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At least 343 records · Page 19Linked to original sources
PubMed1988

Phosphoprotein synthesis and secretion by odontoblasts in rat incisors as revealed by electron microscopic radioautography.

The secretory pathway of dentin phosphoproteins in rat incisors was studied by electron microscopic radioautography after the injection of 3H-serine, and the results were compared with those using 3H-proline as a tracer. Five min after injection of 3H-serine, radioactivity was found in the rough endoplasmic reticulum. At 10 min, silver grains were observed over the spherical portions of the cisface of the Golgi apparatus. At 20 min after injection, silver grains were seen over the cylindrical portions of the transface of the Golgi apparatus. The secretory granules showed the strongest reaction from 20 min to 1 hr. At 45 min, a significant labeled band appeared at the mineralization front. At 1 hr, the labeling at the mineralization front began to appear in the mineralized dentin, and after 12 hr this labeled band was located within the mineralized dentin. The pathway of 3H-proline was essentially the same as that of 3H-serine, but 3H-proline moved more slowly than 3H-serine, especially in transit from the rough endoplasmic reticulum to the Golgi apparatus. Secretory granules were heavily labeled from 30 min to 1 hr after injection of 3H-proline; no labeling was found at the mineralization front at 45 min. The labeling seen initially over the predentin was over the mineralized dentin no earlier than 6 hr after injection. The labeling pattern with 3H-serine is closely related to the localization of phosphoproteins, whereas the pattern with 3H-proline reflects the production of collagen rather than of phosphoproteins. The present radioautographic results indicate that dentin phosphoproteins are related to secretory granules and are secreted by odontoblasts at the mineralization front and also that phosphoproteins are involved in the process of mineralization of the circumpulpal dentin.

Animals↗
PubMed2005

Modulation of 1alpha,25-dihydroxyvitamin D3-membrane associated, rapid response steroid binding protein expression in mouse odontoblasts by 1alpha,25-(OH)2D3.

The rapid, nongenomic effects of 1alpha,25-dihydroxyvitamin D3 (1alpha,25-(OH)2D3 have been related to a 1,25D3-membrane associated, rapid response steroid binding protein or 1,25D3-[MARRS]bp, with a molecular weight of 65 kDa, in several tissues and species. Currently, no information is available concerning the nongenomic responses to 1alpha,25-(OH)2D3 in dental tissues. In order to investigate the expression of 1,25D3-[MARRS]bp in dental cells, in the presence or absence of 1alpha,25-(OH)2D3, we have used rabbit polyclonal antibodies directed against the N-terminus of the 1,25D3-[MARRS]bp (Ab099) that recognizes the 1alpha,25-(OH)2D3 binding protein in chick intestinal basolateral membranes and a mouse odontoblast-like cell line (MO6-G3). Western blotting and flow cytometric analyses with Ab099 specifically detected 1,25D3-[MARRS]bp in MO6-G3 cells. Moreover, 1,25D3-[MARRS]bp was up-regulated, in vivo, in differentiated dental cells. Electron microscopic analysis confirmed the plasma membrane localization of this binding protein and also showed its intracellular presence. Incubation of MO6-G3 cells with different doses of 1alpha,25-(OH)2D3 for 36 h resulted in an inhibition of 1,25D3-[MARRS]bp expression with a maximal effect at 50 nM steroid. In addition, the culture media of MO6-G3 cells contains immunoreactive 1,25D3-[MARRS]bp. Immunogold positive membrane vesicle-like structures are present in the extracellular matrix of MO6-G3 cells. Altogether, these results indicate that the 1,25D3-[MARRS]bp expression in MO6-G3 cells is modulated by 1alpha,25-(OH)2D3. In conclusion, this 1alpha,25-(OH)2D3 binding protein could play an important role in the rapid, nongenomic responses to 1alpha,25-(OH)2D3 in dental cells.

Animals↗
PubMed1983

Effects of denervation on 3H-fucose incorporation by odontoblasts in the mouse incisor.

The present study was designed to determine the effects of denervation on glycoprotein synthesis in the predentinal matrix of the mouse incisor. The inferior alveolar nerve (IAN), superior cervical ganglion (SCG) or both (IAN + SCG) were unilaterally resected in adult mice with the contralateral side remaining intact as a control. Fourteen days after surgery and 4 h prior to killing, 0.2 mCi of 3H-fucose was injected intravenously and mandibles were processed for standard histological and autoradiographic techniques. Silver halide grains were counted over the predentin matrix for 2000 micrometers per tooth. The results showed that the IAN and SCG resection affected 3H-fucose incorporation into the predentinal matrix; however, the highest absolute mean grain counts occurred after IAN + SCG resection. SCG resection increased the amount of 3H-fucose incorporated into the predentinal matrix by 48%, that of IAN by 24% and that of IAN + SCG by 14% as compared to contralateral controls. These data indicate a regulatory role for the nervous system and a possible interaction of neural components in the control of glycoprotein synthesis by odontoblasts in the mouse incisor.

Animals↗
PubMed1986

Type-I collagen production by human odontoblast-like cells in explants cultured on cyanoacrylate films. Electron-immunolocalization of fibronectin at cell/film interface.

Odontoblast-like cells derived from human tooth pulps were maintained in explant culture and grown either on glass coverslips only (used as control) or on glass coverslips coated with cyanoacrylate films. Ultrastructural and cyto-morphometric evidence showed that cells exposed to cyanoacrylate, in contrast to controls, display a significant decrease of rough endoplasmic reticulum and mitochondria. In addition, immunofluorescent staining and radioimmunoassays for type-I collagen suggested disturbances in production for the exposed cells. The use of anti-fibronectin antibodies with electron-microscopic immunoperoxidase-labelling demonstrated that the adherence of cells to cyanoacrylate can involve both adhesion plaques and fibronectin. These results therefore suggest that there were no apparent differences in the adhesion interaction of cells between glass and cyanoacrylate substrates.

Cell Adhesion↗
PubMed1989

Effect of tunicamycin on glycogen accumulation in the stratum intermedium and odontoblasts of rat incisor.

Repeated injection of rats with tunicamycin over two days induced a 1- to 5-fold increase in glycogen. This accumulation occurred in the stratum intermedium of the enamel organ and in young secretory odontoblasts. In rats injected over 3 days, the number of glycogen particles was at least 10 times larger than in control rats, and large glycogen accumulations were observed in the cytosol of these two groups of cells. These results were obtained by staining with periodic acid-thiocarbohydrazide and silver proteinate, a specific method for the detection of glycoconjugates containing vic-glycol groups. The existence of a relationship between these local cytosolic accumulations of glycogen and the developmental stage of certain groups of cells was shown by the changes that occurred in glycogen distribution. The present results suggest that the stratum intermedium supplies energy for precursor transport.

Animals↗
PubMed1993

The influence of fluoride on proteoglycan structure using a rat odontoblast in vitro system.

Using an in vitro rat incisor odontoblast system, the effect of fluoride on proteoglycans was investigated at both the metabolic and structural level. Incisors were removed from 4-week-old rats, split longitudinally, and the pulps removed. Teeth were incubated at 37 degrees C, 5% CO2 in Eagle's Minimum Essential Medium containing 35S-sulfate for 7 hours in the presence of 0 mM, 3 mM, or 6 mM sodium fluoride. Teeth were demineralized in EDTA, proteoglycan was extracted from the residue with 4 M guanidinium chloride, and further purified by anion exchange chromatography. Uptake of radiolabel was monitored by liquid scintillation counting. The resultant products were examined by cellulose acetate electrophoresis, SDS-PAGE, chondroitinase digestion, and amino acid analysis. Differential effects of fluoride were observed in both metabolism and biochemical characterization of proteoglycans following incubation at the two concentrations. Fluoride decreased uptake of the radiolabel but led to an accumulation of glycosaminoglycan within the proteoglycan of the matrix. Chondroitin sulfate was the predominant glycosaminoglycan identified, with the additional presence of dermatan sulfate and heparan sulfate identified. Dermatan sulfate levels increased in 3 mM-treated teeth. Fluoride-treated proteoglycans had a reduced molecular weight (200-90K to 180-79K); this reduction is primarily a result of smaller glycosaminoglycan chains, with limited reduction in the size of the core protein of 6 mM-treated teeth occurring. Such alterations in the biochemical metabolism and hence structure and function of proteoglycan may be implicated in the hypomineralization seen in fluorosis.

Amino Acids↗
PubMed1995

Extracellular processing of dentin matrix protein in the mineralizing odontoblast culture.

Odontoblasts that we prepared from bovine incisors produced a dentin-specific protein, phosphophoryn, and accumulated it in mineralized nodules. The time course of mineralization was detected by measuring osteocalcin and mineral in the nodules. The sequence of developmental expression of proteins in this mineralizing dentin cell culture is very similar to that in bone cells, suggesting a common mechanism for matrix mineralization in bone and dentin. Casein kinase II, which phosphorylates bone phosphoproteins and dentin phosphorylates bone phosphoproteins and dentin phosphophoryn, also emerges coinciding with the initiation of mineralization. Furthermore, we have detected extracellular phosphorylation by casein kinase II of a dentin protein of M(r) 60,000, which we recovered from the phosphophoryn fraction in CaCl2 precipitate.

Animals↗
PubMed1977

Qualitative electron probe analysis of secretory ameloblasts and odontoblasts in the rat incisor.

Rapidly frozen growing rat incisors were freeze fractured and freeze dried in preparation for energy dispersive X-ray emission microanalysis in a scanning electron microscope. Ca levels were found to be elevated in the distal cell body of odontoblasts, whereas Ca was uniformly low over all parts of the cell body of secretory ameloblasts. The results suggest fundamental differences in the mechanisms by which these two cell types process Ca, and that Ca possibly diffuses through the secretory ameloblast layer on its way to the enamel.

Ameloblasts↗
PubMed1977

A comparative study of alkaline phosphatase in calcifying cartilage, odontoblasts and the enamel organ.

The enzyme alkaline phosphatase (AP) (EC 3.1.3.1) in three different calcification areas was studied by means of a spectrophotometric micro method using p-nitrophenylphosphate as a substrate. Rat maxillary incisor odontoblasts and enamel organ from the zones of matrix formation and maturation and tissue from rabbit metatarsal cartilage were allowed to react with the substrate in glycine-NaOH buffer at room temperature. The reaction was found to be linear for a minimum of 20 min. The pH optima for AP from these tissues were in the pH range of 10.0-10.3. In order to compare AP from the four calcification areas different parameters were studied. Heating at 56 degrees C or 60 degrees C for varying times revealed that the enzymes were almost completely inactivated after 10 min. Mg2+ ions activated the enzymes by about 25% at concentrations of 2.5 mM (enamel organ 1.25 mM); while only higher concentrations of Mg2+ had an inactivating effect, Ca2+ and PO3-4 ions were inactivating at varying concentrations. F- ions showed no effect on AP activity at concentrations below 250 mM (enamel organ 125 mM) but caused inactivation of the enzymes at about 50% at 1 M. EDTA was found to be a very effective AP inactivator at concentrations above 0.06 mM, whereas urea did not noticeably affect the enzyme reactions at concentrations below 1 M. At higher concentrations, inactivation was observed. In order to determine AP localization in the epiphyseal plate successive 40-mum-thick, freeze-sectioned slices were analyzed. The activity was highest nearest the zone of cartilage calcification and decreased towards the reserve cell zone. It was concluded that the same AP isoenzyme is present in these quite different calcification loci.

Alkaline Phosphatase↗
PubMed1977

Cathepsin D activity in isolated odontoblasts.

The presence of an acid proteinase with a high activity has been demonstrated in isolated odontoblast-predentine material from dentinogenically active rat incisors. The enzyme was identified as cathepsin D (EC 3.4.23.5). The possible significance of the enzymatic degradation of proteoglycans and glycosaminoglycans in the course of the calcification process is discussed.

Animals↗
PubMed1981

ATP-dependent uptake of Ca2+ by a microsomal fraction from rat incisor odontoblasts.

Intracellular vesicles containing alkaline phosphatase and Ca2+-ATPase activity were isolated in the microsomal fraction from free-dissected odontoblasts of rat incisors. The microsomal fraction was incubated with 45Ca2+ to study Ca2+ uptake. ATP stimulated Ca2+ uptake, whereas little uptake occurred without ATP. The maximal effect was obtained with 3mM ATP. The ATP-dependent uptake was linear for 2 h. Increasing the pH up to pH 8.2 resulted in an increased uptake. Mg2+ was stimulatory with an optimal effect at a 6mM concentration. Increasing concentrations of Ca2+ up to 100 micrometer enhanced the uptake. A correlation between Ca2+ uptake and Ca2+-ATPase in intracellular vesicles as well as a possible function in the calcification process are discussed.

Animals↗
PubMed1979

Separation of odontoblast Ca2+-ATPase and alkaline phosphatase.

Ca2+-ATPase activity was solubilized, partly purified, and separated from nonspecific alkaline phosphatase activity (APase1) of dentinogenically active rat incisor odontoblasts. Attempts were made to extract the enzymes by various agents, such as Triton X-100, deoxycholate, butanol, EDTA, and buffers of decreasing ionic strength. Solubilization by butanol followed by extraction with low concentrations of EDTA proved to be most effective. Purification and separation were done by molecular sieve chromatography. Ca2+-ATPase showed no activity against p-nitrophenyl phosphate (p-NPP) or inorganic pyrophosphate (PPi) and was unaffected by R 8231 [+/-)-6(m-bromophenyl)-5,6-dihydroimidazo(2,1-b)thiazole oxalate]. It was activated by Ca2+ and Mg2+ ions in equimolar concentrations with the substrate. The enzyme was rapidly inactivated in the solubilized state. An apparent molecular weight of about 18,000 was obtained from molecular sieve data. APase, showing activity against ATP, PPi, and p-NPP, was virtually totally inhibited by R 8231. It was activated by Mg2+ ions but slightly reduced in activity by Ca2+ ions. It had an apparent mol. wt. of 79,000. The results provide direct evidence for earlier suggestions of the existence in hard tissue forming cells of two phosphatases active at alkaline pH.

Alkaline Phosphatase↗
PubMed1983

The effect of various fixatives on the extent of the odontoblast process in human dentine.

Unerupted but fully formed human third molar teeth were prepared for ultrastructural examination using three different fixatives; glutaraldehyde, a mixture of glutaraldehyde and p-formaldehyde and a picric acid-formaldehyde solution. These fixatives have reportedly differing rates of penetration of tissue. Odontoblast processes were found to be limited to the inner-third of crown dentine in all teeth, irrespective of the fixative used.

Adult↗
PubMed1984

A different approach to immersion fixation of human dental pulp and odontoblast processes.

A low-speed diamond-edge rotary saw microtome was used to prepare freshly extracted human teeth for fixation. The teeth were sliced transversely 900 microns thick using saline as a coolant; the slices were immersed in glutaraldehyde fixative within 10 min of tooth extraction. After flat-embedding in Araldite, sections were reduced to 70 microns thickness and examined with light microscopy. Selected areas were processed for electron microscopy. In the light microscope, the entire pulp appeared to be well fixed. Electron microscopy showed that the contents of most of the tubules near the predentine were well fixed and microfilaments and microtubules were present in odontoblast processes. The quality of fixation with this method was at least as good as other methods applicable to teeth with the advantage that the integrity of the entire dental pulp was preserved.

Adolescent↗
PubMed1984

Further evidence of an intravesicular Ca2+- pump in odontoblasts from rat incisors.

Intracellular vesicles containing alkaline phosphatases were isolated from isolated odontoblasts using several centrifugation techniques, gradient media and filtering procedures. With a combined centrifugation technique using 0.32 M sucrose layered on 1.23 M sucrose, a fraction containing alkaline phosphatases with a 36-40-fold increased specific activity was obtained. This fraction also revealed a high Ca2+-accumulating ability. The vesicle fraction was totally free from mitochondria but to some extent contaminated by lysosomes. Characteristics of Ca2+-uptake were obtained. The Ca2+-uptake was maximal at 37-40 degrees C whereas no Ca2+-accumulated at 4 degrees C. Temperatures above 40 degrees C strongly inhibited Ca2+-uptake. ATP was the most potent stimulator of Ca2+-uptake whereas ITP, GTP, CTP, ADP, PPi and AMP also promoted Ca2+-uptake. Cysteine, EDTA and Triton X-100 were inhibitory to Ca2+-uptake. A correlation between alkaline phosphatases in intracellular vesicles as well as their relation to extracellular matrix vesicles and to the mineralization process is suggested.

Alkaline Phosphatase↗
PubMed1985

Freeze-fracture electron microscopy of the nuclear envelope of the human odontoblast.

The nuclear envelope was studied in several planes on freeze-fracture replicas. The inner and outer nuclear membranes were similar. Each presented two fracture faces, one with a higher intra-membranous particle density than the other. The perinuclear cisterna was bounded by outer and inner nuclear membranes about 40 nm apart. The nuclear pores of 85 nm diameter were evenly distributed over the nuclei. The pore density (5/micron2) was low compared with that in many other cells, but was of the same magnitude as is reported for the rat odontoblast.

Adolescent↗
PubMed1988

Transmission electron microscopy of the human odontoblast process in peripheral root dentine.

Various methods of fixation were tried on dentine of 45 premolars from children. Two methods based on immediate or delayed use of liquid nitrogen, as well as a cryoprotector (10 per cent dimethylsulphoxid), gave the best results in transmission electron microscopy. Using these methods, the presence of an odontoblast process could be demonstrated in the inner, middle and peripheral human root dentine. The presence of unmyelinated nerve fibril in outer root dentine supports the hypothesis of direct neural stimulation in peripheral dentine.

Adolescent↗