RESUMEN
The POU5F1 gene encodes one of the 'core' transcription factors necessary to establish and maintain pluripotency in mammals. Its function depends on its precise level of expression, so its transcription has to be tightly regulated. To date, few conserved functional elements have been identified in its 5' regulatory region: a distal and a proximal enhancer, and a minimal promoter, epigenetic modifications of which interfere with POU5F1 expression and function in in vitro-derived cell lines. Also, its permanent inactivation in differentiated cells depends on de novo methylation of its promoter. However, little is known about the epigenetic regulation of POU5F1 expression in the embryo itself. We used the rabbit blastocyst as a model to analyze the methylation dynamics of the POU5F1 5' upstream region, relative to its regulated expression in different compartments of the blastocyst over a 2-day period of development. We evidenced progressive methylation of the 5' regulatory region and the first exon accompanying differentiation and the gradual repression of POU5F1 Methylation started in the early trophectoderm before complete transcriptional inactivation. Interestingly, the distal enhancer, which is known to be active in naïve pluripotent cells only, retained a very low level of methylation in primed pluripotent epiblasts and remained less methylated in differentiated compartments than the proximal enhancer. This detailed study identified CpGs with the greatest variations in methylation, as well as groups of CpGs showing a highly correlated behavior, during differentiation. Moreover, our findings evidenced few CpGs with very specific behavior during this period of development.
Asunto(s)
Blastocisto/metabolismo , Metilación de ADN , Factor 3 de Transcripción de Unión a Octámeros/metabolismo , Secuencias Reguladoras de Ácidos Nucleicos , Animales , Secuencia de Bases , Islas de CpG , Desarrollo Embrionario , Femenino , Factor 3 de Transcripción de Unión a Octámeros/genética , ConejosRESUMEN
Because of the potential use of embryonic stem cells (ESC), especially for genetic modifications, there is great interest in establishing domestic animals-related ESCs. Unfortunately, despite considerable efforts, validated ESC lines in species other than mice and primates are yet to be isolated. In this paper, we will summarize the current knowledge on bovine ESCs in an attempt to understand why derivation of domestic animal ESC is still unsuccessful and we will discuss some promising future approaches.
Asunto(s)
Bovinos/embriología , Bovinos/fisiología , Embrión de Mamíferos/citología , Células Madre Embrionarias/fisiología , Trasplante de Células Madre/veterinaria , Animales , Células Cultivadas , Femenino , MasculinoRESUMEN
Despite their biological and biotechnological interest, pluripotent embryonic stem cell lines (ES cells) have been isolated from cultured embryos only in a very limited number of mammalian species. Here we review the main molecular mechanisms that have been shown in mouse or primates to regulate the maintenance of pluripotency in vitro. We describe the main signaling pathways that participate in the self-renewal of ES cells and provide an outlook on the epigenetic associated mechanisms. We also propose a practical approach to stem cell differentiation that examines the relationships between the genotype of embryos and their culture conditions and consider nuclear reprogramming as a valuable approach in ES cell derivation in farm animals.
Asunto(s)
Animales Domésticos/embriología , Reprogramación Celular/fisiología , Células Madre Embrionarias/citología , Células Madre Pluripotentes/citología , Animales , Técnicas de Cultivo de Célula/veterinaria , Diferenciación Celular , Proliferación Celular , Separación Celular , Epigénesis Genética/fisiología , Genotipo , Modelos Biológicos , Transducción de Señal/fisiologíaRESUMEN
Mice have recently been successfully cloned from embryonic stem (ES) cells. However, these fast dividing cells provide a heterogeneous population of donor nuclei, in terms of cell cycle stage. Here we used metaphases as a source of donor nuclei because they offer the advantage of being both unambiguously recognizable and synchronous with the recipient metaphase II oocyte. We showed that metaphases from ES cells can provide a significantly higher development rate to the morula or blastocyst stage (56--70%) than interphasic nuclei (up to 28%) following injection into a recipient oocyte. Selective detachment of mitotic cells after a demecolcin treatment greatly facilitates and accelerates the reconstruction of embryos by providing a nearly pure population of cells in metaphase and did not markedly affect the developmental rate. Most of the blastocysts obtained by this procedure were normal in terms of both morphology and ratio of inner cell mass and total cell number. After transfer into pseudopregnant recipients at the one- or two-cell stage, the ability of metaphase to be fully reprogrammed was demonstrated by the birth of two pups (1.5% of activated oocytes). Although the implantation rate was quite high (up to 32.9% of activated oocytes), the postimplantation development was characterized by a high and rapid mortality. Our data provide a clear situation to explore the long-lasting effects that can be induced by early reprogramming events.
Asunto(s)
Clonación de Organismos , Embrión de Mamíferos/fisiología , Metafase , Técnicas de Transferencia Nuclear , Células Madre/ultraestructura , Animales , Blastocisto/fisiología , Ciclo Celular , Tamaño de la Célula , ADN/análisis , Implantación del Embrión , Transferencia de Embrión , Embrión de Mamíferos/citología , Desarrollo Embrionario y Fetal , Citometría de Flujo , Interfase , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Mórula/fisiología , Oocitos/ultraestructuraRESUMEN
IGF-II is abundant in the nascent mesoderm of the gastrulating mouse embryo. Its function at this developmental stage is unknown. We investigated it by following the in vitro and in vivo differentiation of several androgenetic, biparental, parthenogenetic, and androgenetic Igf2 -/- murine ES cell lines; these cells differed in endogenous IGF-II levels because Igf2 is paternally expressed in the mouse embryo in most tissues. The expression of mesoderm markers and the subsequent formation of muscle structures were correlated with endogenous IGF-II level during teratoma formation and during in vitro differentiation. In addition, the absence of Igf2 in androgenetic Igf2 -/- ES cells led to a severe impairment of mesoderm development, demonstrating the dependence of the preferential mesoderm development of androgenetic ES cells upon Igf2 activity, among the numerous known imprinted genes. The addition of exogenous IGF-II to in vitro differentiation culture medium led to a specific increase in the expression of mesoderm markers. Thus, we propose a novel model in which the binding of IGF-II to its principal signaling receptor, IGF1R, at the surface of mesoderm precursor cells increases the formation of mesoderm cells.
Asunto(s)
Factor II del Crecimiento Similar a la Insulina/metabolismo , Mesodermo/citología , Mesodermo/metabolismo , Animales , Diferenciación Celular/efectos de los fármacos , Línea Celular , Gástrula/citología , Gástrula/efectos de los fármacos , Gástrula/metabolismo , Eliminación de Gen , Regulación del Desarrollo de la Expresión Génica/efectos de los fármacos , Corazón/efectos de los fármacos , Corazón/embriología , Inmunohistoquímica , Hibridación in Situ , Factor II del Crecimiento Similar a la Insulina/genética , Factor II del Crecimiento Similar a la Insulina/farmacología , Mesodermo/efectos de los fármacos , Ratones , Ratones Noqueados , Fibras Musculares Esqueléticas/citología , Fibras Musculares Esqueléticas/efectos de los fármacos , Fibras Musculares Esqueléticas/metabolismo , Proteínas Musculares/metabolismo , Miocardio/citología , Miocardio/metabolismo , Trasplante de Neoplasias , ARN Mensajero/genética , ARN Mensajero/metabolismo , Receptor IGF Tipo 2/metabolismo , Células Madre/citología , Células Madre/efectos de los fármacos , Células Madre/metabolismo , Teratoma/genética , Teratoma/metabolismoRESUMEN
Cadherins are calcium-dependent cell adhesion receptors with strong morphoregulatory functions. To mediate functional adhesion, cadherins must interact with actin cytoskeleton. Catenins are cytoplasmic proteins that mediate the interactions between cadherins and the cytoskeleton. In addition to their role in cell-cell adhesion, catenins also participate in signaling pathways that regulate cell growth and differentiation. Cadherins and catenins appear to be involved in melanocyte development and transformation. Here, we investigated the function of cadherin-catenin complexes in the normal development and transformation of melanocytes by studying the patterns of expression of the cell-cell adhesion molecules, E-, N- and P-cadherin, and the expression of their cytoplasmic partners, alpha-, beta- and gamma-catenin during murine development. Similar analyses were performed in vitro using murine melanoblast, melanocyte, and melanoma cell lines in the presence and absence of keratinocytes, the cells with which melanocytes interact in vivo. Overall, the results suggest that the expression of cadherins and catenins is very plastic and depends on their environment as well as the transformation status of the cells. This plasticity is important in fundamental cellular mechanisms associated with normal and pathological ontogenesis, as well as with tumorigenesis.
Asunto(s)
Cadherinas/biosíntesis , Proteínas del Citoesqueleto/biosíntesis , Melanocitos/metabolismo , Piel/metabolismo , Transactivadores , Animales , Animales Recién Nacidos , Diferenciación Celular , Línea Celular , Transformación Celular Neoplásica , Dermis/metabolismo , Desmoplaquinas , Células Epidérmicas , Epidermis/metabolismo , Folículo Piloso/citología , Folículo Piloso/metabolismo , Queratinocitos/citología , Queratinocitos/metabolismo , Melanocitos/citología , Melanoma Experimental , Ratones , Ratones Endogámicos C57BL , Piel/citología , Piel/embriología , Células Tumorales Cultivadas , alfa Catenina , beta Catenina , gamma CateninaRESUMEN
Melanocytes derived from pluripotent neural crest cells migrate initially in the dorsolateral pathway between the ectoderm and dermomyotome. To understand the role of specific proteins involved in this cell migration, we looked for a cellular model that mimics the in vivo behavior of melanoblasts, and that allows functional studies of their migration. We report here that wild-type embryonic stem (ES) cells are able to follow the ventral and dorsolateral neural crest pathways after being grafted into chicken embryos. By contrast, a mutant ES cell line deficient for beta1 integrin subunits, proteins involved in cell-extracellular interactions, had a severely impaired migratory behavior. Interestingly, ES cells deficient for Kit, the tyrosine kinase receptor for the stem cell factor (SCF), behaved similarly to wild-type ES cells. Thus, grafting mouse ES cells into chicken embryos provides a new cellular system that allows both in vitro and in vivo studies of the molecular mechanisms controlling dorsolateral migration.
Asunto(s)
Movimiento Celular/fisiología , Melanocitos/fisiología , Glicoproteínas de Membrana , Oxidorreductasas , Proteínas Proto-Oncogénicas c-kit/genética , Animales , Sitios de Unión , Biomarcadores , Línea Celular , Embrión de Pollo , Proteínas de Unión al ADN/genética , Inducción Embrionaria , Endotelina-3/genética , Fibronectinas/metabolismo , Colorantes Fluorescentes/metabolismo , Regulación del Desarrollo de la Expresión Génica , Integrina beta1/genética , Integrina beta1/metabolismo , Oxidorreductasas Intramoleculares/genética , Ratones , Ratones Mutantes , Factor de Transcripción Asociado a Microftalmía , Monofenol Monooxigenasa/genética , Mutación , Sistema Nervioso/citología , Sistema Nervioso/embriología , Proteínas/genética , Receptor de Endotelina B , Receptores de Endotelina/genética , Factores de Transcripción de la Familia Snail , Trasplante de Células Madre , Factores de Transcripción/genética , beta-Galactosidasa/genética , beta-Galactosidasa/metabolismoRESUMEN
Similar amounts of N-cadherin and cadherin-7, the prototypes of type I and type II cadherin, induced cell-cell adhesion in murine sarcoma 180 transfectants, Ncad-1 and cad7-29, respectively. However, in the initial phase of aggregation, Ncad-1 cells aggregated more rapidly than cad7-29 cells. Isolated Ncad-1 and cad7-29 cells adhered and spread in a similar manner on fibronectin (FN), whereas aggregated cad7-29 cells were more motile and dispersed than aggregated Ncad-1 cells. cad7-29 cells established transient contacts with their neighbors which were stabilized if FN-cell interactions were perturbed. In contrast, Ncad-1 cells remained in close contact when they migrated on FN. Both beta-catenin and cadherin were more rapidly downregulated in cad7-29 than in Ncad-1 cells treated with cycloheximide, suggesting a higher turnover rate for cadherin-7-mediated cell-cell contacts than for those mediated by N-cadherin. The extent of FN-dependent focal adhesion kinase phosphorylation was much lower if the cells had initiated N-cadherin-mediated rather than cadherin-7-mediated cell adhesion before plating. On grafting into the embryo, Ncad-1 cells did not migrate and remained at or close to the graft site, even after 48 h, whereas grafted cad7-29 cells dispersed efficiently into embryonic structures. Thus, the adhesive phenotype of cadherin-7-expressing cells is regulated by the nature of the extracellular matrix environment which also controls the migratory behavior of the cells. In addition, adhesions mediated by different cadherins differentially regulate FN-dependent signaling. The transient contacts specifically observed in cadherin- 7-expressing cells may also be important in the control of cell motility.
Asunto(s)
Cadherinas/metabolismo , Movimiento Celular , Proteínas de la Matriz Extracelular/metabolismo , Transactivadores , Animales , Cadherinas/genética , Adhesión Celular , Moléculas de Adhesión Celular/metabolismo , Agregación Celular , Tamaño de la Célula , Trasplante de Células , Embrión de Pollo , Cicloheximida/farmacología , Proteínas del Citoesqueleto/metabolismo , Regulación hacia Abajo/efectos de los fármacos , Fibronectinas/metabolismo , Quinasa 1 de Adhesión Focal , Proteína-Tirosina Quinasas de Adhesión Focal , Integrinas/metabolismo , Ratones , Microscopía por Video , Fosforilación , Proteínas Tirosina Quinasas/metabolismo , Transducción de Señal , Transfección , Células Tumorales Cultivadas , beta CateninaRESUMEN
We have analyzed the interaction of neural crest cells with fragments of fibronectin corresponding to the different spliced variants of the COOH-terminal cell-binding domain (COOH-ter CBD). We have shown that this domain can support cell adhesion and migration and that both the IIICS and HepII regions are involved in these events. The rate of locomotion is high, although undirectional, compared to that of whole fibronectin. Interactions with the COOH-ter CBD are controlled by alpha4beta1 and maybe other beta1 integrins and cell-surface proteoglycans. These receptors act cooperatively to mediate attachment, spreading, and migration on fibronectin.
Asunto(s)
Moléculas de Adhesión Celular/metabolismo , Fibronectinas/metabolismo , Cresta Neural/fisiología , Fragmentos de Péptidos/metabolismo , Animales , Adhesión Celular/genética , Moléculas de Adhesión Celular/genética , Movimiento Celular/genética , Células Cultivadas , Fibronectinas/genética , Variación Genética , Inmunohistoquímica , Integrina beta1/aislamiento & purificación , Cresta Neural/citología , Fragmentos de Péptidos/genética , Codorniz/embriologíaRESUMEN
Interactions between cells and extracellular matrix play a crucial role during development by controlling tissue remodelling and cell migration. Integrins are the main family of cell surface receptors for extracellular matrix. The knockout of integrin genes in mouse embryos has provided new insights into the function of these receptors during embryonic development and morphogenesis. The lethality observed either during embryonic life or after birth suggests that many integrins are essential.