Patent Application
20120148538
This patent application claims the benefit of priority from Korean Patent Application No. 10-2010-0127022, filed on Dec. 13, 2010 and No. 10-2011-0069292, filed on Jul. 13, 2011, the contents of which are incorporated herein by reference.
1. Field of the Invention
The present invention relates to a composition for hard tissue formation and dentin or dental pulp regeneration, more precisely a composition for hard tissue formation and dentin or dental pulp regeneration using ameloblasts, apical bud cells, or its culture fluid as an active ingredient.
2. Description of the Related Art
Odontoblasts, being attached to dentin, are columnar cells forming dentin (Victor, E.; Arana-Chavez, V. E.; Massa, L F. OdontOblasts: the cells forming and maintaining dentine. The International Journal of Biochemistry & Cell Biology, 2004 36: 1367-73. The final differentiation of odontoblasts is regulated by the ectoderm derived inner dental epithelium. It has been known so far that a variety of factors are involved in the differentiation of odontoblasts, which are exemplified by various growth factors secreted in basement membrane and enamel knot, DMPI, and DMP4 (Lisi S, Peterkov R, Peterka M, Vonesch J L, Ruch J V, Lesot H. Tooth morphogenesis and pattern of odontoblast differentiation. Connect Tissue Res. 2003; 44, 1:167-70; Smith A J, Lesot H. Induction and regulation of crown dentinogenesis: embryonic events as a template for dental tissue repair? Crit. Rev Oral Biol Med. 2001; 12:425-37). Laminin alpha2, one of constituents of basement membrane, regulates DSPP expression during the differentiation of odontoblasts (Yuasa K, Fukumoto S, Kamasaki Y, Yamada A, Fukumoto E, Kanaoka K, Saito K, Harada H, Arikawa-Hirasawa E, Miyagoe-Suzuki Y, Takeda S, Okamoto K, Kato Y, Fujiwara T. Laminin alpha2 is essential for odontoblast differentiation regulating dentin sialoprotein expression. J Biol. Chem. 2004 Mar. 12; 279(11):10286-92). A. George et al reported that DMPI and DMP4 regulate the differentiation of odontoblasts (Narayanan, K.; Srinivas, R.; Ramachandran, A. Nao, J.; Quinn, B. George, A. Differentiation of embryonic mesenchymal cells to odontoblast-like cells by overexpression of dentin matrix protein 1. PNAS, 2001, 98 (8), 14516-21; Narayanan, K.; Gajjeraman, S.; Ramachandran, A.; Hao, J.; George, A. Dentin matrix protein 1 regulates dentin sialophosphoprotein gene transcription during early odontoblast differentiation. J Biol. Chem. 2006, 281(28), 19064-71; Hao, J.; Narayanan, K.; Muni, T.; Ramachandran, A.; George, A. Dentin Matrix Protein 4, a Novel Secretory Calcium-binding Protein That Modulates Odontoblast Differentiation. J Biol. Chem. 2007, 282(21), 15357-65). It has been also reported that the growth factor of enamel knot could regulate the differentiation of odontoblasts (Thesleff, I.; Ker, S. V.; Jernvall, J. Enamel Knots as Signaling Centers Linking Tooth Morphogenesis and Odontoblast Differentiation. Adv. Dent. Res., 2001, 15, 14-8). It has recently been suggested that insulin growth factor, retinoic acid, epithermal growth factor, and neuronal growth factor are also the factors inducing odontoblast differentiation (Lesot, H.; Lisi, S.; Peterkova, R.; Peterka, M.; Mitolo, V.; Ruch, J. V. Epigenetic Signals during Odontoblast Differentiation. Adv. Dent. Res., 2001, 15, 8-13; Arany, S.; Koyota, S.; Sugiyama, T. Nerve growth factor promotes differentiation of odontoblast-like cells. J Cell Biochem. 2009, 106(4), 539-45). However, those factors involved in odontoblast differentiation including DMPI and DMP4 are not the ones secreted specifically in epithelial cells. Therefore, based on the theory that inner dental epithelium regulates the final step of odontoblast differentiation, it is necessarily investigated to identify a factor inducing odontoblast differentiation from ameloblasts originated from inner dental epithelium and its products.
Human dental pulp stem cells (hDPSCs) are easy to isolate from human third molar, which are differentiated into odontoblasts and osteoblasts, and have the similar characteristics to mesenchymal stem cells (d'Aquino R, De Rosa A, Laino G, Caruso F, Guida L, Rullo R, Checchi V, Laino L, Tirino V, Papaccio G., Human dental pulp stem cells: from biology to clinical applications., J Exp Zool B Mol Dev Evol. 2009 Jul. 15; 312B (5):408-15). Gronthos, et al had succeeded in isolation of human dental pulp stem cells and then demonstrated that the differentiation of the dental pulp stem cells into odontoblasts, chondrocytes, adipocytes, and nerve cells could be possible (Gronthos S, Mankani M, Brahim J, Robey P G, Shi S. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci USA. 2000 Dec. 5; 97(25):13625-30; Iohara K, Meng L, Ito M, Tomokiyo A, Matsushita K, Nakashima M. Side population cells isolated from porcine dental pulp tissue with self-renewal and multipotency for dentinogenesis, chondrogenesis; adipogenesis, and neurogenesis. Stem Cells. 2006 November; 24(11):2493-503. Epub 2006 July 27).
Dental pulp is a loose connective tissue supporting dentin, which is composed of cells, extracellular matrix, blood vessels, nerve, and lymph ducts. Dental pulp is involved in the maintenance, support and continuous formation of dentin. Dental pulp has sensory function, and delivers nutrition to dentin, and provides protection for pulp by forming tertiary dentin (Histogenesis. Oral Tissues., 145-162, Park J C, et al., Komoonsa). However, the conventional method to treat dentin-pulp disease, mainly focused on the conservation of dentin-pulp, has disadvantages of weakening of treated teeth and high chance of re-infection (Kim J Y, Xin X, Moioli E K, Chung J, Lee C H, Chen M, Fu S Y, Koch P D, Mao J J., Regeneration of Dental-Pulp-like Tissue by Chemotaxis-Induced Cell Homing., Tissue Eng Part A., 2010, Jun. 24; Murray P E, Garcia-Godoy F, Hargreaves K M., Regenerative endodontics: a review of current status and a call for action., J. Endod., 2007, April; 33(4):377-90). There have been many attempts to generate dental pulp like tissues in previous studies. And some factors such as DMPI, FGF, and BMP7 have been approved to be, effective in dental pulp regeneration. But, in the treatment of these factors, normal arrangement of odontoblasts on the surface of dentin has not been observed at all (Prescott R S, Alsanea R, Fayad M I, Johnson B R, Wenckus C S, Hao J, John A S, George A, In vivo generation of dental pulp-like tissue by using dental pulp stem cells, a collagen scaffold, and dentin matrix protein 1 after subcutaneous transplantation in mice., J. Endod. 2008 April; 34(4):421-6).
Rodent incisors have a special epithelial structure, referred to as the ‘apical bud,’ at the apical end, which continuously grows. The apical bud contains inner enamel epithelium, outer enamel epithelium, and stellate reticulum, and the inner enamel epithelium differentiates into ameloblasts (Harada H, Ohshima H. New perspectives on tooth development and the dental stem cell niche. Arch Histol Cytol 2004 March; 67(1):1-11; Ohshima H, Nakasone N, Hashimoto E, Sakai H, Nakakura-Ohshima K, Harada H. The eternal tooth germ is formed at the apical end of continuously growing teeth. Arch Oral Biol. 2005 February; 50(2):153-7. Epub 2004 November 23). Jin Y et al have recently reported that dental pulp cells were differentiated into odontoblasts when epithelial and mesenchymal cells were co-cultured using tooth germ conditioned medium (Yu, J.; Deng, Z.; Shi, J.; Zhai, H.; Nie, X.; Zhuang, H.; Li, Y.; Jin, Y. Differentiation of dental pulp stem cells into regular-shaped dentin-pulp complex induced by tooth germ cell conditioned medium. Tissue Eng., 2006, 12(11), 3097-105; Yu J, Wang Y, Deng Z, Tang L, Li Y, Shi J, Jin Y. Odontogenic capability: bone marrow stromal stem cells versus dental pulp stem cells. Biol Cell. 2007 August; 99(8):465-74). It was additionally reported that when dental pulp cells were transplanted together with apical bud cells, enamel-dentin complex was formed (Yu, J.; Jin, F.; Deng, Z.; Li, Y.; Tang, L.; Shi, Jin, Y. Epithelial-mesenchymal cell ratios can determine the crown morphogenesis of dental pulp stem cells. Stem Cells Dev., 2008, 17(3), 475-82). These results suggest that epithelium derived factors play an important role in odontoblast differentiation. In particular, Honda et al reported that when epithelial and mesenchymal cells were sequentially seeded, tooth-like structure was formed (Honda, M. J.; Tsuchiya, S.; Sumita, Y.; Sagara, H.; Ueda, M. The sequential seeding of epithelial and mesenchymal cells for tissue-engineered tooth regeneration. Biomaterials, 2007, 28(4), 680-9). That is, epithelial-mesenchymal interactions are important and necessary for dentinogenesis. However, it has not been identified specifically which factor of epithelium can induce the differentiation of odontoblasts.
Recently, proteomic methods have been widely applied to various studies. For example, mineralized tissues, such as dentin and enamel, are used in proteomic analysis. Proteomic analysis reports have been made for enamel and ameloblasts. However, proteomic research has not been performed on secretory factors of ameloblasts (Park E S, Cho H S, Kwon T G, Jang S N, Lee S H, An C H, Shin H I, Kim J Y, Cho J Y. Proteomics analysis of human dentin reveals distinct protein expression profiles. J Proteome Res. 2009 March; 8(3):1338-46; Mangum J E, Veith P D, Reynolds E C, Hubbard M J. Towards second-generation proteome analysis of murine enamel-forming cells. Eur J Oral Sci. 2006 May; 114 Suppl 1:259-65; discussion 285-6, 382).
Thus, the present inventors studied the effect of epithelial cells on the differentiation of odontoblasts to develop a novel composition for hard tissue formation and dentin or dental pulp regeneration. As a result, the present inventors completed this invention by confirming that ameloblasts, apical bud cells, or its culture fluid could accelerate the differentiation of odontoblasts and osteoblasts, increase DSPP promoter activity, and induce regeneration of dental pulp of dental pulp stem cells, and at the same time form a huge amount of hard tissues in vivo, so it can be used effectively as an active ingredient for the composition for hard tissue formation and dentin or dental pulp regeneration.
It is an object of the present invention to provide a composition for hard tissue formation and dentin or dental pulp regeneration comprising ameloblasts, apical bud cells, or its culture fluid as an active ingredient.
To achieve the above object, the present invention provides a method for dentin or dental pulp regeneration containing the step of administering a pharmaceutically effective dose of ameloblasts, apical bud cells, or its culture fluid to a subject.
The present invention also provides a method for promoting hard tissue formation containing the step of administering a pharmaceutically effective dose of ameloblasts, apical bud cells, or its culture fluid to a subject.
The present invention further provides a pharmaceutical composition for dentin or dental pulp regeneration comprising ameloblasts, apical bud cells, or its culture fluid as an active ingredient.
In addition, the present invention provides a pharmaceutical composition for promoting hard tissue formation comprising ameloblasts, apical bud cells, or its culture fluid as an active ingredient.
The ameloblasts, apical bud cells, or its culture fluid of the present invention induces the differentiation of odontoblasts and osteoblasts, increases DSPP promoter activity, promotes dental pulp regeneration, and induces hard tissue formation significantly in vivo, so that it can be effectively used for a composition for promoting hard tissue formation and dentin or dental pulp regeneration.
The application of the preferred embodiments of the present invention is best understood with reference to the accompanying drawings, wherein:
ABCs: apical bud cells;
MDPC-23: mouse odontoblast cell line;
hDPSCs: human dental pulp stem cells; and
MG63: human osteoblast cell line.
A: microphotograph of separated apical bud cells; and
B: photograph showing the expressions of ameloblastin and amelogenin mRNA.
control: the MDPC-23 only group;
co-culture: the group co-cultured MDPC-23 and apical bud cells;
A: a graph showing the relative expression level of DSPP mRNA;
B: a graph showing the relative expression level nestin mRNA;
C: a graph showing the relative expression level of BSP mRNA;
D: a graph showing the comparison of proliferation between the control and the co-culture group;
E: a graph showing the quantitative analysis of type I collagen protein expression;
F: a graph showing the quantitative analysis of DSP protein expression; and
G: a set of photographs showing the expressions of DSP, BSP and type I collagen.
(control)hDPSCs: the dental pulp stem cells only group; and
(co-culture)hDPSCs+ABCs: the group co-cultured dental pulp stem cells and apical bud cells.
control: the osteoblasts only group;
co-culture: the group co-cultured ameloblasts(apical bud cells) and osteoblasts;
A: a graph showing the relative expression level of Runx2 mRNA;
B: a graph showing the relative expression level of osterix mRNA;
C: a graph showing the relative expression level of type I collagen mRNA;
D: a graph showing the relative expression level of ALP mRNA;
E: a set of photographs showing the expression of BSP protein; and
F: a graph showing the quantitative analysis of BSP protein expression in the control and the co-culture group.
A: DSP promoter activity;
B: BSP promoter activity;
C: calcium accumulation confirmed by alizarin red S staining;
PA-CM: apical bud cells culture fluid; and
KB-CM: oral epithelial cells culture fluid.
hDPSCs: the dental pulp stem cells only group (A and D);
hDPSCs+BMP-2: the BMP-2-treated dental pulp stem cells group (B and E);
hDPSCs+PA-CM: the PA-CM-treated dental pulp stem cells group (C and F); and
G: a graph showing the hard tissue formations of hDPSCs, hDPSCs+BMP-2, and hDPSCs+PA-CM.
A: the dental pulp stem cells (hDPSCs) only group;
B: the rhBMP-2-treated dental pulp stem cells group, arrows indicate the cells entrapped in mineralized matrix;
C: the apical bud cells culture fluid-treated dental pulp stem cell group, black arrows indicate odontoblast processes of differentiating odontoblasts; and
D: a scanning electron micrograph (SEM) showing the differentiated odontoblasts in the apical bud cells culture fluid-treated dental pulp stem cells group, white arrows indicate odontoblast processes of differentiating odontoblasts.
hDPSCs: the dental pulp stem cells only group;
hDPSCs+BMP-2: the BMP-2-treated dental pulp stem cells group; and
hDPSCs+PA-CM: the PA-CM-treated dental pulp stem cells group.
hDPSCs: the dental pulp stem cells only group.
A: DSPP promoter activity after noggin treatment in apical bud cells culture fluid; and
B: result of Western blotting with odontoblasts treated with periostin-neutralized conditioned medium.
Hereinafter, the present invention is described in detail.
The present invention provides a method for dentin or dental pulp regeneration containing the step of administering a pharmaceutically effective dose of ameloblasts, apical bud cells, or its culture fluid to a subject.
The present invention also provides a pharmaceutical composition for dentin or dental pulp regeneration comprising ameloblasts, apical bud cells, or its culture fluid as an active ingredient.
The ameloblasts herein are preferably ameloblast-lineage cells, but not always limited thereto.
The dentin or dental pulp herein is preferably dentin-pulp complex, but not always limited thereto.
The culture fluid herein is preferably the one cultured for 0-10 days from the beginning of differentiation, and more preferably the one cultured for 3-7 days, and most preferably cultured for 3 days.
The apical bud cells culture fluid herein is preferably prepared by the following steps, but not always limited hereto.
1) culturing mouse primary apical bud cells (ABSs) until reaching 90% of confluence;
2) culturing the cells in the medium supplemented with ascorbic acid and i-glycerophosphate;
3) collecting the medium after 3 days in culture;
4) filtering the medium; and
5) precipitating proteins in the medium, followed by eliminating salts therein.
In a preferred embodiment of the present invention, differentiation of apical bud cells into ameloblasts was investigated. As a result, the expression of ameloblast differentiation markers by apical bud cells was confirmed after 3 days in culture (see
In a preferred embodiment of the present invention, it was confirmed that differentiated odontoblasts secreted DSPP, the noncollageneous protein playing an important role in dentin formation. To confirm the increase of DSPP expression in odontoblasts, apical bud cells were co-cultured with odontoblasts. As a result, it was confirmed that the expression of DSPP was almost double the amount (see
In a preferred embodiment of the present invention, it was investigated whether nestin expressed in differentiated odontoblasts was increased. First, apical bud cells were co-cultured with odontoblasts, followed by real-time PCR. As a result, it was confirmed that nestin level was increased 4 times as high as that in the control (see
In a preferred embodiment of the present invention, it was investigated whether or not DSP protein forming DSPP and type I collagen, the most abundant collagenous protein in dentin, were increased. To do so, apical bud cells were co-cultured with odontoblasts, followed by Western blotting. As a result, it was confirmed that the expressions of those proteins were increased in experimental groups, compared with those of control (see
In a preferred embodiment of the preset invention, it was investigated whether apical bud cells induced odontoblast differentiation of dental pulp stem cells. To do so, dental pulp stem cells were co-cultured with apical bud cells. As a result, the expression level of DSPP, marker differentiated odontoblasts, increased in dental pulp stem cells co-cultured with apical bud cells (see
In a preferred embodiment of the present invention, it was investigated whether dental pulp stem cells could induce regeneration of dental pulp when apical bud cells culture fluid was treated. First, apical bud cells culture fluid was treated in tooth-like environment. As a result, it was confirmed that pulp-like tissues were formed (see
In a preferred embodiment of the present invention, the effect of apical bud cells culture fluid on DSPP promoter activity was investigated. The promoter activity was measured by using various apical bud cells culture fluids. As a result, DSPP promoter activity was increased in all apical bud cells culture fluids. Particularly, apical bud cells culture fluid after 3 days in culture was most effective in increasing DSPP promoter activity (see
In a preferred embodiment of the present invention, it was investigated if the confirmed characteristics above were unique ones of epithelium. To do so, KB cells (oral epithelial cells) were used for the same experiment as above. As a result, KB cells culture fluid had no influence on DSPP promoter activity (see
In a preferred embodiment of the present invention, proteomic analysis was performed to investigate what type of protein is contained in apical bud cells culture fluid. As a result, 113 proteins were identified (see
In a preferred embodiment of the present invention, the effect of periostin confirmed by western blotting on apical bud cells culture fluid was investigated. As a result, periostin-neutralization in apical bud cells culture fluid did not alter the effects of apical bud cells culture fluid on the odontoblast differentiation (see
Therefore, it was confirmed from the co-culture of ameloblasts, apical bud cells, or its culture fluid with odontoblasts that the expressions of DSPP and nestin were increased and at the same time the formations of DSP and type I collagen were increased as well. Moreover, apical bud cells culture fluid had the effect of inducing DSPP promoter activity, inducing dental pulp regeneration, and increasing calcium accumulation. Thus, the said ameloblasts, apical bud cells, or its culture fluid can be effectively used as an active ingredient for the composition for dentin or dental pulp regeneration.
To be applied to the medicine, the ameloblasts, apical bud cells, or its culture fluid of the present invention can additionally include one or more effective ingredients having the same or similar function to the ameloblasts, apical bud cells, or its culture fluid.
The ameloblasts, apical bud cells, or its culture fluid can be administered orally or parenterally and be used in general forms of pharmaceutical formulation. That is, the ameloblasts, apical bud cells, or its culture fluid of the present invention can be prepared for oral or parenteral administration by mixing with generally used diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents and surfactants. Solid formulations for oral administration are tablets, pills, powders, granules and capsules. These solid formulations are prepared by mixing the ameloblasts, apical bud cells, or its culture fluid of the present invention with one or more suitable excipients such as starch, calcium carbonate, sucrose or lactose, gelatin, etc. Except for the simple excipients, lubricants, for example magnesium stearate, talc, etc, can be used. Liquid formulations for oral administrations are suspensions, solutions, emulsions and syrups, and the above-mentioned formulations can contain various excipients such as wetting agents, sweeteners, aromatics and preservatives in addition to generally used simple diluents such as water and liquid paraffin. Formulations for parenteral administration are sterilized aqueous solutions, water-insoluble excipients, suspensions, emulsions, lyophilized preparations and suppositories. Water insoluble excipients and suspensions can contain, in addition to the active compound or compounds, propylene glycol, polyethylene glycol, vegetable oil like olive oil, injectable ester like ethylolate, etc. Suppositories can contain, in addition to the active compound or compounds, witepsol, macrogol, tween 61, cacao butter, laurin butter, glycerogelatin, etc.
The effective dosage of the ameloblasts, apical bud cells, or its culture fluid of the present invention can be determined according to weight, age, gender, health condition, diet, administration frequency, administration method, excretion and severity of a disease. The dosage is 0.001˜100 mg/kg per day, and preferably 0.1˜10 mg/kg per day, and administration frequency is preferably 1˜6 times a day.
The ameloblasts, apical bud cells, or its culture fluid of the present invention can be administered alone or together with surgical operation, radiotherapy, hormone therapy, chemotherapy and biological regulators.
The present invention also provides a method for promoting hard tissue formation containing the step of administering a pharmaceutically effective dose of ameloblasts, apical bud cells, or its culture fluid to a subject.
The present invention further provides a pharmaceutical composition for promoting hard tissue formation comprising ameloblasts or its culture fluid as an active ingredient.
The ameloblasts herein are preferably ameloblast-lineage cells, but not always limited thereto.
The present invention also provides a pharmaceutical composition for promoting hard tissue formation comprising apical bud cells or its culture fluid as an active ingredient.
The culture fluid herein is preferably the one cultured for 0-10 days from the beginning of differentiation, and more preferably the one cultured for 3-7 days, and most preferably cultured for 3 days.
The apical bud cells culture fluid herein is preferably prepared by the following steps, but not always limited hereto.
1) culturing mouse primary apical bud cells until reaching 90% of confluence;
2) culturing the cells in the medium supplemented with ascorbic acid and J-glycerophosphate;
3) collecting the medium after 3 days in culture;
4) filtering the medium; and
5) precipitating proteins in the medium, followed by eliminating salts therein.
In a preferred embodiment of the present invention, the effect of ameloblasts on the differentiation of osteoblasts was investigated. First, expression levels of Runx2, osterix, type I collagen, ALP and BSP, the genes involved in osteoblast differentiation, were measured by real-time PCR and western blotting. As a result, the expressions were all increased significantly. The effect of ameloblasts on the expressions of type collagen and osterix was also investigated. As a result, the expression levels of type I collagen and osterix were significantly increased in osteoblasts co-cultured with ameloblasts compared to the control (see
In a preferred embodiment of the present invention, to investigate the effects of apical bud cells culture fluid on hard tissue formation, dental pulp stem cells were mixed with HA/TCP and then transplanted into the subcutaneous tissues of nude mice. As a result, it was confirmed that apical bud cells culture fluid induced hard tissue formation (see
In a preferred embodiment of the present invention, immunohistochemistry was performed to investigate the characteristics of the hard tissue formed by apical bud cells culture fluid. As result, the hard tissue was confirmed to have bone characteristics by identifying BSP mainly expressed in bones (see
Therefore, it was confirmed that the ameloblasts, apical bud cells and their culture fluids could increase the expressions of Runx2 and osterix which are essential for osteoblast differentiation, increase the expression of type I collagen which is abundant in extracellular matrix approximately 2.5-fold compared to the control, and increase the expression of ALP approximately 7-fold. Particularly, apical bud cells culture fluid induced hard tissue formation and the hard tissue contained BSP, the matrix protein expressed mainly in bones, confirmed by immunohistochemistry. Thus, the said ameloblasts, apical bud cells, or its culture fluid can be effectively used as an active ingredient for a pharmaceutical composition for promoting hard tissue formation.
Practical and presently preferred embodiments of the present invention are illustrative as shown in the following Examples, Experimental Examples and Manufacturing Examples.
However, it will be appreciated that those skilled in the art, on consideration of this disclosure, may make modifications and improvements within the spirit and scope of the present invention.
Three cell lines cultured at 37° C. in a 5% CO2 humidified atmosphere were used in this invention. MDPC-23, the mouse odontoblast cell line, and MG63, the human osteoblast cell line, were grown and maintained in Dulbecco's Modified Eagle's Medium (Invitrogen) supplemented with 10% heat-inactivated fetal bovine serum. KB carcinoma cells, the human oral epithelial cells, were grown in MEM supplemented with 10% heat-inactivated fetal bovine serum.
The lower incisors were separated from anesthetized mice at postnatal day 7. Apical bud was enzymatically isolated therefrom by using a needle. The isolated tissue was cultured in DMEM/F12. Epithelial cells were isolated by treating trypsin at different concentrations. The isolated cells were cultured in keratinocyte serum-free medium (GIBCO-BRL, USA) until reaching confluence. After reaching confluence, the cells were cultured in DMEM supplemented with 10% heat-inactivated FBS.
Human dental pulp stem cells were isolated from the wisdom teeth of 10 adults (18-22 years of age) at the Seoul National University Dental Hospital. The experimental protocol was approved by the hospital's Institutional Review Board, and the patients provided informed consent. The isolation was performed according to the method of Jung H S et al (Jung H S, Lee D S, Lee J H, Park S J, Lee G, Seo B M, et al. Directing the differentiation of human dental follicle cells into cementoblasts and/or osteoblasts by a combination of HERS and pulp cells. J Mol. Histol. 2011; 42:227-35.). Briefly, the teeth were cracked and opened, and the pulp tissues were removed gently with forceps, minced into explants, and placed in 60 mm culture dishes. The explants were cultured in DMEM. To culture apical bud cells simultaneously with odontoblasts, dental pulp stem cells or osteoblasts, transwell dishes (3450-clear, Corning, USA) were used. Apical bud cells were cultured in the insert of the transwell dish, and odontoblasts, dental pulp stem cells or osteoblasts were cultured in the base of the dish, respectively. When confluence reached 80-90%, the insert was combined with the base, and differentiation was induced using differentiation medium supplemented with 50 mg/ml ascorbic acid and 10 mM β-glycerophosphate for 10 days (
Apical bud cells were seeded at the density of 7.5×105 cells on 100 mm dishes. When confluence reached 90%, the cells were cultured in differentiation medium supplemented with 50 mg/ml ascorbic acid and 10 mM 8-glycerophosphate. The day before differentiation was regarded as day 0. On day 0 and day 3, the cells were washed twice with PBS, and differentiation medium without FBS/EGF was added. The conditioned medium was collected three times at 8 hour intervals. After filtration using a 0.2-μm pore filter (Nalgene, USA), 200 ml of harvested conditioned medium was concentrated using ammonium sulfate (80 g) precipitation and dialyzed against PBS at a low temperature to remove salts.
To confirm the differentiation apical cells into ameloblasts, total RNA was extracted. cDNA was synthesized by using 2 μg of total RNA, 1 ul of reverse transcriptase, and 0.5 μg of oligo (dT). The synthesized cDNA was used for real-time PCR. Real-time PCR was performed on an ABI PRISM 7500 sequence detection system (Applied Biosystems) using SYBR GREEN PCR Master Mix (Takara, Japan). The PCR conditions were 94° C. for 1 min followed by 95° C. for 15 sec and 60° C. for 34 sec for 40 cycles. The relative differences in PCR results were calculated using the comparative cycle threshold (CT) method. Primer sequences are shown in Table 1.
As a result, as shown in
To investigate whether apical bud cells induce odontoblast differentiation, the following experiments were performed. DSPP, the noncollageneous protein playing an important role in dentin formation, is regarded as a specific marker of differentiated odontoblasts. So, the present inventors co-cultured odontoblasts with apical bud cells and analyzed the expression of DSPP by real time PCR and western blotting. Particularly, PCR and western blotting were performed as follows:
Total RNA was extracted from odontoblasts, dental pulp stem cells and osteoblasts with TRIzol reagent. cDNA was synthesized by using 2 μg of total RNA, 1 ul of reverse transcriptase, and 0.5 μg of oligo (dT). The synthesized cDNA was used for real-time PCR. Real-time PCR was performed on an ABI PRISM 7500 sequence detection system (Applied Biosystems) using SYBR GREEN PCR Master Mix (Takara, Japan). The PCR conditions were 94° C. for 1 min followed by 95° C. for 15 sec and 60° C. for 34 sec for 40 cycles. The relative differences in PCR results were calculated using the comparative cycle threshold (CT) method. Primer sequences are shown in Table 1.
As a result, as shown in
To isolate protein, cells were washed with PBS, followed by centrifugation at 1,000×g for 5 minutes at a low temperature. After removal of the supernatant, the pellet was resuspended in lysis buffer (100 mM Tris, pH 7.4, 350 mM NaCl, 10% glycerol, 1% Nonidet P-40, 1 mM EDTA, 1 mM dithiothreitol, 1× protease inhibitor) (SigmaAldrich, St. Louis, Mo., USA) and incubated for 15 min on ice. Cell debris was eliminated by centrifugation at 16,000×g for 15 minutes at a low temperature. Then, supernatant was obtained. 30 μg of protein was separated by electrophoresis and transferred onto a PVDF membrane. The membrane was blocked with 5% nonfat dry milk in PBS containing 0.1% Tween 20 (PES-T) and reacted with antibodies against DSP, BSP and type I collagen (1:1000). After washing, the membrane was incubated with anti-rabbit IgG conjugated with horseradish peroxidase (1:5000, Santa Cruz Biotechnology, USA) for 1 hr. Labeled protein bands were detected using an ECL system (enhanced chemiluminescence system) (Amersham Biosciences).
As a result, as shown in
To investigate whether apical bud cells induce dental pulp stem cells differentiation, dental pulp stem cells were co-cultured with apical bud cells, followed by real time PCR and Western blotting by the same manner as described in <Experimental Example 1>.
As a result, as shown in
The expressions of Runx2, osterix, type I collagen, ALP and BSP were investigated by real time PCR by the same manner as described in <1-1> and Western blotting by the same manner as described in <1-2>.
<3-1> Promotion of osteoblast differentiation confirmed by real time PCR
The expression levels of Runx2 and osterix, the transcription factors playing an essential role in osteoblast differentiation, increased in osteoblasts co-cultured with apical bud cells compared to control (
To investigate whether apical bud cells induce osteoblast differentiation, the expression of BSP, the gene involved in osteoblast differentiation, was investigated by Western blotting.
As a result, as shown in
To select the most effective apical bud cells culture fluid for odontoblast differentiation, the effects of various apical bud cells culture fluids (days 0, 3, and 7) on DSPP promoter activity in MDPC-23 cells were investigated by luciferase assay.
As a result, as shown in
Hereinbefore, it was confirmed that ameloblasts promoted odontoblast differentiation in vitro, and increased the expression of DSPP that was important for dentin formation. In this example, if the substance secreted by apical bud cells could affect DSPP promoter activity was investigated. Various apical bud cells culture fluids (days 0, 3, and 7) were prepared and used for the following experiments. Odontoblasts were seeded in a 24-well plate at the density of 5×104 cells/well. After 24 hours, the cells were transfected with Lipofectamine Plus™ reagent. For each transfection, 0.4 mg of pGL3 basic (control) and DSPP promoter were used. Transfected cells were treated with apical bud cells culture fluid or oral epithelial cells culture fluid for 48 hrS. Then, luciferase activity was measured with luminometer (FLUOStar, Germany).
As a result, as shown in
<5-1> Confirmation of Sternness of Dental Pulp Stem Cells (hDPSCs)
To ascertain the sternness of isolated hDPSCs by explant culture, immunofluorescence staining was performed.
Particularly, human dental pulp stem cells were fixed in 4% paraformaldehyde for 30 min at 4° C. After permeabilization with 0.15% Triton X-100/PBS, nonspecific binding of the antibodies was blocked using 2% bovine serum albumin. Cells were incubated with primary anti-CD44 (550538, BD Pharmigen, San Jose, Calif., USA) and STRO-1 antibodies (MAB1038, R&D Systems, Minneapolis, Minn., USA) for 16 hrS at 4° C. After primary antibody incubation, the cells were washed twice with PBS and incubated with a fluorescent labeled secondary anti-mouse antibody for 1 hr in the dark. DAPI was used to identify cell nuclei. After washing, samples were mounted and analyzed by fluorescent microscopy.
Isolated hDPSCs expressed both STRO-1 and CD-44. As a result, as shown in
Dental pulp stem cells are very useful material for dental tissue regeneration based on tissue engineering methods. Dental pulp stem cells are easily isolated from human wisdom teeth and can be differentiated into various cells (Mantesso A, Sharpe P, Dental stem cells for tooth regeneration and repair. Expert Opin Biol Ther. 2009 September; 9(9):1143-54). Many of previous reports showed that hard tissue could be formed by using dental pulp stem cells (Prescott, R. S.; Alsanea, R.; Fayad, M. I.; Johnson, B. R.; Wenckus, C. S.; Hao, J.; John, A. S.; George, A. In vivo generation of dental pulp-like tissue by using dental pulp stem cells, a collagen scaffold, and dentin matrix protein 1 after subcutaneous transplantation in mice. J. Endod., 2008, 34(4), 421-6; Huang, G. T.; Yamaza, T.; Shea, L. D.; Djouad, F.; Kuhn, N. Z.; Tuan, R. S.; Shi, S. Stem/Progenitor cell-mediated de novo regeneration of dental pulp with newly deposited continuous layer of dentin in an in vivo model. Tissue Eng Part A., 2010, 16(2), 605-15). Considering that apical bud cells culture fluid induced odontoblast differentiation, the present inventors tried to evaluate its effect in vivo. Dental pulp stem cells treated with or without concentrated apical bud cells culture fluid were mixed with HA/TCP, which were transplanted into the subcutaneous tissues of nude-mice. Twelve weeks later, the tissues were histologically observed. BMP-2 was used as a positive control, because it is well known that BMP-2 induces hard tissue formation of dental pulp stem cells.
As a result, as shown in
<5-3> Alizarin red S staining
To compare calcification, calcium accumulation was investigated by alizarin red S staining. Odontoblasts were seeded on 35-mm dishes and cultured in differentiation media for 2 weeks with or without apical bud cells culture fluid, followed by alizarin red S staining. On day 0, day 3, day 7, and day 10, each dish was washed three times with PBS and fixed in 4% paraformaldehyde (PFA). After fixing, the cells were washed three times with water, and stained with a 1% alizarin solution (Sigma Aldrich, St. Louis, Mo., USA) for 20 minutes. The excessive staining solution was washed off with water. The stained part was photographed by optical microscope and the density of the part was measured.
As shown in
<6-1> Promotion of Differentiation of Dental Pulp Stem Cells into Odontoblasts by Treatment of Apical Bud Cells Culture Fluid
To investigate if the treatment of apical bud cells culture fluid could promote the differentiation of dental pulp stem cells to odontoblasts, dental pulp stem cells (1.0×107 cells) were mixed with 100 mg hydroxyapatite/tricalcium phosphate (HA/TCP) ceramic powder (Zimmer Inc., Warsaw, Ind., USA) with or without 50 μg of apical bud cells culture fluid (PA-CM) and were then transplanted subcutaneously into nude-mice (NIH-bg-nu/nu-xid, Harlan Sprague Dawley, Indianapolis, Ind., USA). Samples were obtained after 6 and 12 weeks, respectively, fixed in 4% paraformaldehyde, and decalcified in a 10% ethylenediaminetetra-acetic acid (EDTA, pH 7.4) solution for a week. The samples were washed, dehydrated, and embedded in paraffin. The paraffin block was sectioned in 5 μm thickness, and the sections were stained with hematoxylin-eosin (H-E). For immunohistochemistry, the sections proceeded to deparaffin and hydration, followed by reaction with 0.6% H2O2/methanol for 20 minutes. After blocking with PBS containing 1% bovine serum albumin, the sections were reacted with DSP, BSP and human nuclei antibodies (1:100) at a low temperature. Secondary anti-rabbit IgG antibodies were incubated with the sections at room temperature for 30 min, which were then reacted with the avidin-biotin-peroxidase complex (Vector Laboratory, Burlingame, Canada). Signals were converted using a DAB kit (Vector Laboratory, Burlingame, Canada). The sections were washed, dehydrated and sealed, followed by observation under optical microscope. For scanning electron microscopy (SEM), samples were fixed in 0.1 M cacodylate buffer (pH 7.3) containing 2.5% glutaraldehyde for 30 min and in 0.1 M cacodylate buffer (pH 7.4) containing 1% osmium tetroxide for 1 hr. After rapid dehydration through an ethanol gradient, critical point drying, and sputter coating with gold, cells were observed by SEM (S-4700, HITACHI, Tokyo, Japan).
As a result, as shown in
To investigate the characteristics of hard tissue formed similarly to dentin-pulp complex, immunohistochemistry was used by the same manner as described in Example <6-1>. Anti-human nuclei antibody was used to confirm the origin of the hard tissue.
BSP and DSP are regarded as specific markers of osteoblast and odontoblast differentiation. DSP expression was observed weakly in the dental pulp stem cells only group (
However, negative control showed negative staining (
Apical bud cells culture fluid was treated to the general tooth-like environment where dental pulp exists. Thereafter, tissue formation was investigated.
As a result, as shown in
After eliminating dental pulp completely, human tooth was sliced, followed by sterilization. The sterilized tooth slices were treated with dental pulp stem cells (5.0×105) and with or without apical bud cells culture fluid (8 ug), which were transplanted subcutaneously into nude-mice (NIH-bg-nu/nu-xid, Harlan Sprague Dawley, Indianapolis, Ind., USA). Samples were obtained after 12 weeks, fixed in 4% paraformaldehyde, and decalcified in a 10% ethylenediaminetetra-acetic acid (EDTA, pH 7.4) solution for a week. The samples were washed, dehydrated, and embedded in paraffin. The paraffin block was sectioned in 5 um thickness, and the sections were stained with hematoxylin-eosin (H-E). To confirm histological characteristics, immunohistochemistry was performed using nestin antibody expressed in dentinal tubule and human specific h-nuclei antigen.
As a result, as shown in
As shown in
To investigate whether the newly formed hard tissue was originated from human dental pulp stem cells, genomic DNA was extracted from the cells isolated from sectioned slices. Human Alu sequence was amplified by using 2 ul of the extracted genomic DNA. As a positive control, 1.0 mg/mL human DNA was used, and 1.0 mg/mL nude mouse genomic DNA was used as a negative control. Human Alu sequence was amplified by PCR as follows; predenaturation at 94□ for 5 minutes, denaturation at 94° C. for 30 seconds, annealing at 58° C. for 30 seconds, polymerization at 72° C. for 45 seconds, 35 cycles from denaturation to polymerization. The PCR products were confirmed by electrophoresis performed on a 2% agarose gel. Primer sequences are shown in Table 1.
As a result, as shown in
To confirm whether the promotion effect of apical bud cells conditioned medium on odontoblast differentiation and hard tissue formation was attributed to BMP (bone morphogenetic protein) having the effect of promoting the differentiation of dental pulp stem cells and hard tissue formation, the present inventors blocked BMP activity in conditioned medium with a BMP antagonist, noggin and evaluated DSPP promoter activity.
As a result, there were no changes in DSPP promoter activity after the BMP antagonist treatment, suggesting that conditioned medium affects DSPP promoter activity by factors that are irrelevant to BMP (
As a result, as shown in
Periostin was identified in Example 10. Thus, it was further investigated if periostin played any part in apical bud cells culture fluid. The effect of periostin on odontoblast differentiation was investigated by using periostin-neutralized conditioned medium (PNSF).
As a result, as shown in
Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended Claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| KR10-2010-0127022 | Dec 2010 | KR | national |
| KR10-2011-0069292 | Jul 2011 | KR | national |
