RESUMO
Temporal expression patterns and activity of two cyclooxygenase (COX-1 and COX-2) isoforms were analysed during early chick embryogenesis to evaluate their roles in development. COX-2 inhibition with etoricoxib resulted in significant structural anomalies such as anophthalmia (born without one or both eyes), phocomelia (underdeveloped or truncated limbs), and gastroschisis (an opening in the abdominal wall), indicating its significance in embryogenesis. Furthermore, the levels of PGE2, PGD2, PGF2α, and TXB2 were assessed using quantitative LC-MS/MS to identify which effector prostanoid (s) had their synthesis initiated by COX-2. COX-2 inhibition was only shown to reduce the level of PGE2 significantly, and hence it could be inferred that the later could be largely under the regulation of activated COX-2 in chick embryos. The compensatory increase in the activity of COX-1 observed in the etoricoxib-treated group helped to maintain the levels of PGD2, PGF2α, and TXB2. Though the roles of these three prostanoids in embryogenesis need to be further clarified, it appears that their contribution to the observed developmental anomalies is minimal. This study has shown that COX-2 is functionally active during chick embryogenesis, and it plays a central role in the structural configuration of several organs and tissues through its downstream effector molecule PGE2.
Assuntos
Proteínas Aviárias/metabolismo , Embrião de Galinha/embriologia , Ciclo-Oxigenase 2/metabolismo , Dinoprostona/metabolismo , Animais , Proteínas Aviárias/genética , Embrião de Galinha/anormalidades , Embrião de Galinha/efeitos dos fármacos , Embrião de Galinha/metabolismo , Galinhas , Ciclo-Oxigenase 2/genética , Inibidores de Ciclo-Oxigenase 2/farmacologia , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacosRESUMO
Cyclopia is a congenital anomaly characterized by the presence of a single or partially divided eye in a single orbit at the body midline. This condition is usually associated with other severe facial malformations, such as the absence of the nose and, on rare occasions, the presence of a proboscis located above the ocular structures. The developmental origin of cyclopia in vertebrates is the failure of the embryonic prosencephalon to divide properly during the formation of the two bilateral eyes. Although the developmental origin of the cyclopia-associated proboscis is not clear, it has been suggested that this unique structure results from the disrupted morphogenesis of the olfactory placodes, the main organizers of the developing nose. In this study, we report a spontaneous congenital case of cyclopia with a proboscis-like appendage in a chick embryo. By means of both conventional histology and immunohistochemical methods, we have analyzed this anomaly in detail to suggest an alternative identity for the anatomical embryonic features of cyclopic vertebrate embryos displaying a proboscis. Our findings are discussed in the context of previously reported cases of cyclopia, and provide additional insight into this complex congenital malformation.
Assuntos
Embrião de Galinha/anormalidades , Holoprosencefalia/veterinária , Animais , Holoprosencefalia/embriologia , Holoprosencefalia/patologia , Imuno-HistoquímicaRESUMO
BACKGROUND: Temperature and relative humidity (RH) are very important factors affecting embryo development, hatchability, and posthatch performance. This study aimed at characterizing embryonic metabolic and behavioural response to a harsh incubation environment generated by manipulations (elevations and drops) in these two key factors. This study was aimed at establishing patterns of metabolic and behavioural response, as well as mortality and the development of malformations, all of which can potentially be used in monitoring incubating operations and diagnosing problems with faulty equipment. RESULTS: Of all the parameters monitored throughout embryonic development the ones shown to be most affected were: albumen-weight to egg-weight ratio (AR); yolk-weight to egg-weight ratio (YR); embryo-weight to egg-weight ratio (ER); heart rate (HR); voluntary movements per minute (VMM); mortality rates; malformation prevalence and type. The most significant changes in the evolution of AR and YR throughout incubation involved delay and reduction in the amplitude of the expected drop in albumen and yolk levels, reflecting lower nutrient consumption by the embryo. ER tended to grow more slowly and remain lower than the established normal, especially in embryos challenged with temperature treatments. HR and VMM were considered to be strong indicators of embryonic stress, as all treatments applied resulted in elevated heart rate and decreased embryo movement. Mortality rates for both temperature-related treatments were higher during the first four days of incubation. Changes in relative humidity have produced less radical effects on mortality. Malformation rates were higher for embryos subjected to high incubation temperatures and were most prominently related to the abdominal wall, head, skull and limbs. Overall, manipulations in environmental (incubator) temperature during incubation produced more drastic changes in embryo development than humidity-related manipulations, especially where mortality and malformation rates were concerned. CONCLUSIONS: This paper describes changes in embryonic metabolism and behaviour, as well as in mortality and malformation rates, in response to manipulations in environmental temperature and relative humidity. Together with further studies, these patterns may prove helpful in the diagnosis of equipment malfunctions relating to temperature or relative humidity.
Assuntos
Embrião de Galinha/crescimento & desenvolvimento , Umidade , Temperatura , Albuminas/metabolismo , Animais , Embrião de Galinha/anormalidades , Temperatura Baixa , Gema de Ovo/metabolismo , Frequência Cardíaca , MovimentoRESUMO
Cephalothoracopagus embryos are conjoined twins, who share parts of their heads, necks and bodies. Our study aims at presenting a detailed morphological analysis of a cephalothoracopagus chick embryo of developmental stage 31. Because none of the existing theories can explain the genesis of the phenotype of this embryo, we also suggest a hypothesis, which explains it. Beside the cephalothoracopagus embryo, we investigated five control embryos. With the aid of the high-resolution episcopic microscopy (HREM) technique, we created digital volume data and three-dimensional (3D) computer models of the organs and arteries of the embryos. We used the 3D models for topological analysis and for measuring the diameters of the great intrathoracic arteries. The malformed embryo showed two body backs, each containing a notochord, spinal cord and dorsal aorta. The body backs continued into separated lower bodies. The embryo had a single, four-chambered heart, single respiratory tract and single upper alimentary tract. The topology of the pharyngeal arch arteries was normal, and the diameters of these arteries were similar to that of the control embryos. We classified the embryo we investigated as a yet unknown malformation and suggest a hypothesis explaining its genesis.
Assuntos
Embrião de Galinha/anormalidades , Animais , Anormalidades Cardiovasculares/embriologia , Anormalidades Cardiovasculares/patologia , Anormalidades Cardiovasculares/veterinária , Simulação por Computador , Imageamento Tridimensional/métodos , Microscopia Acústica/métodos , Modelos Anatômicos , Gêmeos Unidos/embriologia , Gêmeos Unidos/patologiaRESUMO
Maternal diseases like diabetes mellitus may cause developmental defects. Supplementation with folic acid and vitamin C during the periconceptional period has been shown to prevent some neural tube and congenital heart defects. Hearts were dissected from 5 days-old White Leghorn chick embryos, the cells isolated and cultured in micromass under diabetic conditions, with and without folic acid and vitamin C. Contractile activity, cell viability (resazurin reduction) and protein assays were performed. Results indicated diabetic conditions reduced contractile activity and cell viability, whilst vitamin C (100 µM) and folic acid (1 mM) administered concurrently significantly improved them to values comparable with the control. Day 3 chick embryos in ovo were injected with glucose+hydroxybutyrate or a combination of these and vitamins. Diabetic conditions caused gross and histological malformations, but these effects were abrogated by vitamin supplement. Teratogenic effects on heart development could possibly be prevented by vitamin supplementation during pregnancy.
Assuntos
Ácido Ascórbico/farmacologia , Complicações do Diabetes/prevenção & controle , Ácido Fólico/farmacologia , Cardiopatias Congênitas/prevenção & controle , Vitaminas/farmacologia , Ácido 3-Hidroxibutírico/toxicidade , Animais , Antioxidantes/farmacologia , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , Embrião de Galinha/anormalidades , Glucose/toxicidade , Coração , Cardiopatias Congênitas/etiologia , Teratogênicos/toxicidadeRESUMO
The toxic potential of cadmium (Cd) is well-documented for young and adult vertebrates, but it is still poorly understood in the early stages of development. In this study, cadmium effects were investigated on Gallus gallus embryos after injection of CdCl(2) (5µM and 50µM) within the egg air chamber, and incubation for 48 and 72h. After exposure, morphological and enzymatic analyses for glucose-6-phosphate dehydrogenase (G6PDH) and glutathione S-transferase (GST) were performed. Critical morphological abnormalities occurred after exposure to the highest concentration of cadmium, mainly in the cephalic region, indicating the powerful teratogenic effect of Cd to chick embryos. Cd exposure did not alter enzymatic activities when compared to the control group, but the levels of G6PDH activity were highest in older embryos at stage 19, indicating that antioxidant defenses are not so robust in the earliest embryo stages.
Assuntos
Cádmio/toxicidade , Embrião de Galinha/efeitos dos fármacos , Poluentes Ambientais/toxicidade , Teratogênicos/toxicidade , Animais , Embrião de Galinha/anormalidades , Embrião de Galinha/enzimologia , Glucosefosfato Desidrogenase/metabolismo , Glutationa Transferase/metabolismoRESUMO
Infants with intrauterine growth retardation are prone to intestinal disorders. The morphological and molecular mechanisms that lead to these complications are not completely understood and suitable experimental models are necessary. The aim of this study was to characterize mesenteric artery (MA) reactivity, small intestine morphometry and intestinal expression of vascular endothelial growth factor (VEGF) in a chicken model of hypoxia-induced fetal growth restriction. Chicken embryos (15 and 19 incubation days) and hatchlings (<3-h-old and 1-d-old) were incubated under hypoxic (15% O2 from day 0 to day 19 of incubation) or normoxic conditions. Vascular reactivity was studied using wire miography. Intestinal morphometry was assessed in hematoxyline-eosine-stained sections. VEGF mRNA expression was determined by RT-PCR analysis. Hypoxia increased the responsiveness of chicken embryo MAs to the adrenergic agonist norepinephrine, the polypeptide endothelin (ET)-1, and the nitric oxide donor sodium nitroprusside and decreased the responsiveness to the endothelium-dependent relaxant agonist acetylcholine. However, the majority of these alterations, with the exception of the hyperresponsiveness to ET-1, were not present in the hypoxic hatchlings. When intestinal histology was analyzed, subtle hypoxia-induced changes were noted in the villi and the muscularis propria from the hatchlings. Hypoxic incubation also diminished the expression of VEGF mRNA in the terminal ileum of the hatchlings. In conclusion, chronic moderate hypoxia during incubation results in subtle but significant alterations in chicken MA reactivity, small intestine morphology and VEGF expression. Whether these alterations may have a direct effect on the functional status of the intestine remains to be investigated.
Assuntos
Embrião de Galinha/anormalidades , Hipóxia/patologia , Hipóxia/fisiopatologia , Íleo/patologia , Artérias Mesentéricas/fisiopatologia , Animais , Animais Recém-Nascidos , Galinhas , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Regulação da Expressão Gênica no Desenvolvimento , Hipóxia/embriologia , Hipóxia/genética , Hipóxia/metabolismo , Íleo/embriologia , Íleo/metabolismo , Artérias Mesentéricas/efeitos dos fármacos , Artérias Mesentéricas/embriologia , RNA Mensageiro/metabolismo , Fatores de Tempo , Fator A de Crescimento do Endotélio Vascular/genética , Fator A de Crescimento do Endotélio Vascular/metabolismo , Vasoconstrição , Vasoconstritores/farmacologia , Vasodilatação , Vasodilatadores/farmacologiaRESUMO
The potential of arsenic to induce neural tube defects (NTDs) remains a topic of controversy. In our previous study, oxidative stress and altered DNA methylation were observed in arsenic-exposed animal models. However, the correlation between these conditions was not fully understood. Therefore, our present aim was to determine whether arsenic exposure results in altered reactive oxygen species levels that affect DNA methylation and may contribute to NTDs in chick embryos. We demonstrated that arsenic-induced NTDs were associated with oxidative stress. Increased intracellular oxidative species and DNA methylation changes were observed following arsenic exposure. These changes were accompanied by a decrease in manganese superoxide dismutase activity. Furthermore, a significant decrease in DNA methyltransferase (DNMT) 1 and 3a expression was observed following arsenic exposure. The known antioxidant N-acetyl-l-cysteine, a known antioxidant, ameliorated global DNA hypomethylation and the decreased DNMT 1 and 3a expression observed during arsenic exposure. In addition, arsenic caused a significant decrease in S-adenosylmethionine (SAM) and significant increase in S-adenosylhomocysteine (SAH). This effect resulted in a significant reduction of the SAM/SAH ratio, which may also contribute to DNA hypomethylation. In conclusion, oxidative stress and reduction in SAM/SAH ratio during arsenic exposure in chick embryos seem to modulate DNA methylation and contribute to arsenic-induced NTDs via epigenetic mechanisms.
Assuntos
Arsênio/farmacologia , Embrião de Galinha/anormalidades , Embrião de Galinha/efeitos dos fármacos , Defeitos do Tubo Neural/induzido quimicamente , Estresse Oxidativo/efeitos dos fármacos , Acetilcisteína/farmacologia , Animais , Epigênese Genética , Feminino , Glutationa Peroxidase/metabolismo , Malondialdeído/metabolismo , Espécies Reativas de Oxigênio/metabolismo , S-Adenosil-Homocisteína/metabolismo , S-Adenosilmetionina/metabolismo , Superóxido Dismutase/metabolismoRESUMO
Early in the history of the thalidomide disaster, chick embryos were "eliminated" as useful in the study of thalidomide. One reason for that conclusion was that many of the early experiments were flawed. We employed a number of experiments to expose chick embryos to thalidomide. Our data show that thalidomide does cause limb reduction defects in chick embryos as long as the embryos are directly exposed to the drug. The most useful techniques are implanting thalidomide-soaked beads into the embryo immediately adjacent to the limb territory or soaking presumptive chick limb territories in thalidomide and then grafting the explants to a host embryo celom. Thalidomide affects the chick limb grafted to a host embryo in a dose response fashion. Furthermore, S-thalidomide and S-EM12 are more teratogenic than R-thalidomide and R-EM12.
Assuntos
Anormalidades Induzidas por Medicamentos , Embrião de Galinha/efeitos dos fármacos , Extremidades/embriologia , Deformidades Congênitas dos Membros , Teratogênicos/toxicidade , Talidomida/toxicidade , Anormalidades Induzidas por Medicamentos/embriologia , Anormalidades Induzidas por Medicamentos/etiologia , Anormalidades Induzidas por Medicamentos/patologia , Animais , Embrião de Galinha/anormalidades , Relação Dose-Resposta a Droga , Extremidades/crescimento & desenvolvimento , Deformidades Congênitas dos Membros/induzido quimicamente , Deformidades Congênitas dos Membros/embriologia , Deformidades Congênitas dos Membros/patologia , Talidomida/administração & dosagemRESUMO
Patterning of the developing vertebrate limb along the anterior-posterior axis is controlled by the zone of polarizing activity (ZPA) via the expression of Sonic hedgehog (Shh) and along the proximal-distal axis by the apical ectodermal ridge (AER) through the production of fibroblast growth factors (FGFs). ZPA grafting, as well as ectopic application of SHH to the anterior chick limb bud, demonstrate that digit patterning is largely influenced by these secreted factors. Although signal transduction pathways have been well characterized for SHH and for FGFs, little is known of how these signals are regulated extracellularly in the limb. The present study shows that alteration of the extracellular environment through trypsin treatment can have profound effects on digit patterning. These effects appear to be mediated by the induction of Shh in host tissues and by ectopic AER formation, implicating the extracellular matrix in regulating the signaling activities of key patterning genes in the limb.
Assuntos
Padronização Corporal/efeitos dos fármacos , Embrião de Galinha/embriologia , Regulação da Expressão Gênica no Desenvolvimento , Proteínas Hedgehog/fisiologia , Botões de Extremidades/embriologia , Tripsina/farmacologia , Animais , Padronização Corporal/fisiologia , Embrião de Galinha/anormalidades , Colagenases/farmacologia , Ectoderma/fisiologia , Ectoderma/transplante , Indução Embrionária , Matriz Extracelular/fisiologia , Feminino , Fibrinolisina/farmacologia , Fatores de Crescimento de Fibroblastos/fisiologia , Botões de Extremidades/anormalidades , Botões de Extremidades/efeitos dos fármacos , Botões de Extremidades/metabolismo , Botões de Extremidades/transplante , Masculino , Camundongos , Morfogênese/efeitos dos fármacos , Pâncreas/embriologia , Transdução de Sinais , Transplante Heterólogo , Transplante Heterotópico , Asas de Animais/anormalidades , Asas de Animais/embriologiaRESUMO
VATER association represents a cluster of Vertebral, Anal, Tracheo-Esophageal, Radial and Renal malformations, and caudal regression syndrome is an entity consisting of a spectrum of congenital anomalies of lower spine and hips associated with genitourinary and lower limb defects. The concurrence of various malformations may be explained by a common defect in blastogenesis, but direct evidence is yet to be accumulated. Here, by the use of autofluorescence and the teratogenic effect of adriamycin, we demonstrated that adriamycin administered to eggs of White Leghorns distributes to the caudal portion of the embryo and foregut epithelium and induces caudal regression and tracheal and pulmonary agenesis. The induction of caudal regression syndrome-like anomaly was developmental stage and dose dependent. Embryos with caudal regression demonstrated tracheoesophageal anomalies, one of the defects included in VATER association. The stages at which anomalies were produced corresponded to that of human embryos between days 22 and 26 (Carnegie stages 10-11). In view of the antitumor activity of adriamycin by intercalating to double-stranded DNA of undifferentiated cells undergoing rapid cell division, it is possible that adriamycin had preferentially attacked cells in the caudal end where pronounced proliferation takes place during this narrow period of greatest susceptibility.
Assuntos
Anormalidades Induzidas por Medicamentos/patologia , Anormalidades Múltiplas/induzido quimicamente , Embrião de Galinha , Doxorrubicina/efeitos adversos , Esôfago/anormalidades , Traqueia/anormalidades , Animais , Embrião de Galinha/anormalidades , Embrião de Galinha/anatomia & histologia , Embrião de Galinha/efeitos dos fármacos , Modelos Animais de Doenças , HumanosRESUMO
PROBLEM: The authors review embryofetal pathologies in humans caused by antibodies to maternal autoantigens and paternal alloantigens. They consider the variable percentages of miscarriages, developmental delays, intrauterine growth retardation, perinatal deaths and birth defects of unknown etiology, because a part of these percentages may be caused by analog human isoantibodies to the studied ones in the chick embryos. METHOD OF STUDY: A total of 81 chick embryos whose dams had been immunized against soluble foreign transitory antigens and soluble paternal alloantigens from chick embryos have been macroscopically analyzed. The development was interrupted at random to know anomalies then existing; but 29/81 eggs (35.8%) were incubated until hatching. Each class of anomaly was analyzed by statistical methods; 66 control embryos were studied using the same methods. RESULTS: Transmission of the induced isoantibodies to the embryos caused: monstrosity 8.6%; death by functional abnormality 3.7%; digested embryos 7.4%; malformation 1.2%; developmental delay 30.8%; developmental delay together with intraovo growth retardation 11.1; intraovo growth retardation 15.1%; normal 25.9%. Of the mentioned 29 eggs, 19 embryos died before being born, six died in under 1 week, but only four poults survived more than 1 week. Three chicks exhibited congenital abnormalities: transitory ataxia and dysphagia, and one of them also scoliosis, while a fourth remained healthy. CONCLUSION: If pathogenic activity by these isoantibodies can be shown to occur naturally in humans, as has been postulated, it could account for some miscarriage, developmental delay, fetal and perinatal death and birth defects of currently unknown etiology.
Assuntos
Anormalidades Múltiplas/imunologia , Antígenos/imunologia , Autoantígenos/imunologia , Embrião de Galinha/imunologia , Isoanticorpos/imunologia , Anormalidades Múltiplas/mortalidade , Animais , Embrião de Galinha/anormalidades , Embrião de Galinha/embriologia , Desenvolvimento EmbrionárioRESUMO
There is increasing concern over the widespread use of perfluorinated chemicals, which accumulate in various tissues and penetrate the mammalian fetus. A chick model was established for the rapid evaluation of teratogenicity of these chemicals, an important issue because developmental defects often occur at lower exposures than those required for adult systemic toxicity. Chicken eggs were injected with varying doses of perfluorooctanoic acid prior to incubation. Observed were defects in hatching, increased incidence of splayed legs, and interference with the appropriate development of yellow plumage. All these defects are potentially related to essential molecular/biochemical and functional development of the chick. Because of the relationship between structural defects and vulnerability of the developing brain, our model points to the need to evaluate neurobehavioral teratogenicity, which may involve even lower doses.
Assuntos
Caprilatos/toxicidade , Embrião de Galinha/efeitos dos fármacos , Poluentes Ambientais/toxicidade , Fluorocarbonos/toxicidade , Membro Posterior/anormalidades , Modelos Animais , Pigmentação/efeitos dos fármacos , Teratogênicos/toxicidade , Animais , Embrião de Galinha/anormalidades , Galinhas/anormalidades , Desenvolvimento Embrionário/efeitos dos fármacosRESUMO
The lymph heart is a sac-like structure on either side of avian tail. In some adult birds, it empties the lymph from the copulatory organ; however, during embryonic development, it is thought to circulate extra-embryonic lymph. Very little is known about the origin, innervation and the cellular changes it undergoes during development. Using immunohistochemistry and gene expression profiling we show that the musculature of the lymph heart is initially composed solely of striated skeletal muscle but later develops an additional layer composed of smooth myofibroblasts. Chick-quail fate-mapping demonstrates that the lymph heart originates from the hypaxial compartments of somites 34-41. The embryonic lymph heart is transiently innervated by somatic motoneurons with no autonomic input. In comparison to body muscles, the lymph heart has different sensitivity to neuromuscular junction blockers (sensitive only to decamethonium). Furthermore, its abundant bungarotoxin-positive acetylcholinesterase receptors are unique as they completely lack specific acetylcholinesterase activity. Several lines of evidence suggest that the lymph heart may possess an intrinsic pacing mechanism. Finally, we assessed the function of the lymph heart during embryogenesis and demonstrate that it is responsible for preventing embryonic oedema in birds, a role previously thought to be played by body skeletal muscle contractions.
Assuntos
Embrião de Galinha/embriologia , Sistema Linfático/embriologia , Animais , Embrião de Galinha/anormalidades , Embrião de Galinha/patologia , Quimera , Coturnix/embriologia , Edema/embriologia , Sistema Linfático/inervação , Sistema Linfático/patologia , Microscopia Eletrônica de Transmissão , Músculo Esquelético/embriologia , Somitos/embriologiaRESUMO
Ocular anomalies seen in children with fetal alcohol syndrome (FAS) suggest that ocular structures are sensitive to alcohol exposure during their development. This study was designed to investigate the effect of in ovo ethanol (EtOH) exposure on retinal development and myelinization of optic nerve fibers at an ultra structural level in a chick embryo model system. Prior to incubation, fertilized chicken eggs were injected once with 100 microl of either 0.9% NaCl (vehicle control), or EtOH solutions at different doses (10, 30, or 50%, v:v in 0.9% NaCl) into their air sacs and incubated at 37.5 degrees C and saturation humidity. On day 20 embryos were analyzed in terms of their viability and growth and the optic cups including the optic nerves were dissected out. Specimens were processed for electron microscopy (EM). Results showed that, EtOH significantly decreased the viability of chick embryos (P < 0.045), and caused significant prenatal growth retardation (P < 0.004) in a dose-dependant manner. Light microscopy of semi thin sections revealed that prenatal exposure to EtOH resulted in both retinal degeneration and optic nerve hypoplasia (P < 0.001) in a dose-dependant manner. EM revealed that a dose-dependant decrease in the number of myelinated nerve fibers was profound in groups exposed to EtOH (P < 0.001). Furthermore, the myelin coats observed were thinner than those seen in control embryos. In groups exposed to EtOH myelin sheets were unorganized and contained vacuolar structures in between them. The tissue in between the cells and optic nerve fibers, on the other hand, lost its intact appearance with vacuolar and vesicular structures in between them. In addition, the optic nerve fibers contained granular accumulations in EtOH exposed groups. A dose dependent degeneration was also observed in retinas of EtOH exposed groups. The effect of EtOH was profound in pigment epithelium (PE), inner plexiform layer (IPL), and ganglion cell layer (GC). Mitochondrial deficiencies, and alterations in melanin granule number and distribution dominated the defects seen in PE. On the other hand, EM findings of all the affected layers were suggestive of induced cell death in EtOH exposed groups. Thus, this study suggests retinal development with the emphasis on melanin pigmentation in PE and optic nerve myelinization as potential targets of prenatal EtOH exposure and discusses potential mechanisms of EtOH action on these tissues.
Assuntos
Anormalidades Induzidas por Medicamentos , Depressores do Sistema Nervoso Central/toxicidade , Embrião de Galinha/efeitos dos fármacos , Etanol/toxicidade , Nervo Óptico/efeitos dos fármacos , Retina/efeitos dos fármacos , Animais , Embrião de Galinha/anormalidades , Relação Dose-Resposta a Droga , Perda do Embrião/induzido quimicamente , Peso Fetal/efeitos dos fármacos , Hiperplasia/induzido quimicamente , Hiperplasia/embriologia , Fibras Nervosas Mielinizadas/efeitos dos fármacos , Fibras Nervosas Mielinizadas/patologia , Nervo Óptico/anormalidades , Doenças do Nervo Óptico/induzido quimicamente , Doenças do Nervo Óptico/embriologia , Doenças do Nervo Óptico/patologia , Retina/anormalidades , Retina/patologia , Degeneração Retiniana/induzido quimicamente , Degeneração Retiniana/embriologia , Degeneração Retiniana/patologiaRESUMO
The anatomical and histological alterationsthat affect chick embryos from hens immunizedwith antigens from chick embryos, butwhich are foreign to the immune system of thehen, are reported here for the first time. Theimportance of these antigens, the maternalantibodies that they induce, and the injuriesthat these produce in the embryo can clearlybe seen in the results reported. These results,obtained by means of experimental immunizationin hens, may also hypothetically takeplace in humans (women) through naturalimmunization because analogous antigensfrom the embryo cross her placenta.Thus 81 eggs of immunized hens werestudied, of which 60 displayed morphologicalterations of diverse intensity, especiallydevelopmental delay and growth retardation.Of these, three embryos 57 pih, 4 and 7 pidwere chosen for their delay in growth, duringthe period of organogenesis. Their anatomicalalterations were studied and an exhaustive andqualitative histological analysis was carriedout. Each section was compared with those ofcontrol embryos which underwent the sametime of incubation or were at the same stage ofdevelopment. Embryonic growth retardationwas evident in the smallest size of the embryosbut also there were developmental delay ofsome organs and cells. Among other strikinganomalies, the following were observed: invasionof the neural crest cells into the mesencephalonand rombencephalon lumen;malformation of the infundibulum; disintegrationof dermatomes and myotomes; a loosearrangement of mesenchymal tissue; a delay inthe development of the heart and bloodislands cells, etc. Some of the observed anomalieswere related to birth defects that alsoaffected other chicks in the same experiment,as published elsewhere (AU)
No disponible
Assuntos
Animais , Embrião de Galinha/anormalidades , Mesoderma/anormalidades , Malformações do Sistema Nervoso/diagnóstico , Neuro-Hipófise/anormalidades , Antígenos/uso terapêutico , ImunizaçãoRESUMO
Cyp26a1, a gene required for retinoic acid (RA) inactivation during embryogenesis, was previously identified as a potential Tbx1 target from a microarray screen comparing wild-type and null Tbx1 mouse embryo pharyngeal arches (pa) at E9.5. Using real-time PCR and in situ hybridization analysis of Cyp26a1 and its two functionally related family members Cyp26b1 and c1, we demonstrate reduced and/or altered expression for all three genes in pharyngeal tissues of Tbx1 null embryos. Blockade of Cyp26 function in the chick embryo using R115866, a specific inhibitor of Cyp26 enzyme function, resulted in a dose-dependent phenocopy of the Tbx1 null mouse including loss of caudal pa and pharyngeal arch arteries (paa), small otic vesicles, loss of head mesenchyme and, at later stages, DiGeorge Syndrome-like heart defects, including common arterial trunk and perimembranous ventricular septal defects. Molecular markers revealed a serious disruption of pharyngeal pouch endoderm (ppe) morphogenesis and reduced staining for smooth muscle cells in paa. Expression of the RA synthesizing enzyme Raldh2 was also up-regulated and altered Hoxb1 expression indicated that RA levels are raised in R115866-treated embryos as reported for Tbx1 null mice. Down-regulation of Tbx1 itself was observed, in accordance with previous observations that RA represses Tbx1 expression. Thus, by specifically blocking the action of the Cyp26 enzymes we can recapitulate many elements of the Tbx1 mutant mouse, supporting the hypothesis that the dysregulation of RA-controlled morphogenesis contributes to the Tbx1 loss of function phenotype.
Assuntos
Anormalidades Múltiplas/enzimologia , Anormalidades Múltiplas/genética , Embrião de Galinha/anormalidades , Inibidores das Enzimas do Citocromo P-450 , Sistema Enzimático do Citocromo P-450/genética , Síndrome de DiGeorge/enzimologia , Animais , Benzotiazóis/farmacologia , Embrião de Galinha/enzimologia , Síndrome de DiGeorge/genética , Síndrome de DiGeorge/patologia , Regulação para Baixo , Masculino , Camundongos , Camundongos Knockout , Ácido Retinoico 4 Hidroxilase , Proteínas com Domínio T/genética , Tretinoína/metabolismo , Triazóis/farmacologiaAssuntos
Embrião de Galinha/efeitos dos fármacos , Anormalidades Craniofaciais/induzido quimicamente , Dibenzodioxinas Policloradas/toxicidade , Animais , Embrião de Galinha/anormalidades , Anormalidades Craniofaciais/embriologia , Relação Dose-Resposta a Droga , Poluentes Ambientais/toxicidade , Anormalidades do Olho/induzido quimicamente , Anormalidades do Olho/embriologia , Maxila/anormalidades , Maxila/efeitos dos fármacos , Teratogênicos/toxicidadeRESUMO
Talpid3 is a classical chicken mutant with abnormal limb patterning and malformations in other regions of the embryo known to depend on Hedgehog signaling. We combined the ease of manipulating chicken embryos with emerging knowledge of the chicken genome to reveal directly the basis of defective Hedgehog signal transduction in talpid3 embryos and to identify the talpid3 gene. We show in several regions of the embryo that the talpid3 phenotype is completely ligand independent and demonstrate for the first time that talpid3 is absolutely required for the function of both Gli repressor and activator in the intracellular Hedgehog pathway. We map the talpid3 locus to chromosome 5 and find a frameshift mutation in a KIAA0586 ortholog (ENSGALG00000012025), a gene not previously attributed with any known function. We show a direct causal link between KIAA0586 and the mutant phenotype by rescue experiments. KIAA0586 encodes a novel protein, apparently specific to vertebrates, that localizes to the cytoplasm. We show that Gli3 processing is abnormal in talpid3 mutant cells but that Gli3 can still translocate to the nucleus. These results suggest that the talpid3 protein operates in the cytoplasm to regulate the activity of both Gli repressor and activator proteins.