RESUMEN
The present study was performed to examine how transforming growth factor ß (TGF-ß) in root-surrounding tissues on deciduous teeth regulates the differentiation induction into odontoclasts during physiological root resorption. We prepared root-surrounding tissues with (R) or without (N) physiological root resorption scraped off at three regions (R1-R3 or N1-N3) from the cervical area to the apical area of the tooth and measured both TGF-ß and the tartrate-resistant acid phosphatase (TRAP) activities. The TGF-ß activity level was increased in N1-N3, whereas the TRAP activity was increased in R2 and R3. In vitro experiments for the receptor activator of nuclear factor-κB (NF-κB) ligand (RANKL)-mediated osteoclast differentiation revealed that proteins from N1-N3 and R1-R3 enhanced the TRAP activity in RAW264 cells. A genetic study indicated that the mRNA levels of TGF-ß1 in N1 and N2 were significantly increased, and corresponded with levels of osteoprotegerin (OPG). In contrast, the expression level of RANKL was increased in R2 and R3. Our findings suggest that TGF-ß is closely related to the regulation of OPG induction and RANKL-mediated odontoclast differentiation depending on the timing of RANKL and OPG mRNA expression in the root-surrounding tissues of deciduous teeth during physiological root resorption.
Asunto(s)
Resorción Radicular , Diente Primario/metabolismo , Factor de Crecimiento Transformador beta/metabolismo , Animales , FN-kappa B/genética , FN-kappa B/metabolismo , Osteoclastos/metabolismo , Osteoprotegerina/genética , Osteoprotegerina/metabolismo , Ligando RANK/genética , Ligando RANK/metabolismo , Porcinos , Fosfatasa Ácida Tartratorresistente/genética , Fosfatasa Ácida Tartratorresistente/metabolismo , Diente Primario/citología , Diente Primario/fisiología , Factor de Crecimiento Transformador beta/genéticaRESUMEN
All-trans retinoic acid and bone morphogenetic protein 2 (BMP2) synergistically induced an alkaline phosphatase (ALP) activity, one of the osteoblastic differentiation markers, and promoted the extracellular matrix calcification in a myoblastic C2C12 cell culture system. The induced ALP mRNA was not suppressed in the presence of a protein synthesis inhibitor, suggesting that the de novo protein synthesis does not influence this induction. There are three isotypes for the retinoic acid receptor (RARα, RARß, RARγ). Both the ALP activity and the extracellular matrix calcification were inhibited by the addition of the specific siRNA for RARγ, but not by that for RARα or RARß. When the effects of the RAR subtype-specific agonists on the ALP activity in the presence of BMP2 were examined, the RARγ-specific agonist was the most effective. The ALP activity induced by any RAR subtype-specific agonist was inhibited by the addition of the specific siRNA for RARγ, but not by that for RARα or RARß. These results suggest that a RARγ-dependent functional crosstalk is present between the retinoic acid and BMP2 signaling to induce osteogenic transdifferentiation in myoblastic C2C12 cells.
Asunto(s)
Proteína Morfogenética Ósea 2/fisiología , Transdiferenciación Celular/efectos de los fármacos , Receptores de Ácido Retinoico/fisiología , Fosfatasa Alcalina/biosíntesis , Fosfatasa Alcalina/metabolismo , Animales , Calcificación Fisiológica/efectos de los fármacos , Línea Celular , Cicloheximida/farmacología , Regulación hacia Abajo , Sinergismo Farmacológico , Humanos , Ratones , Mioblastos/metabolismo , Osteoblastos/citología , Osteoblastos/fisiología , Inhibidores de la Síntesis de la Proteína/farmacología , ARN Interferente Pequeño/farmacología , Receptores de Ácido Retinoico/agonistas , Retinoides/farmacología , Tretinoina/farmacología , Receptor de Ácido Retinoico gammaRESUMEN
BACKGROUND: Enamel extracts are biologically active and capable of inducing osteogenesis and cementogenesis, but the specific molecules carrying these activities have not been ascertained. The purpose of this study was to identify osteogenic factors in porcine enamel extracts. METHODS: Enamel proteins were separated by size-exclusion chromatography into four fractions, which were tested for their osteogenic activity on osteoblast-like cells (ST2) and human periodontal ligament (HPDL) cells. RESULTS: Fraction 3 (Fr.3) and a transforming growth factor-beta 1 (TGF-beta1) control reduced alkaline phosphatase (ALP) activity in ST2 but enhanced ALP activity in HPDL cells. The enhanced ALP activity was blocked by anti-TGF-beta antibodies. Furthermore, using a dual-luciferase reporter assay, we demonstrated that Fr.3 can induce the promoter activity of the plasminogen activator inhibitor type 1 (PAI-1) gene. CONCLUSION: These results show that the osteoinductive activity of enamel extracts on HPDL cells is mediated by TGF-beta1.
Asunto(s)
Proteínas del Esmalte Dental/aislamiento & purificación , Factor de Crecimiento Transformador beta1/aislamiento & purificación , Fosfatasa Alcalina/efectos de los fármacos , Animales , Células Cultivadas , Proteínas del Esmalte Dental/farmacología , Humanos , Mitógenos/farmacología , Osteoblastos/efectos de los fármacos , Osteogénesis/efectos de los fármacos , Ligamento Periodontal/citología , Ligamento Periodontal/efectos de los fármacos , Inhibidor 1 de Activador Plasminogénico/genética , Regiones Promotoras Genéticas/efectos de los fármacos , Porcinos , Extractos de Tejidos , Factor de Crecimiento Transformador beta1/farmacologíaRESUMEN
Proteoglycans and their constituent glycosaminoglycan (GAG) have been proposed to be involved in the inhibition of mineralization in unmineralized tissue, predentin. Among the proteoglycans secreted by odontoblasts, we focused on the large chondroitin sulfate proteoglycan, versican, for its large binding capacity for calcium ions. The aims of this study were the determination of the full-length sequence and splicing variants of the porcine versican, and the detection of versican in the porcine predentin. The complete coding sequence of the porcine versican mRNA was cloned to be 11,775 nucleotides long and encode 3,924 amino acids, and four splicing variants, V0, V1, V2 and V3, were characterized in the isolated porcine cartilage cells. The number of potential GAG attachment sites was 15 in the V0 variant, 13 in the V1 variant, 2 in the V2 variant and 0 in the V3 variant. They were deposited in DDBJ. The V1 variant was determined by RT-PCR in the odontoblasts, dental papilla cells, dental follicle cells, periodontal ligament cells, dental pulp cells, and gingival cells of pigs, although a small amount of the V0 valiant was found in the dental papilla cells. The predentin was prepared from developing porcine permanent incisor tooth germs and its soluble proteins were extracted in order to be partially characterized by protein and proteinase profiles. The versican V1 cleavage products were detected in the predentin extract by Western blotting analysis. These results suggested that the versican splice variant V1 implicates both the control of the mineralization and the activities of the predentin metalloproteinases, because it has 13 GAG chains that bind a large amount of calcium.
RESUMEN
Dentin sialophosphoprotein (DSPP) is critical for proper mineralization of tooth dentin, and mutations in DSPP cause inherited dentin defects. Dentin phosphoprotein (DPP) is the C-terminal cleavage product of DSPP that binds collagen and induces intrafibrillar mineralization. We isolated DPP from individual pigs and determined that its N-terminal and C-terminal domains are glycosylated and that DPP averages 155 phosphates per molecule. Porcine DPP is unstable at low pH and high temperatures, and complexing with collagen improves its stability. Surprisingly, we observed DPP size variations on SDS-PAGE for DPP isolated from individual pigs. These variations are not caused by differences in proteolytic processing or degrees of phosphorylation or glycosylation, but rather to allelic variations in Dspp. Characterization of the DPP coding region identified 4 allelic variants. Among the 4 alleles, 27 sequence variations were identified, including 16 length polymorphisms ranging from 3 to 63 nucleotides. None of the length variations shifted the reading frame, and all localized to the highly redundant region of the DPP code. The 4 alleles encode DPP domains having 551, 575, 589, or 594 amino acids and completely explain the DPP size variations. DPP length variations are polymorphic and are not associated with dentin defects.
Asunto(s)
Dentina/metabolismo , Proteínas de la Matriz Extracelular/genética , Proteínas de la Matriz Extracelular/metabolismo , Polimorfismo Genético/genética , Alelos , Secuencia de Aminoácidos , Animales , Proteínas de la Matriz Extracelular/química , Glicosilación , Concentración de Iones de Hidrógeno , Datos de Secuencia Molecular , Fosforilación , Desnaturalización Proteica , Procesamiento Proteico-Postraduccional , Alineación de Secuencia , Porcinos , TemperaturaRESUMEN
The activities of two proteases--enamelysin (MMP-20) and kallikrein 4 (KLK4)--are necessary for dental enamel to achieve its high degree of mineralization. We hypothesize that the selected enamel protein cleavage products which accumulate in the secretory-stage enamel matrix do so because they are resistant to further cleavage by MMP-20. Later, they are degraded by KLK4. The 32-kDa enamelin is the only domain of the parent protein that accumulates in the deeper enamel. Our objective was to identify the cleavage sites of 32-kDa enamelin that are generated by proteolysis with MMP-20 and KLK4. Enamelysin, KLK4, the major amelogenin isoform (P173), and the 32-kDa enamelin were isolated from developing porcine enamel. P173 and the 32-kDa enamelin were incubated with MMP-20 or KLK4 for up to 48 h. Then, the 32-kDa enamelin digestion products were fractionated by reverse-phase high-performance liquid chromatography (RP-HPLC) and characterized by Edman sequencing, amino acid analysis, and mass spectrometry. Enamelysin cleaved the 32-kDa enamelin only after it was deglycosylated. Kallikrein 4 digestion of the 32-kDa enamelin generated nine major cleavage products, six of which were successfully characterized. After 12 h of digestion with KLK4, all of the 32-kDa enamelin had been cleaved, but some cleavage products persisted after 48 h of digestion.
Asunto(s)
Proteínas del Esmalte Dental/metabolismo , Calicreínas/metabolismo , Metaloproteinasas de la Matriz/metabolismo , Amelogénesis/fisiología , Amelogenina , Animales , Western Blotting , Cromatografía Líquida de Alta Presión/métodos , Esmalte Dental/enzimología , Esmalte Dental/metabolismo , Proteínas del Esmalte Dental/análisis , Electroforesis en Gel de Poliacrilamida , Espectrometría de Masas , Metaloproteinasa 20 de la Matriz , Péptido-N4-(N-acetil-beta-glucosaminil) Asparagina Amidasa/metabolismo , Isoformas de Proteínas/análisis , Análisis de Secuencia de Proteína , Porcinos , Factores de Tiempo , Calcificación de Dientes/fisiologíaRESUMEN
The purpose of this study was to identify the periodontal regeneration factors of enamel protein extracts that induce cementum and bone regeneration in vivo. Cementum regeneration, one aspect of periodontal ligament regeneration, was examined using a buccal dehiscence model of dogs. Enamel matrix protein fractions were prepared from developing porcine incisors. Cementum-regeneration activity was found to reside in a protein aggregate composed of amelogenins and sheath proteins extracted from newly formed secretory enamel. Cementum-regeneration activity was not observed in protein fractions containing only amelogenin or its derivatives. The sheath proteins were purified to homogeneity and tested for alkaline phosphatase (ALP)-inducing activity on human periodontal ligament (HPDL) cells. The induction of ALP was observed following application of the 17-kDa sheath protein but not of the lower-molecular-weight sheath proteins. Although transforming growth factor-beta1 also shows ALP-inducing activity, contamination with growth factors was excluded because synthetic peptides (based on the sheath protein's sequence) also showed ALP-inducing activity. The 17-kDa sheath protein showed both cytodifferentiation and cementum-regeneration activity, but it is unclear whether its cementum-regeneration activity is derived from its ALP-inducing activity on HPDL cells.
Asunto(s)
Proteínas del Esmalte Dental/uso terapéutico , Ligamento Periodontal/efectos de los fármacos , Regeneración/efectos de los fármacos , Fosfatasa Alcalina/efectos de los fármacos , Pérdida de Hueso Alveolar/tratamiento farmacológico , Amelogenina , Animales , Regeneración Ósea/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Células Cultivadas , Cemento Dental/efectos de los fármacos , Esmalte Dental/química , Proteínas del Esmalte Dental/aislamiento & purificación , Modelos Animales de Enfermedad , Perros , Humanos , Porcinos , Extractos de Tejidos , Germen Dentario/química , Factor de Crecimiento Transformador beta/farmacología , Factor de Crecimiento Transformador beta1RESUMEN
Dentin sialophosphoprotein (DSPP) is a major secretory product of odontoblasts and is critical for proper tooth dentin formation. During dentinogenesis, DSPP is proteolytically cleaved into smaller subunits. These cleavages are proposed activation steps, and failure to make these cleavages is a potential cause of developmental tooth defects. We tested the hypothesis that dentin-resident matrix metalloproteinases catalyze the cleavages that process DSPP. We defined the exact DSPP cleavages that are catalyzed by proteases during crown formation by isolating DSPP-derived proteins from developing porcine molars and characterizing their N-terminal sequences and apparent size on SDS-PAGE and Western blots. The in vivo DSPP cleavage sites were on the N-terminal sides of Thr(200), Ser(330), Val(353), Leu(360), Ile(362), Ser(377), Ser(408), and Asp(458). The initial DSPP cleavage is between dentin glycoprotein (DGP) and dentin phosphoprotein (DPP), generating dentin sialoprotein (DSP)/DGP and DPP. Gelatin and casein zymograms identified MMP-2, MMP-20, and KLK4 in the dentin extracts. MMP-2 and MMP-20 were purified from over 150 g of porcine dentin powder and incubated with DSP-DGP and DPP. These enzymes show no activity in further cleaving DPP. MMP-20 cleaves DSP-DGP to generate DSP and DGP. MMP-20 also cleaves DSP at multiple sites, releasing N-terminal DSP cleavage products ranging in size from 25 to 38 kDa. MMP-2 makes multiple cleavages near the DSP C terminus, releasing larger forms of DGP, or "extended DGPs." Exact correspondence between DSPP cleavage sites that occur in vivo and those generated in vitro demonstrates that MMP-2 and MMP-20 process DSPP into smaller subunits in the dentin matrix during odontogenesis.
Asunto(s)
Metaloproteinasa 20 de la Matriz/metabolismo , Metaloproteinasa 2 de la Matriz/metabolismo , Sialoglicoproteínas/metabolismo , Secuencia de Aminoácidos , Animales , Sitios de Unión , Western Blotting , Catálisis , Electroforesis en Gel de Poliacrilamida , Datos de Secuencia Molecular , PorcinosRESUMEN
Dentin sialophosphoprotein (DSPP) is a major secretory product of odontoblasts and is critical for proper dentin formation. DSPP is believed to be processed into only two structural/functional domains: dentin sialoprotein (DSP) and dentin phosphoprotein (DPP). Here we report the isolation and characterization of a third domain of DSPP, designated dentin glycoprotein (DGP). DGP was isolated from a guanidine/EDTA extract of porcine tooth dentin by ion exchange, hydroxyapatite affinity, size exclusion, and RP-HPL chromatography. Endoproteinase lysine C digestion products of DGP were characterized by Edman sequencing and mass spectrometry. The porcine DGP backbone is the 81-amino acid segment of DSPP (Ser392 to Gly472) between the DSP and DPP domains. DGP has four phosphorylated serine residues (Ser453, Ser455, Ser457, and Ser462) and one glycosylated asparagine (Asn397). There are no other post-translational modifications. DGP is a stains-all positive protein with an apparent molecular mass on SDS-PAGE of 19 kDa, which is reduced by glycopeptidase A digestion to 16 kDa. A variety of glycans can be linked to Asn397. All are complex biantennary structures with a common N-linked pentasaccharide core (mannose3-N-acetylglucosamine2), most with a fucosyl residue on the innermost N-acetylglucosamine. The alpha1-3 and alpha1-6 arms are always galactose beta1-4 N-acetylglucosamine beta1-2 mannose, and either or both arms can be unsialidated or monosialidated. The calculated monoisotopic molecular masses of the different glycosylated forms of the DGP phosphoprotein are: unsialidated 10,523 and 10,670, monosialidated 10,815 and 10,961, and disialidated 11,106, and 11,252 Da, with the disialidated forms being the most abundant.
Asunto(s)
Sialoglicoproteínas/química , Sialoglicoproteínas/fisiología , Acetilglucosamina/química , Secuencia de Aminoácidos , Aminoácidos/química , Animales , Asparagina/química , Secuencia de Carbohidratos , Carbohidratos/química , Cromatografía , Cromatografía Líquida de Alta Presión , Cromatografía por Intercambio Iónico , Durapatita/química , Durapatita/farmacología , Ácido Edético/química , Electroforesis en Gel Bidimensional , Electroforesis en Gel de Poliacrilamida , Glucosa/química , Guanidina/química , Iones , Manosa/química , Espectrometría de Masas , Metaloendopeptidasas/química , Datos de Secuencia Molecular , FN-kappa B/metabolismo , Oligosacáridos/química , Oxígeno/metabolismo , Péptido-N4-(N-acetil-beta-glucosaminil) Asparagina Amidasa/química , Fosfoproteínas/química , Polisacáridos/química , Unión Proteica , Conformación Proteica , Estructura Terciaria de Proteína , Proteínas Recombinantes de Fusión/química , Homología de Secuencia de Aminoácido , Relación Estructura-Actividad , Porcinos , Factores de Tiempo , Diente/embriologíaRESUMEN
Dentin sialoprotein (DSP) is a glycoprotein that is critical for proper tooth dentin formation, but little is known about the nature of its carbohydrate attachments and other post-translational modifications. We have isolated DSP from pig dentin and demonstrate that it is a proteoglycan. Polyclonal antibodies were raised in chicken against recombinant pig DSP, and used to identify native DSP in fractions of tooth dentin proteins extracted from developing pig molars. Amino acid analyses and characterization of lysylendopeptidase cleavage products confirmed that the purified protein was DSP, and that Arg391 is at the DSP C terminus. On SDS-PAGE and on urea gels, DSP appeared as a smear extending from 280 to 100 kDa, but in the presence of beta-mercaptoethanol the top of the DSP smear disappeared. The high molecular weight material was likely comprised of covalent DSP dimers connected by a disulfide bridge at Cys205. Oligosaccharides were released from DSP following N- and O-linked glycosidase digestions, but these digestions had little effect on the apparent molecular weight of DSP on SDS-PAGE, when compared with the significant reduction following chondroitinase ABC digestion. Glycosaminoglycanases with assorted glycosaminoglycan (GAG) cleavage specificities coupled with Western analyses of the cleaved GAG "stubs" demonstrated that the DSP GAG attachments contain chondroitin 6-sulfate, but not keratan sulfate, heparan sulfate, chondroitin, or chondroitin 4-sulfate. DSP binds biotin-labeled hyaluronic acid, and such binding is inhibited by the addition of unlabeled hyaluronic acid. We conclude that DSP is a proteoglycan and that GAG attachments are the predominant structural feature of porcine DSP.
Asunto(s)
Sulfatos de Condroitina/análisis , Glicosaminoglicanos/análisis , Glicosaminoglicanos/química , Proteoglicanos/química , Sialoglicoproteínas/química , Porcinos , Secuencia de Aminoácidos , Animales , Sulfatos de Condroitina/química , Dimerización , Proteínas de la Matriz Extracelular , Glicósido Hidrolasas/metabolismo , Glicosilación , Humanos , Ácido Hialurónico/metabolismo , Ratones , Datos de Secuencia Molecular , Peso Molecular , Fosfoproteínas , Precursores de Proteínas , Estructura Cuaternaria de Proteína , Proteoglicanos/genética , Proteoglicanos/aislamiento & purificación , Proteoglicanos/metabolismo , Ratas , Sialoglicoproteínas/genética , Sialoglicoproteínas/aislamiento & purificación , Sialoglicoproteínas/metabolismo , Porcinos/genéticaRESUMEN
OBJECTIVES: It has been shown that Emdogain (EMD) containing enamel matrix derivative has cementum- and osteo-promotive activities in vivo and in vitro. Nevertheless, the commercial sale of EMD was halted because it has some possible risk for infectiosity. At present, Emdogain Gel (Emd-Gel) containing the EMD heated to avoid the infectiosity is commercially available. The purpose of this study was to compare the in vitro bioactivities of Emd-Gel and EMD. MATERIAL AND METHODS: Healthy human periodontal ligament (HPDL) cells were used to study the effect of Emd-Gel and EMD on cell differentiation. The HPDL cells exposed to Emd-Gel and EMD were evaluated for the following effects: (i) alkaline phosphatase (ALP) activity; (ii) mitogenic (MTT) assay; (iii) biomineralization activity; (iv) gene expressions using reverse transcription-polymerase chain reaction (RT-PCR). The effect of EMD with or without heat treatment was examined for ALP activity on the cell differentiation. RESULTS: The effect of Emd-Gel on ALP activity was greater than that of EMD. It was confirmed from the effect of EMD with heat treatment at 60 degrees C, 80 degrees C and 100 degrees C on the ALP activity. The effect of Emd-Gel on the biomineralization activity was also greater than that of the EMD. The Emd-Gel has a stronger effect for the expression of osteoblast-like phenotype than the EMD. CONCLUSION: The results indicate that the Emd-Gel has greater bioactivities than the EMD in vitro.
Asunto(s)
Proteínas del Esmalte Dental/farmacología , Ligamento Periodontal/efectos de los fármacos , Alginatos/química , Fosfatasa Alcalina/efectos de los fármacos , Calcificación Fisiológica/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , División Celular/efectos de los fármacos , Células Cultivadas , Colorantes , Proteínas del Esmalte Dental/química , Electroforesis en Gel de Poliacrilamida , Geles , Regulación de la Expresión Génica/efectos de los fármacos , Calor , Humanos , Mitógenos/farmacología , Osteoblastos/efectos de los fármacos , Osteoblastos/metabolismo , Ligamento Periodontal/citología , Fenotipo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Sales de Tetrazolio , TiazolesRESUMEN
Dentin sialophosphoprotein (DSPP) is a chimeric glycoprotein with dentin sialoprotein (DSP) on its N-terminus and dentin phosphoprotein (DPP) on its C-terminus. We have constructed and screened a unidirectional cDNA library derived from the pulp organ of developing pig teeth, and isolated cDNA clones encoding DSP-only, as well as two DSPP clones with alternative sequences in their 3' coding regions. The DSP-only transcript has an open reading frame of 386 codons, and is generated through the use of a polyadenylation signal within intron 4, immediately following the DSP coding region. the use of this polyadenylation signal deletes the DPP coding region and places a TGA translation termination signal as the fourth codon following the exon 4-encoded segment. The DSPP cDNAs contain open reading frames of 593 and 600 codons. Northern blots hybridized to radiolabeled DSP probes showed bands at 1.4, 2.5, 4.4, and 4.8 kb. Cloning and characterization of reverse transcriptase polymerase chain reaction products confirmed the existence of mRNA encoding pDSP386, pDSPP593, and pDSPP600in vivo, but also suggested that DNA sequence redundancies in the DSPP coding region make it prone to cloning artifacts.