RESUMEN
The present paper considers a multidimensional view of the standard for the development process of human fetuses. An efficient method by which to find a multidimensional standard curve for the development process of human fetuses is proposed in which a logistic function with three parameters is utilized as an underlying model and a nonlinear regression method is applied. The proposed method also identifies an approximate prediction region, which can be efficiently applied to diagnose fetal malformation.
Asunto(s)
Desarrollo Fetal , Feto/anatomía & histología , Modelos Estadísticos , Algoritmos , Pueblo Asiatico , Anomalías Congénitas/diagnóstico , Largo Cráneo-Cadera , Retardo del Crecimiento Fetal/diagnóstico , Feto/anomalías , Cabeza/anatomía & histología , Cabeza/embriología , Humanos , Húmero/anatomía & histología , Húmero/embriología , Japón , Funciones de Verosimilitud , Modelos Logísticos , Análisis Multivariante , Valores de Referencia , Muslo/anatomía & histología , Muslo/embriología , Tórax/anatomía & histología , Tórax/embriologíaRESUMEN
Reg I (regenerating gene product I) is a growth factor that plays a central role in the generation and regeneration of the gastric mucosal architecture. On the other hand, mouse Reg I mRNA is expressed at the highest levels in the small intestine among the gastrointestinal tissues. In the current study, with the aim to clarify the role of Reg I protein in the small intestine, the temporal and spatial pattern of Reg I expression and the phenotype of Reg I-knockout mice in the tissue were examined. In the wild-type mice, immunohistochemistry localized Reg I protein expression in absorptive cells located in the lower half of the intestinal villi. Reg I expression was undetectable until embryonic day 13 (E13), when the fetal intestine still lacks villous structure; however, it dramatically increased at E17 along with the formation and maturation of the fetal intestinal villi. In the small intestine of the adult Reg I-knockout mice, less densely packed, round-shaped aberrant morphology of the absorptive cells was observed light microscopically, and electron microscopical examination revealed a strikingly loose connection of these cells to the basement membrane. Antiproliferating cell nuclear antigen staining and anti-Ki67 staining demonstrated the marked decrease in the number of proliferating cells in the small intestinal mucosa of the knockout mice. The cell migration speed visualized by one shot labeling of 5-bromodeoxyuridine was significantly slower in the knockout mice. These phenotypes of Reg I-knockout mice emerged, in accordance with the temporal pattern of Reg I expression described above, from E17. Reg I was considered to be a regulator of cell growth that is required to generate and maintain the villous structure of the small intestine.
Asunto(s)
Proliferación Celular , Mucosa Intestinal/citología , Intestino Delgado/citología , Litostatina/fisiología , Microvellosidades/ultraestructura , Animales , Procesos de Crecimiento Celular , Movimiento Celular , Femenino , Regulación del Desarrollo de la Expresión Génica , Mucosa Intestinal/ultraestructura , Intestino Delgado/ultraestructura , Litostatina/genética , Masculino , Ratones , Ratones Endogámicos ICR , Ratones Noqueados , Fenotipo , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa InversaRESUMEN
Using a mouse exo utero system to examine the effects of fetal jaw movement on the development of condylar cartilage, we assessed the effects of restraint of the animals' mouths from opening, by suture, at embryonic day (E)15.5. We hypothesized that pre-natal jaw movement is an important mechanical factor in endochondral bone formation of the mandibular condyle. Condylar cartilage was reduced in size, and the bone-cartilage margin was ill-defined in the sutured group at E18.5. Volume, total number of cells, and number of 5-bromo-2'-deoxyuridine-positive cells in the mesenchymal zone were lower in the sutured group than in the non-sutured group at E16.5 and E18.5. Hypertrophic chondrocytes were larger, whereas fewer apoptotic chondrocytes and osteoclasts were observed in the hypertrophic zone in the sutured group at E18.5. Analysis of our data revealed that restricted fetal TMJ movement influences the process of endochondral bone formation of condylar cartilage.
Asunto(s)
Placa de Crecimiento/embriología , Mandíbula/embriología , Cóndilo Mandibular/embriología , Animales , Antimetabolitos , Apoptosis/fisiología , Bromodesoxiuridina , Recuento de Células , Tamaño de la Célula , Condrocitos/patología , Desarrollo Fetal , Edad Gestacional , Hipertrofia , Mesodermo/patología , Ratones , Ratones Endogámicos ICR , Ratones Endogámicos , Osteoclastos/patología , Osteogénesis/fisiología , Técnicas de SuturaRESUMEN
To establish an in vivo experimental system for developmental endocrinology research, AtT-20 cells, a corticotropic tumor cell line, were transplanted by exo utero manipulation into mouse embryos on embryonic day 14. The induced tumor secreted ACTH in situ, and the circulating ACTH level was elevated. This was the first model for studying the regulation of ACTH in the mouse fetal adrenal in vivo and the first continuous ACTH treatment model in rodent fetuses. The changes in the adrenal gland from the tumor-induced embryos were analyzed by light microscopic morphometry, immunohistochemistry for steroidogenic enzymes, and electron microscopy. In the treated adrenal, the volume of the inner cortical zone was significantly larger than that in controls. In the inner zone, cell density was decreased, and average cell size was increased, whereas bromodeoxyuridine-incorporation was not increased. The enlarged inner zone cells expressed an enhanced level of cytochrome P45011beta, the corticosterone-synthesizing enzyme, and the serum corticosterone level was increased. Electron microscopy showed an active form of the organelles involved in steroidogenesis. These findings indicate that ACTH stimulates both adrenocortical hypertrophy and steroidogenesis in fetal mice. Potential perspectives of the novel paradigm in this research for molecular developmental endocrine study are discussed.
Asunto(s)
Glándulas Suprarrenales/embriología , Hormona Adrenocorticotrópica/metabolismo , Feto/fisiología , Feto/cirugía , Trasplante de Neoplasias , Adenohipófisis , Neoplasias Hipofisarias/metabolismo , Trasplante Heterotópico , Glándulas Suprarrenales/metabolismo , Glándulas Suprarrenales/patología , Animales , Corticosterona/sangre , Inmunohistoquímica , Ratones/embriología , Microscopía Electrónica , Neoplasias Hipofisarias/patología , Células Tumorales CultivadasRESUMEN
In order to study the reaction mechanism of RNase Rh from Rhizopus niveus, the rates of cleavage of four 2',3'-cyclic nucleotides by mutant enzymes of RNase Rh, H46F, H109F, E105Q, and K108L were measured. H46F is virtually inactive towards cyclic nucleotides, but H109F hydrolyzed these substrates at 0.7-4.5% of the rates of the native RNase Rh. The other mutants hydrolyzed 2',3'-cyclic nucleotides at 15-20% of the rates of the native enzyme. Relative enzymatic activities towards four cyclic nucleotides of H109F in the hydrolysis reaction (2nd step) were much higher than in the transphosphorylation reaction (the 1st step). In the presence of a 13-fold excess of uridine, H109F catalyzed the transphosphorylation reaction of 2',3'-cyclic AMP (A>p) to ApU. However, this reaction was not catalyzed by H46F mutant or native RNase Rh. These results showed that His46 is crucial to the hydrolysis reaction, and to the reversed reaction of the transphosphorylation reaction. We suggest that His46 in RNase Rh plays a major role in these reactions by acting as a base catalyst to activate water and the 5'-hydroxyl group of nucleosides, respectively.
Asunto(s)
Endorribonucleasas/metabolismo , Histidina/genética , Histidina/fisiología , Rhizopus/enzimología , Sitios de Unión/genética , Sitios de Unión/fisiología , Fosfatos de Dinucleósidos/biosíntesis , Endorribonucleasas/genética , Concentración de Iones de Hidrógeno , Hidrólisis/efectos de los fármacos , Cinética , Mutación/genética , Mutación/fisiología , Fosforilación , Rhizopus/química , Rhizopus/genéticaRESUMEN
The long form of the leptin receptor (Ob-Rb) has a cytoplasmic domain which activates the JAK-STAT signal transduction pathway. It is related to appetite and energy expenditure and is expressed in various parts of the brain in adults. In embryos, however, the detailed distribution of Ob-Rb expression sites and the function of the leptin-Ob-Rb system remain unclear, although leptin is detected in human cord plasma and leptin mRNA is detected in mouse embryos. In this study, we investigated the Ob-Rb mRNA expression pattern in the brains of mouse embryos and newborn mice by RT-PCR and in situ hybridization. At embryonic day 10.5 (E10.5), Ob-Rb mRNA was already detected in the brain by RT-PCR. By in situ hybridization, Ob-Rb mRNA was observed in the ventricular zone of the rhombencephalon at E11.5. At E12.5, it was also expressed in the ventricular zone of the telencephalon, mesencephalon and cerebellar primordium. From E14. 5 it was expressed in the cortical plate of the telencephalon and the ventricular zone of the thalamus. At E16.5, it was expressed in the premamillary hypothalamic nucleus, superficial gray matter of the superior colliculus, external germinal and Purkinje cell layers of the cerebellum, and facial nucleus. At E18.5, it was expressed in the arcuate nucleus and ventromedial hypothalamic nucleus. These results suggest that the leptin-Ob-Rb system is related to brain development.
Asunto(s)
Encéfalo/embriología , Proteínas Portadoras/genética , Leptina/metabolismo , Receptores de Superficie Celular , Animales , Animales Recién Nacidos , Encéfalo/metabolismo , Embrión de Mamíferos , Femenino , Ratones , Ratones Endogámicos ICR , Embarazo , ARN Mensajero/metabolismo , Receptores de LeptinaRESUMEN
EXTL3 encodes alpha1,4-N-acetylglucosaminyltransferases I and II enzymes, which are involved in chain initiation and elongation of heparan sulfate (HS) biosynthesis. HS proteoglycans are critically involved in a variety of biological phenomena at various levels of complexity in adult and embryonic lives. Dedicated functions of HS proteoglycans are due to variable HS chains that interact with different cellular proteins, and can be regulated by their synthesizing enzymes. EXTL3 protein is also a putative receptor for Reg protein, a growth signal mediator for the beta-cells of the pancreas. The present Northern blot analysis revealed two EXTL3 transcripts (6.2 and 3.4 kb), which were differentially expressed in different mouse adult tissues. The strongest expression was in the adult brain and pancreas. In the adult pancreas, a comparable intensity of both signals was detected. In the embryonic pancreas, the longer transcript was predominant, and showed a biphasic expression pattern with a peak at E11.5, whereas the shorter one showed a steady level of expression throughout the whole period of pancreatic development. By in situ hybridization, the acini of adults and embryos were strong positive for EXTL3 mRNA. Mature islets of Langerhans gave a weak signal, whereas the developing islets showed moderately positive reaction albeit less intense than the acini. In situ hybridization revealed a wide and differential expression pattern of EXTL3 mRNA in embryonic tissues. At the early stages, intense reaction was found in the developing neurons of the brain and spinal cord and in the epithelia of the developing GIT, pancreas, liver and kidney of embryos. Our data suggested that EXTL3 expression is developmentally regulated, and may contribute to the regulated production of HS in different adult and embryonic tissues.
Asunto(s)
Regulación del Desarrollo de la Expresión Génica , N-Acetilglucosaminiltransferasas/genética , Páncreas/enzimología , Animales , Femenino , Ratones , Ratones Endogámicos ICR , N-Acetilglucosaminiltransferasas/metabolismo , Organogénesis , Páncreas/embriología , Embarazo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa InversaRESUMEN
The system for directly manipulating mammalian embryos is an advantage not only to revealing the various developmental evidences but also in evaluating the availability of possible techniques for fetal surgery. "Exo utero development in mice" was reported by Muneoka et. al. and has been one of the most useful techniques in experimental embryology \ including developmental neurobiology and prenatal plastic surgery for malformations. We have applied this method to establish experimental animal models with congenital disorders and examined the mechanisms of normal and abnormal morphogenesis. In this paper, we would like to introduce the technique of exo utero development in combination with a microinjection system in mice embryos.
Asunto(s)
Encéfalo/fisiopatología , Corteza Cerebral/irrigación sanguínea , Infarto Cerebral/diagnóstico , Convulsiones/etiología , Anfetaminas , Encéfalo/patología , Infarto Cerebral/complicaciones , Circulación Cerebrovascular , Niño , Electroencefalografía , Potenciales Evocados Somatosensoriales , Femenino , Humanos , Radioisótopos de Yodo , Yofetamina , Imagen por Resonancia Magnética , Tomografía Computarizada de Emisión , Tomografía Computarizada por Rayos XRESUMEN
To determine the effect of intranasal administration of salmon calcitonin on glucocorticoid-induced osteoporosis in children with nephrosis, we gave 100 U of calcitonin intranasally on alternate days with 1 alpha-hydroxyvitamin D3 to five children, 8 to 12 years of age, with frequently relapsing nephrosis. Four patients with osteoporosis, 10 to 14 years of age, were treated only with 1 alpha-hydroxyvitamin D3 and served as control subjects. Both groups were treated with an almost equal amount of glucocorticoids previously and during this study period. Bone mineral content of the spine was measured by a quantitative computed tomographic technique. The bone mineral content was preserved in both cortical and spongeous areas of the vertebrae during the 16-month period in the calcitonin-treated group but was decreased significantly in the control group. Urinary hydroxyproline and calcium excretion decreased significantly in the calcitonin-treated group. The serum calcium and phosphorus concentrations and the parathyroid function did not change significantly in either group. We conclude that calcitonin suppressed bone resorption and might be useful for the long-term treatment of osteoporosis, in combination with 1 alpha-hydroxyvitamin D3, in children with nephrosis requiring long-term glucocorticoid therapy.
Asunto(s)
Calcitonina/administración & dosificación , Glucocorticoides/efectos adversos , Nefrosis/complicaciones , Osteoporosis/prevención & control , Administración Intranasal , Aerosoles , Densidad Ósea , Niño , Quimioterapia Combinada , Glucocorticoides/administración & dosificación , Humanos , Hidroxicolecalciferoles/administración & dosificación , Nefrosis/tratamiento farmacológico , Nefrosis/metabolismo , Osteoporosis/inducido químicamente , Osteoporosis/metabolismo , Recurrencia , Columna Vertebral/diagnóstico por imagen , Tomografía Computarizada por Rayos XRESUMEN
Using a model of an ectopic corticotrophic tumor transplanted in mouse embryos, we now report several new findings. One relates to fetal adrenocortex-medulla interactions and others to feedback regulation of the pituitary by adrenal products or other factors in mouse embryos.
Asunto(s)
Corteza Suprarrenal/embriología , Médula Suprarrenal/embriología , Hormona Adrenocorticotrópica/metabolismo , Trasplante de Neoplasias , Hipófisis/embriología , Neoplasias Hipofisarias/patología , Animales , Trasplante de Células , Retroalimentación , Feto/fisiología , Ratones/embriologíaRESUMEN
This study was aimed to evaluate the source of endothelin-1 (ET-1) in cirrhotic patients. ET-1 is implicated in the pathogenesis of portal hypertension. However, the mechanism and source for increased plasma ET-1 in cirrhotic patients are still obscure. Plasma ET-1 levels in systemic (SV), superior mesenteric (SMV), and splenic venous (SPV) blood were measured in 23 patients with cirrhosis and 8 controls with normal liver. Fourteen removed spleens were immunohistochemically studied for ET-1, CD34, CD68, and CD20. In situ hybridization was done to localize ET-1 messenger RNA (mRNA). In cirrhosis, ET-1 levels in both SMV and SPV were higher than in SV. ET-1 in SV and SPV were significantly higher in cirrhotic patients than in control patients. Three groups of cells in the spleen expressed both protein and mRNA of ET-1: endothelial cells in the sinus, which were also stained for CD34; cells in the germinal center; and cells in the marginal zone of lymphoid sheaths and follicles, which were also stained for CD20 but not for CD34 and CD68. The ET-1 concentration released from the spleen was in parallel with the grade of ET-1 expression in the spleen. The spleen is one of the major sites of ET-1 release in cirrhotic patients. Endothelial cells of the splenic sinus and possibly B lymphocytes in the germinal center and marginal zone of lymphoid sheaths and follicles seem to be the sites of ET-1 production in the spleen.
Asunto(s)
Endotelina-1/metabolismo , Hipertensión Portal/metabolismo , Mucosa Intestinal/metabolismo , Cirrosis Hepática/complicaciones , Bazo/metabolismo , Adulto , Anciano , Anciano de 80 o más Años , Antígenos CD/análisis , Antígenos CD34/análisis , Antígenos de Diferenciación Mielomonocítica/análisis , Endotelina-1/genética , Femenino , Humanos , Hibridación in Situ , Masculino , Persona de Mediana Edad , Vena Porta/fisiopatología , Presión VenosaRESUMEN
Despite extensive studies on the crucial functions of Ras and c-Myc in cellular proliferation and transformation, their roles in regulating cell adhesion are not yet fully understood. Involvement of Ras in modulating integrin activity by inside-out signaling has been recently reported. However, in contrast to R-Ras, H-Ras was found to exhibit a suppressive effect. Here we show that ectopic expression of a constitutively active H-Rasv12, but not c-Myc alone, in a hemopoietic cell line induces activation of very late Ag-4 (VLA-4, alpha4beta1) integrin without changing its surface expression. Intriguingly, coexpression of H-Rasv12 and c-Myc in these cells results in not only the activation of VLA-4, but also the induction of expression of VCAM-1, the counterreceptor for VLA-4, thereby mediating a marked homotypic cell aggregation. In addition, H-Rasv12-induced VLA-4 activation appears to be partly down-regulated by coexpression with c-Myc. Our results represent an unprecedented example demonstrating a novel role for H-Rasv12 in the regulation of cell adhesion via c-Myc-independent and -dependent mechanisms.