RESUMEN
In early Caenorhabditis elegans embryos, asymmetric cell divisions produce descendants with asynchronous cell cycle times. To investigate the relationship between cell cycle regulation and pattern formation, we have identified a collection of embryonic-lethal mutants in which cell divisions are delayed and cell fate patterns are abnormal. In div (for division delayed) mutant embryos, embryonic cell divisions are delayed but remain asynchronous. Some div mutants produce well-differentiated cell types, but they frequently lack the endodermal and mesodermal cell fates normally specified by a transcriptional activator called SKN-1. We show that mislocalization of PIE-1, a negative regulator of SKN-1, prevents the specification of endoderm and mesoderm in div-1 mutant embryos. In addition to defects in the normally asymmetric distribution of PIE-1, div mutants also exhibit other losses of asymmetry during early embryonic cleavages. The daughters of normally asymmetric divisions are nearly equal in size, and cytoplasmic P-granules are not properly localized to germline precursors in div mutant embryos. Thus the proper timing of cell division appears to be important for multiple aspects of asymmetric cell division. One div gene, div-1, encodes the B subunit of the DNA polymerase alpha-primase complex. Reducing the function of other DNA replication genes also results in a delayed division phenotype and embryonic lethality. Thus the other div genes we have identified are likely to encode additional components of the DNA replication machinery in C. elegans.
Asunto(s)
Tipificación del Cuerpo , Proteínas de Caenorhabditis elegans , Caenorhabditis elegans/embriología , Caenorhabditis elegans/genética , Ciclo Celular/genética , ADN Primasa/genética , Replicación del ADN/genética , Proteínas de Unión al ADN , Factores de Transcripción , Secuencia de Aminoácidos , Animales , División Celular , Polaridad Celular , Mapeo Cromosómico , ADN Primasa/química , Embrión no Mamífero/fisiología , Endodermo/fisiología , Ligamiento Genético , Proteínas del Helminto/química , Proteínas del Helminto/genética , Proteínas del Helminto/metabolismo , Mesodermo/fisiología , Datos de Secuencia Molecular , Mutación , Alineación de Secuencia , Transactivadores/metabolismoRESUMEN
BACKGROUND: The Aurora/Ipl1p-related kinase AIR-2 is required for mitotic chromosome segregation and cytokinesis in early Caenorhabditis elegans embryos. Previous studies have relied on non-conditional mutations or RNA-mediated interference (RNAi) to inactivate AIR-2. It has therefore not been possible to determine whether AIR-2 functions directly in cytokinesis or if the cleavage defect results indirectly from the failure to segregate DNA. One intriguing hypothesis is that AIR-2 acts to localize the mitotic kinesin-like protein ZEN-4 (also known as CeMKLP1), which later functions in cytokinesis. RESULTS: Using conditional alleles, we established that AIR-2 is required at metaphase or early anaphase for normal segregation of chromosomes, localization of ZEN-4, and cytokinesis. ZEN-4 is first required late in cytokinesis, and also functions to maintain cell separation through much of the subsequent interphase. DNA segregation defects alone were not sufficient to disrupt cytokinesis in other mutants, suggesting that AIR-2 acts specifically during cytokinesis through ZEN-4. AIR-2 and ZEN-4 shared similar genetic interactions with the formin homology (FH) protein CYK-1, suggesting that AIR-2 and ZEN-4 function in a single pathway, in parallel to a contractile ring pathway that includes CYK-1. Using in vitro co-immunoprecipitation experiments, we found that AIR-2 and ZEN-4 interact directly. CONCLUSIONS: AIR-2 has two functions during mitosis: one in chromosome segregation, and a second, independent function in cytokinesis through ZEN-4. AIR-2 and ZEN-4 may act in parallel to a second pathway that includes CYK-1.
Asunto(s)
Proteínas de Caenorhabditis elegans , Caenorhabditis elegans/metabolismo , Ciclo Celular/fisiología , Cinesinas/metabolismo , Metafase , Proteínas Serina-Treonina Quinasas/fisiología , Huso Acromático/metabolismo , Animales , Aurora Quinasa B , Aurora Quinasas , Caenorhabditis elegans/citología , Caenorhabditis elegans/embriología , ADN/metabolismoRESUMEN
During cytokinesis of animal cells, the mitotic spindle plays at least two roles. Initially, the spindle positions the contractile ring. Subsequently, the central spindle, which is composed of microtubule bundles that form during anaphase, promotes a late step in cytokinesis. How the central spindle assembles and functions in cytokinesis is poorly understood. The cyk-4 gene has been identified by genetic analysis in Caenorhabditis elegans. Embryos from cyk-4(t1689ts) mutant hermaphrodites initiate, but fail to complete, cytokinesis. These embryos also fail to assemble the central spindle. We show that the cyk-4 gene encodes a GTPase activating protein (GAP) for Rho family GTPases. CYK-4 activates GTP hydrolysis by RhoA, Rac1, and Cdc42 in vitro. RNA-mediated interference of RhoA, Rac1, and Cdc42 indicates that only RhoA is essential for cytokinesis and, thus, RhoA is the likely target of CYK-4 GAP activity for cytokinesis. CYK-4 and a CYK-4:GFP fusion protein localize to the central spindle and persist at cell division remnants. CYK-4 localization is dependent on the kinesin-like protein ZEN-4/CeMKLP1 and vice versa. These data suggest that CYK-4 and ZEN-4/CeMKLP1 cooperate in central spindle assembly. Central spindle localization of CYK-4 could accelerate GTP hydrolysis by RhoA, thereby allowing contractile ring disassembly and completion of cytokinesis.
Asunto(s)
Proteínas de Caenorhabditis elegans , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , División Celular/fisiología , Proteínas Activadoras de GTPasa/metabolismo , Proteínas del Helminto/metabolismo , Huso Acromático/fisiología , Proteínas de Unión al GTP rho/metabolismo , Animales , Caenorhabditis elegans/citología , Niño , Clonación Molecular , Embrión no Mamífero , Femenino , Proteínas Activadoras de GTPasa/genética , Regulación del Desarrollo de la Expresión Génica/fisiología , Proteínas del Helminto/genética , Humanos , Cinesinas/genética , Cinesinas/metabolismo , Masculino , Modelos Biológicos , Mutación/fisiología , Estructura Terciaria de Proteína/genética , Fracciones Subcelulares/metabolismo , Proteínas de Unión al GTP rho/genéticaRESUMEN
BACKGROUND: Assessment of essential fatty acid status requires collection of blood or adipose tissue samples. However, these invasive techniques cannot always be used in studies involving infants, young children, or subjects from whom it is difficult to obtain blood. A body tissue that is easy to access is the buccal mucosa (cheek cells). OBJECTIVE: The objective was to investigate the degree to which fatty acids of cheek cells reflect the fatty acid content of plasma, red blood cells, and the diet. DESIGN: Thirty-one infants aged 12 mo were enrolled. Five infants were fed human milk and 26 infants received formulas that provided a wide range of arachidonic acid and docosahexaenoic acid (DHA) intakes. Cheek cells were collected on a small piece of gauze by gently swabbing the inside of the cheek 3 times. Lipids were extracted from the gauze and the phospholipid fatty acid content of the cheek cells was determined. RESULTS: Cheek cell DHA and arachidonic acid in phospholipids were significantly correlated with DHA and arachidonic acid in plasma [r = 0.61 (P < 0.001) and r = 0.37 (P <0.05), respectively], red blood cells [r = 0.58 (P < 0.001) and r = 0.37 (P < 0.05), respectively], and the diet [r = 0.65 (P < 0.001) and r = 0. 51 (P < 0.01), respectively]. CONCLUSIONS: Given these correlations and the ease and noninvasive nature of this technique, cheek cell fatty acids may serve as a marker of the essential fatty acid content, especially of DHA and arachidonic acid, in plasma, red blood cells, and the diet.
Asunto(s)
Ácidos Araquidónicos/metabolismo , Grasas de la Dieta/metabolismo , Ácidos Docosahexaenoicos/metabolismo , Alimentos Infantiles , Leche Humana , Mucosa Bucal/metabolismo , Análisis de Varianza , Ácidos Araquidónicos/administración & dosificación , Ácidos Araquidónicos/sangre , Grasas de la Dieta/sangre , Ácidos Docosahexaenoicos/administración & dosificación , Ácidos Docosahexaenoicos/sangre , Humanos , Lactante , Reproducibilidad de los ResultadosRESUMEN
The metaphase to anaphase transition is a critical stage of the eukaryotic cell cycle, and, thus, it is highly regulated. Errors during this transition can lead to chromosome segregation defects and death of the organism. In genetic screens for temperature-sensitive maternal effect embryonic lethal (Mel) mutants, we have identified 32 mutants in the nematode Caenorhabditis elegans in which fertilized embryos arrest as one-cell embryos. In these mutant embryos, the oocyte chromosomes arrest in metaphase of meiosis I without transitioning to anaphase or producing polar bodies. An additional block in M phase exit is evidenced by the failure to form pronuclei and the persistence of phosphohistone H3 and MPM-2 antibody staining. Spermatocyte meiosis is also perturbed; primary spermatocytes arrest in metaphase of meiosis I and fail to produce secondary spermatocytes. Analogous mitotic defects cause M phase delays in mitotic germline proliferation. We have named this class of mutants "mat" for metaphase to anaphase transition defective. These mutants, representing six different complementation groups, all map near genes that encode subunits of the anaphase promoting complex or cyclosome, and, here, we show that one of the genes, emb-27, encodes the C. elegans CDC16 ortholog.
Asunto(s)
Anafase/genética , Caenorhabditis elegans/citología , Caenorhabditis elegans/genética , Meiosis/genética , Metafase/genética , Mutación/genética , Complejos de Ubiquitina-Proteína Ligasa , Alelos , Ciclosoma-Complejo Promotor de la Anafase , Animales , Caenorhabditis elegans/embriología , Caenorhabditis elegans/metabolismo , Proteínas de Ciclo Celular/química , Proteínas de Ciclo Celular/genética , Proteínas de Ciclo Celular/metabolismo , Embrión no Mamífero/citología , Embrión no Mamífero/metabolismo , Femenino , Genes de Helminto/genética , Genes Letales/genética , Prueba de Complementación Genética , Histonas/metabolismo , Ligasas/química , Ligasas/genética , Ligasas/metabolismo , Masculino , Madres , Fenotipo , Fosfoproteínas/metabolismo , Subunidades de Proteína , Espermatocitos/citología , Espermatocitos/metabolismo , Tubulina (Proteína)/metabolismo , Ubiquitina-Proteína LigasasRESUMEN
The signalling protein Wnt regulates transcription factors containing high-mobility-group (HMG) domains to direct decisions on cell fate during animal development. In Caenorhabditis elegans, the HMG-domain-containing repressor POP-1 distinguishes the fates of anterior daughter cells from their posterior sisters throughout development, and Wnt signalling downregulates POP-1 activity in one posterior daughter cell called E. Here we show that the genes mom-4 and lit-1 are also required to downregulate POP-1, not only in E but also in other posterior daughter cells. Consistent with action in a common pathway, mom-4 and lit-1 exhibit similar mutant phenotypes and encode components of the mitogen-activated protein kinase (MAPK) pathway that are homologous to vertebrate transforming-growth-factor-beta-activated kinase (TAK1) and NEMO-like kinase (NLK), respectively. Furthermore, MOM-4 and TAK1 bind related proteins that promote their kinase activities. We conclude that a MAPK-related pathway cooperates with Wnt signal transduction to downregulate POP-1 activity. These functions are likely to be conserved in vertebrates, as TAK1 and NLK can downregulate HMG-domain-containing proteins related to POP-1.
Asunto(s)
Proteínas Adaptadoras Transductoras de Señales , Proteínas de Caenorhabditis elegans , Caenorhabditis elegans/genética , Proteínas Quinasas Dependientes de Calcio-Calmodulina/metabolismo , Proteínas de Unión al ADN/genética , Regulación hacia Abajo , Proteínas del Grupo de Alta Movilidad/genética , Péptidos y Proteínas de Señalización Intracelular , Proteínas Quinasas JNK Activadas por Mitógenos , Quinasas Quinasa Quinasa PAM , Quinasas de Proteína Quinasa Activadas por Mitógenos , Proteínas Quinasas Activadas por Mitógenos , Proteínas Proto-Oncogénicas/metabolismo , Proteínas de Pez Cebra , Secuencia de Aminoácidos , Animales , Caenorhabditis elegans/enzimología , Caenorhabditis elegans/metabolismo , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Línea Celular , Clonación Molecular , Activación Enzimática , Regulación del Desarrollo de la Expresión Génica , Genes de Helminto , Humanos , MAP Quinasa Quinasa 4 , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Datos de Secuencia Molecular , Canales de Potasio con Entrada de Voltaje , Proteínas Quinasas/metabolismo , Proteínas Serina-Treonina Quinasas/química , Proteínas Serina-Treonina Quinasas/genética , Proteínas Serina-Treonina Quinasas/metabolismo , Homología de Secuencia de Aminoácido , Transducción de Señal , Proteínas WntRESUMEN
The major microtubule-associated protein in echinoderms is a 77-kDa, WD repeat protein, called EMAP. EMAP-related proteins have been identified in sea urchins, starfish, sanddollars, and humans. We describe the purification of sea urchin EMAP and demonstrate that EMAP binding to microtubules is saturable at a molar ratio of 1 mol of EMAP to 3 mol of tubulin dimer. Unlike MAP-2, MAP-4, or tau proteins, EMAP binding to microtubules is not lost by cleavage of tubulin with subtilisin. In addition to binding to the microtubule polymer, EMAP binds to tubulin dimers in a 1:1 molar ratio. The abundance of EMAP in the egg suggests that it could function to regulate microtubule assembly. To test this hypothesis, we examined the effects of EMAP on the dynamic instability of microtubules nucleated from axoneme fragments as monitored by video-enhanced differential interference contrast microscopy. Addition of 2.2 microM EMAP to 21 microM tubulin results in a slight increase in the elongation and shortening velocities at the microtubule plus ends but not at the minus ends. Significantly, EMAP inhibits the frequency of rescue 8-fold without producing a change in the frequency of catastrophe. These results indicate that EMAP, unlike brain microtubule-associated proteins, promotes microtubule dynamics.
Asunto(s)
Proteínas Asociadas a Microtúbulos/aislamiento & purificación , Proteínas Asociadas a Microtúbulos/metabolismo , Microtúbulos/metabolismo , Óvulo/metabolismo , Erizos de Mar/metabolismo , Tubulina (Proteína)/metabolismo , Animales , Western Blotting , Cromatografía DEAE-Celulosa , Cromatografía en Gel , Dimerización , Equinodermos , Electroforesis en Gel de Poliacrilamida , Femenino , Humanos , Cinética , Masculino , Proteínas Asociadas a Microtúbulos/química , Peso Molecular , Cola del Espermatozoide/metabolismo , Estrellas de Mar , Porcinos , Tubulina (Proteína)/aislamiento & purificaciónRESUMEN
Vaults are large ribonucleoprotein particles that have been identified in a wide range of eukaryotic organisms. Although present in thousands of copies per cell, their function remains unknown. In this report, we identify the major vault protein in sea urchins as a 107-kDa polypeptide that copurifies with microtubules and ribosomes. Although initially identified in microtubule preparations, the sea urchin major vault protein is not predominantly microtubule-associated in vivo. Rather, the sea urchin major vault protein is present throughout the cytoplasm in eggs and embryos and in the nucleus in adult somatic cells. Within the nucleus, the sea urchin major vault protein is concentrated in the region of the nucleolus and to punctate regions of the nuclear envelope. In addition, the vault protein localizes to short linear strings juxtaposed to the exterior of the nucleus and extending outward into the cytoplasm. Based on their copurification and intracellular distribution, vaults may be involved in the nucleocytoplasmic transport of ribosomes and/or mRNA.
Asunto(s)
Núcleo Celular/metabolismo , Citoplasma/metabolismo , Ribonucleoproteínas/análisis , Ribonucleoproteínas/química , Erizos de Mar/química , Partículas Ribonucleoproteicas en Bóveda , Animales , Transporte Biológico , Blastocisto/química , Embrión no Mamífero/química , Gástrula/química , Proteínas Asociadas a Microtúbulos/análisis , Microtúbulos/química , Peso Molecular , Óvulo/química , Ratas , Ribonucleoproteínas/aislamiento & purificación , Ribonucleoproteínas/fisiología , Ribosomas/ultraestructura , Erizos de Mar/embriología , SolubilidadRESUMEN
Information from 12 studies is combined to estimate the AIDS incubation distribution with greater precision than is possible from a single study. The analysis uses a hierarchy of parametric models based on a four-parameter generalized F distribution. This general model contains four standard two-parameter distributions as special cases. The cases are the Weibull, gamma, log-logistic, lognormal distributions. These four special cases subsume three distinct asymptotic hazard behaviors. As time increases beyond the median of approximately 10 years, the hazard can increase to infinity (Weibull), can plateau at some constant level (gamma), or can decrease to zero (log-logistic and lognormal). The Weibull, gamma and 'log-logistic distributions' which represent the three distinct asymptotic hazard behaviors, all fit the data as well as the generalized F distribution at the 25 percent significance level. Hence, we conclude that incubation data is still too limited to ascertain the specific hazard assumption that should be utilized in studies of the AIDS epidemic. Accordingly, efforts to model the AIDS epidemic (e.g., back-calculation approaches) should allow the incubation distribution to take several forms to adequately represent HIV estimation uncertainty. It is recommended that, at a minimum, the specific Weibull, gamma and log-logistic distributions estimated in this meta-analysis should all be used in modeling the AIDS epidemic, to reflect this uncertainty.
Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/epidemiología , Modelos Estadísticos , Adulto , Distribución de Chi-Cuadrado , Progresión de la Enfermedad , Europa (Continente)/epidemiología , Humanos , América del Norte/epidemiología , Factores de TiempoRESUMEN
A subset of mRNAs, polyribosomes, and poly(A)-binding proteins copurify with microtubules from sea urchin embryos. Several lines of evidence indicate that the interaction of microtubules with ribosomes is specific: a distinct stalk-like structure appears to mediate their association; ribosomes bind to microtubules with a constant stoichiometry through several purification cycles; and the presence of ribosomes in these preparations depends on the presence of intact microtubules. Five specific mRNAs are enriched with the microtubule-bound ribosomes, indicating that translation of specific proteins may occur on the microtubule scaffolding in vivo.
Asunto(s)
Blastocisto/fisiología , Blastocisto/ultraestructura , Proteínas de Microtúbulos/biosíntesis , Microtúbulos/fisiología , Polirribosomas/fisiología , ARN Mensajero/biosíntesis , Animales , Western Blotting , Electroforesis en Gel de Poliacrilamida , Embrión no Mamífero/fisiología , Femenino , Fertilización , Masculino , Microscopía Electrónica , Proteínas de Microtúbulos/análisis , Microtúbulos/ultraestructura , Óvulo/citología , Óvulo/fisiología , Proteínas de Unión a Poli(A) , Polirribosomas/ultraestructura , ARN Mensajero/análisis , ARN Mensajero/aislamiento & purificación , Proteínas de Unión al ARN/aislamiento & purificación , Proteínas de Unión al ARN/metabolismo , Erizos de Mar/embriología , Espermatozoides/citología , Espermatozoides/fisiologíaRESUMEN
OBJECTIVE: To evaluate the effect of the assumption of no long reporting delays on estimates of AIDS incidence. DESIGN: Reported AIDS cases must be adjusted for reporting delays to estimate AIDS incidence. We compared the adjustments supplied with the Centers for Disease Control and Prevention (CDC) AIDS Public Information Data Set with a set of adjustments that differ with respect to CDC assumption of no long delays. Both methods assume that no changes in delay have occurred throughout the reporting period. METHODS: Probability distributions of reporting delays were calculated from the delay adjustment weights supplied by CDC, and from an alternative method that estimates the probability of long delays from the surveillance data. AIDS incidence estimates from these two approaches were calculated and compared. RESULTS: The CDC adjustments assume that there will be no reporting delays longer than 61 months, whereas the alternative method estimates that 5.9% of case reports will be delayed longer than 61 months. The CDC adjustments result in lower estimates of AIDS incidence and a flattening of the epidemic. CONCLUSIONS: In addition to a 6.2% reduction in total estimated AIDS incidence, the CDC assumption changes the shape of the estimated epidemic. These may result in as much as 4-21% reductions in model estimates of HIV incidence and prevalence.
Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/epidemiología , Métodos Epidemiológicos , Humanos , Incidencia , Factores de Tiempo , Estados Unidos/epidemiologíaRESUMEN
"The objective of this paper is to examine continuation and effectiveness of contraception based on a 1986 survey of more than 3,200 women in rural Sri Lanka. Data on both programme and non-programme methods of contraception are analyzed. Programme methods are defined as including all those methods that are provided through the public or private family planning programmes (namely, oral pills, IUDs, injectables, condoms, female barrier methods and sterilization). Non-programme methods refer to those that are not provided through any structured programme; these methods include calendar rhythm (commonly referred to as 'safe period' in Sri Lanka), withdrawal, abstinence and other traditional methods."
Asunto(s)
Conducta Anticonceptiva , Anticoncepción , Estudios de Evaluación como Asunto , Planificación en Salud , Accesibilidad a los Servicios de Salud , Evaluación de Programas y Proyectos de Salud , Población Rural , Asia , Demografía , Países en Desarrollo , Servicios de Planificación Familiar , Población , Características de la Población , Sri LankaRESUMEN
Previous research in this laboratory, using photoactivatable radioiodinated lipopolysaccharide derivatized with sulfosuccinimidyl-2-(p-azidosalicylamide)-1,3'-dithiopropionate (125I-ASD-LPS), has resulted in the identification of a specific LPS receptor with a molecular mass of approximately 73 kDa on murine lymphocytes and splenic macrophages. The experiments presented in this report investigated whether a similar LPS-binding protein was also expressed on human peripheral blood populations, including monocytes, lymphocytes, neutrophils, platelets, and erythrocytes. Each cell population was incubated with 125I-ASD-LPS, UV irradiated, washed, reduced, and solubilized, and the cell lysates were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by autoradiography. On all of the cell populations, except erythrocytes, a similar 73-kDa LPS-binding protein was present. In addition, each population also expressed lower-molecular-weight secondary LPS-binding proteins, some of which were conserved among the populations. Binding of the photoactivatable LPS probe was found to be both time and temperature dependent. These data support the concept that the 73-kDa LPS-binding protein is conserved on multiple cell types from a variety of species.
Asunto(s)
Células Sanguíneas/química , Proteínas Portadoras/análisis , Glicoproteínas de Membrana , Proteínas de Fase Aguda/análisis , Plaquetas/química , Humanos , Lipopolisacáridos/metabolismo , Peso Molecular , Neutrófilos/químicaAsunto(s)
Infecciones por VIH/epidemiología , Abuso de Sustancias por Vía Intravenosa/epidemiología , Adulto , Métodos Epidemiológicos , Femenino , Infecciones por VIH/mortalidad , Infecciones por VIH/transmisión , Humanos , Estudios Longitudinales , Masculino , Modelos Teóricos , Abuso de Sustancias por Vía Intravenosa/complicaciones , Estados UnidosRESUMEN
Research data describing the prevalence and patterns of behaviors that place persons at increased risk of HIV infection are extremely limited. The scarcity of data has constrained potential applications of surveillance data, research on specific high-risk behaviors, and epidemiological studies. This article critically reviews available research for four population groups: intravenous drug users, homosexual males, and sexually active adolescents and adults. The fallacies inherent in estimating risk group size underscore the need for population-based research that can provide detailed data on sexual and drug use behaviors.
Asunto(s)
Infecciones por VIH/etiología , Homosexualidad , Conducta Sexual , Trastornos Relacionados con Sustancias/complicaciones , Adolescente , Adulto , Femenino , Infecciones por VIH/epidemiología , Infecciones por VIH/transmisión , Humanos , Masculino , Factores de Riesgo , Estados UnidosRESUMEN
This study examines the influence of a selected set of determinants of contraceptive method switching in rural Sri Lanka. Of interest is the question of how change in contraceptive practice at the individual level can account for patterns observed at the aggregate level. Based on calendar data on contraceptive use over a 3-year period, collected for more than 3,000 married women in a 1986 survey, the multivariate analysis shows that women who attain all or a significant proportion of their desired fertility tend to switch to more effective methods. Women who experience method failure tend to switch methods, usually to a type that is more effective. The woman's background determinants of age and education have small but significant effects on method switching, whereas the effect of household economic well-being is not significant. There is strong indication that rural couples are practicing contraception in a nonrandom fashion, switching methods in accordance with changes in their fertility motivations and contraceptive experience.
Asunto(s)
Conducta de Elección , Conducta Anticonceptiva/psicología , Anticoncepción/métodos , Población Rural , Anticoncepción/psicología , Anticoncepción/tendencias , Conducta Anticonceptiva/estadística & datos numéricos , Conducta Anticonceptiva/tendencias , Femenino , Fertilidad , Humanos , Modelos Psicológicos , Motivación , Análisis de Regresión , Sri LankaRESUMEN
Previously we had utilized the spin trap 5,5 dimethyl-1-pyrroline-N-oxide (DMPO) to detect superoxide (.O2-) formation by human neutrophils stimulated with phorbol myristate acetate (PMA) or opsonized zymosan. When N-formyl-methionyl-leucyl-phenylalanine (FMLP) or concanavalin A were substituted as the neutrophil stimulus spin trap evidence of neutrophil free radical production was not detected. Consequently, the hypothesis that DMPO interfered with neutrophil stimulus response coupling was examined. DMPO exhibited a concentration-related inhibition of neutrophil .O2- secretion (ferricytochrome C reduction) following exposure to six different stimuli. The extent of inhibition was stimulus dependent--large (FMLP, concanavalin A), moderate (PMA, opsonized zymosan, A23187), and mild (arachidonic acid). Inhibition was reversible. Onset was nearly instantaneous and was observed even if DMPO was added after stimulus-induced .O2- formation was ongoing. DMPO had only minimal effect on .O2- production by a cell-free NADPH-oxidase membrane preparation. DMPO also inhibited the neutrophil degranulation response for elastase and lactoferrin but not vitamin B12 binding protein. DMPO-mediated inhibition of neutrophil function was not related to alteration in stimulus binding (FMLP or concanavalin A). DMPO had minimal impact on the stimulus-induced rise in intracellular calcium. However, the presence of DMPO resulted in a concentration-dependent depolarization of the resting neutrophil membrane and blunting of the depolarization response to each stimulus examined. These data are of importance to investigators applying spin-trapping techniques to phagocytic cells and suggest DMPO could be used as a tool for investigating neutrophil stimulus-response mechanisms.
Asunto(s)
Óxidos N-Cíclicos/farmacología , Neutrófilos/fisiología , Marcadores de Spin , Ácido Araquidónico , Ácidos Araquidónicos/farmacología , Calcimicina/farmacología , Concanavalina A/farmacología , Grupo Citocromo c/sangre , Gránulos Citoplasmáticos/efectos de los fármacos , Gránulos Citoplasmáticos/fisiología , Humanos , Potenciales de la Membrana/efectos de los fármacos , N-Formilmetionina Leucil-Fenilalanina/farmacología , Neutrófilos/efectos de los fármacos , Neutrófilos/ultraestructura , Proteínas Opsoninas , Superóxidos/sangre , Acetato de Tetradecanoilforbol/farmacología , Zimosan/farmacologíaRESUMEN
Hydroxyl radical (.OH) formation by neutrophils in vitro requires exogenous iron. Two recent studies [Britigan, Rosen, Thompson, Chai & Cohen (1986) J. Biol. Chem. 261, 17026-17032; Winterbourn (1987) J. Clin. Invest. 78, 545-550] both reported that neutrophil degranulation could potentially inhibit the formation of .OH, but differed in their conclusions as to the responsible factor, myeloperoxidase (MPO) or lactoferrin (LF). By using a previously developed spin-trapping system which allows specific on-line detection of superoxide anion (O2-) and .OH production, the impact of MPO and LF release on neutrophil .OH production was compared. When iron-diethylenetriaminepenta-acetic acid-supplemented neutrophils were stimulated with phorbol myristate acetate or opsonized zymosan, .OH formation occurred, but terminated prematurely in spite of continued O2- generation. Inhibition of MPO by azide increased the magnitude, but not the duration, of .OH formation. No azide effect was noted when MPO-deficient neutrophils were used. Anti-LF antibody increased both the magnitude and duration of .OH generation. Pretreatment of neutrophils with cytochalasin B to prevent phagosome formation did not alter the relative impact of azide or anti-LF on neutrophil .OH production. An effect of azide or anti-LF on spin-trapped-adduct stability was eliminated as a confounding factor. These data indicate that neutrophils possess two mechanisms for limiting .OH production. Implications for neutrophil-derived oxidant damage are discussed.
Asunto(s)
Degranulación de la Célula , Hidróxidos/sangre , Hierro/farmacología , Lactoferrina/sangre , Lactoglobulinas/sangre , Neutrófilos/fisiología , Peroxidasa/sangre , Anticuerpos , Azidas/farmacología , Espectroscopía de Resonancia por Spin del Electrón , Radicales Libres , Humanos , Radical Hidroxilo , Técnicas In Vitro , Neutrófilos/efectos de los fármacos , Neutrófilos/enzimología , Consumo de Oxígeno , Superóxido Dismutasa/farmacología , Superóxidos/sangre , Acetato de Tetradecanoilforbol/farmacología , Zimosan/farmacologíaRESUMEN
Activation of human neutrophils leads to secretion of myeloperoxidase (MPO) with resulting generation of several oxidant species including OCl-. Spin trapping techniques employing 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) are being applied increasingly to the investigation of free radical production by in vitro and in vivo experimental systems which contain neutrophils. Because such knowledge is critical to the interpretation of these data, we examined the impact of MPO and MPO-derived oxidants on DMPO spin adduct formation and stability. Addition of increasing concentrations of OCl- to DMPO yielded a number of EPR-detectable products including DMPO-OH. However, the concentration of OCl- required was in excess of that expected under physiologic conditions. Addition of purified human MPO and H2O2 to DMPO yielded EPR spectra consisting of small DMPO-OH peaks. The addition of MPO and H2O2 to preformed DMPO-OH and DMPO-CH3 resulted in rapid destruction of these spin adducts. Thus MPO/H2O2 appeared to both generate and destroy DMPO spin adducts. Neutrophils stimulated with phorbol myristate acetate or opsonized zymosan generated large DMPO-OOH and DMPO-OH peaks as well as small DMPO-CH3 peaks. Addition of the MPO inhibitor azide to the reaction mixture had no effecting on resulting DMPO-OH or DMPO-CH3 peak amplitudes but increased that of DMPO-OOH. These data suggest that MPO-derived oxidants likely have little impact on the nature of EPR spectra resulting from DMPO spin trapping of free radical species following neutrophil stimulation. Because MPO oxidants did appear to react with DMPO the ability of DMPO to protect a biologic target from in vitro MPO injury was examined. DMPO (greater than 10 mM) significantly decreased MPO/H2O2/Cl- -mediated erythrocyte hemolysis as assessed by 51Cr release. The experimental and/or pharmacologic implications of this observation require further study.