RESUMEN

p27BBP/eIF6 is an evolutionarily conserved regulator of ribosomal function. It is necessary for 60S biogenesis and impedes improper joining of 40S and 60S subunits, regulated by protein kinase C or Efl1p. No data on p27BBP/eIF6 during early development of Metazoa are available. We studied the distribution, post-translational changes and association with the cytoskeleton of p27BBP/ eIF6 during Xenopus oogenesis and early development. Results indicate that p27BBP/eIF6 is present throughout oogenesis, partly associated with 60S subunits, partly free and with little cytoskeleton bound. During prophase I, p27BBP/eIF6 is detected as a single band of 27-kDa. Upon maturation induced by progesterone or protein kinase C, a serine-phosphorylated 29 kDa isoform appears and is kept throughout development to the neurula stage. Confocal microscopy showed that the distribution of p27BBP/eIF6 and its association with the cytoskeleton varies according to oogenesis stages. Briefly, in stage 6 oocytes, p27BBP/eIF6 has a limited dot-like distribution, and does not co-localize with cytokeratin, whereas upon maturation it spreads throughout the cytoplasm. After fertilization, a large fraction coalesces around cytomembranes and a cytochalasin B-sensitive co-localization with cytokeratin occurs. RNAse removes p27BBP/eIF6 from the cytokeratin fibres. Developmental data suggest a role of p27BBP/eIF6 in controlling ribosomal availability or regulating cross-talk between ribosomes and the cytoskeleton.

Asunto(s)

Proteínas Portadoras/metabolismo , Citoesqueleto/metabolismo , Proteínas de Filamentos Intermediarios/metabolismo , Oogénesis , Proteínas de Xenopus/metabolismo , Animales , Western Blotting , Proteínas Portadoras/química , Electroforesis en Gel de Poliacrilamida , Factores Eucarióticos de Iniciación , Femenino , Inmunohistoquímica , Proteínas de Filamentos Intermediarios/química , Masculino , Meiosis , Microscopía Confocal , Peso Molecular , Oocitos/efectos de los fármacos , Oocitos/crecimiento & desarrollo , Oocitos/metabolismo , Monoéster Fosfórico Hidrolasas/metabolismo , Fosforilación , Fosfoserina/metabolismo , Progesterona/farmacología , Unión Proteica , Ribosomas/metabolismo , Factores de Tiempo , Proteínas de Xenopus/química , Xenopus laevis , Cigoto/metabolismo

RESUMEN

This work describes the different patterns of expression of integrins and extracellular matrix proteins in normal and transformed mucosa in laryngeal and oropharyngeal carcinomas. Samples from each tumor group were sectioned and examined by immunohistochemistry using monoclonal antibodies raised against integrin chains (alpha2, alpha3, alpha6, beta1 and beta4) and their ligands (laminins 1 and 5, collagen type IV and two fibronectin isoforms: ED-A and ED-B). Controls were provided by samples of tumor-free laryngeal and oropharyngeal mucosa that had been removed during the surgical procedure. We found that the known distinct topographical pattern of integrins and the continuity of basement membrane components was altered in both groups but that the extent of changes was significantly more marked in oropharyngeal tumors, which are known to be more infiltrating and diffusive and to have a bad prognosis. These molecular patterns of expression can be used as an additional prognostic factor as they suggest a greater biological tumor aggressiveness of oropharyngeal tumors. We suggest that performing immunohistochemical analysis on biopsy samples may help in selecting the correct therapeutic strategy for these tumors and enable more accurate follow-up. The above-mentioned molecules may become part of the diagnostic toolbox of head and neck surgical pathologists.

Asunto(s)

Biomarcadores/análisis , Carcinoma de Células Escamosas/diagnóstico , Proteínas de la Matriz Extracelular/análisis , Integrinas/análisis , Neoplasias Laríngeas/diagnóstico , Neoplasias Orofaríngeas/diagnóstico , Carcinoma de Células Escamosas/patología , Humanos , Inmunohistoquímica , Neoplasias Laríngeas/patología , Ligandos , Invasividad Neoplásica , Neoplasias Orofaríngeas/patología

RESUMEN

The inhibitor of apoptosis protein survivin has been implicated in both cell cycle control and apoptosis resistance. To discriminate between these different roles, we used transgenic expression of survivin in the skin as a model for cell proliferation, differentiation, and apoptosis. Transgenic mice expressing survivin under the control of a keratin-14 promoter developed normally, without histologic abnormalities of the skin or hair, epidermal hyperplasia, or developmental abnormalities of basal or suprabasal epidermis. Keratinocyte proliferation assessed under basal conditions, or after ultraviolet-B (UVB) irradiation, or phorbol ester stimulation was unchanged in survivin transgenic mice. In contrast, survivin expression inhibited UVB-induced apoptosis in vitro and in vivo (i.e., sunburn cell formation), whereas it did not affect Fas-induced cell death. When crossed with p53 knockout mice, transgenic expression of survivin in a p53(+/-) background substituted for the loss of a second p53 allele and further inhibited UVB-induced apoptosis. These data provide the first in vivo evidence that survivin inhibits apoptosis and suggest that this pathway may oppose the elimination of cancerous cells by p53.

Asunto(s)

Apoptosis , Proteínas Cromosómicas no Histona/metabolismo , Queratinocitos/citología , Proteínas Asociadas a Microtúbulos , Proteína p53 Supresora de Tumor/metabolismo , Animales , Proteínas Cromosómicas no Histona/genética , Expresión Génica , Humanos , Proteínas Inhibidoras de la Apoptosis , Queratina-14 , Queratinas/genética , Ratones , Ratones Noqueados , Ratones Transgénicos , Proteínas de Neoplasias , Fenotipo , Regiones Promotoras Genéticas , Piel/citología , Piel/metabolismo , Survivin , Proteína p53 Supresora de Tumor/genética , Rayos Ultravioleta

RESUMEN

The ITGB4BP gene encodes for a highly conserved protein, named p27BBP (also known as eIF6), originally identified in mammals as a cytoplasmic interactor of beta4 integrin. In vitro and in vivo studies demonstrated that p27BBP is essential for cell viability and has a primary function in the biogenesis of the 60S ribosomal subunit. Here we report the genomic organization of the human ITGB4BP gene and show that its gene product is expressed with features of a housekeeping element in vitro, but is regulated in a cell specific fashion in vivo. The human gene spans 10 kb and comprises seven exons and six introns. The 5' flanking region shows a TATA-less promoter, canonical CpG islands, and binding sites for serum responsive elements. In cultured cells, p27BBP mRNA and protein are constitutively expressed and stable. A gradual loss of p27BBP mRNA can be observed only after prolonged serum starvation, and heat shock treatment. In contrast, p27BBP mRNA and protein levels in vivo are variable among different organs. More strikingly, immunohistochemical analysis shows that the p27BBP protein is present in a cell specific fashion, even within the same tissue. Taken together, these data show that ITGB4BP gene expression is highly regulated in vivo, possibly by the combination of tissue specific factors and protein synthesis pathways.

Asunto(s)

Proteínas Portadoras/genética , Genes/genética , Proteínas de Filamentos Intermediarios/genética , Secuencia de Aminoácidos , Secuencia de Bases , Northern Blotting , Proteínas Portadoras/metabolismo , ADN/química , ADN/genética , Factores Eucarióticos de Iniciación , Exones , Regulación de la Expresión Génica , Humanos , Proteínas de Filamentos Intermediarios/metabolismo , Intrones , Datos de Secuencia Molecular , Regiones Promotoras Genéticas , ARN Mensajero/genética , ARN Mensajero/metabolismo , Análisis de Secuencia de ADN , Distribución Tisular , Células Tumorales Cultivadas

RESUMEN

BACKGROUND: Signal transduction by mesangial cell (MC) integrins regulates cell growth and survival, extracellular matrix production, and organization. The aim of the study was to investigate human MC integrin modulation by differently glycosylated IgA and macromolecular IgA, which are thought to play a pathogenetic role in IgA nephropathy (IgAN). METHODS: MCs were incubated with purified human polymeric IgA, heat-aggregated IgA, IgA glycoforms generated by enzymatic hydrolysis of saccharide residues and serum fractions from IgAN patients, and controls isolated by lectin affinity and containing IgA with peculiar glycan patterns. Integrins were quantitated by flow cytometry. RESULTS: Cultured MCs highly expressed alphavbeta3 and some alpha3beta1; alphavbeta3 was up-regulated by matrix components (P < 0.02). In vitro desialylated and degalactosylated polymeric human IgA enhanced alphavbeta3 expression on cultured MCs (P < 0.001). Serum IgA glycoforms isolated from IgAN patients with high exposure of internal sugars, GalNAc, Neu5Ac2,6GalNAc, and Man enhanced alphav expression on cultured MCs more than healthy controls. CONCLUSIONS.: These data support the hypothesis that IgA glycation plays a role in modulating the cell-matrix interaction, and that this mechanism can be operating in IgAN.

Asunto(s)

Glomerulonefritis por IGA/inmunología , Glomerulonefritis por IGA/metabolismo , Inmunoglobulina A/metabolismo , Inmunoglobulina A/farmacología , Receptores de Vitronectina/biosíntesis , Anticuerpos Monoclonales , Apoptosis , Células Cultivadas , Matriz Extracelular/metabolismo , Citometría de Flujo , Galactosa/metabolismo , Glicosilación , Humanos , Técnicas para Inmunoenzimas , Técnicas In Vitro , Integrina alfa3beta1 , Integrinas/análisis , Integrinas/biosíntesis , Integrinas/inmunología , Glomérulos Renales/citología , Glomérulos Renales/inmunología , Glomérulos Renales/metabolismo , Sustancias Macromoleculares , Ácido N-Acetilneuramínico/metabolismo , Receptores de Vitronectina/análisis , Receptores de Vitronectina/inmunología

RESUMEN

T cell precursors homed to thymus develop in close contact with stromal cells. Among them, thymic epithelial cells (TEC) are known to exert dominant roles in their survival and functional shaping. Key molecules mediating TEC/thymocytes interactions include cytokines and growth factors secreted by the two cell types and adhesion receptors mediating cell contact. Signaling events triggered in thymocytes by adhesion to epithelial cells have been extensively investigated, whereas little is known on the opposite phenomenon. We have previously investigated this issue in a co-culture system composed of TEC cultures derived from human normal thymus and heterologous thymocytes. We demonstrated that thymocytes adhere to TEC involving beta1 and beta4 integrins and induce the clustering of alpha3beta1 and alpha6beta4 heterodimers at the TEC surface. In addition thymocyte adhesion was followed by activation of NF-kappaB and NF-IL6 gene transcription factors and enhanced IL-6 production. The two latter phenomena were reproduced by the cross-linking of the alpha3, alpha6, beta1 and beta4 integrins, thus implying that the alpha3beta1 and alpha6beta4 heterodimers can signal during thymocyte adhesion. We have extended our previous work investigating in the same experimental setting the inducing activity of non stimulated or activated policlonal or clonal mature T cells as representative of the more mature thymocyte subset. We found that adhesion of unstimulated T cell i) involved beta1, but not beta4 integrin functions at the surface ii) induced the clustering of alpha3beta1, but not alpha2beta1 heterodimers at the TEC surface and iii) up-regulated the nuclear binding activity of NF-kappaB transcription factor and the IL-6 secretion. We propose that alpha3beta1 and alpha6beta4 heterodimers are induced to cluster at the TEC surface recognizing yet unknown cellular ligands differentially expressed during T cell development.

Asunto(s)

Antígenos de Superficie/fisiología , Proteína beta Potenciadora de Unión a CCAAT/fisiología , Integrinas/fisiología , Interleucina-6/genética , FN-kappa B/fisiología , Linfocitos T/fisiología , Timo/citología , Adhesión Celular , Preescolar , Células Epiteliales/fisiología , Regulación de la Expresión Génica , Humanos , Lactante , Integrina alfa3beta1 , Integrina alfa6beta4

RESUMEN

The interface between apoptosis (programmed cell death) and the cell cycle is essential to preserve homeostasis and genomic integrity. Here, we show that survivin, an inhibitor of apoptosis over-expressed in cancer, physically associates with the cyclin-dependent kinase p34(cdc2) on the mitotic apparatus, and is phosphorylated on Thr(34) by p34(cdc2)-cyclin B1, in vitro and in vivo. Loss of phosphorylation on Thr(34) resulted in dissociation of a survivin-caspase-9 complex on the mitotic apparatus, and caspase-9-dependent apoptosis of cells traversing mitosis. These data identify survivin as a mitotic substrate of p34(cdc2)-cyclin B1 and suggest that survivin phosphorylation on Thr(34) may be required to preserve cell viability at cell division. Manipulation of this pathway may facilitate the elimination of cancer cells at mitosis.

Asunto(s)

Apoptosis/fisiología , Proteína Quinasa CDC2/metabolismo , División Celular/fisiología , Proteínas Asociadas a Microtúbulos , Proteínas/química , Proteínas/metabolismo , Secuencia de Aminoácidos , Anticuerpos , Ciclo Celular/fisiología , Células HeLa , Humanos , Proteínas Inhibidoras de la Apoptosis , Cinética , Melanoma , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida , Proteínas de Neoplasias , Fragmentos de Péptidos/química , Fragmentos de Péptidos/inmunología , Fragmentos de Péptidos/metabolismo , Fosforilación , Proteínas/genética , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Survivin , Transfección , Células Tumorales Cultivadas

RESUMEN

The highly conserved protein p27BBP is a cytoplasmic interactor of integrin beta4 expressed in epithelia. p27BBP is found in two pools: one nuclear pool enriched in the perinucleolar region, and one cytoplasmic pool. Deletion of p27BBP in yeast is lethal as a result of loss of the ribosomal 60S subunit. The aim of this study was to investigate the distribution of p27BBP in gut epithelium and its behavior during progression of human colorectal carcinomas. Results indicated that p27BBP is high in rapidly cycling cells and decreased in villous cells committed to apoptotic cell death. In dysplastic adenomas and carcinomas, p27BBP displayed a large increase of its nucleolar component that was superimposable to argyrophylic nucleolar organizing region-associated proteins and was associated with the nuclear matrix. Western blotting confirmed increased p27BBP in dysplastic adenomas and in carcinomas. In particular, p27BBP increased progressively from adenomas to carcinomas and, in the latter, was related to the tumor stage. The overexpression of p27BBP corresponded to mRNA up-regulation in carcinomas, supporting the idea of transcriptional or post-transcriptional regulation of its expression. Results suggested that p27BBP alterations are an early event in the transition from benign to malignant colorectal phenotypes and provide a novel tool in surgical pathology.

Asunto(s)

Proteínas Portadoras/análisis , Neoplasias Colorrectales/química , Proteínas de Filamentos Intermediarios/análisis , Adenoma/química , Animales , Antígenos CD/análisis , Carcinoma/química , Proteínas Portadoras/genética , Factores Eucarióticos de Iniciación , Regulación Neoplásica de la Expresión Génica , Humanos , Integrina beta4 , Proteínas de Filamentos Intermediarios/genética , Mucosa Intestinal/química , Región Organizadora del Nucléolo/química , Conejos , Transcripción Genética

RESUMEN

Inside the thymus, thymic epithelial cells and thymocytes show an interdependent relationship for their functional differentiation and development. As regards possible interdependency for their mutual survival, it is clear that lympho-epithelial adhesion can control the survival of developing thymocytes whereas the effects of lymphoid adhesion on epithelial cell survival have never been described. To address this issue, we performed co-cultures between normal human thymic epithelial cells (TEC) and a mature lymphoid T cell line (H9) or unfractionated thymocytes. TEC were induced to apoptosis by growth factor deprivation and the level of cell death was measured by flow cytometry. TEC stimulated by cell adhesion showed a significant reduced apoptosis when compared to the control and this phenomenon was associated with increased binding activity of NF-(kappa)B, as measured by gel shift analysis. The activation of NF-(kappa)B was necessary to promote survival, since its inhibition by acetyl salicylic acid prevented the promoting effect. The mAb-mediated crosslinking of (alpha)(3)(beta)(1) was considered as a potential inducer of TEC survival, since we have previously demonstrated that the engagement of this integrin was able to induce NF-(kappa)B activation in TEC. The crosslinking of (alpha)(3)(beta)(1), which clustered at the lympho-epithelial contact sites, partially reproduced the promoting activity of cell adhesion. These results highlight that lympho-epithelial adhesion can control the survival of thymic epithelial cells through an intracellular pathway which requires the activation of NF-(kappa)B and is triggered by integrins of the (beta)(1) family.

Asunto(s)

Células Epiteliales/citología , Células Epiteliales/metabolismo , FN-kappa B/metabolismo , Linfocitos T/citología , Timo/citología , Antígenos CD/metabolismo , Apoptosis/efectos de los fármacos , Aspirina/farmacología , Adhesión Celular/efectos de los fármacos , Línea Celular , Tamaño de la Célula/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Técnicas de Cocultivo , ADN/genética , ADN/metabolismo , Dimerización , Relación Dosis-Respuesta a Droga , Células Epiteliales/efectos de los fármacos , Sustancias de Crecimiento/deficiencia , Sustancias de Crecimiento/fisiología , Humanos , Integrina alfa3 , Integrina alfa3beta1 , Integrina beta1/metabolismo , Integrinas/metabolismo , FN-kappa B/antagonistas & inhibidores , Transducción de Señal/efectos de los fármacos , Factor de Transcripción Sp1/metabolismo , Linfocitos T/efectos de los fármacos , Linfocitos T/metabolismo

RESUMEN

Here we investigate the role of the control of apoptosis in normal cell division. We show that interference with the expression or function of the apoptosis inhibitor survivin causes caspase-dependent cell death in the G2/M phase of the cell cycle, and a cell-division defect characterized by centrosome dysregulation, multipolar mitotic spindles and multinucleated, polyploid cells. Use of a dominant-negative survivin mutant or antisense survivin complementary DNA disrupts a supramolecular assembly of survivin, caspase-3 and the cyclin-dependent-kinase inhibitor p21Waf1/Cip1 within centrosomes, and results in caspase-dependent cleavage of p21. Polyploidy induced by survivin antagonists is accentuated in p21-deficient cells, and corrected by exogenous expression of p21. These findings show that control of apoptosis and preservation of p21 integrity within centrosomes by survivin are required for normal mitotic progression.

Asunto(s)

Apoptosis , División Celular , Proteínas Asociadas a Microtúbulos , Proteínas/genética , Proteínas/metabolismo , Caspasa 3 , Caspasas/metabolismo , Línea Celular , Núcleo Celular/metabolismo , Supervivencia Celular , Centrosoma/química , Centrosoma/enzimología , Centrosoma/metabolismo , Inhibidor p21 de las Quinasas Dependientes de la Ciclina , Ciclinas/metabolismo , Citometría de Flujo , Técnica del Anticuerpo Fluorescente , Genes Dominantes/genética , Células HeLa , Humanos , Proteínas Inhibidoras de la Apoptosis , Mitosis , Mutación/genética , Proteínas de Neoplasias , Oligonucleótidos Antisentido/genética , Poliploidía , Proteínas/antagonistas & inhibidores , Proteínas/química , Huso Acromático/química , Huso Acromático/metabolismo , Survivin , Transfección

Asunto(s)

Apoptosis/fisiología , Proteínas Asociadas a Microtúbulos , Proteínas/fisiología , Animales , Muerte Celular/fisiología , División Celular/fisiología , Proteínas Inhibidoras de la Apoptosis , Proteínas de Neoplasias , Neoplasias Experimentales/patología , Neoplasias Experimentales/fisiopatología , Proteínas/genética , Survivin

RESUMEN

p27(BBP/eIF6) is an evolutionarily conserved protein that was originally identified as p27(BBP), an interactor of the cytoplasmic domain of integrin beta4 and, independently, as the putative translation initiation factor eIF6. To establish the in vivo function of p27(BBP/eIF6), its topographical distribution was investigated in mammalian cells and the effects of disrupting the corresponding gene was studied in the budding yeast, Saccharomyces cerevisiae. In epithelial cells containing beta4 integrin, p27(BBP/eIF6) is present in the cytoplasm and enriched at hemidesmosomes with a pattern similar to that of beta4 integrin. Surprisingly, in the absence and in the presence of the beta4 integrin subunit, p27(BBP/eIF6) is in the nucleolus and associated with the nuclear matrix. Deletion of the IIH S. cerevisiae gene, encoding the yeast p27(BBP/eIF6) homologue, is lethal, and depletion of the corresponding gene product is associated with a dramatic decrease of the level of free ribosomal 60S subunit. Furthermore, human p27(BBP/eIF6) can rescue the lethal effect of the iihDelta yeast mutation. The data obtained in vivo suggest an evolutionarily conserved function of p27(BBP/eIF6) in ribosome biogenesis or assembly rather than in translation. A further function related to the beta4 integrin subunit may have evolved specifically in higher eukaryotic cells.

Asunto(s)

Proteínas Portadoras/fisiología , Proteínas de Filamentos Intermediarios/fisiología , Proteínas Nucleares/fisiología , Fosfoproteínas , Ribosomas , Proteínas de Saccharomyces cerevisiae , Secuencia de Aminoácidos , Antígenos Nucleares , Secuencia de Bases , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Nucléolo Celular/metabolismo , Cartilla de ADN , Factores Eucarióticos de Iniciación , Técnica del Anticuerpo Fluorescente Indirecta , Humanos , Inmunohistoquímica , Proteínas de Filamentos Intermediarios/genética , Proteínas de Filamentos Intermediarios/metabolismo , Microscopía Electrónica , Mitosis , Datos de Secuencia Molecular , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Proteínas Ribosómicas , Saccharomyces cerevisiae/genética , Homología de Secuencia de Aminoácido

Asunto(s)

Microscopía Fluorescente/métodos , Animales , Células Cultivadas , Humanos

Asunto(s)

Clonación Molecular/métodos , Hibridación de Ácido Nucleico/métodos , Transducción de Señal , Levaduras

RESUMEN

Progression of the cell cycle and control of apoptosis (programmed cell death) are thought to be intimately linked processes, acting to preserve homeostasis and developmental morphogenesis. Although proteins that regulate apoptosis have been implicated in restraining cell-cycle entry and controlling ploidy (chromosome number), the effector molecules at the interface between cell proliferation and cell survival have remained elusive. Here we show that a new inhibitor of apoptosis (IAP) protein, survivin, is expressed in the G2/M phase of the cell cycle in a cycle-regulated manner. At the beginning of mitosis, survivin associates with microtubules of the mitotic spindle in a specific and saturable reaction that is regulated by microtubule dynamics. Disruption of survivin-microtubule interactions results in loss of survivin's anti-apoptosis function and increased caspase-3 activity, a mechanism involved in cell death, during mitosis. These results indicate that survivin may counteract a default induction of apoptosis in G2/M phase. The overexpression of survivin in cancer may overcome this apoptotic checkpoint and favour aberrant progression of transformed cells through mitosis.

Asunto(s)

Apoptosis/fisiología , Proteínas Asociadas a Microtúbulos , Proteínas/fisiología , Huso Acromático/fisiología , Células 3T3 , Animales , Ciclo Celular/fisiología , Fase G2/fisiología , Células HeLa , Humanos , Proteínas Inhibidoras de la Apoptosis , Ratones , Microtúbulos/fisiología , Mitosis/fisiología , Mutación , Proteínas de Neoplasias , Survivin , Tubulina (Proteína)/fisiología , Proteínas Virales/genética , Proteínas Virales/fisiología

RESUMEN

T-cell precursors develop within the thymus in contact with multiple supportive elements, among which thymic epithelial cells (TEC) are known to exert a dominant role in their homing, survival, and functional differentiation. All these functions are supported by cell-cell contacts and cytokine release. Signaling events triggered in lymphoid cells by adhesion to TEC are well characterized, but little is known about the opposite phenomenon. To address this issue, we derived cultures of TEC from human normal thymus. TEC monolayers were cocultured with thymocytes and immunostained with monoclonal antibodies (MoAbs) to integrin (2, 3, 4, and 6) and beta (beta1 and beta4) chains. Optical and confocal analysis showed that integrins were polarized on TEC at discrete surface locations: 6beta4 lined the basal surface of TEC monolayers, whereas 3beta1 was found mostly at TEC-TEC contacts; it is noteworthy that both 3beta1 and 6beta4 became highly enriched also at the boundaries with adherent thymocytes. Functional studies performed with MoAbs anti-beta1 and -beta4 integrins showed that beta1, and, to a much lower extent, beta4 heterodimers are involved in the TEC-thymocyte adhesion. Thymocyte contact or MoAb-mediated ligation of 3, 6, beta1, and beta4 integrins was investigated as a potential inducer of intracellular signaling in TEC. Thymocyte adhesion or cross-linking of MoAbs bound to integrins clustered at the TEC/thymocyte contact sites led to activation of interleukin-6 (IL-6) gene transcription factors, namely NF-IL6 serine phosphorylation and NF-kappaB nuclear targeting, as well as to increased IL-6 secretion. We propose that integrin clustering occurring during TEC-thymocyte contacts modulates in TEC the gene expression of a cytokine involved in thymocyte growth and functional differentiation.

Asunto(s)

Anticuerpos Monoclonales/farmacología , Antígenos de Superficie/fisiología , Proteínas Potenciadoras de Unión a CCAAT , Comunicación Celular , Proteínas de Unión al ADN/metabolismo , Regulación del Desarrollo de la Expresión Génica , Integrinas/fisiología , Interleucina-6/biosíntesis , FN-kappa B/metabolismo , Proteínas Nucleares/metabolismo , Agregación de Receptores/fisiología , Timo/citología , Factores de Transcripción , Transcripción Genética , Anticuerpos Monoclonales/inmunología , Antígenos CD/inmunología , Proteína delta de Unión al Potenciador CCAAT , Adhesión Celular , Diferenciación Celular , Células Cultivadas , Preescolar , Técnicas de Cocultivo , Dimerización , Células Epiteliales/metabolismo , Humanos , Lactante , Integrina alfa3beta1 , Integrina alfa6beta4 , Integrina beta1/inmunología , Integrina beta4 , Interleucina-6/genética , Ligandos , Agregación de Receptores/efectos de los fármacos

RESUMEN

In all mammalian cells protein phosphatase-1 (PP1) exists in three isoforms, defined as alpha, gamma 1 and delta. Immunofluorescence studies with isoform-specific antibodies indicated that delta, but not alpha or gamma 1, is enriched at focal adhesions in HeLa cells, fibroblasts, endothelial cells and keratinocytes. This was confirmed also by interference reflection microscopy, which indicated that PP1 delta was in areas of tight adhesion of the membrane to the extracellular matrix at sites where the microfilament cytoskeleton is organized. In all the cell types so far considered the PP1 delta in focal adhesions represented only a small aliquot of the total PP1 delta, which was predominantly localized to the nucleus. The association of PP1 delta to focal adhesions was confirmed by the co-immunoprecipitation of PP1 delta with the focal adhesion kinase pp125FAK and with the alpha v integrin. Comparison between the amount of PP1 delta associated with focal adhesion proteins and that of PP1 delta recovered in an anti-PP1 delta immunoprecipitate confirmed that only a minor amount of the enzyme was associated with the focal adhesions. Since some focal adhesion proteins are phosphorylated on Ser/Thr, it is likely that PP1 delta may be involved in the regulation of focal adhesion functions and particularly in the signaling pathway generated by cell-substratum adhesion.

Asunto(s)

Moléculas de Adhesión Celular/análisis , Endotelio Vascular/citología , Isoenzimas/análisis , Proteínas Tirosina Fosfatasas/análisis , Proteínas Tirosina Quinasas/análisis , Células 3T3/química , Células 3T3/enzimología , Animales , Especificidad de Anticuerpos , Antígenos CD/análisis , Western Blotting , Adhesión Celular/fisiología , Dermis/citología , Endotelio Vascular/química , Endotelio Vascular/enzimología , Fibroblastos , Técnica del Anticuerpo Fluorescente , Quinasa 1 de Adhesión Focal , Proteína-Tirosina Quinasas de Adhesión Focal , Células HeLa , Humanos , Integrina alfaV , Isoenzimas/inmunología , Queratinocitos/química , Queratinocitos/citología , Queratinocitos/enzimología , Ratones , Pruebas de Precipitina , Proteína Fosfatasa 1 , Proteínas Tirosina Fosfatasas/inmunología , Ratas , Ratas Endogámicas F344 , Proteínas Tirosina Fosfatasas Clase 2 Similares a Receptores , Venas Umbilicales/citología , Vinculina/análisis

Asunto(s)

Proteínas Portadoras/genética , Mapeo Cromosómico , Cromosomas Humanos Par 20/genética , Genes , Proteínas de Filamentos Intermediarios/genética , Mapeo Cromosómico/métodos , ADN Complementario/análisis , Epidermólisis Ampollosa/genética , Factores Eucarióticos de Iniciación , Humanos , Placenta , Reacción en Cadena de la Polimerasa , Receptores de Laminina/metabolismo , Homología de Secuencia de Ácido Nucleico

RESUMEN

Integrin activation is a multifaceted phenomenon leading to increased affinity and avidity for matrix ligands. To investigate whether cytokines produced during stromal infiltration of carcinoma cells activate nonfunctional epithelial integrins, a cellular system of human thyroid clones derived from normal glands (HTU-5) and papillary carcinomas (HTU-34) was employed. In HTU-5 cells, alphavbeta3 integrin was diffused all over the membrane, disconnected from the cytoskeleton, and unable to mediate adhesion. Conversely, in HTU-34 cells, alphavbeta3 was clustered at focal contacts (FCs) and mediated firm attachment and spreading. alphavbeta3 recruitment at FCs and ligand-binding activity, essentially identical to those of HTU-34, occurred in HTU-5 cells upon treatment with hepatocyte growth factor/scatter factor (HGF/SF). The HTU-34 clone secreted HGF/SF and its receptor was constitutively tyrosine phosphorylated suggesting an autocrine loop responsible for alphavbeta3 activated state. Antibody-mediated inhibition of HGF/SF function in HTU-34 cells disrupted alphavbeta3 enrichment at FCs and impaired adhesion. Accordingly, activation of alphavbeta3 in normal cells was produced by HTU-34 conditioned medium on the basis of its content of HGF/SF. These results provide the first example of a growth factor-driven integrin activation mechanism in normal epithelial cells and uncover the importance of cytokine-based autocrine loops for the physiological control of integrin activation.

Asunto(s)

Antígenos CD/metabolismo , Adhesión Celular/fisiología , Citocinas/fisiología , Factor de Crecimiento de Hepatocito/farmacología , Invasividad Neoplásica/fisiopatología , Glicoproteínas de Membrana Plaquetaria/metabolismo , Movimiento Celular/fisiología , Células Clonales/metabolismo , Citoesqueleto/fisiología , Matriz Extracelular/metabolismo , Citometría de Flujo , Técnica del Anticuerpo Fluorescente , Humanos , Integrina beta1/metabolismo , Integrina beta3 , Metástasis de la Neoplasia , Fosforilación , Proteínas Proto-Oncogénicas c-met/metabolismo , Transducción de Señal , Glándula Tiroides/fisiología , Células Tumorales Cultivadas , Tirosina/metabolismo

RESUMEN

The expression and distribution of integrin chains alpha 2, alpha 3, alpha 5, alpha 6, beta 1, beta 4, collagen type IV, laminin 1 and laminin 5 in oral squamous cell carcinoma (SCC) and oral keratoses with and without dysplasia (OL) have been studied by immunochemistry and western blotting. Focal interruptions of basement membrane protein staining were detected in SCC indicating a loss of continuity, whereas tumour nests were apparently completely surrounded by laminin 1, type IV collagen and laminin 5; the loss of basement membrane components in OL was found in only one specimen showing severe dysplasia. The localisation of integrins showed altered suprabasal and pericellular expression of the alpha 6 chain in all but one SCC, as well as in many OL samples, whereas the beta 4 subunit showed only a faint pericellular redistribution in SCC. In OL, beta 4 was often seen in a normal basally polarised distribution. Western blotting analysis confirmed that alpha 6 protein levels were abnormally high in cancerous lesions, whereas quantitative recovery of the beta 4 subunit in SCC was only minimal, suggesting a dissociation in the synthetic ratios of the two chains of the alpha 6 beta 4 heterodimer in SCC. Because alterations in the polarised expression of integrin alpha 6 beta 4 have been seen during epithelial tumour progression and wound healing, we suggest that the lack of restricted basal polarisation of alpha 6 could be an early but non-specific marker of oral malignancy, indicating that the generation of abnormal signals from the extracellular matrix may be involved.

Asunto(s)

Antígenos CD/metabolismo , Carcinoma de Células Escamosas/metabolismo , Integrinas/metabolismo , Leucoplasia Bucal/metabolismo , Neoplasias de la Boca/metabolismo , Western Blotting , Colágeno/metabolismo , Humanos , Técnicas para Inmunoenzimas , Integrina alfa6 , Laminina/metabolismo , Mucosa Bucal/metabolismo , Proteínas de Neoplasias/metabolismo