Introduction
Thymosin β4 (Tβ4), a 4.9-kDa small peptide composed of 43 amino acids, was first extracted from the thymus and is the most abundant type of thymosin in mammals (1). Tβ4 participates in regulating cell proliferation, differentiation and motility (2). Our previous study demonstrated that Tβ4 expression increases MC3T3-E1 cell viability on titanium (Ti) discs by increasing adhesion and proliferation (3). Tβ4 is expressed and involved in the initiation, formation and differentiation of tooth germ during molar development (4,5). Tβ4-overexpressing transgenic mice exhibit abnormal tooth development resembling enamel hyperplasia (6). Tβ4 knockdown with small interfering RNA (siRNA) significantly decreases mRNA levels of noncollagenous proteins and type I collagen (COL type I) during MDPC-23 odontoblastic cell differentiation (7).
Dentinogenesis is regulated in odontoblasts by a complex signaling cascade that promotes the expression of dentin matrix-associated proteins (8). Dentin is composed of the mineral hydroxyapatite and organic materials including collagen and noncollagenous proteins. Among noncollagenous proteins, bone sialoprotein (BSP) is one of the major proteins in mineralized tissues including bone, dentin, cementum and calcified cartilage (9). BSP is a phosphorylated or sulfurized glycoprotein with high levels of a sialic acid, for example osteopontin, and tends to bind with hydroxyapatite (10,11). BSP serves as the nucleator of primary apatite crystals, and it regulates the direction of ribbon-like apatite crystal growth on collagen during mineralization (12). Protamine increases BSP expression via mitogen-activated protein kinase (MAPK) signaling in osteoblasts (13). Transforming growth factor β1 (TGF-β1) inhibits BSP expression and osteoblast formation from human mesenchymal stem cells via mothers against decapentaplegic homolog 3 (Smad3)/β-catenin signaling (14). Tβ4 increases MC3T3-E1 cell viability by activating the paired box (Pax)/focal adhesion kinase (FAK) and FAK/growth factor receptor-bound protein 2 (Grb2)/Ras/extracellular signal-regulated kinase (ERK) signaling pathways and promoting focal adhesion and proliferation on Ti discs (3). In addition, Tβ4 increases gastric cancer cell migration by down-regulating E-cadherin through the ERK/glycogen synthase kinase 3α/β-catenin signaling pathway (15).
The authors' previous study identified that Tβ4 protein expression was highest in the secretory odontoblast layer during the advanced bell stage of dentinogenesis (7). It was also identified that Tβ4 promotes differentiation and mineralization of the osteoblastic MC3T3-E1 cell line on Ti discs (16). These previous studies indicated that Tβ4 serves as a principle molecule during the formation of mineralized tissues including bone and dentin. However, Tβ4-associated signaling is not fully understood in odontoblasts, and specifically, the association between Tβ4 signaling and BSP has not been elucidated. Therefore, we hypothesized and investigated whether Tβ4 signaling may regulate BSP expression in odontoblasts. To the best of our knowledge, the present study identified for the first time that Tβ4 upregulates BSP by activating ERK and Smad3 signaling in MDPC-23 odontoblastic cells, suggesting its role as a principle regulatory signaling molecule in dentin matrix formation during dentinogenesis.
Materials and methods
Tissue preparation
A total of 3 pregnant adult ICR outbred female mice, 10-weeks old, weighing 50–60 g (Samtako Bio Korea Osan, Gyeonggi-do, Korea), were used. The temperature and humidity was maintained at 23±2°C and 60±10%, respectively. The animals were kept in a 12 h light-dark photoperiod and provided with pelleted mouse chow and tap water ad libitum. The animal protocols were approved by the Institutional Animal Care and Use Committees at Chosun University (Gwangju, Korea), and animal care was performed using specific-pathogen-free systems according to the Guide for the Care and Use of Laboratory Animals (17). The heads of mice at postnatal day 1 (PN1), PN3, PN5, PN15, and PN21 were used in the present study. The heads, dissected from PN1, PN3, and PN5 mice, were fixed in 4% paraformaldehyde (PFA) in diethylpyrocarbonate-treated phosphate-buffer saline (DEPC-PBS, pH 7.4) at 4°C for 24 h. The PN15 and PN21 mice were fixed by the intracardiac perfusion of 4% PFA. The heads of the PN15 and PN21 mice were dissected and fixed an additional 18 h in fresh 4% PFA at 4°C. Tissues were decalcified in a solution of 10% ethylenediaminetetraacetic acid (EDTA) supplemented with 1% PFA at 27–28°C for 4 weeks. After decalcification, the heads were dehydrated by sequential washes in 70, 80, 90, 100 I, 100 II and 100% III at 27–28°C for 1 h and finally in 100% IV ethanol for 18 h. Paraffin-embedded tissues were cut into 6-μm thick sections using a Histocut 820 (Leica Microsystems, Wetzlar, Germany) and were subsequently placed onto glass slides and dried on a 37°C slide warmer overnight.
Synthesis of Tβ4 complementary RNA (cRNA) probes and peptides
Gene-specific probes for the 405-bp Tβ4 cDNA were designed according to methods described previously (5). The pGEM-3Z vector (Promega Corporation, Madison, WI, USA) containing a Tβ4 cDNA insert was linearized by digestion with restriction enzymes (EcoRI or HindIII) to synthesize Tβ4 sense (S) and antisense (AS) cRNA probes using an in vitro transcription kit (Roche Applied Science, Penzberg, Germany). The probes were labeled with digoxigenin (DIG)-11-UTP using a SP6/T7 DIG RNA Labeling kit (Roche Diagnostics, Basel, Switzerland). The full amino acid sequence of the mouse Tβ4 peptide, Ac-SDK PDM AEI EKF DKS KLK KTE TQE KNP LPS KET IEQ EKQ AGE S, was synthesized by solution phase peptide synthesis (A&PEP, Cheongju-si, Chungcheongbuk-do, Korea).
Membrane hybridization
Unlabeled S probes were anchored to the nucleic acid transfer membranes (GE Healthcare Life Sciences, Little Chalfont, UK) using a ultraviolet crosslinker (Stratagene; Agilent Technologies, Inc., Santa Clara, CA, USA). The membrane-anchored unlabeled S probes were incubated with DIG-labeled AS probes mixed with unlabeled S or unlabeled AS (1–10 ng/μl) in the hybridization solution. The DIG-labeled AS probes were reacted with alkaline phosphatase (AP)-conjugated DIG antibodies and then detected using a DIG nucleic acid detection kit (Roche Diagnostics).
In situ hybridization
Tissue sections were deparaffinized sequentially in xylene I and II at 27–28°C for 5 min. For rehydration, the sections were incubated sequentially in 100, 90, 80 and 70% ethanol at 27–28°C for 1 min. Following deparaffinization and hydration, the tissue sections were incubated with proteinase K at 37°C for 12 min and then 4% PFA at 27–28°C for 10 min. Subsequently, sections were immersed in 0.1 M triethanolamine-HCl (TEA-HCl) and 0.25% acetic anhydride (in 0.1 M TEA) to remove background signals. Hybridization was performed with the hybridization mixture (hybridization solution, 1 ng/μl DIG-labeled S or DIG-labeled AS). The sections were washed twice in 2X and 0.2X saline-sodium citrate buffer containing 50% formamide, and then incubated with a 1:500 dilution of AP-conjugated DIG antibodies at 27–28°C for 1 h. This DIG-labeled S or DIG-labeled AS probes analysis was performed using a DIG nucleic acid detection kit (cat. no. 11 175 041 910; Roche Diagnostics), and sections were counterstained with 1% methyl green (10 mg/ml, Vector Laboratories, Inc., Burlingame, CA, USA) at 27–28°C for 20 sec. The stained tissue was observed by optical microscopy (Carl Zeiss AG, Oberkochen, Germany) on bright field for Tβ4 mRNA detection. The expression of Tβ4 mRNA in the tissue was analyzed using a bright field microscope and Axiovision LE 4.6 software (Carl Zeiss AG).
Cell culture
MDPC-23 cells (provided by Dr CT Hanks from University of Michigan, Ann Arbor, MI, USA), an odonto-blastic cell line derived from the dental papilla of fetal mouse molars, were cultured in Dulbecco's modified Eagle medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (Welgene, Inc., Gyeongsan-si, Korea) and 1% antibiotic-antimycotic solution (Welgene, Inc.). Cells were incubated in a humidified chamber maintained with 5% CO2 at 37°C.
Extraction of total RNA and reverse transcription (RT) semi-quantitative polymerase chain reaction (PCR)
Following serum starvation in serum free medium, MDPC-23 cells were treated with 2 μg/ml Tβ4 (Tβ4/MDPC-23) for 24 h (18). Total RNA was extracted from the cells using TRIzol® reagent (Molecular Research Center, Inc., Cincinnati, OH, USA) according to the manufacturer's protocol, and PCR was performed using AmpONE Taq premix (GeneAll Biotechnology, Co., Ltd., Seoul, Korea). The following primers were synthesized by Bioneer, Co., Ltd. (Daejeon, Korea) for RT-PCR analysis: BSP forward, 5′-ACCGGCCACGCTACTTTCTTTAT-3′; BSP reverse, 5′-TCCTCGTCGCTTTCCTTCACTTT-3′; GAPDH forward, 5′-CCATGGAGAAGGCTGGG-3′; GAPDH reverse, 5′-CAAAGTTGTCATGGATGACC-3′. Each PCR reaction consisted of an initial denaturation at 95°C for 2 min followed by three-step cycling: Denaturation at 95°C for 20 sec, annealing at a temperature optimized for each primer pair for 10 sec (BSP, 60°C for 30 cycles; GAPDH, 56°C for 30 cycles), and extension at 72°C for 30 sec. Single bands were observed at the expected sizes of 358 bp for BSP (GenBank #L20232) and 199 bp for GAPDH (GenBank #M33197) by agarose gel electrophoresis. The PCR products were electrophoresed on 1.5% agarose gel buffered with 0.5X Tris-Borate-EDTA (TBE) buffer and stained with ethidium bromide after amplification. The bands were visualized using a Gel-Doc system (BioRad Laboratories, Inc., Hercules, CA, USA). Band intensities were measured to determine differences in mRNA expression using Science Lab Image Gauge software version 3.12 (Fujifilm Corporation, Tokyo, Japan).
Protein extraction and western blot analysis
Following serum starvation in serum free medium, MDPC-23 cells were treated with 2 μg/ml Tβ4 (Tβ4/MDPC-23) at 37°C for 6, 12 or 24 h. TGF-β1 (10 ng/ml; R&D Systems, Inc., Minneapolis, MN, USA) was also added to a group of MDPC-23 cells (TGF-β1/MDPC-23) at 37°C for 30 min. Certain MDPC-23 cells were treated with the mitogen activated protein kinase kinase inhibitor PD98059 (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) or the Smad3 phosphorylation inhibitor SIS3 (Sigma-Aldrich; Merck KGaA) at 5 μM (PD98059/MDPC-23 and SIS3/MDPC-23, respectively) at 37°C for 1 h to examine the effects of these inhibitors alone. In addition, MDPC-23 cells were pretreated with PD98059 and SIS3 for 1 h prior to Tβ4 treatment (Tβ4/PD98059/MDPC-23 and Tβ4/SIS/MDPC-23, respectively). Subsequent to the various treatments, proteins were extracted from the cells using NP-40 lysis buffer [150 mM NaCl, 1% NP-40, 50 mM Tris-HCl (pH 7.4), 2 mM Na3VO4, 2 mM Na4P2O, 50 mM NaF, 2 mM EDTA (pH 7.4), 0.1 μg/ml of leupeptin and 1 μg/ml of aprotinin], and the proteins (30 μg per lane) were electro-phoresed on 7.5% SDS-PAGE gels. Following electrophoresis, proteins were transferred to PVDF membranes and blocked with either 5% non-fat dry milk or 5% bovine serum albumin (BioShop Canada, Inc., Burlington, ON, Canada) at 27–28°C for 1 h in TBS with 0.05% Tween-20 (TBS-T) buffer. The membranes were blotted with specific antibodies at 4°C for 16 h against phosphorylated (p)β-catenin (cat. no. 4176; 1:1,000), β-catenin (cat. no. 8480; 1:1,000), pERK1/2 (cat. no. 9106; 1:2,500), ERK1/2 (cat. no. 9102; 1:2,500), pSmad2 (cat. no. 3108; 1:1,000), pSmad3 (cat. no. 9502; 1:1,000), or Smad2/3 (cat. no. 3102; 1:1,000) from Cell Signaling Technology, Inc., (Danvers, MA, USA); BSP (cat. no. AB1854; 1:2,500) from Merck KGaA; and runt-related transcription factor 2 (Runx2, cat. no. sc-10758; dilution, 1:2,000) or β-actin (cat. no. sc-47778; 1:2,500) from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA). Membranes were then blotted with horseradish peroxidase-conjugated goat anti-rabbit (cat. no. sc-2004; 1:10,000) or mouse-IgG antibodies (cat. no. sc-2005; 1:10,000) at 27–28°C for 1 h as appropriate (Santa Cruz Biotechnology, Inc.). Immunoreactive bands were detected using X-ray film (Fujifilm Corporation) following treatment with enhanced chemiluminescent solution (Merck KGaA). The intensity of expressed bands was measured by densitometry using Science Lab Image Gauge software version 3.12 (Fujifilm Corporation).
Immunofluorescence
MDPC-23 cells were serum starved in serum free medium and then treated with 2 μg/ml Tβ4 and 5 μM PD98059 or SIS3 for 24 h. Cells were fixed in 4% formaldehyde at 27–28°C for 15 min, treated with 0.1 M glycine, then permeabilized with 0.2% Triton X-100 for 5 min, and blocked with 5% normal goat serum (Vector Laboratories, Inc.) at 27–28°C for 1 h. Cells were incubated with a 1:100 dilution of anti-rabbit BSP, pSmad3, β-catenin, or Runx2 antibodies at 4°C overnight. A 1:1,000 dilution of fluorescein isothiocyanate-conjugated goat-anti-rabbit IgG (Santa Cruz Biotechnology, Inc.; cat. no. sc-2012) was used as a secondary antibody. Cells were mounted with DAPI (Vector Laboratories, Inc.) for nuclear staining and images were captured at ×400, magnification using a fluorescence microscope (Carl Zeiss AG). The fluorescence intensity of β-catenin, Runx2 and pSmad3 protein in the nucleus compared with the cytoplasm was measured by ImageJ 1.8.0 software (National Institutes of Health, Bethesda, MD, USA). At least 100 cells were counted in 3 different microscopic fields. The measurement and quantification methods were performed as described previously (19).
Plasmid construction and transfection
The 2.5 kb portion of the mouse BSP gene promoter region from -2,472 to +41 was artificially synthesized (Bioneer, Co., Ltd.; https://www.bioneer.co.kr) and cloned into the Nhe I-Xho I site of the pGL3-basic vector (pGL3-BSP-Luc). The pGL3-basic vector was supplied from Promega Corporation (Madison, WI, USA). All construct identities were verified by DNA sequencing and restriction enzyme digestion. MDPC-23 cells were transfected with 2 μg/ml pGL3-basic vector (pGL3-Luc; 3.85×1011/ml) or 2 μg/ml pGL3-BSP-Luc (2.53×1011/ml) for 48 h using WellFect-EX (Welgene, Inc.) according to the manufacturer's protocol and transfected cells were used subsequent experiment after serum starvation for 16 h.
Luciferase assay
The pGL3-BSP-Luc-transfected MDPC-23 cells were treated with 2 μg/ml Tβ4 (pGL3-BSP-Luc/Tβ4), or 5 μM PD98059 or SIS3 (pGL3-BSP-Luc/PD98059 or pGL3-BSP-Luc/SIS3, respectively), for 24 h after serum starvation in serum free medium. In addition, the pGL3-BSP-Luc/Tβ4 cells were pretreated with PD98059 or SIS3 at 37°C for 1 h prior to Tβ4 treatment (pGL3-BSP-Luc/PD98059 or SIS3/Tβ4) for 24 h. Protein extraction and reaction with luciferase substrates were performed using a luciferase assay kit (Promega Corporation; cat. no. E1500) according to the manufacturer's protocol. Luciferase activity as proxy for BSP expression was measured using a luminometer (Thermo Fisher Scientific, Inc.). The luciferase activity of pGL3-basic vector was used for normalization.
Statistical analysis
All experiments were performed at least in triplicate. Values are expressed as the mean ± standard error of the mean. Statistical analysis was performed using SPSS v25 (IBM Corp., Armonk, NY, USA). Differences between samples among multiple groups were compared by one-way analysis of variance (ANOVA). The Tukey's post hoc method was used to perform pairwise comparisons following ANOVA. P<0.01 was considered to indicate a statistically significant difference.
Results
Tβ4 mRNA is expressed in odontoblasts during postnatal dentinogenesis
To determine DIG-labeled AS binding activity, the hybridization signal between the mixture of DIG-labeled AS and unlabeled S was determined, and membrane-fixed unlabeled S was detected upon the addition of 1 ng/μl of unlabeled S mixture, but was not detected upon the addition of 5 or 10 ng/μl. In addition, the hybridization signal between the mixture of DIG-labeled AS and unlabeled AS, and membrane-fixed unlabeled S was most marked upon addition of the 1 ng/μl unlabeled AS mixture, and was gradually decreased upon addition of the 5 and 10 ng/μl solutions (Fig. 1A). Tβ4 mRNA was increased in odontoblasts at the advanced bell stage (PN5), and was observed in the odonto-blasts of the crown (PN15) and functional stages (PN21) with a pattern similar to that observed in the early bell stage (PN1). Dentin deposition was observed at PN1 during the early bell stage and became thickened with the increase in enamel at PN3 and PN5 during the advanced bell stage (Fig. 1B and C).
Tβ4 increases BSP expression by activating ERK/Runx2 or ERK/β-catenin signaling in MDPC-23 cells
In MDPC-23 cells treated with Tβ4 for 24 h, the levels of BSP mRNA and protein were increased compared with the levels observed in untreated control cells (Fig. 2A). Furthermore, immunofluorescence analysis indicated that Tβ4 treatment increased BSP protein levels compared to the levels observed in untreated control cells (Fig. 2B). To identify the effect of Tβ4 on pERK1/2, pβ-catenin and β-catenin expression, MDPC-23 cells were treated with Tβ4 at different time intervals (5, 10, 15 and 30 min). The levels of pERK1/2 and pβ-catenin increased the most, but β-catenin was decreased at 10 min in MDPC-23/Tβ4 cells compared with that of the control (data not shown). pERK1/2 and pβ-catenin levels were decreased in the PD98059/MDPC-23 and Tβ4/PD98059/MDPC-23 groups compared with those in the Tβ4/MDPC-23 cells. β-catenin levels were increased in the PD98059/MDPC-23 group compared with levels in the Tβ4/MDPC-23 cells. Expression levels of Runx2 and BSP were increased in the Tβ4/MDPC-23 cells compared with that in the untreated control cells, but levels of the 2 proteins were decreased in the PD98059/MDPC-23 and Tβ4/PD98059/MDPC-23 groups compared with that in the Tβ4/MDPC-23 cells (Fig. 2C). Upon Tβ4 treatment for 6–24 h, levels of pβ-catenin were increased but levels of cytosolic and nuclear β-catenin protein were decreased in the Tβ4/MDPC-23 cells compared with levels in the control cells. Cytosolic and nuclear levels of Runx2 protein were increased in the Tβ4/MDPC-23 cells after 6 h of treatment compared with that of the control cells. BSP expression increased time-dependently in the Tβ4/MDPC-23 cells compared with that in the control cells (Fig. 2D). Furthermore, levels of nuclear β-catenin were increased in the Tβ4/PD98059/MDPC-23 cells compared with levels in the Tβ4/MDPC-23 cells, and PD98059 inhibited the Tβ4-induced nuclear localization of Runx2 (Fig. 2E and F).
Tβ4 increases BSP expression by activating Smad3/Runx2 or Smad3/β-catenin signaling in MDPC-23 cells
pSmad2 levels were significantly increased in the TGF-β1/MDPC-23 cells treated for 30 min compared with levels in the control, but pSmad2 was not induced in the Tβ4/MDPC-23 cells. pSmad3 levels were increased in the TGF-β1/MDPC-23 and Tβ4/MDPC-23 cells compared with levels in the control cells (Fig. 3A). Smad2 phosphorylation was not induced in the Tβ4/MDPC-23 cells, but pSmad3 was significantly increased in the Tβ4/MDPC-23 cells treated for 5 to 30 min compared with that in the control (Fig. 3B). In the Tβ4/MDPC-23 cells, the levels of pSmad3 and pβ-catenin were increased compared with the control cells; however, this phosphorylation was decreased in the SIS3/MDPC-23 and Tβ4/SIS3/MDPC-23 groups. β-catenin levels were decreased in the Tβ4/MDPC-23 cells compared with that in the control, but β-catenin levels were similar to the control levels in the SIS3/MDPC-23 and Tβ4/SIS3/MDPC-23 groups. The expression levels of Runx2 and BSP were increased in the Tβ4/MDPC-23 cells compared with expression in the control, but decreased levels were observed in the SIS3/MDPC-23 and Tβ4/SIS3/MDPC-23 groups compared with levels observed in the Tβ4/MDPC-23 cells (Fig. 3C). The levels of cytoplasmic and nuclear pSmad3 were increased from 6–24 h in the Tβ4/MDPC-23 cells compared with that in the control. The expression of BSP was increased in the Tβ4/MDPC-23 cells compared with the expression in the control cells (Fig. 3D). Furthermore, nuclear pSmad3 levels were decreased in the Tβ4/SIS3/MDPC-23 cells compared with that in the Tβ4/MDPC-23 cells, and the nuclear levels of β-catenin were increased in the Tβ4/SIS3/MDPC-23 group (Fig. 3E and F).
Tβ4 increases BSP promoter activity via ERK and Smad3 signaling
Luciferase activity was significantly increased in the pGL3-BSP-Luc cells compared with that in the pGL3-Luc cells, and it was also increased in the pGL3-BSP-Luc/Tβ4 group compared with that in the pGL3-BSP-Luc group (P<0.01). Compared with the pGL-BSP-Luc/Tβ4 cells, the luciferase activity was significantly decreased upon treatment with PD98059 or SIS3. Furthermore, luciferase activity was decreased in the pGL-BSP-Luc/SIS3/Tβ4 cells compared with in the pGL-BSP-Luc/PD98059/Tβ4 cells (Fig. 4A). Fig. 4B is a schematic diagram of the experimental results demonstrating that Tβ4 induced BSP expression via ERK or Smad3 signaling associated with Runx2 and β-catenin in MDPC-23 cells.
Discussion
Odontoblast differentiation occurs actively at the early bell stage, and secretory odontoblasts are present in the cusp and cervical region of developing molars at advanced bell stages (7,20,21). Secretory odontoblasts secrete non-collagenous proteins including BSP, dentin sialoprotein, osteocalcin (OCN) and osteonectin at the advanced bell stage (22–24). Our previous study indicated that Tβ4 protein levels are increased in odonto-blasts at the cusp and cervical region of developing molars in the advanced bell stage, compared with levels in early bell stages (7). Other studies suggested that Tβ4 is associated with enamel development and tooth germ growth (6,25). In the present study, Tβ4 mRNA was markedly expressed in odontoblasts at the cusp region in the advanced bell stage concordantly with the activation of dentin matrix synthesis during dentinogenesis. Therefore, in accordance with previous studies, the marked expression of Tβ4 mRNA in secretory odontoblasts indicated that Tβ4 may regulate odontoblast differentiation or dentin formation during tooth development. Our previous study demonstrated that Tβ4 knockdown remarkably decreases mineralization and mRNA expression of non-collagenous proteins including BSP during MDPC-23 cell differentiation (7). In bone tissue, which is similar to dentin, transgenic BSP knockout mice form undermineralized bones, and their cortical bones are thinner compared with the cortical bones of normal mice (26). These studies suggest that Tβ4 may regulate BSP expression during mineralized tissue development. In the present study, Tβ4 treatment increased BSP mRNA and protein levels in MDPC-23 cells compared with levels in untreated control cells. This suggests that Tβ4 may regulate BSP expression in odontoblasts through intracellular signal transduction during dentinogenesis.
In a pulldown experiment to identify differential interacting proteins, Tβ4 was demonstrated to increase extracellular adenosine 5′-triphosphate (ATP) levels via ecto-ATP synthase on the cell surface (27). Increased ATP was demonstrated to activate P2X purinoreceptor 4 purinergic receptors to promote the migration of endothelial cells. In a recent study, purinergic receptor subtypes, including P2X4, were expressed in dental pulp cells (DPCs) and ATP was revealed to promote the odon-toblastic differentiation and mineralization of DPCs (28). Our previous studies demonstrated autocrine and paracrine actions of Tβ4, similar to results of other studies (27,29). Suppression of Tβ4 expression significantly decreases the mRNA expression of mineralization-associated factors, including BSP, and mineralization in MDPC-23 cells (7). In addition, exogenous Tβ4 increases osteoblast-like cell adhesion on Ti surfaces, but the suppression of Tβ4 expression significantly inhibits this adhesion (3). Exogenous Tβ4 has also been indicated to stimulate angiogenesis through increased endothelial cell differentiation and migration, thereby allowing Tβ4 to function in autocrine and paracrine manners (29). Therefore, based on these data from our studies and additional previous studies, Tβ4 may regulate BSP expression by autocrine or/and paracrine signaling and additional studies are required for determining the receptor of Tβ4 in odontoblasts during dentinogenesis.
Tβ4 is an actin-sequestering peptide that regulates actin polymerization, and Tβ4 may also activate signaling pathways involved with cell migration, adhesion and proliferation, including ERK/β-catenin, Pax/FAK and FAK/Grb2/Ras/ERK in osteoblasts and gastric cancer cells (3,15). Tβ4 is expressed in developing mouse mandibles and is also involved in the initiation, formation and differentiation of tooth germ during molar development (4,5). In a previous study, Tβ4 promoted the odontoblastic differentiation of dental pulp cells by activating MAPKs [p38 MAPK, c-Jun N-terminal kinase (JNK) and ERK], and Smad (Smad1/5/8 and Smad2/3) signaling pathways (30). ERK, p38 and JNK have critical functions in signal transduction during embryo development, immune response and neural canal development in vertebrates (31,32). In addition, MAPKs are the central signal transducers that modulate osteogenesis and bone mass (33,34). ERK1/2 signaling activates Runx2 and therefore OCN expression during osteoblast differentiation (35). In the present study, it was identified that Tβ4 increases pERK1/2 levels and Runx2 expression in MDPC-23 cells. Additionally, Tβ4 increased Runx2 nuclear translocation in MDPC-23 cells. In previous studies, Wnt3a stimulation increased the nuclear translocation of β-catenin, thereby decreasing the expression of Runx2, osterix, alkaline phosphatase (ALP), BSP, and OCN in cementoblasts and dental follicle cells (36,37). In the present study, Tβ4 reduced cytoplasmic and nuclear β-catenin levels in MDPC-23 cells. Considering all these results together, Tβ4 signal transduction increases BSP expression through ERK/Runx2 or ERK/β-catenin in MDPC-23 cells.
Smad proteins are additional important signal transducers associated with tooth development. BMP-2 increases Runx2 expression through the Smad1/5 pathway, which also increases the expression of ALP and OCN through the β-catenin pathway in dental papilla cells (38,39). TGF-β1 inhibits the differentiation of mesenchymal stem cells into osteoblasts by elevating β-catenin levels via Smad3, protein kinase A (PKA) and phosphoinositide 3-kinase (PI3K) signaling, thereby decreasing BSP expression (14). Cytosolic Smad2 or Smad3 translocate into the nucleus by interacting with Smad4, where they regulate the expression of genes associated with bone matrix synthesis including Runx2, ALP, COL type I and OCN in MC3T3-E1 cells (40,41). In a recent study, Tβ4 knockdown decreased Runx2 expression via Smad1/5/8 and PI3K/protein kinase B (Akt) signaling in dental epithelial cells (42). The results of the present study indicated that Tβ4 increased Smad3 phosphorylation and expression of Runx2, but did not increase the phosphorylation of Smad2 in MDPC-23 cells. In addition, Tβ4 increased nuclear pSmad3 levels in MDPC-23 cells. Tβ4 also decreased cytoplasmic and nuclear β-catenin through Smad3 signaling, similarly to pERK1/2 signaling, in MDPC-23 cells. Therefore, the present results indicated that Tβ4 increased BSP expression through Smad3/Runx2, Smad3/β-catenin and Smad3 signal transduction in MDPC-23 cells.
According to the results of the present study, Tβ4 induced BSP expression via ERK and Smad3 signaling in MDPC-23 cells. However, it is necessary to determine which pathway is more important for Tβ4-mediated BSP expression in MDPC-23 cells. A previous study suggested that protamine-induced BSP promoter activation was significantly more suppressed by ERK1/2 inhibitor treatment (U0126) compared with protein kinase C or PKA inhibitor treatment (H7 or KT5720) in ROS 17/2.8 osteoblast-like cells (13). SIS3 treatment inhibits TGF-β1-induced β-catenin transcription and stabilization in mesenchymal stem cells, but these phenomena are not affected by PD98059 treatment (14). Additionally, Tβ4 increases Runx2 expression via Smad1/5/8 and PI3K/Akt signaling to a lesser degree compared with ERK/MAPK signaling in dental epithelial cells (42). In the present study, Tβ4 increased BSP promoter activity, which was decreased by PD98059 or SIS3 treatment in MDPC-23 cells. Notably, BSP promoter activity was significantly more inhibited by SIS3 treatment compared with PD98059 treatment. These results indicated that Tβ4 activated BSP transcription via ERK and Smad3 signaling, and that Smad3 signaling contributed to Tβ4-induced BSP transcription in MDPC-23 cells to a greater extent compared with ERK signaling.
In conclusion, Tβ4 induced BSP in MDPC-23 cells through ERK and Smad3 pathways, suggesting its role as a signaling molecule for regulating BSP secretion in odontoblasts. These events indicate that Tβ4 signaling may be associated with dentin matrix formation in odontoblasts during dentinogenesis. Additional examination of the receptor of Tβ4 in odontoblasts during dentinogenesis is required.