth [27]. The extract from Symphytum officinale rich in phenolic acids (including hydroxybenzoic acid, chlorogenic acid, and p-coumaric acid) characterized by the lack of cytotoxicity, stimulates the viability and metabolism of human skin fibroblast cells [28]. Furthermore, the extract of Persea americana seeds, mostly composed of quinic acid, chlorogenic acid, and their isomers, enhanced the proliferation rate of human skin fibroblasts and keratinocytes and did not affect their cytotoxicity [29]. The extracts from C. japonica are rich in chlorogenic acid, which is known from the literature as a compound affecting, among others, the proliferation of fibroblasts and preferably, acting to improve skin regeneration [30].
The authors believe that the C. japonica extracts are worthy to be investigated in regard to their properties to positively affect the skin, which is related to the presence of valuable compounds. Many researchers suggest that extracts rich in bioactive compounds, as opposed to single compounds, can be characterized by synergistic effects on cells, increasing their proliferation rate and scavenging free radicals [27]. A breakthrough in understanding human skin cells (e.g., fibroblasts, keratinocytes) treated with plant-derived extracts with well-defined and natural ingredients offers a pathway for anti-aging product development. Our research brings us closer to understanding how the C. japonica callus extract may influence the cultured fibroblasts, cells of connective tissue, which number decreases during the aging process of the skin. For the aseptic culture initiation, the seeds were isolated from fresh fruits, surface disinfected, and used as primary explants. The isolated seeds were washed in distilled water for 5 min followed by submerging in 70% (v/v) ethanol for 30 s to degrease the seeds and placed on lignin in a thermostat (26 • C) for 24 h to swell the seeds. After this pretreatment, the seeds were disinfected with commercial bleach at a 50% concentration for 20 min with two drops of Tween 20. They were finally rinsed 5 times in sterilized bi-distilled water and transferred to Murashige and Skoog (MS) [31] medium to obtain the aseptic seedlings, whose parts were the secondary explants for in vitro cultures establishment. All types of culture media consisted of MS basal media solidified with 0.8% (w/v) agar (Sigma-Aldrich, Saint. Louis, MO, USA) supplemented with 30 g L −1 (w/v) sucrose and plant growth regulators at various concentrations. All plant growth regulators originated from Sigma-Aldrich (St. Louis, Saint Louis, MO, USA). After adjusting pH to 5.8, the media were autoclaved at 121 • C for 20 min at 105 kPa. Cultures were incubated in a growth chamber (16/8 h photoperiod, 55 µmol m −2 s −1 light, temp. 21 ± 2 • C).

Phytochemical Analysis
Lyophilized plant samples (100 mg) were ground in a mortar and extracted with 80% (v/v) methanol, using the accelerated solvent extraction system (ASE 200, Dionex, Sunnyvale, CA, USA). Extraction was carried out at 100 • C, operating pressure was 1500 psi. The extracts were evaporated to dryness, suspended in 5% MeOH, and subjected to solid phase extraction (SPE) on Waters SepPak Classic cartridges equilibrated with 5% MeOH. The analytes were eluted with 95% MeOH, evaporated to dryness and reconstituted in 3.000 mL of 90% MeOH. The samples were then stored in −20 • C and centrifuged at 23,000 x g for 15 min before analysis. UHPLC-DAD-ESI-MS analyzes were performed using an ACQUITY UPLC ® chromatographic system (Waters Corp., Milford, MA, USA), equipped with a triple quadrupole mass detector.
The MS analysis was carried out using the scanning method in the positive and negative ionization mode. The MS settings for the negative ionization mode were as follows: the capillary voltage was 2.8 kV; cone voltage was 45 V; source temperature was 140 • C, desolvation temperature was 350 • C, cone gas flow (nitrogen) was 100 L h −1 , desolvation gas flow was 800 L h −1 ; positive ionization: capillary voltage was 3.1 kV, cone voltage was 60 V, other settings were as above. Constituents of the extracts were tentatively identified on the basis of their UV spectra and/or MS data. Chlorogenic acid was quantified on the basis of UV chromatograms, using a calibration curve of chlorogenic acid (y = 182.94x -560.94, R2 = 0.9981). The contents of other phenolics were expressed as chlorogenic acid equivalents.
Extractions and analyzes were performed in triplicate, while the presented results are means-based with standard deviation.

Determination of Total Polyphenolic, Phenolic Acid, and Flavonoid Contents
Samples of lyophilized and powdered biomass were extracted three times with a matched quantity of 80% (v/v) ethanol for 60 min at the boiling point temperature of the extractive mixture under reflux. The extracts were evaporated to dryness under a reduced pressure.
The content of phenolics in the ethanol-water extracts (80%, v/v) was determined spectrophotometrically using Dóka and Bicanic's (2002) [32] modified method, with the Folin-Ciocalteu reagent. Briefly, 0.05 mL of the tested extract was mixed with 3.7 mL of distilled water and 0.25 mL of the Folin-Ciocalteu reagent. The mixture was shaken vigorously and a 20% (w/v) sodium dicarbonate solution (1.0 mL) was added after 1 min. Next, the samples were incubated in the dark for 30 min at room temperature. The absorbance was measured at 760 nm. The concentration of the total phenolic compounds in the extract was expressed as mg of the gallic acid equivalent per gram of the dry plant material weight from a calibration curve of gallic acid (y = 9.8399x + 0.0289, R2 = 9993) in a concentration rate (20-80 µg 10 mL −1 ). The values are expressed as the mean of 6 replications ± SD.
The content of phenolic acids in the ethanol-water extracts (80%, v/v) was determined by a spectrophotometric method described in Polish Pharmacopeia VI (2002) [33] with Arnov's reagent The content of flavonoids in the ethanol-water extracts (80%, v/v) was determined as described by Meda et al. (2005) [34]. Briefly, equal volumes of 2% AlCl 3 in methanol (0.7 mL) and the extract (0.7 mL) were mixed and left for 10 min. The absorbance was measured at 415 nm using a blank sample of water and methanol without AlCl 3 . The total concentration of the flavonoid content was expressed as mg of quercetin per gram of the dry plant material weight, from a calibration curve of quercetin (y = 0.046x − 0.0199, R2 = 0.9991) in a concentration range (3.125-25 µg mL −1 ). The values are expressed as the mean of 6 replications ± SD.

Determination of Antioxidant Activity DPPH, FRAP, CUPRAC Assays
The DPPH assay was conducted according to Studzińska-Sroka et al. [35] with modifications. Briefly, 25 µL of the dry extracts dissolved in DMSO (Sigma-Aldrich, Saint-Louis, MO, USA) at different concentrations (0.3125-5 mg/mL) were mixed with a 175 µL of DPPH (Sigma-Aldrich, St. Louis, MO, USA) solution (39 mg 50 mL −1 of MeOH; the final assay concentrations were 78.13-625 µg mL −1 ). The reaction mixture was shaken and incubated in the dark, at room temperature for 30 min. Absorbance was measured at 517 nm against the blank (25 µL of DMSO and 175 µL of MeOH). The control contains 25 µL of DMSO and 175 µL of DPPH solution. The inhibition of the DPPH radical by the sample was calculated according to the following formula: DPPH scavenging activity (%) = (A0−A1)/A0 × 100%, where A0 is the absorbance of the control and A1 is the absorbance of the sample. Analyses were performed in six replicates. Vitamin C was used as a standard (7.5-80 µg mL −1 ; the final assay concentrations were 0.9375-15 µg mL −1 ). The results were expressed as the IC 50 value corresponds to the concentration of the extract required to inhibit DPPH radical formation by 50% and was determined from the linear regression analysis.
The FRAP assay was performed according to Tiveron et al. [36] with some modifications. The stock solutions of FRAP reagent included 300 mM acetate buffer (pH 3.6), 10 mM 2,4,6-Tris(2-pyridyl)-s-triazine (TPTZ, Sigma-Aldrich, Saint-Louis, MO, USA) solution in 40 mM HCl, and 20 mM FeCl 3 ·6H 2 O (Sigma-Aldrich, Saint-Louis, MO, USA) solution. The working FRAP solution was freshly prepared by mixing 25 mL of acetate buffer, 2.5 mL of TPTZ solution, and 2.5 mL of FeCl 3 ·6H 2 O solution, and then warmed at 37 • C before usage. Briefly, 25 µL of the tested extracts were dissolved in DMSO at different concentrations (0.0125-3.2 mg of extract/mL) was mixed with 175 µL of the FRAP solution (the final assay concentrations were 3.125-400 µg mL −1 ), shaken and incubated at 37 • C for 30 min in the dark condition. Then the absorbance was read at 593 nm. The analysis was performed in six replicates. Vitamin C was used as a standard (0.0125-0.2 mg mL −1 ; the final assay concentrations were 0.195-3.125 µg mL −1 ). The results were expressed as the IC 0.5 , which corresponds to the extract concentration required to produce 0.5 O.D. value.
The CUPRAC assay was conducted according to Apak et al. [37] with modifications. The stock solutions of the CUPRAC reagent included equal parts of acetate buffer (pH = 7.0), 7.5 mM neocuproine (Sigma-Aldrich, St. Louis, MO, USA) solution in 96% ethanol, and 10 mM CuCl 2 ·H 2 0 (Avantor Performance Materials, Gliwice, Poland) solution. Briefly, 50 µL of the dry tested extracts dissolved in DMSO at different concentrations (0.0125-1.6 mg mL −1 ), were mixed with 150 µL of CUPRAC solution (the final assay concentrations were 3.125-400 µg mL −1 ), shaken and incubated at room temperature for 30 min in the dark condition. Then the absorbance was read at 450 nm. The analysis was performed in six replicates. Vitamin C was used as a standard (0.0125-0.1 mg mL −1 ; the final assay concentrations were 3.125-25 µg mL −1 ). The results were expressed as the IC 0.5 which corresponds to the extract concentration required to produce 0.5 O.D. value.

Biological Activity on Fibroblasts
The research was carried out on human skin fibroblasts established from male newborns normal foreskin (CRL-2522, ATCC, Manassas, VA, USA). Fibroblasts were cultured in EMEM medium (Corning, New York, NY, USA) supplemented with 100 µg mL −1 streptomycin (Cytogen, Sinn, Germany), 100 µg mL −1 penicillin (Cytogen, Sinn, Germany), 2 mmol L −1 L-glutamine (Cytogen, Sinn, Germany), and 10% fetal bovine serum (FBS, Corning, NY, USA). The cell line was maintained in aseptic conditions at 37 • C in a humidified, 5% CO 2 incubator and confirmed free of mycoplasma contamination through regular testing (Mycoplasma PCR Test Kit, AppliChem, Darmstadt, Germany). Cells were cultured until 90% confluence. At this point, they were detached from culture dishes with a trypsin solution (2.5%, Biowest, Riverside, MO, USA). After 3 min of incubation, the trypsin was removed, complete growth medium was added, and the cell suspension was transferred into sterile Petri dishes. Cells prepared due to this procedure were used for further investigations.
The cell proliferation ratio was evaluated using the xCELLigence RTCA DP system (Roche Diagnostics, Mannheim, Germany; ACEA Biosciences, San Diego, CA, USA). Real-time measurements of cell proliferation were conducted using 16-well plates (F. Hoffmann-La Roche Ltd., Basel, Switzerland; ACEA Biosciences, San Diego, CA 92121 USA). Gold microelectrodes are attached at the bottom of each well for the impedance-based detection of cells biological status, including attachment and cell number. The voltage of about 20 mV applied to the electrodes during the test does not affect the examined cells. The electrical impedance was measured by the integrated software of the xCELLigence RTCA DP system as a cell index (CI). Cells were seeded into the wells at a density of 10,000 cells/well. Afterward, the cells were treated with callus extracts/fruit extracts/kinetin at different final concentrations: 100, 50, 25, 12.5 µg mL −1 . The control consisted of cells cultured in a medium without addition of the above ligands. Cell proliferation was monitored every 15 min for 72 h. Cells morphology and viability were evaluated using an Axio Vert.A1 microscope (10× and 20× magnitude, Zeiss, Jena, Germany) by means of propidium iodide/Hoechst33342 double staining after 48 h of incubation with different ligand concentrations: 100; 12.5 µg mL −1 and subsequently analyzed with AxioVision software (Zeiss, Jena, Germany). Microscopy analysis was performed on the same selected area on the Petri dish before and after propidium iodide/Hoechst33342 staining.

Statistical Analysis
The collected data from the biotechnological experiments were subjected to a one-way analysis of variance ANOVA, followed by Duncan's post-hoc test. A two-sided P-value of 0.05 was used to declare statistical significance. The Shapiro-Wilk test was used as the normality test of continuous variables. Homogeneity of variance was assessed with the Levene test. A one-way ANOVA followed by Tukey (RIR) post hoc test was used to analyze the relationship between various ligands. Repeated measures of one-way ANOVA with the Tukey-Kramer multiple comparisons test were used to evaluate changes in time for particular ligands. The analysis was made by using Statistica 10 software (StatSoft Inc., Tulsa, OK, USA). Data were presented as mean ± standard deviation and considered statistically significant at p < 0.05.

Conclusions
The stimulation of the proliferation of human skin fibroblasts by C. japonica callus extracts may indicate the prospects for their use in the design of new cosmetic preparations based on plant raw materials.