Research Paper Volume 11, Issue 12 pp 4216—4237
β-catenin-mediated hair growth induction effect of 3,4,5-tri-O-caffeoylquinic acid
- 1 School of Integrative and Global Majors (SIGMA) University of Tsukuba, Tsukuba City, 305-8572, Japan
- 2 Faculty of Life and Environmental Sciences University of Tsukuba, Tsukuba City, 305-8572, Japan
- 3 Alliance for Research on the Mediterranean and North Africa (ARENA) University of Tsukuba, Tsukuba City, 305-8572, Japan
Received: April 23, 2018 Accepted: June 17, 2019 Published: June 29, 2019https://doi.org/10.18632/aging.102048
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Copyright: Bejaoui et al. This is an open‐access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The hair follicle is a complex structure that goes through a cyclic period of growth (anagen), regression (catagen), and rest (telogen) under the regulation of several signaling pathways, including Wnt/ β-catenin, FGF, Shh, and Notch. The Wnt/β-catenin signaling is specifically involved in hair follicle morphogenesis, regeneration, and growth. β-catenin is expressed in the dermal papilla and promotes anagen induction and duration, as well as keratinocyte regulation and differentiation. In this study, we demonstrated the activation of β-catenin by a polyphenolic compound 3,4,5-tri-O-caffeoylquinic acid (TCQA) in mice model and in human dermal papilla cells to promote hair growth cycle. A complete regrowth of the shaved area of C3H mice was observed upon treatment with TCQA. Global gene expression analysis using microarray showed an upregulation in hair growth-associated genes. Moreover, the expression of β-catenin was remarkably upregulated in vivo and in vitro. These findings suggest that β-catenin activation by TCQA promoted the initiation of the anagen phase of the hair cycle.
Hair plays an important role in an individual's general appearance . Hair loss is a common disorder that occurs both in men and women. Although it is not dangerous or severe, it affects people’s quality of life and leads to psychological changes that lower self-esteem and even disturbing an individual capability to fulfill a normal lifestyle [1–3].
The hair follicle (HF) is composed of two compartments, the epidermal (epithelial) and dermal (mesenchymal), and is formed via a coordinated and complicated crosstalk between dermal cells playing the role of inducers and epithelial cells as responders. The mesenchymal is composed of specialized fibroblasts divided into the dermal papilla (DP), located at the proximal end of the HF and surrounded by matrix cells, and the dermal sheath (DS), considered as a reservoir of DP cells . The DP plays an important role in the induction and maintenance of the hair growth cycle by acting as inductive signal while driving the differentiation of epithelial stem cells residing in the bulge area of the HF, and generating the complex follicular product, the shaft, and the sheath [5–8]. In the adult hair, the HF undergo continuous self-renewal and cycling, dividing in three phases anagen, catagen, and telogen . During the growth phase or anagen, the DP regulates the migration of bulge residing stem cells to the bulb region forming the matrix cells that will be proliferating and dividing into the hair shaft and the inner root sheath (IRS) [9,10]. The HF enters then a regression phase known as catagen where the hair matrix cells stop proliferating and the hair is attached to a keratin matrix above the DP . During the third phase (telogen), the follicle is resting and the hair shaft is dislodged in non-active follicle. In order to initiate the transition from telogen to anagen, various signaling pathways play a key role in cell proliferation and differentiation during development and homeostasis of the HF . Previous studies have identified Wnt, FGF, Shh, and Notch signaling and several transcription factors as regulators of the hair cycle. Wnt/β-catenin signaling pathway plays a major role in the development, growth, and proliferation of the HF and the regulation of the activity of embryonic and adult stem cell populations [13,14]. The activation of Wnt/β-catenin is initiated by Wnt ligand that binds to frizzled (FZD) and LRP5/6 co-receptors to form a complex inducing β-catenin activation and translocation to the nucleus. Therefore, β-catenin activates canonical target genes involved in the growth of the HF including, Wnt signaling proteins expressed during anagen, and FGF signaling molecules involved in keratinocytes differentiation [15–17]. Wnt/β-catenin activation in the HF initiates the anagen induction by inducing the proliferation and differentiation of the epithelial matrix cells that produces the hair shaft and IRS .
Studies have shown that the lack of β-catenin inhibit the initiation of hair growth cycle and its activation in the DP promotes postnatal hair growth and the elongation of anagen phase [19–21]. Activating β-catenin expression is therefore considered significant in the initiation of the anagen phase and promotion of hair growth cycle. Recently, drugs like minoxidil and finasteride are used to promote hair growth cycle but they showed side effects [22–24].
In this context, developing a drug with no undesirable side effects is becoming urgent in order to have an alternative therapy for promoting hair growth. Caffeoylquinic acid (CQA) is a phenylpropanoids compound exhibiting several beneficial properties including anti-oxidant, anti-allergic, neuroprotective, and melanogenesis-regulating effects [25–28]. TCQA or 3,4,5-tri-O-caffeoylquinic acid with IUPAC name (3R,5R)-3,4,5-tris[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1-hydroxycyclohexane-1-carboxylic acid, is a CQA derivative and chlorogenic acid (CGA) family member compound, that has a stable albumin affinity and is composed of multi-esters formed between quinic acid and one-to-four residues of trans-cinnamic acids . TCQA has been found to induce a powerful inhibitory activities against aldose reductase, hypertension, hyperglycemia, and Alzheimer's disease without unwanted secondary effects . Moreover, TCQA induces neurogenesis, improves learning and memory in aged mice, and promotes the differentiation of human neural stem cells , however its effect on Wnt/β-catenin signaling pathway and hair growth promotion has not yet been assessed. This study was designed to elucidate the ability of TCQA to activate β-catenin and its target genes to promote hair growth, anagen induction and elongation in 8-weeks-old C3H male mice. Global gene expression analysis was performed to explain the hair growth-promoting effects. Furthermore, β-catenin expression in DP and its effect on DP cell proliferation was evaluated.
3,4,5-tri-O-caffeoylquinic acid (TCQA) promoted hair regrowth in C3H mice
The ability of TCQA to promote hair regrowth was tested in eight-weeks-old male C3H mice. Ten days after shaving, TCQA-treated group exhibited hair regrowth in the shaved area (Figure 1A). TCQA significantly enhanced the hair growth by approximately 40%, 80%, and 120% at day 14, 20, and 30, respectively, compared with the control (Figure 1B). By the end of the treatment period (day 30), the treated group displayed a markedly complete regrowth of the hair in the clipped area. In contrast, for the control group, only 37% hair regrowth area was observed (Figure 1A and 1B). The direction of the growth was random in the treated and untreated mice. These results showed that TCQA stimulated the hair growth cycle. Minoxidil, a widely used drug against alopecia often used as a positive control ,induces hair regrowth in C3H mice within 28 days . Our results showed that TCQA had the same effect as minoxidil in stimulating hair growth cycle. Interestingly, the hair shaft was fully developed and the epidermis and the hair follicle (HF) displayed no sign of inflammation or irritation following TCQA application (Figure 1C). The anagen phase is divided into six sub-stages that goes from I to VI and starting the third phase the HFs development can be distinguished. As shown in Figure 1C (indicated by arrows), the HF from the TCQA-treated mice were at advanced stage of anagen phase. The results indicated that TCQA induced the transition of the hair cycle from telogen to anagen phase accelerating hair growth in vivo.
Figure 1. TCQA promoted hair regrowth in C3H mice skin. (A) The back skin of eight-weeks-old male C3H mice was shaved and treated daily with topical application of 1 wt% TCQA (1 g TCQA in 100 ml milli-Q water) and with milli-Q water (control) for 30 days. (B) The area of the new generated coat was measured by ImageJ. (C) Skin from treated area from TCQA-treated group and control group were cut at thickness of 10 µM and visualized under the microscope. *Statistically significant (P ≤0.05) difference between control and TCQA-treated group. **Statistically significant (P ≤0.01) difference between control and TCQA-treated mice.
Gene expression changes in C3H mice skin caused by 3,4,5-tri-O-caffeoylquinic acid (TCQA)
Microarray analysis was conducted from skin collected from the treated area with TCQA and milli-Q water to elucidate the mechanism behind the observed hair growth promoting effect of TCQA. The expression of 1235 genes was modulated by TCQA out of which, 435 were upregulated while 800 downregulated. Genes relevant in β-catenin binding, epidermal growth factor, transcription regulation, and Wnt signaling were upregulated (Figure 2A). On the other hand, genes involved in glycosylation, protein binding, and β-catenin degradation complex were downregulated (Figure 2B). A volcano plot was created to compare the gene expression in the control group vs TCQA group (Figure 2C). TCQA significantly upregulated 435 genes (2-fold change; red) and downregulated 800 genes (2-fold change; green), while the gray color represents the other genes (
Figure 2AB. Transcriptome changes induced by TCQA, 1235 genes were significantly selected: 435 were upregulated and 800 downregulated. (A) Summary of the functional categories of upregulated genes in response to TCQA treatment. (B) Summary of the functional categories of downregulated genes in response to TCQA treatment. Analyses for the down and upregulated genes were performed individually using Database for Annotation, Visualization and Integrated Discovery v6.8 (DAVID). Bars represent the number of genes implicated in each category. *Statistically significant (P ≤0.01). **Statistically significant (P ≤0.001). ***Statistically significant (P ≤0.0001).
Figure 2CD. Transcriptome changes induced by TCQA, 1235 genes were significantly selected: 435 were upregulated and 800 downregulated. (C) Hierarchical clustering of the genes altered after treatment with TCQA using Euclidean distance and average linkage algorithm of the TIGR Mev version 3.0.3 software (The Institute for Genomic Research, MD, USA). Horizontal stripes represent genes and columns represent control and TCQA. The significant fold change in gene expression is 2-fold change (control vs TCQA). (D) The volcano plot represents the regulated genes between the control and TCQA. The red color represents the upregulated genes, the green color the downregulated genes, and the grey color the unregulated genes. The expression of the genes above or below, left or right, the lines differed more than 2-fold change between the control and TCQA group.
Genes with 2-fold change in expression (control vs TCQA) were subjected to hierarchical clustering that generated five clusters. In the first cluster (enrichment Score: 1.53), TCQA regulated genes including Wnt2b, Dock2, Rasgrp2, Agbl4, and Dgki that are relevant for protein binding (P=0.0048), Ras signaling pathway (P=0.023), and intracellular signal transduction (P=0.017), and microtubule (P=0.0018) (Figure 2D). Moreover, a regulation of genes including, Ctnnb1, Wls, Rassf1, and Map3k12 that plays a role in ATP binding (P=0.023), kinase activity (P=0.0152), Wnt signaling (P=0.02152), and phosphorylation (P=0.025) was observed in cluster two (enrichment score: 0.83). The third cluster with enrichment score of 0.29 is composed of genes that are significant for cell adhesion (P=0.0049), cAMP signaling pathway (P=0.02), and neuroactive ligand-receptor interaction (P=0.0049). The last two clusters with an enrichment score of 0.89 and 0.55, respectively, represent the genes that were downregulated upon treatment with TCQA. Those genes are significant for metal binding (P=0.0045), Wnt signaling repression (P=0.0015), and cell surface receptor linked signal transduction (P=0.0175) (Figure 2D).
Tables 1, 2, 3, and 4 summarize the significantly modulated genes and their biological activities. An upregulation in the expression of canonical Wnt-associated genes, Ctnnb1, Wls,Wnt2b, and Wnt4 was observed (Table 1). Notch, FGF, and Rac/Ras pathway-related genes were upregulated as well. Genes significant for keratinocytes differentiation, including Foxn1, Rps3 were upregulated. In addition, the expression of genes involved in cell differentiation, cell cycle, ATP binding, and oxidation-reduction process like Sapcd2, Smchd1, and Txnrd1, were enhanced by TCQA (Table 2). Genes associated with telogen phase, repression of Wnt signaling, β-catenin degradation, and aging (Ldb3, Ak1, Gsk3b, Tcf3, Soct, and Nfatc1), were downregulated (Tables 3 and 4).
Table 1. Top upregulated anagen-associated genes in TCQA-treated mice (vs control) *.
|Gene symbol||Gene name||Biological function||Fold-change||P value **|
|Fgf1||Fibroblast growth factor 1||Hair morphogenesis||3.22||0.026|
|Ctnnb1||Catenin (cadherin associated protein), beta 1||Cell differentiation; hair follicle morphogenesis; hair cycle process; positive regulation of fibroblast growth factor||3.2||0.043|
|Wnt4||Wingless-related MMTV integration site 4||Hair morphogenesis||2.87||0.047|
|Tspan10||Tetraspanin 10||Notch signaling promotion||2.86||0.011|
|RBPj||Recombination signal binding protein for immunoglobulin kappa J region-like||Hair fate determination of hair follicular stem cells||2.72||0.003|
|AlpL||Alkaline phosphatase||Dermal papilla marker||2.33||0.007|
|Dlx||Distal-less homeobox||Regulator of hair follicle differentiation and cycling||2.31||0.034|
|Rps3||Ribosomal protein S3||Positive regulation of NF-kB required for anagen maintenance||2.17||0.000017|
|Wnt2b||Wingless related MMTV integration site 2b||Hair morphogenesis||2.16||0.0002|
|Foxn1||Forkhead box N1||Keratinocyte differentiation; hair follicle development||2.06||0.00015|
|Krt14||Keratin 14||Formation of epithelial hair buds; hair cycle||2.04||0.002|
|Corin||Corin serine peptidase||Dermal papilla marker upregulated during anagen||2.03||0.006|
|Fgf2||Fibroblast growth factor 2||Hair follicle growth||2.02||0.006|
|*Genes functions were obtained from Mouse Genome Informatics (MGI).|
|**ANOVA was performed to assess the level of significance between groups. The gene expression was considered significant when fold change was ≥ 2-fold (control vs TCQA).|
Table 2. Top upregulated genes associated with the observed hair growth in TCQA-treated mice (vs control) *.
|Gene symbol||Gene name||Biological function||Fold- change||P value|
|Smchd1||SMC hinge domain containing 1||ATP binding||6.83||0.021|
|Dock2||Dedicator of cyto-kinesis 2||Positive regulation of Rac protein signal transduction||2.78||0.00014|
|Rassf1||Ras association (RalGDS/AF-6) domain family member 1||Ras protein signal transduction ; cell cycle||2.69||0.007|
|Sapcd2||Suppressor APC domain containing 2||Cell proliferation; cell cycle||2.66||0.005|
|Txnrd1||Thioredoxin reductase 1||Oxidation-reduction process; protection against oxidative stress||2.63||0.001|
|Tada3||Transcriptional adaptor 3||Stabilization and activation of the p53||2.58||0.011|
|Fmo4||Flavin containing monooxygenase 4||Oxidation-reduction process||2.49||0.0003|
|Cyp11a1||Cytochrome P450, family 11, subfamily a, polypeptide 1||Oxidation-reduction process||2.42||0.003|
|Kif1b||Kinesin family member 1B||ATP binding||2.3||0.004|
|Rasgrp2||RAS, guanyl releasing protein 2||Ras activation||2.28||0.0004|
|Agbl4||ATP/GTP binding protein-like 4||ATP binding||2.2||0.0001|
|Dgki||Diacylglycerol kinase, iota||Ras protein signal transduction regulation||2.17||1.26E-07|
|Plk2||Polo-like kinase 2||Ras protein signal transduction||2.17||0.027|
|Map3k12||Mitogen-activated protein kinase kinase kinase 12||ATP binding, cell-cycle progression||2.11||0.004|
|*Genes functions were obtained from Mouse Genome Informatics (MGI).|
|**ANOVA was performed to assess the level of significance between groups. The gene expression was considered significant when fold change was ≥ 2-fold (control vs TCQA)|
Table 3. Top downregulated genes in TCQA-treated mice (vs control)*.
|Gene symbol||Gene name||Biological function||Fold-change||P value|
|Ldb3||LIM domain binding 3||Regulator of transcription during telogen||-8.65||0.040|
|Cryab||Crystallin, alpha B||Negative regulator of apoptosis||-6.89||0.035|
|Ak1||Adenylate kinase 1||Cell cycle arrest||-6.24||0.027|
|Dst||Dystonin||Cell cycle arrest||-5.34||0.027|
|Gsk3b||Glycogen synthase kinase 3 beta||Phosphorylation of β-catenin||-5.08||0.002|
|Tcf3||Transcription factor 3||Wnt/β-Catenin repression||-4.72||0.042|
|Soct||Sclerostin||Negative regulation of|
|Aebp1||AE binding protein 1||Regulator of telogen hair follicle||-3.8||0.015|
|Satb1||Special AT-rich sequence binding protein 1||Regulator of transcription during telogen||-3.36||0.026|
|H2afv||H2A histone family||Stem cell quiescence||-3.31||0.040|
|Egr1||Early growth response 1||Negative regulation of|
Wnt/β-Catenin; upregulated with aging
|Igfbp4||Insulin-like growth factor binding protein 3||Negative regulation of|
|lL-6||Interleukin 6||Inflammation response||-2.44||0.026|
|Shisa3||Shisa family member 3||Negative regulator of|
|Abra||Actin-binding Rho activating protein||Regulator of transcription during telogen||-2.22||0.046|
|Nfatc1||Nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1||Stem cells quiescence||-2.09||0.011|
|*Genes functions were obtained from Mouse Genome Informatics (MGI).|
|**ANOVA was performed to assess the level of significance between groups. The gene expression was considered significant when fold change was ≥ 2-fold (control vs TCQA)|
Table 4. Telogen-associated genes downregulated by TCQA*.
|Cell cycle arrest||Ak1,Dst|
|Regulation of transcription||Ldb3,Abra, Satb, Cebpd1,Synpo2, Aebp1, Rora,lrrfip|
|Negative regulator of cell growth||Igfbp4|
|Signal transduction||Hspb6, Obscn|
|Carbohydrate metabolic process||Pygm, Gpd1, Agl|
|Aging||Jun, Egr1, Fos|
|*Genes functions were obtained from Mouse Genome Informatics (MGI).|
3,4,5-tri-O-caffeoylquinic acid (TCQA) stimulated β-catenin expression in vivo
TCQA-treated mice were observed to have an accelerated anagen phase and at the same time Ctnnb1 gene expression was observed to be upregulated based on microarray analyses results, the effect of TCQA on β-catenin expression was further determined in mice skin tissue. Results revealed that β-catenin expression in TCQA-treated mice skin was increased in the HF, in the area where the dermal papilla (DP) cells are, in the root sheath, and in the bulb area (Figure 3A). In case of the control mice, β-catenin expression was located in the epidermis and the upper part of the dermis (Figure 3A). In addition, the gene expression of Ctnnb1 in treated skin tissues was enhanced up to 2.3-fold compared with the control (Figure 3B). This upregulation of Ctnnb1 expression was followed by an increase in β-catenin protein expression level as shown in Figures 3C and 3D.
Figure 3AB. TCQA enhanced β-catenin expression in the hair follicle. (A) Immunohistochemistry was performed to measure β-catenin expression in the hair follicle and the epidermis in skin collected from the treated area from mice dorsal skin at 30 days after treatment. The figure is divided into four panels, the first panel is the phase, the second is DAPI to stain the nucleus, the third is for β-catenin staining, and the last panel is a merge between β-catenin and the nucleus. (B) Ctnnb1 mRNA relative expression was measured after treatment with TCQA at 30 days after treatment. The mRNA level was quantified using TaqMan real-time PCR from RNA extracted from the treated area (TCQA or milli-Q water) from the mice dorsal back.
Figure 3C-E. TCQA enhanced β-catenin expression in the hair follicle. (C) β-catenin protein expression was determined at the end of the treatment period. The protein was extracted from the treated area from the mice dorsal part, and western blot was carried away. (D) Band intensities was done assessed using LI-COR system. Results represent the mean ± SD of three independent experiments. *Statistically significant (P ≤0.05) difference between control and TCQA-treated mice. **Statistically significant (P ≤0.01) difference between control and TCQA-treated mice. (E) Summary of the up and downregulated genes modulated by TCQA compared with the control. The red color represents the upregulated genes and the green color the downregulated genes.
Figure 3E illustrates the summary of the modulated genes by TCQA. β-catenin target genes that are involved in HF development and keratinocyte differentiation including, Foxn1, Dlx, Fgf, and others, were upregulated. In contrast, genes that inhibit Wnt/β-catenin signaling including Gsk3b,Tcf3, and Igfbp4 were downregulated (Figure 3E). These results indicated that the observed hair regrowth effect appears to be caused by increased β-catenin expression following TCQA treatment.
3,4,5-tri-O-caffeoylquinic acid (TCQA) increased the proliferation of hair bulb cells
To determine the cytotoxic effect of TCQA, if any, on the cells that reside in the bulb area of the HF, a proliferation assay (MTT assay) of human epidermal melanocytes (HEM) and human hair follicle dermal papilla cells (HFDPC) was conducted. The cells were treated with 0, 5, 10, 15, and 25 µM TCQA for 48 and 72 h. Results showed that TCQA was not cytotoxic to the cells at all concentrations and in fact, the proliferation of the cells was stimulated (Figure 4A and 4B).
Figure 4. TCQA stimulated hair bulb cells proliferation. (A) Cell proliferation of human epidermal melanocytes (HEM) was assessed after 48 and 72 h treatment with various concentrations of TCQA. (B) Cell proliferation of human hair follicle dermal papilla cells (HFDPCs) was assessed after 48 and 72 h treatment with various concentrations of TCQA. (C) ATP content determination after treatment with 5 and 10 µM of TCQA and 0.1 µM of minoxidil (Minox) used as positive control. (D) Gene expression of ALPL (Alkaline Phosphatase) after 6 and 12 h treatment with 0, 10 µM TCQA, and 0.1 Minox. The mRNA level was quantified using TaqMan real-time PCR after treatment. Results represent the mean ± SD of three independent experiments. *Statistically significant (P ≤0.05) difference between control and treated cells. **Statistically significant (P ≤0.01) difference between control and treated cells. ##Statistically significant (P ≤0.01) difference between Minox-treated cells and TCQA-treated cells.
3,4,5-tri-O-caffeoylquinic acid (TCQA) increased the ATP content of human hair follicle dermal papilla cells (HFDPCs)
The number of hair matrix and the size of the HF is determined by DP cells. 10 µM of TCQA significantly enhanced the ATP content of DP cells by around 60% after 48 h treatment (Figure 4C). This result was supported by the microarray analyses that showed an upregulation in genes related to ATP binding.
3,4,5-tri-O-caffeoylquinic acid (TCQA) induced alkaline phosphatase (ALPL) and β-catenin expression in human hair follicle dermal papilla cells (HFDPCs)
Alkaline phosphatase (ALP) is known to be a marker of DP cells. As microarray results showed an upregulation in its gene expression, the validation using DP cells was carried out. Results showed an upregulation in ALPL expression after 6 and 12 h treatment (Figure 4D) confirming that TCQA stimulated the proliferation of DP cells.
The absence of β-catenin in DP cells results to an early entry to catagen phase . To confirm the effect of TCQA on β-catenin stimulation, its protein and gene expression levels in HFDPCs were evaluated. β-catenin was observed to be stimulated by 10 µM TCQA after 12 h treatment, and this expression level was maintained until after 24 h (Figure 5A and 5B). Moreover, according to the immunocytochemistry results, TCQA caused the accumulation and nuclear translocation of β-catenin (Figure 5C). The expression of β-catenin gene (CTNNB1) was significantly upregulated after 6 and 12 h treatment with 10 µM TCQA (Figure 5D) suggesting that TCQA promoted hair growth by activating β-catenin expression in the DP at the onset or early stage of anagen phase.
Figure 5AB. TCQA stimulated β-catenin expression in human hair follicle dermal papilla cells (HFDPCs). (A) β-catenin protein expression after 12 and 24 h treatment with 0 and 10 µM TCQA and 0.1 µM Minox. (B) Band intensities was done using LI-COR system after 12 h and 24 h treatment.
Figure 5CD. TCQA stimulated β-catenin expression in human hair follicle dermal papilla cells (HFDPCs). (C) Immunocytochemistry of β-catenin expression in HFDPC after 24 h treatment with 0, 10 µM TCQA and 0.1 µM Minox. Scale bar=25 µm; magnificence 40 X. (D) Gene expression of CTNNB1 (β-catenin) after treatment with 0 and 10 µM TCQA, and 0.1 µM Minox for 6 h and 12 h. The mRNA level was quantified using TaqMan real-time PCR after treatment.
3,4,5-tri-O-caffeoylquinic acid (TCQA) upregulated β-catenin expression in human hair follicle dermal papilla cells (HFDPCs) after inhibition with XAV939
XAV939 inhibits the activation of β-catenin stimulating its phosphorylation and non-translocation to the nucleus . Here, HFDPCs were treated with various concentration of XAV939 for 48 h and 10 µM XAV939 was used for further experiment as it didn’t show any cytotoxicity effect on the cells (Figure 5E). After that, the cells were treated with 10 µM XAV939 for 6 and 12 h and results showed that CTNNB1 expression was significantly decreased upon treatment confirming the inhibitory effect of XAV939 on Wnt/ β-catenin signaling (Figure 5F). The cells were then treated with 10 µM XAV939 (6 and 12 h) and then with 10 µM TCQA (6 and 12 h). Results showed that treatment with TCQA significantly upregulated CTNNB1 expression suppressing XAV939 inhibition. Finally, after co-treatment with XAV939 and TCQA, the gene expression of β-catenin was maintained higher than after treatment with the inhibitor only. These results further proved the activation of β-catenin by TCQA in DP promoting hair growth cycle.
Figure 5EF. TCQA stimulated β-catenin expression in human hair follicle dermal papilla cells (HFDPCs) (E) Cell proliferation of HFDPC was assessed after 48 h treatment with various concentrations of XAV939 (β-catenin inhibitor). (F) Gene expression expressions of CTNNB1 (β-catenin) after treatment with 10 µM XAV939 for 6 and 12 h, with 10 µM XAV939 for 6 and 12 h then with 10 µM TCQA for 6 h and 12 h (XAV939/TCQA), and finally with co-treatment of 10 µM XAV939 and 10 µM TCQA for 6 and 12 h (XAV939+TCQA). Results represent the mean ± SD of three independent experiments. *Statistically significant (P ≤0.05) difference between control and treated cells. **Statistically significant (P ≤0.01) difference between control and treated cells. ##Statistically significant (P ≤0.01) difference between Minox-treated cells and TCQA-treated cells.
The hair follicle (HF) goes through a life-long cyclical transformations, progressing through stages of growth, regression, and quiescence, and is considered an established model to study the pathways that govern proliferation, differentiation, and growth .
Here, we showed that stimulating Wnt//β-catenin activation with a polyphenolic compound 3,4,5-tri-O-caffeoylquinic acid (TCQA) promoted hair growth in vivo and in vitro. TCQA induced a complete hair recovery in the shaved area of the back of eight-week-old C3H mice (Figure 1A and 1B). The observed results were similar to what have been reported for minoxidil hair regrowth stimulating effect in C3H mice . The HF from TCQA-treated mice displayed a developed morphology compared to control mice (Figure 1C). In addition, during the anagen phase, the inferior segment of the HF is present and grow to form the hair bulb surrounding the dermal papilla (DP), and the hair shaft becomes rooted deep in the sebaceous gland and the dermis . The appearance of the HF from TCQA-treated mice indicates that the hair is in the anagen phase. The anagen phase can be further classified into six sub-stages from anagen I to anagen VI . The regeneration of the HF can be morphologically distinguished starting anagen III and keeps growing until at least anagen VI where the HF reaches its full length, and is entirely surrounded by the IRS, and the bulb and DP reach their optimum size . As shown in Figure 1C, TCQA-treated mice HF are in advanced stage of anagen phase of the hair cycle confirming that TCQA promoted the transition of the telogen phase to the anagen phase.
Several molecular pathways including, Wnt/ β-catenin, Shh, Notch, and FGF are responsible for the maintenance of the HF, the differentiation of the hair matrix cells, and the regulation of the hair growth cycle [38,39]. An upregulation of genes involved in Wnt/β-catenin signaling, β-catenin binding, and transcription, and a downregulation in genes relevant in glycosylation, protein binding, and β-catenin degradation complex was observed in TCQA-treated group (Figure 2).
TCQA upregulated Wnt/β-catenin-related genes,Wnt2b, Wls, Wnt4, and Ctnnb1 (Table 1). β-catenin targets Foxn1 involved in the activation of the matrix cells that differentiated to form the hair shaft to regenerate the HF [40–42]. The HFs of TCQA-treated mice were in the anagen phase and this was clearly caused by increased Wnt proteins level known to initiate HF development, and in addition, by the upregulation of β-catenin and its target Foxn1. Various studies have shown that β-catenin is strongly expressed during anagen phase in the DP and in the outer root sheath, and the absence of β-catenin induces a premature catagen phase [40,43,44]. In this study, TCQA caused β-catenin to move to the DP, upregulated its expression in mice treated skin confirming that the HF is in the anagen phase (Figure 3). Fibroblast growth factors (FGF) pathway-related genes Fgf1 and Fgf2 are required, respectively, in the promotion of the anagen phase in telogenic C57BL/6 mice, and the stimulation of hair growth [38,45]. In Table 1, we observed an upregulation of these genes. The increase in FGF-related genes expression may be attributed to the stimulation of Wnt/β-catenin as the absence of Wnt/β-catenin signaling alters FGF signaling genes . Microarray results also revealed an upregulation in the expression of Notch signaling-associated genes including, RBPj and Tspan10. RBPj binds to Notch in the nucleus to trans-activate the transcription of hair growth-associated genes, and the mutation of which is associated with hair loss and impaired matrix cell differentiation, and Tspan10 is involved in the regulation of hair growth [46–49]. More specifically, the expression of several transcription factors regulated by Notch such as Dlx3 was enhanced. Mutation in Dlx3 causes alopecia due to hair shaft differentiation failure [17,50]. On the other hand, an upregulation in DP marker was observed including Alpl and Corin (Table 1). Alkaline phosphatase (ALP) is known to be marker of DP cells expressed through the hair cycle, as for Corin is reported to be upregulated in DP during anagen phase . A summary of TCQA-modulated genes linked to cell cycle, ATP binding, and oxidation-reduction process is presented in Table 2, and one of these genes is Smchd1 with an ATP binding function (Table 2). During the changes of hair cycle from telogen to anagen phase in guinea-pig, ATP content increase following by a development of the size of the HF and an expansion in DNA content .
Other studies have described the role of Wnt/β-catenin and its interaction with AKT and ERK pathways to promote hair growth [31,52]. In this paper, an upregulation of Wnt/β-catenin and its interaction with other pathways that are linked to hair growth was observed.
Rac/Ras-related genes are involved in cell migration, homeostatic, structural plasticity, and memory [53–55]. It has been reported that Rac/Ras pathway is expressed in the inner ear and may affect hair cell development, and Rho and Rac protein are activated by Wnt/ β-catenin signaling and this activation is required for vertebrate gastrulation [18,56–58]. TCQA modulated Rac/Ras- genes, Rasgrp,Dock2, Rassf1,Dgki, and Plk2 (Table 2). The effect of Wnt/β-catenin on Rac/Ras pathway regulation and involvement in hair growth stimulation has not yet been assessed, but here, we report for the first time that TCQA can, through Wnt/ β-catenin signaling activates Rac/Ras pathway, and as a result promoted hair development.
TCQA downregulated genes repressing Wnt/β-catenin pathway including, Gsk3b, Tcf3, Igfbp4, and Shisa3 (Table 3). Gsk3b phosphorylates β-catenin leading to its degradation and non-translocation to the nucleus inducing catagen phase in the HF . Tcf3 and Igfbp4 inhibit Wnt/ β-catenin signaling during neocortical development [60,61]. Other genes were negatively modulated by TCQA like Aebp1 and Nfatc1. Aebp1 is only expressed in the HF at telogen phase and it is known to regulate MAPK pathway . Nfatc1 regulates HF stem cells quiescence, and is upregulated during telogen, and its expression level decreases during the transition from telogen to anagen in order to reduce the quiescence of stem cells promoting the proliferation [63–65]. A downregulation in genes upregulated with aging such as Egr1 and Fos was observed (Table 4). Here, we introduce TCQA as drug to accelerate hair cycle and prevent hair aging and loss.
The HF goes through a continual cycle regulated by the DP that maintains the stem cells niche during telogen and its activates them during anagen [7,65,66]. As mentioned earlier in this paper, the ATP content increases during anagen promoting the expansion of the size of DP . TCQA not only stimulated the proliferation of human hair follicle dermal papilla cells (HFDPCs) but also the ATP content (Figure 4A and 4C) and this is correlated with the upregulation of Smchd1 in vivo (Table 2). In the DP, β-catenin activity is strongly associated with the anagen phase prolongation, and it direct the hair shaft morphogenesis while regulating the expression of secreted growth factors . After treatment with TCQA, the gene and the protein expression of β-catenin was strongly enhanced in the DP and this explains the fast entry of TCQA-treated mice HFs into the anagen phase (Figures 1 and 5).
On the other hand, a knockdown of Tankyrase known to play a role in the activation of Wnt/ β-catenin leads to tumorigenesis . XAV939 is a small molecule that inhibit Tankyrase inducing β-catenin phosphorylation and non-activation in lung adenocarcinoma A549 cell . The inhibitory effect of XAV939 on β-catenin in DP cells has not yet been checked. In this study, XAV939 downregulated β-catenin gene expression (CTNNB1) in HFDPCs, however, after treatment with TCQA, CTNNB1 expression significantly upregulated again (Figure 5F). Moreover, after a co-treatment of XAV939 and TCQA, CTNNB1 expression remained unchanged proving that TCQA target specifically β-catenin and inhibit its phosphorylation.
In summary, the activation of β-catenin stimulated the expression of Wnt proteins, Rac/Ras pathway, and hair growth-associated genes include FGF- and Notch-related genes promoting the transition from telogen to anagen, anagen initiation and elongation, hair matrix differentiation, and hair shaft development (Figure 3E).
Furthermore, the observed stimulation of hair growth cycle was supported by the downregulation of telogen- and aging-associated genes that caused bulge stem cells to migrate and differentiate promoting the anagen induction. The repression of Wnt signal inhibitors contributed to further enhance the effect of β-catenin and Wnt proteins activation.
Clinical studies would be however necessary to validate the observed hair growth promotion effect of TCQA. The potential effect of the activation of β-catenin by TCQA on hair pigmentation and follicular melanocytes will be looked at as β-catenin regulates the transcription factor of the melanogenesis enzyme microphthalmia-associated transcription factor (MITF).
Materials and Methods
Synthesized 3,4,5-tri-O-caffeoylquinic acid (TCQA) with 97% purity was provided by Dr. Kozo Sato from Synthetic Organic Chemistry Laboratories, the FUJIFILM Corporation (Kanagawa, Japan). For the in vivo experiment, TCQA was prepared by first dissolving in a small volume of 70% ethanol and then diluted in purified water. For the in vitro assay, a highly concentration of TCQA was dissolved in 70% ethanol and then diluted in cell culture medium.
Eight-weeks-old male C3H mice were purchased from Charles River Laboratories, Japan Inc. (Kanagawa, Japan) and housed individually in cages at Gene Research Center of the University of Tsukuba. After one week of acclimatization, the mice were randomly assigned to experimental groups (n=5 for each group) TCQA-treated group and milli-Q water treated group (control group). The mice were anesthetized using isoflurane (Wako Pure Chemical Industries, Tokyo, Japan), then the telogen hair on the dorsal part of the mice back were shaved using hair clipper in order to induce the anagen phase. Each mouse then received a topical application of 1% TCQA or water daily for four weeks. The dorsal part of the shaved area was observed and photographed daily starting on the 14th day after treatment. At the end of the treatment period, the mice were sacrificed by cervical spine dislocation and the skin collected from the treated area were divided into four parts and washed with phosphate-buffered saline (PBS), then immediately immersed in liquid nitrogen and kept at −80 °C. The ImageJ processing program (National Institutes of Health, Bethesda, USA) was used to measure the hair regrowth in the treated area. The experiment was approved by the Animal Study Committee of the University of Tsukuba (No.17-060) and the procedures were handled according to the guidelines of the Care and Use and Use of Animals approved by the Council of the Physiological Society of Japan.
RNA used as a template were extracted from skin tissues collected from treated area of mice dorsal part using ISOGEN solution (Nippon Gene, Tokyo, Japan) following the manufacturer’s instructions. The total RNA extracted were then amplified and labeled. The labeled fragmented aRNA was then hybridized to the Affymetrix mouse Array strips (Affymetrix, Santa Clara, USA). The GeneChip (Mouse Genome 430 2.0 Array) was washed, stained, and scanned using Affymetrix GeneAtlas Imaging Station to obtain the mRNA expression of various genes from mouse genome. The gene ontology, biological process, and fold-change in gene expression (2-fold change, control vs TCQA) were then analyzed using Transcriptome Analysis Console (TAC) Software (version 4.0.1) and database for annotation, visualization, and integrated discovery (DAVID) bioinformatics resources 6.8 [69,70]. The average signal log2 (control vs TCQA) was subjected to hierarchical clustering using Euclidean distance and average linkage algorithm of the TIGR Mev version 3.0.3 software (The Institute for Genomic Research, MD, USA).
Skin tissues from mice treated with TCQA and milli-Q water were collected, embedded in optimum cutting temperature (OCT) compound, and then cut at a thickness of 10 µM. The sections were then dried and fixed in 4% paraformaldehyde (SIGMA, Saint Louis, USA) and washed in different solutions of PBS, 20 mM glycine/PBS (SIGMA, Saint Louis, USA), and 0.1% v/v Triton X-100 /PBS (SIGMA, Saint Louis, USA). The skin samples were then blocked and immersed in a solution of 1:100 dilution of rabbit anti- β-catenin (Abcam, Rockford, USA) for overnight at 4°C in a wet chamber. Then washing in 0.1% v/v Triton X-100 /PBS was conducted. The samples were incubated with Alexa 594-conjugated anti-rabbit (Abcam, Rockford, USA) for 1 h at room temperature (RT) and stained with Hoechst and mounted in antifade solution (p-phenylenediamine, PBS, and glycerol).
Cells and cell culture
Human hair follicle dermal papilla cells (HFDPCs) were purchased from Cell Application Inc. (Tokyo, Japan). HFDPCs were maintained in papilla cell growth medium (Toyobo, Osaka, Japan) supplemented with growth factors: fetal calf serum, insulin transferrin triiodothyronine, bovine pituitary extract, and cyproterone solution (Toyobo, Osaka, Japan).
Human epidermal melanocytes (HEM) were purchased from Gibco Invitrogen cell culture. HEM were maintained in Medium 254 (Gibco, South America) supplemented with human melanocyte growth supplement HMGS (Gibco). The medium was changed every other day until the cells were 60% confluent and ready to be subcultured.
The cells were kept under sterile conditions at 37 °C in 75-cm2 flask (BD Falcon, England, UK) in a humidified atmosphere of 5% CO2. The viability of the cells was determined using trypan blue exclusion method.
Cell proliferation assay
The effect of TCQA on cell proliferation was assessed using the 3-(4,5-dimethyl-thiazol-2-y1) 2,5-diphenyl tetrazolium bromide or MTT assay (Dojindo, Kumamoto, Japan). The cells were seeded in 96-well plate at 3×105 cells/well at 37 °C. After 24 h seeding, the growth medium was replaced by various concentrations of TCQA and incubated for 48 h and 72 h. MTT reagent (5 mg/ml) was added to the cells and incubated further for 8 h followed by an addition of 10% sodium dodecyl sulfate (SDS) and incubation overnight. Absorbance was measured at 570 nm using microplate reader (Powerscan HT, NJ, USA). The viability of the cells was quantiﬁed as the percentage (%) of living cells relative to the control (untreated cells). To detect any change in the morphology, the cells were observed using a contrast microscope (Leica Microsystems, Wetzlar, Germany).
Adenosine triphosphate (ATP) assay
Luminescence luciferase assay kit (Toyo Ink, Tokyo, Japan) was used to measure the ATP content. HFDPCs were seeded in 96-well plate at 3×105 cells/ 100 µl well for 24 h, then the medium was replaced by fresh culture medium containing various concentrations of TCQA or 0.1 µM of the positive control minoxidil (Tokyo Chemical Industry, Tokyo, Japan). After 24 h and 48 h, the plate was incubated for 15 min at RT, then 100 µl of ATP reagent was added, followed by homogenization, and 1 min incubation in the dark. Then, 150 µl of the suspension was transferred to white 96-well plate and incubated for 10 min at RT. Intracellular ATP content was measured by luminescence and calculated as the percentage (%) of TCQA treated-cells relative to the control (untreated cells).
HFDPCs were seeded at a density of 5×105 cells per 100-mm petri dish. The cells were allowed to attach overnight and then the growth medium was replaced with a fresh one containing 0 and 10 µM of TCQA or 0.1 µM minoxidil used as positive control (Tokyo Chemical Industry, Tokyo, Japan). HFDPCs were treated as well with only 10 µM XAV939 (SIGMA, Saint Louis, USA), then with 10 µM XAV939 following by a further incubation with 10 µM TCQA (XAV939/TCQA), and finally co-treated with 10 µM XAV939 and TCQA simultaneously (XAV939+TCQA). After 6 and 12 h treatment, the growth medium was removed, and the cells washed with cold PBS before the total RNA was extracted using ISOGEN kit (Nippon Gene, Tokyo, Japan) following the manufacturer’s instructions. The RNA concentration was assessed using a NanoDrop 2000 spectrophotometer (NanoDrop Technologies, Massachusetts, USA).
Quantitative real-time PCR analysis
The extracted RNAs were used as templates for reverse transcription PCR using SuperScript III reverse transcription kit (Invitrogen, CA, USA). The cycling protocol is as follows: 95 °C for 10 min, 40 cycles of 95 °C for 15 s, and 60 °C for 1 min. TaqMan Universal PCR mix and TaqMan probes specific to Ctnnb1 (Mm 00483039_ m1), CTNNB1 (Hs99999168_m1), and ALPL (Hs01029144) (Applied Biosystems, CA, USA) were used for real-time PCR. The real-Time PCR was performed using 7500 Fast Real-Time PCR Software 1.3.1 (Applied Biosystems, CA, USA). Gapdh (Mm99999915_g1) and GAPDH (Hs 02786624_ g1) (Applied Biosystems, CA, USA) were used as endogenous control. All reactions were run in triplicates.
HFDPCs were seeded at density of 5×105 cells per 100-mm petri dish. After overnight incubation, the medium was removed and the cells were treated with 10 µM TCQA and 0.1 µM minoxidil (Tokyo Chemical Industry, Tokyo, Japan). After 12 h and 24 h treatment, total protein extraction was achieved using radio-immunoprecipitation assay (RIPA) buffer (SIGMA, Saint Louis, USA) and protease inhibitor following the manufacturer’s instructions.
Proteins from tissues collected from treated area at mice dorsal part were also extracted. The skin sections were crushed using a homogenizer in RIPA buffer (SIGMA, Saint Louis, USA) and protease inhibitor following the manufacturer’s instructions.
Protein samples (15 µg) were quantified using 2-D Quant kit according to manufacturer’s instructions (GE Healthcare, Chicago, USA).
The protein samples were resolved in 10% sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to polyvinylidene difluoride membrane (PVDF) (Millipore, NJ, USA). The proteins were blotted with β-catenin 71-2700 (Thermo Fisher Scientific, Massachusetts, USA) and GAPDH sc32233 (Santa Cruz Biotechnology, Texas, USA) primary antibodies and incubated with the second antibody goat anti-rabbit IRDye 800 CW or IRDye 680 LT goat anti-mouse and the expression detected using LI-COR Odyssey Infrared Imaging System (LI-COR, NE, USA).
The cells were seeded at density of 3×104/well in lab-tek slides chambers (SIGMA, Saint Louis, USA), and then allowed to attached for overnight at 37 °C. HFDPCs were treated with 0, and 10 µM TCQA and 0.1 µM Minox for 24 h. The medium was then removed and the cells were washed with 0.1% v/v Triton X-100 /PBS (SIGMA, Saint Louis, USA). After 1 h incubation at RT with the blocking solution, the first antibody rabbit anti- β-catenin (Abcam, Rockford, USA) was added for overnight at 4 °C. Therefore, the cells were immersed in a solution of 1:10000 dilution of Alexa 594-conjugated anti-rabbit (Abcam, Rockford, USA) and mounted with DAPI.
Results were expressed as mean ± standard deviation (SD). Statistical analysis was performed using Student’s t-test when comparing two value sets (control vs TCQA). P value of ≤0.05 was considered significant. ANOVA (One-way between-subject ANOVA unpaired) was performed to assess the level of significance between treated groups in vivo. The gene in gene expression was considered significant when change in expression was at least 2-fold (control vs TCQA). ANOVA (one way between-subject ANOVA unpaired) was performed to assess the level of significance between Minox and TCQA-treated cells; A P value of ≤0.05 was considered significant.
We would like to thank Dr. Kozo Sato for providing synthesized TCQA. We are also grateful for the help extended by Dr. Hiromi Yanagisawa and Dr. Aiko Sada for the analysis, and Dr. Kazunori Sasaki for animal experiment.
Conflicts of Interest
The authors declare that there are no conflicts of interest related to this work.
This study was partially supported by Japan Science and Technology Agency (JST), the Japan International Cooperation Agency’s (JICA), Science and Technology Research Partnership for Sustainable Development (SATREPS), and the Ministry of Education, Culture, Sports, Science, and Technology (MEXT).
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