RESUMO
BACKGROUND: At birth, marsupial neonates have precociously developed forelimbs. The development of the tammar wallaby (Macropus eugenii) hindlimbs lags significantly behind that of the forelimbs. This differs from the grey short-tailed opossum, Monodelphis domestica, which has relatively similar fore- and hindlimbs at birth. This study examines the expression of the key patterning genes TBX4, TBX5, PITX1, FGF8, and SHH in developing limb buds in the tammar wallaby. RESULTS: All genes examined were highly conserved with orthologues from opossum and mouse. TBX4 expression appeared earlier in development than in the mouse, but later than in the opossum. SHH expression is restricted to the zone of polarising activity, while TBX5 (forelimb) and PITX1 (hindlimb) showed diffuse mRNA expression. FGF8 is specifically localised to the apical ectodermal ridge, which is more prominent than in the opossum. CONCLUSIONS: The most marked divergence in limb size in marsupials occurs in the kangaroos and wallabies. The faster development of the fore limb compared to that of the hind limb correlates with the early timing of the expression of the key patterning genes in these limbs.
Assuntos
Padronização Corporal/genética , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Botões de Extremidades/crescimento & desenvolvimento , Botões de Extremidades/metabolismo , Macropodidae/crescimento & desenvolvimento , Fatores Etários , Animais , Primers do DNA/genética , Fatores de Crescimento de Fibroblastos/metabolismo , Proteínas Hedgehog/metabolismo , Técnicas Histológicas , Hibridização In Situ , Botões de Extremidades/ultraestrutura , Macropodidae/metabolismo , Microscopia Eletrônica de Varredura , Especificidade da Espécie , Proteínas com Domínio T/metabolismoRESUMO
Dorsoventral fibers in the presumptive dermis of the chick limb bud reported first by Hurle's group in 1989 are now revealed as bundles of fibrillin microfibrils (Isokawa et al., 2004). The bundles, which could be called oxytalan fibers at the light microscopic level, are aligned perpendicularly to the overlying ectoderm and form a unique fiber array, originating directly from the basal lamina. This well-oriented organization is beneficial in examining the process of in vivo bundling of microfibrils into oxytalan fibers. In this study, sections through the presumptive limb dermis were preferentially prepared from chick embryos at Days 4-6 (ED4-6). Immunohistochemically, fibrillin-positive dots representing cross-sectioned surfaces of individual fibers, increased in size from ED4 to 6, but their number per unit area remained constant. Ultrastructurally, a single oxytalan fiber at ED4 consisted of â¼15 microfibrils; the latter number increased fourfold from ED4 to 5 and threefold from ED5 to 6. Oxytalan fibers were all closely associated with mesenchymal cell; notably, the fibers at ED5 and 6 were held in a shallow ditch on the cell body or by lamellipodial cytoplasmic protrusion. In the sites of cell-fiber adhesion, microfibrils in the periphery of an oxytalan fiber appeared to adhere directly or by means of short flocculent strands to a nearby cell membrane; the latter showed a thickening of plasmalemma and its undercoat, indicating the presence of adhesive membrane specification. These findings suggest that the bundling of microfibrils is a progressive and closely cell-associated process.
Assuntos
Embrião de Galinha/embriologia , Embrião de Galinha/metabolismo , Derme/embriologia , Derme/metabolismo , Proteínas da Matriz Extracelular/metabolismo , Microfibrilas/metabolismo , Proteínas dos Microfilamentos/metabolismo , Animais , Membrana Celular/ultraestrutura , Embrião de Galinha/ultraestrutura , Derme/ultraestrutura , Fibrilinas , Botões de Extremidades/embriologia , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Microscopia Eletrônica de Varredura , Microscopia Eletrônica de TransmissãoRESUMO
Oral-facial-digital type I (OFDI) syndrome is an X-linked male lethal developmental disorder. It is ascribed to ciliary dysfunction and characterized by malformation of the face, oral cavity, and digits. Conditional inactivation using different Cre lines allowed us to study the role of the Ofd1 transcript in limb development. Immunofluorescence and ultrastructural studies showed that Ofd1 is necessary for correct ciliogenesis in the limb bud but not for cilia outgrowth, in contrast to what was previously shown for the embryonic node. Mutants with mesenchymal Ofd1 inactivation display severe polydactyly with loss of antero-posterior (A/P) digit patterning and shortened long bones. Loss of digit identity was found to be associated with a progressive loss of Shh signaling and an impaired processing of Gli3, whereas defects in limb outgrowth were due to defective Ihh signaling and to mineralization defects during endochondral bone formation. Our data demonstrate that Ofd1 plays a role in regulating digit number and identity during limb and skeletal patterning increasing insight on the functional role of primary cilia during development.
Assuntos
Osso e Ossos/embriologia , Cílios/fisiologia , Botões de Extremidades/embriologia , Proteínas/metabolismo , Animais , Western Blotting , Pesos e Medidas Corporais , Imunofluorescência , Proteínas Hedgehog/metabolismo , Técnicas Histológicas , Hibridização In Situ , Marcação In Situ das Extremidades Cortadas , Fatores de Transcrição Kruppel-Like/metabolismo , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Masculino , Camundongos , Microscopia Eletrônica de Transmissão , Proteínas do Tecido Nervoso/metabolismo , Síndromes Orofaciodigitais/embriologia , Transdução de Sinais/fisiologia , Proteína Gli3 com Dedos de ZincoRESUMO
The extent to which the nuclear organisation of a gene impacts on its ability to be expressed, or whether nuclear organisation merely reflects gene expression states, remains an important but unresolved issue. A model system that has been instrumental in investigating this question utilises the murine Hox gene clusters encoding homeobox-containing proteins. Nuclear reorganisation and chromatin decondensation, initiated towards the 3' end of the clusters, accompanies activation of Hox genes in both differentiation and development, and might be linked to mechanisms underlying colinearity. To investigate this, and to delineate the cis-acting elements involved, here we analyse the nuclear behaviour of a 3' Hoxb1 transgene transposed to the 5' end of the Hoxd cluster. We show that this transgene contains the cis-acting elements sufficient to initiate ectopic local nuclear reorganisation and chromatin decondensation and to break Hoxd colinearity in the primitive streak region of the early embryo. Significantly, in rhombomere 4, the transgene is able to induce attenuated nuclear reorganisation and decondensation of Hoxd even though there is no detectable expression of the transgene at this site. This shows that reorganisation of chromosome territories and chromatin decondensation can be uncoupled from transcription itself and suggests that they can therefore operate upstream of gene expression.
Assuntos
Padronização Corporal/genética , Núcleo Celular/genética , Desenvolvimento Embrionário/genética , Proteínas de Homeodomínio/genética , Transgenes/genética , Animais , Diferenciação Celular/genética , Núcleo Celular/ultraestrutura , Cromatina/genética , Montagem e Desmontagem da Cromatina/genética , Elementos de DNA Transponíveis/genética , Regulação da Expressão Gênica no Desenvolvimento/genética , Genes Homeobox/genética , Botões de Extremidades/embriologia , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Camundongos , Camundongos Transgênicos , Linha Primitiva/embriologia , Linha Primitiva/metabolismo , Linha Primitiva/ultraestrutura , Rombencéfalo/embriologia , Rombencéfalo/metabolismo , Rombencéfalo/ultraestruturaRESUMO
Recently canonical Wnt signaling in the ectoderm has been shown to be required for maintenance of the apical ectodermal ridge (AER) and for dorsoventral signaling. Using conditional gain- and loss-of-function beta-catenin alleles, we have studied the role of mesenchymal beta-catenin activity during limb development. Here, we show that loss of beta-catenin results in limb truncations due to a defect in AER maintenance. Stabilization of beta-catenin also results in truncated limbs, caused by a premature regression of the AER. Concomitantly, in these limbs, the expression of Bmp2, Bmp4 and Bmp7, and of the Bmp target genes Msx1, Msx2 and gremlin, is expanded in the mesenchyme. Furthermore, we found that the expression of Lmx1b, a gene exclusively expressed in the dorsal limb mesenchyme and involved in dorsoventral patterning, is reduced upon loss of beta-catenin activity and is expanded ventrally in gain-of-function limbs. However, the known ectodermal regulators Wnt7a and engrailed 1 are expressed normally. This suggests that Lmx1b is also regulated, in part, by a beta-catenin-mediated Wnt signal, independent of the non-canoncial Wnt7a signaling pathway. In addition, loss of beta-catenin results in a severe agenesis of the scapula. Concurrently, the expression of two genes, Pax1 and Emx2, which have been implicated in scapula development, is lost in beta-catenin loss-of-function limbs; however, only Emx2 is upregulated in gain-of-function limbs. Mesenchymal beta-catenin activity is therefore required for AER maintenance, and for normal expression of Lmx1b and Emx2.
Assuntos
Padronização Corporal , Extremidades/embriologia , Regulação da Expressão Gênica no Desenvolvimento , beta Catenina/fisiologia , Alelos , Animais , Biomarcadores/análise , Proteínas Morfogenéticas Ósseas/metabolismo , Citocinas , Proteínas de Ligação a DNA/metabolismo , Proteínas de Homeodomínio/metabolismo , Peptídeos e Proteínas de Sinalização Intercelular/metabolismo , Proteínas com Homeodomínio LIM , Botões de Extremidades/embriologia , Botões de Extremidades/ultraestrutura , Deformidades Congênitas dos Membros/genética , Fator de Transcrição MSX1/metabolismo , Mesoderma/fisiologia , Camundongos , Camundongos Mutantes , Escápula/embriologia , Fatores de Transcrição/metabolismo , Regulação para Cima , Proteínas Wnt/metabolismoRESUMO
Interactions between chondrocytes and their extracellular matrix are partly mediated by beta1-integrin receptors. Recent studies have shown that beta1-integrins co-localize with a variety of cytoskeletal complexes, signaling proteins and growth factor receptors. Since mechanosensitive ion channels and integrins have been proposed to participate in skeletal mechanotransduction, in this study, we investigated the possible co-localization of beta1-integrins with two ion channels and a P-type ATPase in mouse limb-bud chondrocytes. The alpha subunits of Na, K-ATPase, the epithelial sodium channel (ENaC) and the voltage activated calcium channel (VACC) were immunostained in organoid cultures derived from limb-buds of 12-day-old mice using well-characterized antibodies. Indirect immunofluorescence revealed abundant expression of beta1-integrins and each of the selected systems in limb-bud chondrocytes. Two-fluorochrome immunostaining demonstrated that beta1-integrin, Na, K-ATPase, ENaC and VACC co-localize in chondrocytes. Co-imunoprecipitation experiments revealed co-localization and association of integrins with ENaC, VACC and Na, K-ATPase. Cellular responses and signaling cascades initiated by the influx of calcium or sodium through putative mechanosensitive channels may be regulated more effectively if such channels were organized around integrins with receptors, kinases and cytoskeletal complexes clustered about them. The close proximity of ATPase ion pumps such as Na, K-ATPase to chondrocyte mechanoreceptor complexes could facilitate rapid homeostatic responses to the ionic perturbations brought about by activation of mechanically gated cation channels and efficiently regulate the intracellular milieu of chondrocytes.
Assuntos
Canais de Cálcio/metabolismo , Condrócitos/metabolismo , Integrina beta1/metabolismo , Botões de Extremidades/metabolismo , Mecanorreceptores/metabolismo , Canais de Sódio/metabolismo , ATPase Trocadora de Sódio-Potássio/metabolismo , Sequência de Aminoácidos , Animais , Western Blotting , Diferenciação Celular/fisiologia , Sobrevivência Celular/fisiologia , Condrócitos/ultraestrutura , Epitélio/metabolismo , Feminino , Imunofluorescência , Botões de Extremidades/ultraestrutura , Mecanorreceptores/fisiologia , Mecanorreceptores/ultraestrutura , Camundongos , Microscopia Eletrônica , Dados de Sequência Molecular , Técnicas de Cultura de Órgãos , Estimulação Física , Testes de Precipitina , Gravidez , Transdução de Sinais/fisiologiaRESUMO
The effects of selected quinolones (levofloxacin, lomefloxacin, temafloxacin and grepafloxacin) on growth and differentiation of murine limb buds were studied in vitro. Ciprofloxacin and ofloxacin served as controls. We used limb buds from 12-day-old mouse embryos that were grown for 6 days in a serum-free, standard or magnesium-deficient medium. Besides evaluation under a dissecting microscope, we used electron microscopy to characterize the effects in detail. The following results are noteworthy. (1) Comparing the effects of standard and magnesium-deficient medium after 3 and 6 days in culture, we found ultrastructural changes after 6 days only. (2) Direct comparison of ofloxacin (racemate) and levofloxacin (L-enantiomer) showed that they had a similar, rather low, potential for affecting cartilage development. (3) The effects of temafloxacin and ciprofloxacin were more pronounced in magnesium-deficient medium, but those of the other drugs were not. (4) Grepafloxacin was the most active quinolone in this assay. It impaired growth and differentiation of limb buds at 30 mg/l; at higher concentrations the explants did not grow. With lower concentrations of 10 mg grepafloxacin/l, no effects were detectable under a dissecting microscope but characteristic changes were seen by electron microscopy. We observed electron-dense aggregates on and within chondrocytes, detachment of the cell membrane from the matrix with matrix-free pericellular areas around chondrocytes, and swelling of cell organelles such as mitochondria and rough endoplasmic reticulum. (5) The affinity of grepafloxacin for divalent cations (Mg2+, Ca2+) was studied by measuring the fluorescence of grepafloxacin solution at various concentrations of Mg2+ and Ca2+. Grepafloxacin showed a relatively high affinity for Ca2+ in the fluorescence assay, which was more pronounced than the affinities of six other fluoroquinolones tested before.
Assuntos
Anormalidades Induzidas por Medicamentos , Anti-Infecciosos/toxicidade , Embrião de Mamíferos/efeitos dos fármacos , Fluoroquinolonas , Botões de Extremidades/efeitos dos fármacos , Piperazinas/toxicidade , Animais , Cálcio/deficiência , Relação Dose-Resposta a Droga , Feminino , Técnicas In Vitro , Levofloxacino , Botões de Extremidades/anormalidades , Botões de Extremidades/ultraestrutura , Magnésio/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos , Ofloxacino/toxicidade , Gravidez , Quinolonas/toxicidadeRESUMO
The role of major cellular serine/threonine-specific protein phosphatases, protein phosphatase 1 and 2A, was investigated during chicken cartilage differentiation under in vitro conditions. Activity of protein phosphatase 2A decreased parallel to differentiation of chondrogenic cells, whereas activity of protein phosphatase 1 remained unchanged as assayed in the supernatants of the homogenised chicken limb bud micromass cell cultures. When okadaic acid, a potent inhibitor of protein phosphatase 1 and 2A was applied in 20 nM concentration for 4 h during the second and third culturing days, it significantly increased the size of metachromatic cartilage areas measured in 6-day-old colonies. Following okadaic acid treatments, a significant inhibition in the activity of protein phosphatase 2A was found, while the activity of protein phosphatase 1 was unaffected as measured an days 2 and 3. TRITC-phalloidin labelling demonstrated that okadaic acid disorganised actin filaments and induced rounding of chondrogenic cells. This deterioration of actin filaments was reversible. Electron microscopy and biochemical analysis of colonies revealed that the ultrastructure and major components of cartilage matrix remained unchanged under the effect of okadaic acid. Okadaic acid-treatment applied to cultures containing predominantly differentiated chondrocytes (after day 4) did not influence the cartilage formation. 3H-thymidine and bromodeoxyuridine incorporation-assays demonstrated enhanced cell proliferation in the okadaic acid-treated colonies compared to that of the untreated ones. Our results indicate, for the first time, that protein phosphatase 2A is involved in the regulation of chondrogenesis. Inhibition of protein phosphatase 2A with okadaic acid may result in increased chondrogenesis via modulation of proliferation and cytoskeletal organisation, as well as via alteration of protein kinase A-signaling pathway of the chondrogenic cells.
Assuntos
Cartilagem/embriologia , Condrócitos/metabolismo , Condrogênese/fisiologia , Botões de Extremidades/embriologia , Ácido Okadáico/farmacologia , Fosfoproteínas Fosfatases/metabolismo , Citoesqueleto de Actina/efeitos dos fármacos , Citoesqueleto de Actina/metabolismo , Citoesqueleto de Actina/ultraestrutura , Animais , Cartilagem/metabolismo , Cartilagem/ultraestrutura , Diferenciação Celular/efeitos dos fármacos , Diferenciação Celular/fisiologia , Divisão Celular/efeitos dos fármacos , Divisão Celular/fisiologia , Células Cultivadas/efeitos dos fármacos , Células Cultivadas/metabolismo , Células Cultivadas/ultraestrutura , Embrião de Galinha , Condrócitos/efeitos dos fármacos , Condrócitos/ultraestrutura , Condrogênese/efeitos dos fármacos , Citoesqueleto/efeitos dos fármacos , Citoesqueleto/metabolismo , Citoesqueleto/ultraestrutura , Relação Dose-Resposta a Droga , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Fosfoproteínas Fosfatases/efeitos dos fármacos , Fosforilação/efeitos dos fármacos , Proteína Fosfatase 1 , Proteína Fosfatase 2 , Transdução de Sinais/efeitos dos fármacos , Transdução de Sinais/fisiologiaRESUMO
Midkine (MK) is a heparin-binding growth/differentiation factor implicated in the control of development and repair of various tissues. Upon fracture of the murine tibia, MK was found to be transiently expressed during bone repair. MK was immunohistochemically detected in spindle-shaped mesenchymal cells at the fracture site on day 4 after fracture and in chondrocytes in the area of endochondral ossification on day 7. MK expression was decreased on day 14 and scarcely seen on day 28 when bone repair was completed. This mode of MK expression is reminiscent of MK expression during development. MK was expressed in hypertrophic chondrocytes of the prebone cartilage rudiments on embryonic day 14 in mouse embryos. MK was also strongly expressed in the epiphyseal growth plate. MK was localized intracellularly during both bone repair and development, and this localization was confirmed by immunoelectron microscopy for embryonic chondrocytes. When MK cDNA was transfected into ATDC5 chondrogenic cells and overexpressed, the majority of transfected cells with strong MK expression showed enhanced chondrogenesis as revealed by increased synthesis of sulfated glycosaminoglycans, aggrecan, and type II collagen. These results suggest that MK plays important roles in chondrogenesis and contributes to bone formation and repair.
Assuntos
Proteínas de Transporte/biossíntese , Condrogênese/fisiologia , Proteínas da Matriz Extracelular , Consolidação da Fratura/fisiologia , Osteogênese/fisiologia , Agrecanas , Animais , Animais Recém-Nascidos , Northern Blotting , Proteínas de Transporte/genética , Linhagem Celular , Condrócitos/metabolismo , Condrócitos/ultraestrutura , Condrogênese/genética , Citocinas/biossíntese , Citocinas/genética , DNA Complementar/genética , Embrião de Mamíferos , Lâmina de Crescimento/citologia , Lâmina de Crescimento/metabolismo , Imuno-Histoquímica , Lectinas Tipo C , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Camundongos , Camundongos Endogâmicos ICR , Microscopia Imunoeletrônica , Midkina , Osteogênese/genética , Proteoglicanas/biossíntese , TransfecçãoRESUMO
During vertebrate limb development the distal apex of the limb bud ectoderm is induced to form the apical ectodermal ridge (AER). The presence of the AER is required for the continued outgrowth of the limb bud. Classical embryological studies have led to the hypothesis that a secreted mesenchymal factor is required to maintain the AER. We have undertaken a detailed analysis of Dactylaplasia (Dac) mice, a semidominant mutant which displays missing central digits in the fore- and hindlimbs of heterozygous animals and monodactyly in homozygous animals. Our data show that Dac mice have a defect in the maintenance of the AER. At E10.5, the mutant AER is found to be morphologically normal. However, by E11.5 the central aspect of the AER degenerates leaving the anterior and posterior AER intact. In homozygous mice both the central and anterior AER degenerate, while the posterior extremity of the AER is unaffected. Analysis of BrdU incorporation reveals that degeneration of the AER is due to a lack of cell proliferation in the mutant AER. The loss of the AER leads to a reduction in cell proliferation in the subridge mesenchyme at E11.5. The data represent direct genetic evidence for the existence of an AER maintenance activity that is distinct from AER induction and differentiation. Moreover, the data suggest that the role of the AER maintenance factor is to promote cell proliferation in the ridge. Based on our findings, we propose a model for AER maintenance in the vertebrate limb.
Assuntos
Ectoderma/patologia , Botões de Extremidades/anormalidades , Dedos do Pé/anormalidades , Animais , Apoptose , Cruzamentos Genéticos , Ectoderma/fisiologia , Embrião de Mamíferos/ultraestrutura , Feminino , Genes Recessivos , Heterozigoto , Homozigoto , Botões de Extremidades/ultraestrutura , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Mutantes , Microscopia Eletrônica de Varredura , Gravidez , Dedos do Pé/embriologiaRESUMO
The treefrog Eleutherodactylus coqui is a direct developer--it has no tadpole stage. The limb buds develop earlier than in metamorphosing species (indirect developers, such as Xenopus laevis). Previous molecular studies suggest that at least some mechanisms of limb development in E. coqui are similar to those of other vertebrates and we wished to see how limb morphogenesis in this species compares with that in other vertebrates. We found that the hind limb buds are larger and more advanced than the forelimbs at all stages examined, thus differing from the typical amniote pattern. The limb buds were also small compared to those in the chick. Scanning and transmission electron microscopy showed that although the apical ectoderm is thickened, there was no apical ectodermal ridge (AER). In addition, the limb buds lacked the dorsoventral flattening seen in many amniotes. These findings could suggest a mechanical function for the AER in maintaining dorsoventral flattening, although not all data are consistent with this view. Removal of distal ectoderm from E. coqui hindlimb buds does not stop outgrowth, although it does produce anterior defects in the skeletal pattern. The defects are less severe when the excisions are performed earlier. These results contrast with the chick, in which AER excision leads to loss of distal structures. We suggest that an AER was present in the common ancestor of anurans and amniotes and has been lost in at least some direct developers including E. coqui.
Assuntos
Anuros/embriologia , Evolução Biológica , Ectoderma/ultraestrutura , Botões de Extremidades/ultraestrutura , Animais , Membro Anterior/embriologia , Membro Posterior/embriologia , Microscopia Eletrônica , Microscopia Eletrônica de Varredura , MorfogêneseRESUMO
In the rat hind limb bud aged between prenatal days 14 and 16, immunoreactions of fibronectin in the apical ectodermal ridge were localized on the plasma membranes of epidermal cells and cytoplasmic projections of the underlying mesenchymal cells, which are in contact with the basal lamina. Those of integrin alpha 3 and alpha 5 subunits also appeared on such areas. Definite immunoreactions of fibronectin and both integrin subunits were seen in cell to cell contact areas of mesenchymal cells which are associated with the marginal vein, or with each other forming solid cell cords, and appeared on the basal plasma membrane of endothelial cells of the growing capillaries arising from the marginal vein. These findings suggest that fibronectin may work as a ligand for alpha 3 beta 1 and/or alpha 5 beta 1 integrins expressed by the mesenchymal and vasoformative cells in developing limb bud.
Assuntos
Antígenos CD/análise , Fibronectinas/análise , Integrinas/análise , Botões de Extremidades/química , Botões de Extremidades/ultraestrutura , Animais , Membrana Celular/química , Epiderme/química , Epiderme/embriologia , Epiderme/ultraestrutura , Feminino , Integrina alfa3 , Integrina alfa5 , Junções Intercelulares/química , Junções Intercelulares/ultraestrutura , Botões de Extremidades/embriologia , Mesoderma/química , Mesoderma/ultraestrutura , Microscopia Imunoeletrônica , Gravidez , Ratos , Ratos WistarRESUMO
The importance of cyclic nucleotides in the regulation of the processes of differentiation and embryonic development is known. The possible role that cyclic adenosine monophosphate (cAMP) plays during the development of the posterior limb of Bufo bufo is studied by the cytochemical localization of adenylate cyclase (AC), an enzyme that catalyzes the synthesis of the cyclic nucleotide. The method is based on the reaction between the enzyme AC and its specific substrate AMP-PNP (5'-adenylylimidodiphosphate) in the presence of lead. The lead precipitates that form as secondary reaction products are evidence of enzymatic activity. Reaction products are present only at the epithelial level in the limb bud; initially, such products are visible only at the base of the bud, particularly on the epithelial fascia located at the boundary with the body. During successive elongation and toe formation, AC activity is only present on the cells of the proximal portion of each new segment. Enzymatic activity is never present in correspondence to the ectodermal apical crest. cAMP is probably not involved in the processes of cellular proliferation but, rather, in the processes of inducing differentiation of the internal mesenchymal cells.
Assuntos
Adenilil Ciclases/análise , Embrião não Mamífero/enzimologia , Membro Posterior/enzimologia , Botões de Extremidades/enzimologia , Animais , Bufo bufo , Diferenciação Celular , AMP Cíclico/biossíntese , Epitélio/enzimologia , Epitélio/ultraestrutura , Membro Posterior/embriologia , Membro Posterior/crescimento & desenvolvimento , Larva , Botões de Extremidades/embriologia , Botões de Extremidades/crescimento & desenvolvimento , Botões de Extremidades/ultraestrutura , Microscopia Eletrônica , Morfogênese/fisiologiaRESUMO
Programmed cell death or apoptosis is an essential process during the morphogenesis of a large number of structures. Evidence obtained over the past few years indicates that, in some cases, the generation of reactive oxygen species (ROS) is an important event during the course of apoptosis. Using an in vitro culture system in which digit individualization of developing limbs normally occurs, we assayed the effect of different antioxidants on the cell death that takes place at interdigits. The addition of phenol, dimethyl sulfoxide, or 2',7'-dichlorodihydrofluorescein diacetate (DCDHF-DA) to murine developing limbs in culture prevented digit individualization as well as the typical interdigital cell death. Two ROS-sensitive dyes, 3-(4,5-dimethylthiazol)-2,5-diphenyl tetrazolium bromide and DCDHF-DA, stained interdigits and the so-called "necrotic zones," implying that they contain cells under oxidative stress. Very few interdigital cells were doubly stained with the ROS probes and two cell death indicators (i.e., acridine orange and propidium iodide), suggesting that they detect a different stage during the course of apoptosis. Furthermore, we found cells stained for ROS that did not express a specific macrophage marker and in a few cases were seen surrounded by a macrophage. Surprisingly, many regions of the midgestation mouse embryo that are undergoing cell death correlated with those that have a markedly higher level of ROS. Our data suggest that the generation of oxidative stress is a common requirement for cell death that occurs during mouse embryonic development.
Assuntos
Antioxidantes/farmacologia , Apoptose , Fluoresceínas/farmacologia , Botões de Extremidades/citologia , Botões de Extremidades/fisiologia , Espécies Reativas de Oxigênio/fisiologia , Animais , Apoptose/efeitos dos fármacos , Dimetil Sulfóxido/farmacologia , Embrião de Mamíferos , Desenvolvimento Embrionário e Fetal/efeitos dos fármacos , Desenvolvimento Embrionário e Fetal/fisiologia , Corantes Fluorescentes , Botões de Extremidades/ultraestrutura , Macrófagos/citologia , Macrófagos/fisiologia , Macrófagos/ultraestrutura , Camundongos , Microscopia Confocal , Morfogênese/efeitos dos fármacos , Técnicas de Cultura de Órgãos , Fenol/farmacologiaRESUMO
The outermost surface cell layer of the developing embryo, the periderm, arises from the initial single layer of ectoderm and is eventually exfoliated from the stratified epidermis, which has the same ectodermal origin. In this study, monoclonal antibodies against chicken limb bud ectoderm were generated and screened for those which stained the periderm. Four separate antibodies termed PD2, 3, 7 and 9 were obtained from 180 mixed hybridomas. These PD antibodies stained the periderm selectively at all stages examined (stage 20-42). By correlating the results of immunohistochemistry with observations made by transmission electron microscopy, it was revealed that PD antibodies stained both the squamous periderm at an early stage and rounded bulging peridermal cells just before exfoliation. Therefore we feel that PD antibodies may be useful in further systematic investigations of the development and function of the chicken embryonic periderm.
Assuntos
Anticorpos Monoclonais/imunologia , Antígenos de Diferenciação/imunologia , Ectoderma/imunologia , Epiderme/embriologia , Animais , Anticorpos Monoclonais/química , Embrião de Galinha , Ectoderma/ultraestrutura , Epiderme/imunologia , Epitélio/embriologia , Epitélio/imunologia , Botões de Extremidades/ultraestruturaRESUMO
Rat hind limb buds, aged between prenatal days 14 and 18, were used for electron microscopy and immunocytochemistry of fibronectin, laminin and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling staining indicative of DNA fragmentation. Fibronectin and laminin were actively synthesized in the rough endoplasmic reticulum of epidermal cells in the apical ectodermal ridge between prenatal days 14 and 15, but most cells underwent apoptosis after prenatal day 15. As the regression of the apical ectodermal ridge progressed, mesenchymal cells associated with the marginal veins were successively incorporated into the endothelium devoid of the basal lamina. No mitotic figures of endothelial cells were recognized either in the marginal vein or in the surrounding growing capillaries. Extracellular matrix components connected the adjacent mesenchymal cells, with the endothelium of such vessels immunoreacting to fibronectin and laminin. In addition, fibronectin-immunoreactive networks among the interstices of the mesenchymal cell cords developed in the avascular zone between the epidermis and the growing capillaries at prenatal day 15, but became inconspicuous at prenatal day 16. These results indicate that the apoptosis of the epidermal cells is the major reason for the regression of the apical ectodermal ridge, and that the capillary ingrowth from the marginal veins to the avascular zone is accelerated by transformation of mesenchymal cells to endothelial ones. Fibronectin and laminin seem to play crucial roles in capillary growth, especially in the adhesion between endothelial cells of the pre-existing vessels and mesenchymal cells.
Assuntos
Botões de Extremidades/irrigação sanguínea , Animais , Apoptose , Biotina , Capilares/embriologia , Capilares/metabolismo , Capilares/ultraestrutura , Fragmentação do DNA , DNA Nucleotidilexotransferase/metabolismo , Nucleotídeos de Desoxiuracil , Fibronectinas/biossíntese , Membro Posterior/embriologia , Imuno-Histoquímica , Laminina/biossíntese , Botões de Extremidades/metabolismo , Botões de Extremidades/ultraestrutura , Microscopia Imunoeletrônica , Ratos , Ratos Wistar , Veias/embriologia , Veias/metabolismo , Veias/ultraestruturaRESUMO
Cell death constitutes a basic mechanism accounting for many morphogenetic and histogenetic events during normal and abnormal development of embryonic organs and tissues. This article focuses on the major areas of mesodermal cell death occurring during vertebrate limb development. In early stages of limb development, cell death appears to reduce the amount of mesodermal tissue destined to form the anlage of the autopodium. In later stages, cell death plays a role sculpturing the shape of the digits. The morphology of the dying cells corresponds with apoptosis, but internucleosomal DNA fragmentation by endonuclease activation does not appear to be a precocious feature. The cell death program can be inhibited in vivo and in vitro by changing the environmental conditions of the prospective dying cells up to 6-10 h before death. In this review, we survey possible factors controlling the establishment of the cell death program. Information concerning the biochemical basis of cell death in the developing limb is also revised. Finally, the possible role of genes whose pattern of expression is coincident with the dying processes is discussed.
Assuntos
Apoptose/fisiologia , Embrião de Galinha/ultraestrutura , Botões de Extremidades/citologia , Botões de Extremidades/fisiologia , Animais , Apoptose/genética , Comunicação Celular/fisiologia , Embrião de Galinha/citologia , Embrião de Galinha/fisiologia , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Botões de Extremidades/ultraestrutura , Lisossomos/enzimologia , Lisossomos/ultraestrutura , Camundongos , Microscopia Eletrônica/métodos , Microscopia Eletrônica de Varredura/métodosRESUMO
The biological consequences of constitutive fibroblast growth factor-4 (fgf-4) expression were investigated in chimeric embryos prepared between wild-type host embryos and murine ES cells transfected with a construct in which expression of the murine fgf-4 gene was directed by the phosphoglycerate kinase (PGK-1) promoter. The embryos exhibit abnormalities of the limbs and the anterior central nervous system (CNS). The limb phenotype comprised the induction of outgrowth along the lateral ridge between the definitive fore and hind limbs resembling the early phases of limb development. The CNS defects comprised a complete absence, or marked reduction in forebrain and midbrain structures and rudimentary or absent eye development. Constitutive expression of fgf-4 was also accompanied by ectopic expression of the sonic hedgehog (shh) and msx-1 genes in the lateral ridge. These findings indicate that FGF exhibits multiple activities in early development which include the ability to induce the expression of early markers of limb development in the lateral ridge.
Assuntos
Anormalidades Múltiplas/genética , Fatores de Crescimento de Fibroblastos/biossíntese , Regulação da Expressão Gênica no Desenvolvimento , Botões de Extremidades/embriologia , Deformidades Congênitas dos Membros , Proteínas Proto-Oncogênicas/biossíntese , Fatores de Transcrição , Animais , Sistema Nervoso Central/anormalidades , Quimera , Primers do DNA , Embrião de Mamíferos/ultraestrutura , Feminino , Fator 4 de Crescimento de Fibroblastos , Marcadores Genéticos , Proteínas de Homeodomínio/biossíntese , Hibridização In Situ , Botões de Extremidades/ultraestrutura , Fator de Transcrição MSX1 , Camundongos , Microscopia Eletrônica de Varredura , Fosfoglicerato Quinase/genética , Reação em Cadeia da Polimerase , Gravidez , Regiões Promotoras Genéticas , Células-Tronco , TransfecçãoRESUMO
Previous studies in this lab have shown that chondrogenesis is affected in growth plates of rats exposed to microgravity, and in micromass cultures of embryonic limb mesenchyme differentiating in space. In order to provide a three dimensional aspect not seen in the micromass system, and a tissue homogeneity not possible with explants of limb or limb elements, and to alleviate certain difficulties regarding crew time and stowage, we began culturing embryonic limb cells in Rotating Wall Vessels (RWV). First, these cells were attached to beads, and grown for up to 65 days in a type of RWV known as STLV at the Johnson Space Center. During this time, the cells and beads aggregated and the aggregates continued to increase in size, and differentiated into Alcian blue staining chondrocytes. Because our intent was to use these aggregates for implanting into bony defects in addition to their use in studies of chondrogenic regulation at 1g and microgravity, aggregates of these cells without beads were grown in the commercially available version of the STLV, and their ability to ossify when subcutaneously implanted assessed.