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1.
J Periodontal Res ; 53(5): 727-735, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-29732558

RESUMEN

BACKGROUND AND OBJECTIVE: Growth factors are frequently incorporated into scaffolds to promote periodontal regeneration but many currently used scaffolds do not encourage cell migration towards the dentogingival junction. We examined the proliferation and migration of human gingival fibroblasts in a novel, physically robust, collagen-Vicryl™ membrane loaded with fibronectin (FN) and/or insulin-like growth factor (IGF-I). Biocompatibility of the membranes was evaluated in rat dorsal skin. MATERIAL AND METHODS: Chemotaxis was examined in Boyden chambers and cell migration by confocal imaging of membranes, which were fabricated from rat tail type I collagen with embedded Vicryl knitted mesh, IGF-I (50, 100 ng/mL) and FN (10 µg/mL). Membranes (Vicryl alone, collagen+Vicryl, collagen+Vicryl+IGF-I, collagen+Vicryl+FN') were implanted subcutaneously in 8 rats and were evaluated by histomorphometry after 7 and 14 days. RESULTS: IGF-I (50 or 100 ng/mL) promoted chemotaxis compared with vehicle controls (P = .02, P = .001, respectively). IGF-I did not affect cell proliferation. Incorporation of FN retarded time-dependent release of IGF-I from collagen gels. Three dimensional confocal microscopy imaging of cell migration through collagen+Vicryl membranes showed enhanced migration in the IGF+FN group compared to all other groups at 8, 10 and 14 days (P < .05). In a rat skin model, implanted membranes were surrounded by thin collagen capsules and mild inflammatory infiltrates. CONCLUSION: Incorporation of FN into IGF-I-loaded collagen+Vicryl membranes reduced IGF release from collagen and increased the migration of human gingival fibroblasts. The new membrane may promote healing and reformation of the dentogingival junction.


Asunto(s)
Movimiento Celular/efectos de los fármacos , Colágeno/farmacología , Fibroblastos/efectos de los fármacos , Membranas Artificiales , Adulto , Animales , Materiales Biocompatibles/farmacología , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Quimiotaxis/fisiología , Fibronectinas/farmacología , Humanos , Factor I del Crecimiento Similar a la Insulina/farmacología , Masculino , Microscopía Confocal , Permeabilidad , Poliglactina 910/farmacología , Ratas , Ratas Sprague-Dawley
2.
J Dent Res ; 84(12): 1127-32, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16304441

RESUMEN

We aimed to analyze the differential gene expression in various murine dental tissues, expecting to find novel factors that are involved in tooth formation. We here describe the identification of a novel ameloblast-specific gene, amelotin (AMTN), by differential display polymerase chain-reaction (DD-PCR) analysis of microdissected ameloblasts, odontoblasts, dental pulp, and alveolar bone cells of 10-day-old mouse incisors. The conceptually translated protein sequence was unique and showed significant homology only with its human orthologue. The amelotin genes from mouse and human displayed a similar exon-intron structure and were expressed from loci on chromosomes 5 and 4, respectively, which have been associated with various forms of amelogenesis imperfecta. Expression of amelotin mRNA was restricted to maturation-stage ameloblasts in developing murine molars and incisors. Amelotin protein was efficiently secreted from transfected cells in culture. Taken together, our findings suggest that amelotin is a novel factor produced by ameloblasts that plays a critical role in the formation of dental enamel.


Asunto(s)
Ameloblastos/metabolismo , Proteínas del Esmalte Dental/análisis , Proceso Alveolar/citología , Proceso Alveolar/metabolismo , Amelogénesis/genética , Animales , Cromosomas Humanos Par 4/genética , Proteínas del Esmalte Dental/genética , Pulpa Dental/citología , Pulpa Dental/metabolismo , Exones/genética , Humanos , Intrones/genética , Ratones , Odontoblastos/metabolismo , Odontogénesis/genética , Reacción en Cadena de la Polimerasa/métodos , Homología de Secuencia
3.
J Dent Res ; 94(5): 697-705, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25715379

RESUMEN

Amelotin (AMTN) is a relatively recently discovered enamel protein that is predominantly expressed by ameloblasts during the maturation stage of amelogenesis and is present at lower levels in the junctional epithelium of erupted teeth. Previous studies have suggested a function of this protein in enamel mineralization and cell attachment. Genetic mouse models have been instrumental in defining the role of many enamel-related proteins, but a genetic mouse model lacking the Amtn gene has not been reported. Here, we describe the generation of amelotin-deficient mice and the analysis of their enamel phenotype in comparison with that of wild-type animals. Ablation of AMTN expression resulted in mechanically inferior enamel of mandibular incisors that showed chipping and fractures at the incisal edge. Enamel mineralization was delayed, resulting in hypomineralized inner enamel and structural defects in the outer enamel. Erupted enamel close to the gingival margin showed increased surface roughness. The expression levels of the enamel matrix proteins AMEL, AMBN, ENAM, and ODAM and the enamel proteases MMP-20 and KLK-4 were not significantly altered, although the expression of KLK-4 was delayed. The morphology of ameloblasts showing prominent Tomes' processes during the secretory stage was not altered, and there was no indication of disruption of cell structures or activities, but a residual layer, presumably consisting of organic material, remained at the enamel surface close to the gingival margin. The integrity of the dentogingival attachment at the junctional epithelium appeared unaffected by AMTN deficiency. These observations indicate that AMTN plays a subtle yet critical role in enamel biomineralization, particularly during the establishment of the outer and surface enamel layers. This role appears to be largely independent of other enamel proteins.


Asunto(s)
Hipoplasia del Esmalte Dental/genética , Proteínas del Esmalte Dental/genética , Ameloblastos/patología , Amelogénesis/genética , Amelogenina/análisis , Animales , Adhesión Celular/fisiología , Esmalte Dental/ultraestructura , Hipoplasia del Esmalte Dental/patología , Proteínas del Esmalte Dental/análisis , Inserción Epitelial/patología , Encía/patología , Péptidos y Proteínas de Señalización Intracelular , Calicreínas/análisis , Metaloproteinasa 20 de la Matriz/análisis , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos , Ratones Transgénicos , Microscopía Electrónica de Transmisión , Fenotipo , Proteínas/análisis , Calcificación de Dientes/genética
4.
Clin Exp Metastasis ; 18(3): 253-60, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11315099

RESUMEN

Bone sialoprotein (BSP) and osteopontin (OPN) are prominent, mineral-associated proteins in the extracellular matrix of bone that have been implicated in the metastatic activity of cancer cells. The expression of BSP, which is normally restricted to mineralizing tissues, has been observed in cancers with a high propensity for forming bone metastases. To investigate the relationship between BSP expression and the formation of bone metastases we have conducted an initial study of the expression of BSP in 10 intraductal breast carcinoma bone metastases using immunostaining and in situ hybridization, and compared the expression with OPN. The metastases were characterized by the infiltration of tumour cells into bone with extensive bone resorption evident. Moderate to strong staining for BSP was observed in all (100%) carcinomas, which also expressed BSP mRNA as determined by in situ hybridization. Variable staining for BSP was also observed in the mineralized bone and expression of BSP mRNA could be observed in osteoblastic cells on the bone surface and in some osteocytes at sites of bone remodelling. Contrary to a previous report, BSP expression could be demonstrated by PCR in three breast cancer cell lines, MCF-7, T47-D and MDA-MB-231. Moreover, in sub-cutaneous tumours formed by MDA-MB-231 breast cancer cells injected into athymic mice, higher immunostaining for BSP was seen in large ulcerating tumours in which mineral deposits were formed. In contrast to BSP, staining for OPN in bone metastases was generally restricted to the interface between tumor cells and bone surface of the carcinomas. While OPN staining was also observed in the cytoplasm of osteoclasts, which showed strong hybridization to a digoxygenin-labelled OPN cRNA probe, expression of OPN was not clearly detectable in the tumour cells. These studies provide the first demonstration of BSP expression by tumour cells in bone metastases and support the concept that BSP may have a role in targeting metastatic cells to bone. Expression of OPN in bone metastases appears to be related to increased bone resorptive activity by osteoclasts.


Asunto(s)
Neoplasias Óseas/metabolismo , Neoplasias Óseas/secundario , Neoplasias de la Mama/patología , Sialoglicoproteínas/metabolismo , Animales , Humanos , Inmunohistoquímica , Hibridación in Situ , Ratones , Ratones Desnudos , Osteopontina , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Células Tumorales Cultivadas
5.
J Med Chem ; 33(9): 2635-40, 1990 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-2391702

RESUMEN

A number of 1-(omega-aminoalkyl)-5-hydroxy-2-(4-hydroxyphenyl)indoles were synthesized and studied for their binding affinities for the calf uterine estrogen receptor and estrogen antagonistic activities. Highest binding affinities were found with derivatives bearing a methyl group in position 3 and a hexamethylene chain between the indole and amino nitrogen atoms. Values for relative binding affinity (RBA) are between 20 and 30 for derivatives 5b, 5c, 5f, and 5h (17 beta-estradiol = 100). In the mouse uterine weight test, no significant agonistic (estrogenic) activity was observed up to a daily dose of 125 micrograms/animal, except for derivatives 5c, 5j, and 5l. 2-Phenylindoles with amino (5b), pyrrolidino (5f), piperidino (5h), and morpholino (5k) groups as the amino function completely suppressed estrone-stimulated uterine growth as a dose of 125 micrograms/animal (100% antagonism). Therefore, these derivatives can be considered as first examples of nonsteroidal pure antiestrogens.


Asunto(s)
Antagonistas de Estrógenos/síntesis química , Indoles/síntesis química , Aminas/síntesis química , Aminas/metabolismo , Aminas/farmacología , Animales , Sitios de Unión , Bovinos , Fenómenos Químicos , Química , Antagonistas de Estrógenos/metabolismo , Antagonistas de Estrógenos/farmacología , Femenino , Indoles/metabolismo , Indoles/farmacología , Ratones , Morfolinas/síntesis química , Morfolinas/metabolismo , Morfolinas/farmacología , Piperidinas/síntesis química , Piperidinas/metabolismo , Piperidinas/farmacología , Pirrolidinas/síntesis química , Pirrolidinas/metabolismo , Pirrolidinas/farmacología , Receptores de Estrógenos/efectos de los fármacos , Receptores de Estrógenos/metabolismo , Relación Estructura-Actividad , Útero/efectos de los fármacos
6.
J Endocrinol ; 167(1): 183-95, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11018766

RESUMEN

Aryl hydrocarbon receptor (AhR) ligands are environmental contaminants found in cigarette smoke and other sources of air pollution. The prototypical compound is TCDD (2,3,7, 8-tetrachlorodibenzo-p-dioxin), also known as dioxin. There is an increasing body of knowledge linking cigarette smoking to osteoporosis and periodontal disease, but the direct effects of smoke-associated aryl hydrocarbons on bone are not well understood. Through the use of resveratrol (3,5,4'-trihydroxystilbene), a plant antifungal compound that we have recently demonstrated to be a pure AhR antagonist, we have investigated the effects of TCDD on osteogenesis. It was postulated that TCDD would inhibit osteogenesis in bone-forming cultures and that this inhibition would be antagonized by resveratrol. We employed the chicken periosteal osteogenesis (CPO) model, which has been shown to form bone in vitro in a pattern morphologically and biochemically similar to that seen in vivo, as well as a rat stromal cell bone nodule formation model. In the CPO model, alkaline phosphatase (AP) activity was reduced by up to 50% (P<0.01 vs control) in the presence of 10(-9) M TCDD and these effects were reversed by 10(-6) M resveratrol (P<0.05 vs TCDD alone). TCDD-mediated inhibition of osteogenesis was restricted primarily to the osteoblastic differentiation phase (days 0-2) as later addition did not appear to have any effects. Message levels for important bone-associated proteins (in the CPO model) such as collagen type I, osteopontin, bone sialoprotein and AP were inhibited by TCDD, an effect that was antagonized by resveratrol. Similar findings were obtained using the rat stromal bone cell line. TCDD (at concentrations as low as 10(-10)M) caused an approximately 33% reduction in AP activity, which was abrogated by 3. 5x10(-7) M resveratrol. TCDD also induced a marked reduction in mineralization ( approximately 75%) which was completely antagonized by resveratrol. These data suggest that AhR ligands inhibit osteogenesis probably through inhibition of osteodifferentiation and that this effect can be antagonized by resveratrol. Since high levels of AhR ligands are found in cigarette smoke, and further since smoking is an important risk factor in both osteoporosis and periodontal disease, it may be postulated that AhR ligands are the component of cigarette smoke linking smoking to osteoporosis and periodontal disease. If so, resveratrol could prove to be a promising preventive or therapeutic agent for smoking-related bone loss.


Asunto(s)
Inhibidores Enzimáticos/farmacología , Osteogénesis/efectos de los fármacos , Dibenzodioxinas Policloradas/antagonistas & inhibidores , Receptores de Hidrocarburo de Aril/antagonistas & inhibidores , Estilbenos/farmacología , Fosfatasa Alcalina/metabolismo , Animales , Biomarcadores/análisis , Células de la Médula Ósea/efectos de los fármacos , Calcificación Fisiológica/efectos de los fármacos , Técnicas de Cultivo de Célula , Diferenciación Celular/efectos de los fármacos , Embrión de Pollo , Colágeno/biosíntesis , Dibenzodioxinas Policloradas/metabolismo , Dibenzodioxinas Policloradas/farmacología , Ratas , Resveratrol , Estilbenos/metabolismo
7.
J Dent Res ; 82(12): 1002-7, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14630903

RESUMEN

Tooth development is mediated by sequential and reciprocal interactions between dental epithelium and mesenchyme under the molecular control of secreted growth factors and responsive transcription factors. We have previously identified the transcription factor Krox-26 as a potential regulator of tooth formation in mice. The purpose of this study was to investigate a potentially similar role for the human KROX-26 orthologue. We cloned the KROX-26 gene and found its single mRNA transcript (2.4 kb) to be expressed in multiple adult tissues. During fetal development, KROX-26 is expressed in the epithelial component of the developing tooth organ during early bud and cap stages as well as in osteoblasts of craniofacial bone and the developing tongue. The KROX-26 gene was mapped to chromosome 10q11.21, a locus that has been associated with permanent tooth agenesis (He-Zhao deficiency). These results indicate a potential function for KROX-26 in the molecular regulation of tooth formation in humans.


Asunto(s)
Anodoncia/genética , Mapeo Cromosómico , Proteínas de Unión al ADN/genética , Odontogénesis/fisiología , Factores de Transcripción/genética , Dedos de Zinc/genética , Adulto , Cromosomas Humanos Par 10/genética , Epitelio/metabolismo , Humanos , Osteoblastos/metabolismo , ARN Mensajero/genética , Cráneo/embriología , Lengua/embriología , Germen Dentario/embriología , Germen Dentario/metabolismo
8.
Arch Oral Biol ; 45(7): 551-62, 2000 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10785518

RESUMEN

The expression of bone sialoprotein (BSP) is normally restricted to mineralized connective tissues of bones and teeth where it has been associated with mineral crystal formation. However, recent studies have revealed ectopic expression of BSP in various lesions, including oral and extraoral carcinomas, in which it has been associated with the formation of microcrystalline deposits and the metastasis of cancer cells to bone. To develop a model to study the induction of BSP in carcinoma development, BSP expression in squamous-cell carcinomas induced by chemical carcinogen in the hamster cheek-pouch epithelium was investigated. Hamster BSP cDNA was first isolated and characterized, then used to prepare probes for Northern and in situ hybridization. The protein sequence of hamster BSP displayed 86% amino acid identity with a consensus mammalian BSP sequence and retained polyglutamate sequences, the RGD sequence and sites of phosphorylation, glycosylation and sulphation. The tissue-specific expression of hamster BSP mRNA and protein was confirmed by in situ hybridization and immunolocalization in developing tissues. Squamous-cell carcinomas induced in the buccal pouches of 5-week-old male Syrian golden hamsters treated with chemical carcinogen had BSP mRNA and BSP in the proliferating neoplastic epithelium. In contrast, neither BSP mRNA nor the protein could be detected in the stroma within which islands of the transformed tissue had formed. Thus, the hamster cheek pouch is a well-characterized model that can be used to study the induced expression of BSP in association with the development of squamous-cell carcinomas.


Asunto(s)
Huesos/metabolismo , Carcinoma de Células Escamosas/metabolismo , Regulación de la Expresión Génica/fisiología , Mucosa Bucal/metabolismo , Neoplasias de la Boca/metabolismo , Sialoglicoproteínas/metabolismo , Diente/metabolismo , 9,10-Dimetil-1,2-benzantraceno , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Carcinógenos , Carcinoma de Células Escamosas/inducido químicamente , Carcinoma de Células Escamosas/genética , Transformación Celular Neoplásica/inducido químicamente , Transformación Celular Neoplásica/genética , Transformación Celular Neoplásica/metabolismo , Mejilla , Cricetinae , Modelos Animales de Enfermedad , Sialoproteína de Unión a Integrina , Masculino , Mesocricetus , Datos de Secuencia Molecular , Neoplasias de la Boca/inducido químicamente , Neoplasias de la Boca/genética , Distribución Aleatoria , Sialoglicoproteínas/genética
9.
Eur J Biochem ; 217(1): 275-80, 1993 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-7693461

RESUMEN

Soluble ependymins from the predominant protein constituents in the cerebrospinal fluid from many orders of teleost fish. Furthermore, these glycoproteins also exist in a bound form associated with the extracellular matrix. Ependymins are synthesized in meningeal fibroblasts. In goldfish, their synthesis is increased during the regeneration of the optic nerve and they share several characteristics with molecules involved in cell contact phenomena. In this study, we show by a calcium overlay technique that ependymins from goldfish and rainbow trout are able to bind 45Ca2+. However, nearly all of this Ca(2+)-binding capacity is lost after digestion with sialidase. Furthermore, circular-dichroism spectra from FPLC-purified rainbow trout ependymins have been recorded in the presence and absence of Ca2+. Below 250 nm, the CD spectrum showed a characteristic minimum of ellipticity at 217 nm typical of beta structures. This signal is independent of the Ca2+ concentration. In contrast, the complex signal at 250-310 nm mainly decreased with increasing Ca2+ concentration indicating changes in the environment of aromatic side chains.


Asunto(s)
Calcio/metabolismo , Carpa Dorada/metabolismo , Proteínas del Tejido Nervioso/metabolismo , Oncorhynchus mykiss/metabolismo , Ácidos Siálicos/metabolismo , Animales , Antígenos CD/análisis , Antígenos de Diferenciación de Linfocitos T/análisis , Antígenos CD57 , Proteínas del Tejido Nervioso/química , Proteínas del Tejido Nervioso/inmunología , Conformación Proteica , Ácidos Siálicos/análisis
10.
Crit Rev Oral Biol Med ; 11(3): 279-303, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11021631

RESUMEN

Osteopontin (OPN) is a highly phosphorylated sialoprotein that is a prominent component of the mineralized extracellular matrices of bones and teeth. OPN is characterized by the presence of a polyaspartic acid sequence and sites of Ser/Thr phosphorylation that mediate hydroxyapatite binding, and a highly conserved RGD motif that mediates cell attachment/signaling. Expression of OPN in a variety of tissues indicates a multiplicity of functions that involve one or more of these conserved motifs. While the lack of a clear phenotype in OPN "knockout" mice has not established a definitive role for OPN in any tissue, recent studies have provided some novel and intriguing insights into the versatility of this enigmatic protein in diverse biological events, including developmental processes, wound healing, immunological responses, tumorigenesis, bone resorption, and calcification. The ability of OPN to stimulate cell activity through multiple receptors linked to several interactive signaling pathways can account for much of the functional diversity. In this review, we discuss the structural features of OPN that relate to its function in the formation, remodeling, and maintenance of bones and teeth.


Asunto(s)
Sialoglicoproteínas , Secuencia de Aminoácidos , Animales , Remodelación Ósea , Adhesión Celular , Regulación de la Expresión Génica , Humanos , Datos de Secuencia Molecular , Odontogénesis , Osteopontina , Estructura Secundaria de Proteína , Sialoglicoproteínas/química , Sialoglicoproteínas/genética , Sialoglicoproteínas/fisiología , Transducción de Señal , Relación Estructura-Actividad , Distribución Tisular
11.
J Biol Chem ; 276(21): 18282-9, 2001 May 25.
Artículo en Inglés | MEDLINE | ID: mdl-11278774

RESUMEN

Osteogenic differentiation involves a cascade of coordinated gene expression that regulates cell proliferation and matrix protein formation in a defined temporo-spatial manner. Here we have used differential display to identify a novel zinc finger transcription factor (AJ18) that is induced during differentiation of bone cells in vitro and in vivo. The 64-kDa protein, encoded by a 7- kilobase mRNA, contains a Krüppel-associated box (KRAB) domain followed by 11 successive C(2)H(2) zinc finger motifs. AJ18 mRNA, which is also expressed in kidney and brain, is developmentally regulated in embryonic tibiae and calvariae, with little expression in neonate and adult animals. During osteogenic differentiation in vitro AJ18 mRNA is expressed as cells approach confluence and declines as bone formation occurs. Using bacterially expressed, His-tagged AJ18 in a target detection assay, we identified a consensus binding sequence of 5'-CCACA-3', which forms part of the consensus element for Runx2, a master gene for osteogenic differentiation. Overexpression of AJ18 suppressed Runx2-mediated transactivation of an osteocalcin promoter construct in transient transfection assays and reduced alkaline phosphatase activity in bone morphogenetic protein-induced C3H10T1/2 cells. These studies, therefore, have identified a novel zinc finger transcription factor in bone that can modulate Runx2 activity and osteogenic differentiation.


Asunto(s)
Desarrollo Óseo , Proteínas de Unión al ADN , Proteínas de Neoplasias , Proteínas Represoras , Factores de Transcripción/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Subunidad alfa 1 del Factor de Unión al Sitio Principal , Datos de Secuencia Molecular , Ratas , Alineación de Secuencia , Análisis de Secuencia , Factores de Transcripción/metabolismo , Dedos de Zinc
12.
J Mol Evol ; 36(6): 578-85, 1993 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-8350351

RESUMEN

Ependymins represent the predominant protein constituents in the cerebrospinal fluid of many teleost fish and they are synthesized in meningeal fibroblasts. Here, we present the ependymin sequences from the herring (Clupea harengus) and the pike (Esox lucius). A comparison of ependymin homologous sequences from three different orders of teleost fish (Salmoniformes, Cypriniformes, and Clupeiformes) revealed the highest similarity between Clupeiformes and Cypriniformes. This result is unexpected because it does not reflect current systematics, in which Clupeiformes belong to a separate infradivision (Clupeomorpha) than Salmoniformes and Cypriniformes (Euteleostei). Furthermore, in Salmoniformes the evolutionary rate of ependymins seems to be accelerated mainly on the protein level. However, considering these inconstant rates, neither neighbor-joining trees nor DNA parsimony methods gave any indication that a separate euteleost infradivision exists.


Asunto(s)
Proteínas del Líquido Cefalorraquídeo/genética , Peces/clasificación , Proteínas del Tejido Nervioso/genética , Salmonidae/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cipriniformes/clasificación , Cipriniformes/genética , ADN/genética , Peces/líquido cefalorraquídeo , Peces/genética , Genes , Datos de Secuencia Molecular , Proteínas del Tejido Nervioso/líquido cefalorraquídeo , Filogenia , Reacción en Cadena de la Polimerasa , Salmonidae/líquido cefalorraquídeo , Salmonidae/clasificación , Alineación de Secuencia , Homología de Secuencia , Especificidad de la Especie
13.
Crit Rev Oral Biol Med ; 10(1): 79-98, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10759428

RESUMEN

The search for a protein nucleator of hydroxyapatite crystal formation has been a focus for the isolation and characterization of the major non-collagenous proteins in bone. Of the proteins characterized to date, bone sialoprotein (BSP) has emerged as the only bona fide candidate for nucleation. BSP is a highly glycosylated and sulphated phosphoprotein that is found almost exclusively in mineralized connective tissues. Characteristically, polyglutamic acid and arginine-glycine-aspartate (RGD) motifs with the ability to bind hydroxyapatite and cell-surface integrins, respectively, have been conserved in the protein sequence. Expression of the BSP gene, which is induced in newly formed osteoblasts, is up-regulated by hormones and cytokines that promote bone formation and down-regulated by factors that suppress bone formation. Thus, BSP has the biophysical and chemical properties of a nucleator, and its temporo-spatial expression coincides with de novo mineralization in bone and cementum. Moreover, BSP has been associated with mineral crystal formation in several pathologies, including breast carcinomas. However, the ability of BSP to mediate cell attachment and to signal through the RGD motif points to alternate functions for BSP which need further investigation. In combination, the hydroxyapatite-binding polyglutamic acid sequences and the RGD provide bi-functional entities through which BSP may mediate the targeting and attachment of normal and metastasizing cells to the bone surface.


Asunto(s)
Durapatita/química , Sialoglicoproteínas/fisiología , Secuencia de Aminoácidos , Animales , Adhesión Celular , Cristalización , Regulación de la Expresión Génica , Humanos , Sialoproteína de Unión a Integrina , Datos de Secuencia Molecular , Proteínas de Neoplasias , Sialoglicoproteínas/química , Sialoglicoproteínas/genética , Sialoglicoproteínas/metabolismo
14.
Biochem Cell Biol ; 79(6): 737-46, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11800014

RESUMEN

Bone sialoprotein (BSP) and osteopontin (OPN) are sulphated and phosphorylated sialoglycoproteins that regulate the formation of hydroxyapatite crystals during de novo bone formation. To gain insights into the relationship between the synthesis and posttranslational modification of BSP and OPN and the mineralization of bone, pulse-chase studies were conducted on cultures of newly forming bone nodules produced by fetal rat calvarial cells in vitro. Cultures were pulse labelled with 35SO4, or with either 32PO4 or [gamma-32P]ATP to study intracellular and extracellular phosphorylation, respectively, and chased in isotope-free medium for various times up to 24 h. The presence of radiolabelled BSP and OPN was determined in the cells, in culture medium, and in various tissue compartments obtained by dissociative extraction with 4 M GuHCl (G1), 0.5 M EDTA (E), and again with 4 M GuHCl (G2) and a bacterial collagenase digestion of the demineralized collagenous tissue residue. With each isotope employed, radiolabelled BSP and OPN were detected in the E extract within the 1-h chase period and increased in amount with time. Similarly, 35SO4- and 32PO4-labelled BSP increased in the G2 extract, but OPN was not detected. In the G1 extract the 35SO4-labelled BSP decreased with chase time, whereas the 32PO4-labelled BSP increased. No differences were evident in the profiles of BSP labelled with 32PO4 or [gamma-32P]ATP. In the absence of beta-glycerophosphate, which is required for optimal mineralization of the bone nodules, 35SO4-labelled BSP was increased in the medium and G1 extract and decreased in the E extract and G2 extract after 3 h. In addition to differences in the tissue compartmentalization of BSP and OPN, these studies indicate that 35SO4 is lost from BSP during mineralization and that isoforms of BSP exist with a selective affinity for the organic and mineral phases. Moreover, the additional phosphorylation of BSP and OPN catalyzed by ectokinase activity does not appear to alter the distribution of these sialoproteins.


Asunto(s)
Desarrollo Óseo/fisiología , Procesamiento Proteico-Postraduccional/fisiología , Sialoglicoproteínas/biosíntesis , Animales , Calcificación Fisiológica/fisiología , Células Cultivadas , Sialoproteína de Unión a Integrina , Osteopontina , Radioisótopos de Fósforo/metabolismo , Fosforilación , Ratas , Sialoglicoproteínas/metabolismo , Cráneo , Radioisótopos de Azufre/metabolismo
15.
J Biol Chem ; 276(17): 14100-9, 2001 Apr 27.
Artículo en Inglés | MEDLINE | ID: mdl-11278659

RESUMEN

The immunosuppressant cyclosporin A (CsA) markedly inhibits collagen degradation by an intracellular phagocytic pathway in fibroblasts, an effect that can lead to massive gingival overgrowth. We used a collagen bead model of collagen phagocytosis to determine whether CsA inhibits internalization by blocking efflux of calcium from endoplasmic reticulum (ER) and mitochondrial calcium stores. CsA caused dose-dependent inhibition of phagocytosis of collagen-coated (but not bovine serum albumin-coated) beads. Chelation of intracellular Ca(2+) with BAPTA/AM or inhibition of Ca(2+)-ATPase of ER stores with thapsigargin reduced collagen bead phagocytosis. Measurement of intracellular calcium by ratio fluorometry showed increases in response to collagen-coated beads. Preincubation with CsA or thapsigargin caused a >3-fold decrease in intracellular calcium elevations in response to stimulation with collagen beads. Direct measurements of Ca(2+) in mitochondrial and ER stores showed that CsA only slightly inhibited collagen bead-induced discharge of calcium from mitochondria, but almost completely blocked discharge from ER stores. We reduced the numbers of mitochondria with chronic ethidium bromide treatment to test for the importance of ER/mitochondrial interactions. In these cells, CsA delayed collagen bead-induced calcium discharge from mitochondria. Collectively, these data indicate that CsA inhibits collagen phagocytosis by blocking calcium release from ER stores and may perturb functional interactions between the ER and mitochondria that regulate calcium stores.


Asunto(s)
Colágeno/metabolismo , Ciclosporina/farmacología , Animales , Sitios de Unión , Western Blotting , Calcio/metabolismo , Células Cultivadas , Quelantes/farmacología , Relación Dosis-Respuesta a Droga , Ácido Egtácico/análogos & derivados , Ácido Egtácico/farmacología , Retículo Endoplásmico/metabolismo , Inhibidores Enzimáticos/farmacología , Fibroblastos/metabolismo , Citometría de Flujo , Humanos , Cinética , Potenciales de la Membrana , Mitocondrias/metabolismo , Fagocitosis/efectos de los fármacos , Ratas , Albúmina Sérica Bovina/metabolismo , Transducción de Señal , Temperatura , Tapsigargina/farmacología , Factores de Tiempo
16.
J Biol Chem ; 276(34): 31969-77, 2001 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-11423540

RESUMEN

Cells in mechanically active environments can activate cytoprotective mechanisms to maintain membrane integrity in the face of potentially lethal applied forces. Cytoprotection may be mediated by expression of membrane-associated cytoskeletal proteins including filamin A, an actin-binding protein that increases the rigidity of the subcortical actin cytoskeleton. In this study, we tested the hypotheses that applied forces induce the expression of filamin A specifically and that this putative protective response inhibits cell death. Magnetically generated forces were applied to protein-coated magnetite beads bound to human gingival fibroblasts, cells with constitutively low basal levels of filamin A mRNA and protein. Forces applied through collagen or fibronectin, but not bovine serum albumin or poly-l-lysine-coated beads, increased mRNA and protein content of filamin A by 3-7-fold. Forces had no effect on the expression of other filamin isotypes or other cytoskeletal proteins. This effect was dependent on the duration of force and was blocked by anti-beta(1) integrin antibodies. Force also stimulated a 60% increase in expression of luciferase under the control of a filamin A promoter in transiently transfected Rat2 fibroblasts and was dependent on Sp1 transcription factor binding sites located immediately upstream of the transcription start site. Experiments with actinomycin D-treated cells showed that the increased filamin A expression after force application was due in part to prolongation of mRNA half-life. Antisense filamin oligonucleotides blocked force-induced filamin A expression and increased cell death by >2-fold above controls. The force-induced regulation of filamin A was dependent on intact actin filaments. We conclude that cells from mechanically active environments can couple diverse signals from forces applied through beta-integrins to up-regulate the production of cytoprotective cytoskeletal proteins, typified by filamin A.


Asunto(s)
Proteínas Contráctiles/biosíntesis , Encía/citología , Integrina beta1/metabolismo , Proteínas de Microfilamentos/biosíntesis , Animales , Secuencia de Bases , Células Cultivadas , Proteínas Contráctiles/genética , Cartilla de ADN , Fibroblastos/citología , Fibroblastos/metabolismo , Filaminas , Encía/metabolismo , Humanos , Proteínas de Microfilamentos/genética , Regiones Promotoras Genéticas , Ratas , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Factor de Transcripción Sp1/metabolismo
17.
Proc Natl Acad Sci U S A ; 101(35): 12969-73, 2004 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-15317945

RESUMEN

B7-H3, a member of the B7 family of the Ig superfamily proteins, is expressed on the surface of the antigen-presenting cells and down-regulates T cell functions by engaging an unknown counterreceptor on T cells. Although B7-H3 is ubiquitously expressed, its potential nonimmune functions have not been addressed. We found that B7-H3 is highly expressed in developing bones during embryogenesis and that its expression increases as osteoblast precursor cells differentiate into mature osteoblasts. In vitro bone formation by osteoblastic cells was inhibited when B7-H3 function was interrupted by the soluble recombinant protein B7-H3-Fc. Analysis of calvarial cells derived from neonatal B7-H3 knockout (KO) mice revealed normal numbers of osteoblast precursor cells possessing a normal proliferative capacity. However, the B7-H3-deficient calvarial cells exhibited impaired osteogenic differentiation, resulting in decreased mineralized bone formation in vitro. These results suggest that B7-H3 is required for the later phase of osteoblast differentiation. Although B7-H3 KO mice had no gross skeletal abnormalities, they displayed a lower bone mineral density in cortical (but not trabecular) bones compared with WT controls. Consistent with the reduced bone mineral density, the femurs of B7-H3 KO mice were more susceptible to bone fracture compared with those of WT mice. Taken together, these results indicate that B7-H3 and its unknown counterreceptor play a positive regulatory role in bone formation. In addition, our findings identified B7-H3 as another molecule that has a dual role in the bone-immune interface.


Asunto(s)
Antígeno B7-1/fisiología , Huesos/fisiología , Diferenciación Celular/fisiología , Osteoblastos/fisiología , Animales , Antígenos B7 , Antígeno B7-1/genética , Antígeno B7-1/inmunología , Huesos/inmunología , Diferenciación Celular/inmunología , Femenino , Masculino , Ratones , Ratones Noqueados , Osteoblastos/inmunología
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