RESUMEN
Hypoxia is an important selective force in the clonal evolution of tumours. Through HIF-1 and other transcription factors combined with tumour-specific genetic alterations, hypoxia is a dominant factor in the angiogenic phenotype. Cellular adaptation to hypoxia is an important requirement of tumour progression independent of angiogenesis. The adaptive changes, insofar as they alter hypoxia-induced apoptosis, are likely to determine responsiveness to antiangiogenic strategies. To investigate this adaptation of tumour cells to hypoxia, we recreated in vitro the in vivo situation of chronic intermittent exposure to low-oxygen levels. The colon carcinoma cell lines HT29 and HCT116 were subjected to 40 episodes of sublethal hypoxia (4 h) three times a week. The resulting two hypoxia-conditioned cell lines have been maintained in culture for more than 2 years. In both cell lines changes in doubling times occurred: in HT29 an increase, and in HCT116 a decrease. Cell survival in response to hypoxia and to DNA damage differed strikingly in the two cell lines. The HT29 hypoxia-conditioned cells were more resistant than the parental line to a 24 h hypoxic challenge, while those from HCT116 surprisingly were more sensitive. Sensitivity to cisplatin in vitro was also significantly different for the hypoxia-conditioned compared with the parental lines, suggesting a change in pathways leading to apoptosis following DNA damage signaling. The growth of both conditioned cell lines in vivo as xenografts in immunodeficient (SCID) mice was more rapid than their parental lines, and was accompanied in each by evidence of enhanced vascular proliferation as a consequence of the hypoxia-conditioning. Thus the changes in apoptotic susceptibility were independent of altered angiogenesis. The derivation of these lines provides a model for events within hypoxic regions of colon cancers, and for the acquisition of resistance and sensitivity characteristics that may have therapeutic implications for the use of antiangiogenesis drugs.
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Apoptosis , Hipoxia de la Célula , Neoplasias del Colon/patología , Neovascularización Patológica , Adaptación Fisiológica , Animales , Proliferación Celular , Supervivencia Celular , Daño del ADN , Resistencia a Antineoplásicos , Femenino , Humanos , Inmunohistoquímica , Etiquetado Corte-Fin in Situ , Ratones , Ratones SCID , Trasplante Heterólogo , Células Tumorales CultivadasRESUMEN
We reviewed hearing recovery in 3,430 patients with sudden deafness reported between 1989 and 1998 in Japan, evaluated using standards of the Research Group on Sudden Deafness of the Ministry of Health and Welfare of Japan. Complete recovery was seen in 30.8%, marked in 24.7%, slight in 23.3% and no change in 21.8%. No remarked improvement in recovery of hearing was seen in patients with sudden deafness in these 10 years. The number of patients studied in evaluating the efficacy of therapies may thus affect results. Complete recovery from sudden deafness was nearly 30% in proportion to the increase of number of patients studied in the literature. At least 200 patients should be studied to make a reliable evaluation.
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Pérdida Auditiva Súbita/tratamiento farmacológico , Humanos , Resultado del TratamientoRESUMEN
Ectodomain shedding is an important mechanism to regulate the biological activities of membrane proteins. We focus here on the signaling mechanism of the ectodomain shedding of heparin-binding epidermal growth factor (EGF)-like growth factor (pro HB-EGF). Lysophosphatidic acid (LPA), a ligand for seven-transmembrane G protein-coupled receptors, stimulates the shedding of pro HB-EGF, which constitutes a G protein-coupled receptor-mediated transactivation of the EGF receptor. Experiments using a series of inhibitors and overexpression of mutant forms of signaling molecules revealed that the Ras-Raf-MEK signal is essential for the LPA-induced shedding. In addition, the small GTPase Rac is involved in the LPA-induced shedding, possibly to promote MEK activation. 12-O-Tetradecanoylphorbol-13-acetate is another potent inducer of pro HB-EGF shedding. We also demonstrate that the LPA-induced pathway is distinct from the 12-O-tetradecanoylphorbol-13-acetate-induced pathway and that these pathways constitute a dual signaling cascade that regulates the shedding of pro HB-EGF.
Asunto(s)
Factor de Crecimiento Epidérmico/química , Factor de Crecimiento Epidérmico/metabolismo , Lisofosfolípidos/farmacología , Receptores de Superficie Celular/química , Receptores de Superficie Celular/metabolismo , Transducción de Señal , Androstadienos/farmacología , Animales , Western Blotting , Membrana Celular/metabolismo , Células Cultivadas , Chlorocebus aethiops , Relación Dosis-Respuesta a Droga , Activación Enzimática , Inhibidores Enzimáticos/farmacología , GTP Fosfohidrolasas/metabolismo , Factor de Crecimiento Similar a EGF de Unión a Heparina , Péptidos y Proteínas de Señalización Intercelular , Ligandos , Quinasas de Proteína Quinasa Activadas por Mitógenos/metabolismo , Modelos Biológicos , Mutación , Plásmidos/metabolismo , Proteína Quinasa C/metabolismo , Estructura Terciaria de Proteína , Proteínas Proto-Oncogénicas c-raf/metabolismo , Acetato de Tetradecanoilforbol , Factores de Tiempo , Activación Transcripcional , Transfección , Células Vero , Wortmanina , Proteínas ras/metabolismoRESUMEN
A mitochondrial outer membrane protein of approximately 22 kDa (1C9-2) was purified from Vero cells assessing immunoreactivity with a monoclonal antibody, and the cDNA was cloned based on the partial amino acid sequence of the trypsin-digested fragments. 1C9-2 had 19-20% sequence identity to fungal Tom22, a component of the preprotein translocase of the outer membrane (the TOM complex) with receptor and organizer functions. Despite such a low sequence identity, both shared a remarkable structural similarity in the hydrophobicity profile, membrane topology in the Ncyt-Cin orientation through a transmembrane domain in the middle of the molecule, and the abundant acidic amino acid residues in the N-terminal domain. The antibodies against 1C9-2 inhibited the import of a matrix-targeted preprotein into isolated mitochondria. Blue native polyacrylamide gel electrophoresis of digitonin-solubilized outer membranes revealed that 1C9-2 is firmly associated with TOM40 in the approximately 400-kDa complex, with a size and composition similar to those of the fungal TOM core complex. Furthermore, 1C9-2 complemented the defects of growth and mitochondrial protein import in Deltatom22 yeast cells. Taken together, these results demonstrate that 1C9-2 is a functional homologue of fungal Tom22 and functions as a component of the TOM complex.
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Adenosina Trifosfatasas/química , Proteínas Bacterianas , Proteínas Portadoras/química , Proteínas de Escherichia coli , Membranas Intracelulares/enzimología , Proteínas de la Membrana/metabolismo , Proteínas de Transporte de Membrana , Mitocondrias/enzimología , Receptores de Superficie Celular , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Western Blotting , Fraccionamiento Celular , Chlorocebus aethiops , Clonación Molecular , Técnica del Anticuerpo Fluorescente , Proteínas Fúngicas/química , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Prueba de Complementación Genética , Células HeLa , Humanos , Membranas Intracelulares/metabolismo , Sustancias Macromoleculares , Proteínas de la Membrana/química , Proteínas de la Membrana/genética , Mitocondrias/metabolismo , Proteínas de Transporte de Membrana Mitocondrial , Proteínas del Complejo de Importación de Proteínas Precursoras Mitocondriales , Proteínas Mitocondriales , Datos de Secuencia Molecular , Peso Molecular , Subunidades de Proteína , Transporte de Proteínas , Canales de Translocación SEC , Proteína SecA , Alineación de Secuencia , Células Vero , Levaduras/citología , Levaduras/genética , Levaduras/crecimiento & desarrollo , Levaduras/metabolismoRESUMEN
CD9 and CD63 belong to a tetramembrane-spanning glycoprotein family called tetraspanin, and are involved in a wide variety of cellular processes, but the structure-function relationship of this family of proteins has yet to be clarified. CD9 associates with diphtheria toxin receptor (DTR), which is identical to the membrane-anchored form of heparin-binding EGF-like growth factor (proHB-EGF). CD9 upregulates the diphtheria toxin (DT) binding activity of DTR/proHB-EGF, while CD63 does not upregulate the DT binding activity in spite of the fact that this protein also associates with DTR/proHB-EGF on the cell surface. CD9 molecules localize on the cell surface, while those of CD63 localize predominantly at lysosomes and intracellular compartments. We made CD9/CD63 chimeric molecules and then studied their intracellular localization and upregulation activities. The C-terminal regions of CD63, which includes the lysosome sorting motif, showed a strong inhibitory effect on the expression of the chimeric proteins at the cell surface, while mutants lacking the lysosome sorting motif delivered more efficiently on the cell surface, indicating that the lysosome sorting motif contributes to the inhibitory effect of the C-terminal region. However, the N-terminal half of this family of proteins containing the 1st to 3rd transmembrane domains also seems to influence the cell surface expression. For the upregulation of DT binding activity the large extracellular loop (EC2) of CD9 was essential, while the remaining regions influenced the upregulation activity by changing the efficiency of cell surface expression. From these results we discussed the structure-function relationship of this family of proteins.
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Antígenos CD/metabolismo , Toxina Diftérica/metabolismo , Glicoproteínas de Membrana , Glicoproteínas de Membrana Plaquetaria/metabolismo , Proteínas Recombinantes de Fusión/genética , Fracciones Subcelulares/ultraestructura , Animales , Antígenos de Superficie , Técnicas In Vitro , Lisosomas/ultraestructura , Ratones , Unión Proteica/fisiología , Estructura Terciaria de Proteína/fisiología , Ratas , Proteínas Recombinantes de Fusión/metabolismo , Tetraspanina 29 , Tetraspanina 30 , Regulación hacia Arriba/fisiologíaRESUMEN
ISSUES: Cell Preparation Methods Standardized fixation and optimal staining Sampling of cervix, sampling error, homogenization of sample, subsampling Assessment of liquid-based preparations: efficacy and economic impact Training and transitional procedures before full implementation of new technologies Criteria for Sample Adequacy Clinician responsibility for collecting and providing representative sample to laboratory Collection instruments, number of slides Cellular content of samples: evidence of transformation zone (TZ) sampling, number of squamous cells present, obscuring factors Screening issues CONSENSUS POSITION The conventional cervical smear remains the standard method of cervical cancer screening but has limitations in individual test sensitivity and specificity. Sample takers should: (1) receive appropriate training in sample collection, (2) be held responsible for providing the laboratory with appropriate samples, and (3) have their performance monitored. The instruments used for sampling should collect cells from both the ectocervix and endocervix; optimally, TZ sampling, represented by the presence of endocervical or squamous metaplastic cells, should be identifiable in samples other than atrophic specimens. The adequacy of a specimen (as judged microscopically) does not guarantee that it is representative of the cervix. Each cytology report should include a comment on cellular content/adequacy of the specimen. Liquid-based preparations may overcome many of the inherent problems with the conventional cervical smear. ONGOING ISSUES: We need further data on the cost-effectiveness of making two slides from cervical specimens and/or using two samplers rather than a single one. Do we have enough information to make recommendations as to the appropriate type of sampler to be used in particular situations, such as routine screening? What is the best method of screening for/detecting endocervical glandular neoplasia? How are such terms as unsatisfactory and inadequate defined in cervical cytology classifications other than the Bethesda System? What number and types of epithelial cells should be present (visualized) in a cervical smear or liquid-based preparation for it to be considered adequate? Do we need to have evidence of TZ sampling in specimens taken during the follow-up period after treatment of squamous intraepithelial lesion or after detection of endocervical glandular neoplasia? What criteria for obscuring factors, such as blood and inflammation, should be used in assessing adequacy? Cost-benefit analyses of utilizing liquid-based preparations are needed. Should we inform women about the technical details of the test methods available or chosen by the laboratory? Are women in a position to decide which method is the most appropriate to assess their cervical scrape sample? We need to obtain more information about the properties of proprietary liquid fixative/transport media with respect to inactivation of viral pathogens, tuberculosis and other bacterial pathogens and suitability for immunobiologic and molecular tests, etc. We need to obtain more information on the use of stoichiometric stains and the limitations of Papanicolaou stain for image analysis systems. The use of liquid-based preparations for nongynecologic cytopathology and ancillary tests must be considered, including criteria for adequacy. We need to obtain more information on the time required for and best methods of training experienced cytotechnologists to become competent at assessing liquid-based cervical preparations.
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Cuello del Útero/citología , Prueba de Papanicolaou , Manejo de Especímenes/normas , Frotis Vaginal/normas , Biología Celular/educación , Femenino , Humanos , Tamizaje Masivo/métodos , Tamizaje Masivo/normas , Garantía de la Calidad de Atención de Salud/normas , Responsabilidad Social , Manejo de Especímenes/métodos , Coloración y Etiquetado/métodos , Fijación del Tejido/métodos , Revelación de la Verdad , Neoplasias del Cuello Uterino/diagnóstico , Neoplasias del Cuello Uterino/patología , Neoplasias del Cuello Uterino/prevención & control , Frotis Vaginal/economía , Frotis Vaginal/instrumentación , Frotis Vaginal/métodosRESUMEN
Electrocardiographic abnormalities were pointed out in a 51-year-old Japanese male whose major complaint was dizziness. His electrocardiogram showed a complete right bundle branch block, and a prolonged His bundle-ventricle (HV) interval of 100 msec. Two members of his family died of heart disease and 3 members, including a case of sudden death, presented an abnormal electrocardiogram of the Brugada-type with persistent ST segment elevation in the right precordial leads and right bundle branch block. The signal-averaged examination was made in the children of cases that died with the diagnosis of sudden death. Four cases showed a tendency of delay in the HV interval and a positive finding in the late potential. Further studies are necessary to clarify the relationship between electrocardiographic abnormalities of the Brugada-type and atrioventricular conduction disorder as well as to clarify the genetic basis of this disorder.
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Fibrilación Ventricular/genética , Fibrilación Ventricular/fisiopatología , Adolescente , Adulto , Anciano , Bloqueo de Rama/genética , Bloqueo de Rama/fisiopatología , Electrocardiografía , Femenino , Humanos , Masculino , Persona de Mediana Edad , LinajeAsunto(s)
Neoplasias del Apéndice , Adolescente , Adulto , Anciano , Carcinoma in Situ , Niño , Preescolar , Femenino , Humanos , Masculino , Persona de Mediana EdadAsunto(s)
Adenocarcinoma , Neoplasias del Apéndice , Adolescente , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana EdadAsunto(s)
Adenoma , Neoplasias del Apéndice , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana EdadAsunto(s)
Neoplasias del Apéndice , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
Effects of beta-adrenergic stimulation on the membrane potential and intracellular Na+, K+, Cl- activities and pH (pHi) were examined in isolated guinea-pig ventricular muscles using conventional and ion-selective microelectrodes. Isoproterenol (1 microM) produced a transient membrane depolarization followed by a slight hyperpolarization in quiescent papillary muscles. Although the isoproterenol (1 microM)-induced depolarization was not blocked by tetrodotoxin (10 microM), nifedipine (10 microM), Cs+ (5 mM), Ba2+ (0.3 mM), amiloride (1 mM) or ouabain (10 microM), it was significantly attenuated by anthracene-9-carboxylic acid (9 AC, 1 mM), a Cl(-)-channel blocker. Intracellular K+ activity increased, whereas intracellular Na+ activity slightly decreased during beta-adrenergic stimulation. Intracellular Cl- activity significantly decreased during the isoproterenol-induced depolarization of the resting membrane potential, which was attenuated by 9 AC. Isoproterenol significantly decreased pHi, which was enhanced by amiloride. 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid(DIDS, 1 mM), a stilbene derivative possessing blocking action on Cl-/HCO3- exchange system and Na+/HCO3- symport system, failed to affect the isoproterenol-induced acidosis, but pretreatment with 2-deoxyglucose (2-DG, 5.5 mM) or iodoacetic acid(IAA, 0.3 mM) abolished the isoproterenol-induced pHi decrease. Thus, beta-adrenergic stimulation decreased aiCl, aiNa and pHi, and increased aiK. The decrease in aiCl may be ascribed to the activation of Cl- channels, and opposite changes in aiNa and aiK appear to be due to the beta-adrenoceptor mediated activation of Na+/K+ pump. Acceleration of glycolysis during beta-adrenergic stimulation may be responsible for the intracellular acidosis. These changes in intracellular ionic activities may play a role in the modulation of electromechanical response to beta-adrenergic stimulation.
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Cloro/metabolismo , Miocardio/metabolismo , Potasio/metabolismo , Receptores Adrenérgicos beta/fisiología , Sodio/metabolismo , Animales , Femenino , Cobayas , Ventrículos Cardíacos , Concentración de Iones de Hidrógeno , Técnicas In Vitro , Isoproterenol/farmacología , Masculino , Potenciales de la Membrana/efectos de los fármacosAsunto(s)
Adenoma , Neoplasias del Apéndice , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana EdadAsunto(s)
Neoplasias del Apéndice/secundario , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
OBJECTIVE: The aims were to examine the effect of beta adrenergic stimulation on the intracellular pH (pHi) and to compare it with that of alpha adrenergic stimulation in ventricular myocardium. METHODS: Using conventional and ion selective electrodes membrane potential and pHi were measured simultaneously in quiescent papillary muscles of guinea pigs in HEPES or bicarbonate buffered solution. Isoprenaline and propranolol (1 microM) plus phenylephrine (30 microM) were used to stimulate beta and alpha adrenoceptors, respectively. In order to evaluate underlying mechanism(s) of beta adrenoceptor mediated pHi change, effects of Na(+)-H+ exchange, Cl(-)-HCO3- exchange, Na(+)-HCO3- symport, and glycolysis blockers on the pHi change were examined. RESULTS: Isoprenaline (1 microM) produced a decrease in pHi of 0.08(SEM 0.01) pH units and a transient depolarisation of the resting membrane. The isoprenaline induced intracellular acidosis was blocked by the beta 1 blocker atenolol (10 microM) but not by the beta 2 blocker ICI 118,551 (0.1 microM). Forskolin also produced a decrease in pHi of 0.06(0.03) pH units. In contrast, alpha adrenergic stimulation produced an increase in pHi, which was abolished by 1 mM amiloride, an Na(+)-H+ exchange blocker. In the presence of amiloride, the isoprenaline induced decrease in pHi was rather enhanced. 4,4'-Diisothiocyanostilbene-2,2'-disulphonic acid (DIDS, 1 mM), a blocker of Cl(-)-HCO3- exchange and the Na(+)-HCO3- symport system, failed to affect the isoprenaline induced pHi decrease in bicarbonate buffered solution. However, pretreatment with 2-deoxyglucose or iodoacetic acid abolished the isoprenaline induced pHi decrease. CONCLUSIONS: beta 1 Adrenoceptor stimulation causes intracellular acidosis via the enhanced glycolysis, and the Na(+)-H+ exchange system appears to play a compensatory role. The beta 1 adrenoceptor mediated intracellular acidosis may modulate inotropic response to adrenergic stimulation in ventricular myocardium.
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Isoproterenol/farmacología , Miocardio/metabolismo , Propranolol/farmacología , Receptores Adrenérgicos beta 1/efectos de los fármacos , Antagonistas Adrenérgicos beta/farmacología , Amilorida/farmacología , Animales , Atenolol/farmacología , Colforsina/farmacología , Técnicas de Cultivo , Femenino , Cobayas , Ventrículos Cardíacos/metabolismo , Concentración de Iones de Hidrógeno , Masculino , Potenciales de la Membrana/efectos de los fármacos , Fenilefrina/farmacología , Propanolaminas/farmacología , Estimulación QuímicaRESUMEN
Computerized morphological analysis of the cell nuclei was performed on 66 cases (2222 nuclei) of aspirated materials from breast tumors: 25 benign cases (302 nuclei), 41 malignant cases (1420 nuclei). Its diagnostic significance and the correlation between nuclear analysis and clinical staging were studied. Nuclear diagram and intranuclear chromatin distribution pattern were evaluated using computer system named 6400. The malignant tumor had larger, more round-shaped nuclei and less uniform chromatin distribution. Under tnm classification, stage IV tumors had larger, more flattened nuclei and more irregular chromatin distribution pattern than the others. Computerized morphological analysis of breast tumors may give a quantitative aspect to classical diagnostic process. Furthermore, this analytical method provides information on clinical stage of breast cancer.