Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 21
Filtrar
1.
Reprod Fertil Dev ; 26(5): 703-16, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23759283

RESUMO

Human embryonic stem (ES) cells have been proposed as a renewable source of pluripotent cells that can be differentiated into various cell types for use in research, drug discovery and in the emerging area of regenerative medicine. Exploitation of this potential will require the development of ES cell culture conditions that promote pluripotency and a normal cell metabolism, and quality control parameters that measure these outcomes. There is, however, relatively little known about the metabolism of pluripotent cells or the impact of culture environment and differentiation on their metabolic pathways. The effect of two commonly used medium supplements and cell differentiation on metabolic indicators in human ES cells were examined. Medium modifications and differentiation were compared in a chemically defined and feeder-independent culture system. Adding serum increased glucose utilisation and altered amino acid turnover by the cells, as well as inducing a small proportion of the cells to differentiate. Cell differentiation could be mitigated by inhibiting p38 mitogen-activated protein kinase (p38 MAPK activity). The addition of Knockout Serum Replacer also increased glucose uptake and changed amino acid turnover by the cells. These changes were distinct from those induced by serum and occurred in the absence of detectable differentiation. Induction of differentiation by bone morphogenetic protein 4 (BMP4), in contrast, did not alter metabolite turnover. Deviations from metabolite turnover by ES cells in fully defined medium demonstrated that culture environment can alter metabolite use. The challenge remains to understand the impact of metabolic changes on long-term cell maintenance and the functionality of derived cell populations.


Assuntos
Aminoácidos/metabolismo , Metabolismo dos Carboidratos/fisiologia , Meios de Cultura , Células-Tronco Embrionárias/metabolismo , Glucose/metabolismo , Técnicas de Cultura de Células , Diferenciação Celular , Linhagem Celular , Células-Tronco Embrionárias/citologia , Humanos
2.
Genome Res ; 20(2): 155-69, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19952138

RESUMO

Differentiation of mouse embryonic stem cells (mESCs) is accompanied by changes in replication timing. To explore the relationship between replication timing and cell fate transitions, we constructed genome-wide replication-timing profiles of 22 independent mouse cell lines representing 10 stages of early mouse development, and transcription profiles for seven of these stages. Replication profiles were cell-type specific, with 45% of the genome exhibiting significant changes at some point during development that were generally coordinated with changes in transcription. Comparison of early and late epiblast cell culture models revealed a set of early-to-late replication switches completed at a stage equivalent to the post-implantation epiblast, prior to germ layer specification and down-regulation of key pluripotency transcription factors [POU5F1 (also known as OCT4)/NANOG/SOX2] and coinciding with the emergence of compact chromatin near the nuclear periphery. These changes were maintained in all subsequent lineages (lineage-independent) and involved a group of irreversibly down-regulated genes, at least some of which were repositioned closer to the nuclear periphery. Importantly, many genomic regions of partially reprogrammed induced pluripotent stem cells (piPSCs) failed to re-establish ESC-specific replication-timing and transcription programs. These regions were enriched for lineage-independent early-to-late changes, which in female cells included the inactive X chromosome. Together, these results constitute a comprehensive "fate map" of replication-timing changes during early mouse development. Moreover, they support a model in which a distinct set of replication domains undergoes a form of "autosomal Lyonization" in the epiblast that is difficult to reprogram and coincides with an epigenetic commitment to differentiation prior to germ layer specification.


Assuntos
Período de Replicação do DNA/genética , Desenvolvimento Embrionário/genética , Estudo de Associação Genômica Ampla , Animais , Diferenciação Celular/genética , Linhagem Celular , Cromatina/genética , Ilhas de CpG/genética , Regulação para Baixo/genética , Células-Tronco Embrionárias/citologia , Epigênese Genética/genética , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Camadas Germinativas/crescimento & desenvolvimento , Proteínas de Homeodomínio/genética , Camundongos , Proteína Homeobox Nanog , Fator 3 de Transcrição de Octâmero/genética , Células-Tronco Pluripotentes/citologia , Regiões Promotoras Genéticas/genética , Fatores de Transcrição SOXB1/genética , Transcrição Gênica/genética
3.
J Cell Sci ; 123(Pt 10): 1796-804, 2010 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-20427322

RESUMO

The formation and differentiation of multipotent precursors underlies the generation of cell diversity during mammalian development. Recognition and analysis of these transient cell populations has been hampered by technical difficulties in accessing them in vivo. In vitro model systems, based on the differentiation of embryonic stem (ES) cells, provide an alternative means of identifying and characterizing these populations. Using a previously established mouse ES-cell-based system that recapitulates the development of the ectoderm lineage we have identified a transient population that is consistent with definitive ectoderm. This previously unidentified progenitor occurs as a temporally discrete population during ES cell differentiation, and differs from the preceding and succeeding populations in gene expression and differentiation potential, with the unique ability to form surface ectoderm in response to BMP4 signalling.


Assuntos
Antígenos de Diferenciação/metabolismo , Proteína Morfogenética Óssea 4/metabolismo , Ectoderma/embriologia , Neurogênese , Animais , Antígenos de Diferenciação/genética , Proteína Morfogenética Óssea 4/genética , Linhagem Celular , Linhagem da Célula , Embrião de Mamíferos , Células-Tronco Embrionárias , Imunofluorescência , Perfilação da Expressão Gênica , Camundongos , Transdução de Sinais/genética , Proteínas Smad/metabolismo
4.
Am J Physiol Cell Physiol ; 300(6): C1270-9, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21346154

RESUMO

There is an increasing appreciation that amino acids can act as signaling molecules in the regulation of cellular processes through modulation of intracellular cell signaling pathways. In culture, embryonic stem (ES) cells can be differentiated to a second, pluripotent cell population, early primitive ectoderm-like cells in response to biological activities within the conditioned medium MEDII. The amino acid l-proline has been identified as a component of MEDII required for ES cell differentiation. Here, we define the primary l-proline transporter on ES and early primitive ectoderm-like cells as sodium-coupled neutral amino acid transporter 2 (SNAT2). SNAT2 uptake of l-proline can be inhibited by the addition of millimolar concentrations of other substrates. The addition of excess amino acids was used to regulate the uptake of l-proline by ES cells, and the effect on differentiation was analyzed. The ability of SNAT2 substrates, but not other amino acids, to prevent changes in morphology, gene expression, and differentiation kinetics suggested that l-proline uptake through SNAT2 was required for ES cell differentiation. These data reveal an unexpected role for amino acid uptake and the amino acid transporter SNAT2 in regulation of pluripotent cells in culture and provides a number of specific, inexpensive, and nontoxic culture additives with the potential to improve the quality of ES cell culture.


Assuntos
Sistema A de Transporte de Aminoácidos/metabolismo , Diferenciação Celular/fisiologia , Células-Tronco Embrionárias/fisiologia , Prolina/metabolismo , Sistema A de Transporte de Aminoácidos/genética , Aminoácidos/metabolismo , Animais , Células Cultivadas , Meios de Cultivo Condicionados/química , Meios de Cultivo Condicionados/metabolismo , Embrião de Mamíferos/fisiologia , Células-Tronco Embrionárias/citologia , Camundongos
5.
Am J Physiol Cell Physiol ; 298(5): C982-92, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20164384

RESUMO

The development of cell therapeutics from embryonic stem (ES) cells will require technologies that direct cell differentiation to specific somatic cell lineages in response to defined factors. The initial step in formation of the somatic lineages from ES cells, differentiation to an intermediate, pluripotent primitive ectoderm-like cell, can be achieved in vitro by formation of early primitive ectoderm-like (EPL) cells in response to a biological activity contained within the conditioned medium MEDII. Fractionation of MEDII has identified two activities required for EPL cell formation, an activity with a molecular mass of <3 kDa and a second, much larger species. Here, we have identified the low-molecular-weight activity as l-proline. An inhibitor of l-proline uptake, glycine, prevented the differentiation of ES cells in response to MEDII. Supplementation of the culture medium of ES cells with >100 M l-proline and some l-proline-containing peptides resulted in changes in colony morphology, cell proliferation, gene expression, and differentiation kinetics consistent with differentiation toward a primitive ectoderm-like cell. This activity appeared to be associated with l-proline since other amino acids and analogs of proline did not exhibit an equivalent activity. Activation of the mammalian target of rapamycin (mTOR) signaling pathway was found to be necessary but not sufficient for l-proline activity; addition of other activators of the mTOR signaling pathway failed to alter the ES cell phenotype. This is the first report describing a role for amino acids in the regulation of pluripotency and cell differentiation and identifies a novel role for the imino acid l-proline.


Assuntos
Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/fisiologia , Células-Tronco Pluripotentes/citologia , Células-Tronco Pluripotentes/fisiologia , Prolina/farmacologia , Animais , Linhagem Celular , Regulação da Expressão Gênica , Glicina/farmacologia , Humanos , Peptídeos e Proteínas de Sinalização Intracelular/genética , Peptídeos e Proteínas de Sinalização Intracelular/metabolismo , Leucina/farmacologia , Camundongos , Prolina/metabolismo , Proteínas Serina-Treonina Quinases/genética , Proteínas Serina-Treonina Quinases/metabolismo , Transdução de Sinais , Serina-Treonina Quinases TOR
6.
Stem Cells ; 27(12): 2941-51, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19750540

RESUMO

gamma-Secretase is a membrane-associated protease with multiple intracellular targets, a number of which have been shown to influence embryonic development and embryonic stem (ES) cell differentiation. This paper describes the use of the gamma-secretase inhibitor N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT) to evaluate the role of gamma-secretase in the differentiation of pluripotent stem cells to the germ lineages. The addition of DAPT did not prevent the formation of primitive ectoderm-like cells from ES cells in culture. In contrast, the addition of DAPT during primitive ectoderm-like cell differentiation interfered with the ability of both serum and BMP4 to induce a primitive streak-like intermediate and resulted in the preferential formation of neurectoderm. Similarly, DAPT reduced the formation of primitive streak-like intermediates from differentiating human ES cells; the culture conditions used resulted in a population enriched in human surface ectoderm. These data suggest that gamma-secretase may form part of the general pathway by which mesoderm is specified within the primitive streak. The addition of an E-cadherin neutralizing antibody was able to partially reverse the effect of DAPT, suggesting that DAPT may be preventing the formation of primitive streak-like intermediates and promoting neurectoderm differentiation by stabilizing E-cadherin and preventing its proteolysis.


Assuntos
Secretases da Proteína Precursora do Amiloide/metabolismo , Diferenciação Celular , Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/enzimologia , Células-Tronco Pluripotentes/citologia , Células-Tronco Pluripotentes/enzimologia , Secretases da Proteína Precursora do Amiloide/antagonistas & inibidores , Animais , Proteína Morfogenética Óssea 4/metabolismo , Caderinas/metabolismo , Diferenciação Celular/efeitos dos fármacos , Linhagem Celular , Dipeptídeos/farmacologia , Células-Tronco Embrionárias/efeitos dos fármacos , Humanos , Camundongos , Células-Tronco Pluripotentes/efeitos dos fármacos , Inibidores de Proteases/farmacologia , Transdução de Sinais
7.
Nucleic Acids Res ; 33(4): 1309-22, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15741184

RESUMO

We report the sequence, conservation and cell biology of a novel protein, Psc1, which is expressed and regulated within the embryonic pluripotent cell population of the mouse. The Psc1 sequence includes an RS domain and an RNA recognition motif (RRM), and a sequential arrangement of protein motifs that has not been demonstrated for other RS domain proteins. This arrangement was conserved in a second mouse protein (BAC34721). The identification of Psc1 and BAC34721 homologues in vertebrates and related proteins, more widely throughout evolution, defines a new family of RS domain proteins termed acidic rich RS (ARRS) domain proteins. Psc1 incorporated into the nuclear speckles, but demonstrated novel aspects of subcellular distribution including localization to speckles proximal to the nuclear periphery and localization to punctate structures in the cytoplasm termed cytospeckles. Integration of Psc1 into cytospeckles was dependent on the RRM. Cytospeckles were dynamic within the cytoplasm and appeared to traffic into the nucleus. These observations suggest a novel role in RNA metabolism for ARRS proteins.


Assuntos
Proteínas Nucleares/análise , Proteínas Nucleares/química , Proteínas/análise , Proteínas/química , Proteínas de Ligação a RNA/análise , Proteínas de Ligação a RNA/química , Transporte Ativo do Núcleo Celular , Sequência de Aminoácidos , Animais , Sítios de Ligação , Células COS , Núcleo Celular/química , Núcleo Celular/metabolismo , Estruturas do Núcleo Celular/química , Chlorocebus aethiops , Sequência Conservada , Citoplasma/química , Estruturas Citoplasmáticas/química , DNA Complementar/química , DNA Complementar/isolamento & purificação , Evolução Molecular , Camundongos , Microtúbulos/metabolismo , Dados de Sequência Molecular , Proteínas Nucleares/metabolismo , Estrutura Terciária de Proteína , Proteínas/metabolismo , Proteínas de Ligação a RNA/metabolismo
8.
Mech Dev ; 141: 32-39, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27373508

RESUMO

The developmental outcomes of preimplantation mammalian embryos are regulated directly by the surrounding microenvironment, and inappropriate concentrations of amino acids, or the loss of amino acid-sensing mechanisms, can be detrimental and impact further development. A specific role for l-proline in the differentiation of embryonic stem (ES) cells, a cell population derived from the blastocyst, has been shown in culture. l-proline acts as a signalling molecule, exerting its effects through cell uptake and subsequent metabolism. Uptake in ES cells occurs predominantly through the sodium-coupled neutral amino acid transporter 2, Slc38a2 (SNAT2). Dynamic expression of amino acid transporters has been shown in the early mammalian embryo, reflecting functional roles for amino acids in embryogenesis. The expression of SNAT2 and family member Slc38a1 (SNAT1) was determined in mouse embryos from the 2-cell stage through to the early post-implantation pre-gastrulation embryo. Key changes in expression were validated in cell culture models of development. Both transporters showed temporal dynamic expression patterns and changes in intracellular localisation as differentiation progressed. Changes in transporter expression likely reflect different amino acid requirements during development. Findings include the differential expression of SNAT1 in the inner and outer cells of the compacted morula and nuclear localisation of SNAT2 in the trophectoderm and placental lineages. Furthermore, SNAT2 expression was up-regulated in the epiblast prior to primitive ectoderm formation, an expression pattern consistent with a role for the transporter in later developmental decisions within the pluripotent lineage. We propose that the differential expression of SNAT2 in the epiblast provides evidence for an l-proline-mediated mechanism contributing to the regulation of embryonic development.


Assuntos
Sistema A de Transporte de Aminoácidos/genética , Diferenciação Celular/genética , Desenvolvimento Embrionário/genética , Células-Tronco Embrionárias Murinas , Animais , Embrião de Mamíferos , Regulação da Expressão Gênica no Desenvolvimento , Camundongos , Células-Tronco Pluripotentes/metabolismo , Prolina/metabolismo , Nicho de Células-Tronco/genética
9.
PLoS One ; 11(10): e0163244, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27723793

RESUMO

Multiple pluripotent cell populations, which together comprise the pluripotent cell lineage, have been identified. The mechanisms that control the progression between these populations are still poorly understood. The formation of early primitive ectoderm-like (EPL) cells from mouse embryonic stem (mES) cells provides a model to understand how one such transition is regulated. EPL cells form from mES cells in response to l-proline uptake through the transporter Slc38a2. Using inhibitors of cell signaling we have shown that Src family kinases, p38 MAPK, ERK1/2 and GSK3ß are required for the transition between mES and EPL cells. ERK1/2, c-Src and GSK3ß are likely to be enforcing a receptive, primed state in mES cells, while Src family kinases and p38 MAPK are involved in the establishment of EPL cells. Inhibition of these pathways prevented the acquisition of most, but not all, features of EPL cells, suggesting that other pathways are required. L-proline activation of differentiation is mediated through metabolism and changes to intracellular metabolite levels, specifically reactive oxygen species. The implication of multiple signaling pathways in the process suggests a model in which the context of Src family kinase activation determines the outcomes of pluripotent cell differentiation.


Assuntos
Diferenciação Celular , Sistema de Sinalização das MAP Quinases , Células-Tronco Embrionárias Murinas/metabolismo , Células-Tronco Pluripotentes/enzimologia , Proteínas Quinases p38 Ativadas por Mitógeno/metabolismo , Quinases da Família src/metabolismo , Animais , Técnicas de Cultura de Células , Ativação Enzimática , Camundongos , Espécies Reativas de Oxigênio/metabolismo
10.
Int J Dev Biol ; 46(4): 449-58, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12141431

RESUMO

Molecular and cellular analysis of early mammalian development is compromised by the experimental inaccessibility of the embryo. Pluripotent embryonic stem (ES) cells are derived from and retain many properties of the pluripotent founder population of the embryo, the inner cell mass. Experimental manipulation of these cells and their environment in vitro provides an opportunity for the development of differentiation systems which can be used for analysis of the molecular and cellular basis of embryogenesis. In this review we discuss strengths and weaknesses of the available ES cell differentiation methodologies and their relationship to events in vivo. Exploitation of these systems is providing novel insight into embryonic processes as diverse as cell lineage establishment, cell progression during differentiation, patterning, morphogenesis and the molecular basis for cell properties in the early mammalian embryo.


Assuntos
Biologia do Desenvolvimento/métodos , Endopeptidases , Regulação da Expressão Gênica no Desenvolvimento , Animais , Adesão Celular , Proteínas de Ciclo Celular/metabolismo , Diferenciação Celular , Divisão Celular , Linhagem da Célula , DNA Complementar/metabolismo , Ectoderma/metabolismo , Embrião de Mamíferos/citologia , Regulação da Expressão Gênica , Camundongos , Modelos Biológicos , Proteínas/metabolismo , RNA/metabolismo , Proteínas Repressoras/metabolismo , Separase , Células-Tronco/citologia , Fatores de Tempo , Transcrição Gênica
11.
ScientificWorldJournal ; 2: 690-700, 2002 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-12805994

RESUMO

Recent interest in the generation of neural lineages by differentiation of embryonic stem cells arises from the opportunities represented by a developmentally normal, unlimited source of material that can be manipulated genetically with precision. Several experimental approaches, which differ conceptually, in the route of differentiation and the characteristics of the resulting cell population have been reported. In this review we undertake a comparative analysis of these approaches and their suitability for experimental investigation or implantation.


Assuntos
Diferenciação Celular/fisiologia , Proteínas do Tecido Nervoso , Neurônios/citologia , Células-Tronco/citologia , Animais , Diferenciação Celular/efeitos dos fármacos , Linhagem da Célula/efeitos dos fármacos , Linhagem da Célula/fisiologia , Separação Celular/métodos , Humanos , Proteínas de Filamentos Intermediários/biossíntese , Nestina , Neurônios/metabolismo , Células-Tronco/efeitos dos fármacos , Tretinoína/farmacologia
12.
Biores Open Access ; 3(3): 98-109, 2014 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-24940561

RESUMO

Endoderm formation in the mammalian embryo occurs first in the blastocyst, when the primitive endoderm and pluripotent cells resolve into separate lineages, and again during gastrulation, when the definitive endoderm progenitor population emerges from the primitive streak. The formation of the definitive endoderm can be modeled using pluripotent cell differentiation in culture. The differentiation of early primitive ectoderm-like (EPL) cells, a pluripotent cell population formed from embryonic stem (ES) cells, was used to identify and characterize definitive endoderm formation. Expression of serine peptidase inhibitor, Kazal type 3 (Spink3) was detected in EPL cell-derived endoderm, and in a band of endoderm immediately distal to the embryonic-extra-embryonic boundary in pregastrula and gastrulating embryos. Later expression marked a region of endoderm separating the yolk sac from the developing gut. In the embryo, Spink3 expression marked a region of endoderm comprising the distal visceral endoderm, as determined by an endocytosis assay, and the proximal region of the definitive endoderm. This region was distinct from the more distal definitive endoderm population, marked by thyrotropin-releasing hormone (Trh). Endoderm expressing either Spink3 or Trh could be formed during EPL cell differentiation, and the prevalence of these populations could be influenced by culture medium and growth factor addition. Moreover, further differentiation suggested that the potential of these populations differed. These approaches have revealed an unexpected complexity in the definitive endoderm lineage, a complexity that will need to be accommodated in differentiation protocols to ensure the formation of the appropriate definitive endoderm progenitor in the future.

13.
PLoS One ; 7(6): e38645, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22701686

RESUMO

Two lineages of endoderm develop during mammalian embryogenesis, the primitive endoderm in the pre-implantation blastocyst and the definitive endoderm at gastrulation. This complexity of endoderm cell populations is mirrored during pluripotent cell differentiation in vitro and has hindered the identification and purification of the definitive endoderm for use as a substrate for further differentiation. The aggregation and differentiation of early primitive ectoderm-like (EPL) cells, resulting in the formation of EPL-cell derived embryoid bodies (EPLEBs), is a model of gastrulation that progresses through the sequential formation of primitive streak-like intermediates to nascent mesoderm and more differentiated mesoderm populations. EPL cell-derived EBs have been further analysed for the formation of definitive endoderm by detailed morphological studies, gene expression and a protein uptake assay. In comparison to embryoid bodies derived from ES cells, which form primitive and definitive endoderm, the endoderm compartment of embryoid bodies formed from EPL cells was comprised almost exclusively of definitive endoderm. Definitive endoderm was defined as a population of squamous cells that expressed Sox17, CXCR4 and Trh, which formed without the prior formation of primitive endoderm and was unable to endocytose horseradish peroxidase from the medium. Definitive endoderm formed in EPLEBs provides a substrate for further differentiation into specific endoderm lineages; these lineages can be used as research tools for understanding the mechanisms controlling lineage establishment and the nature of the transient intermediates formed. The similarity between mouse EPL cells and human ES cells suggests EPLEBs can be used as a model system for the development of technologies to enrich for the formation of human ES cell-derived definitive endoderm in the future.


Assuntos
Técnicas de Cultura de Células/métodos , Diferenciação Celular/fisiologia , Corpos Embrioides/ultraestrutura , Endoderma/ultraestrutura , Mesoderma/ultraestrutura , Células-Tronco Pluripotentes/ultraestrutura , Linha Primitiva/ultraestrutura , Animais , Primers do DNA/genética , Citometria de Fluxo , Perfilação da Expressão Gênica , Peroxidase do Rábano Silvestre/farmacocinética , Camundongos , Microscopia Eletrônica de Varredura , Microscopia Eletrônica de Transmissão , Células-Tronco Pluripotentes/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Reação em Cadeia da Polimerase Via Transcriptase Reversa
14.
PLoS One ; 5(9): e12555, 2010 Sep 03.
Artigo em Inglês | MEDLINE | ID: mdl-20838439

RESUMO

BACKGROUND: Embryonic stem (ES) cells hold considerable promise as a source of cells with therapeutic potential, including cells that can be used for drug screening and in cell replacement therapies. Differentiation of ES cells into the somatic lineages is a regulated process; before the promise of these cells can be realised robust and rational methods for directing differentiation into normal, functional and safe cells need to be developed. Previous in vivo studies have implicated fibroblast growth factor (FGF) signalling in lineage specification from pluripotent cells. Although FGF signalling has been suggested as essential for specification of mesoderm and endoderm in vivo and in culture, the exact role of this pathway remains unclear. METHODOLOGY/PRINCIPAL FINDINGS: Using a culture model based on early primitive ectoderm-like (EPL) cells we have investigated the role of FGF signalling in the specification of mesoderm. We were unable to demonstrate any mesoderm inductive capability associated with FGF1, 4 or 8 signalling, even when the factors were present at high concentrations, nor any enhancement in mesoderm formation induced by exogenous BMP4. Furthermore, there was no evidence of alteration of mesoderm sub-type formed with addition of FGF1, 4 or 8. Inhibition of endogenous FGF signalling, however, prevented mesoderm and favoured neural differentiation, suggesting FGF signalling was required but not sufficient for the differentiation of primitive ectoderm into primitive streak-like intermediates. The maintenance of ES cell/early epiblast pluripotent marker expression was also observed in cultures when FGF signalling was inhibited. CONCLUSIONS/SIGNIFICANCE: FGF signalling has been shown to be required for the differentiation of primitive ectoderm to neurectoderm. This, coupled with our observations, suggest FGF signalling is required for differentiation of the primitive ectoderm into the germ lineages at gastrulation.


Assuntos
Ectoderma/metabolismo , Fatores de Crescimento de Fibroblastos/metabolismo , Linha Primitiva/metabolismo , Transdução de Sinais , Animais , Técnicas de Cultura de Células , Diferenciação Celular , Linhagem Celular , Ectoderma/citologia , Ectoderma/embriologia , Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Mesoderma/embriologia , Mesoderma/metabolismo , Linha Primitiva/citologia , Linha Primitiva/embriologia , Ratos , Ratos Wistar
15.
PLoS One ; 5(7): e11702, 2010 Jul 22.
Artigo em Inglês | MEDLINE | ID: mdl-20661472

RESUMO

CRTR-1 is a member of the CP2 family of transcription factors. Unlike other members of the family which are widely expressed, CRTR-1 expression shows specific spatio-temporal regulation. Gene targeting demonstrates that CRTR-1 plays a central role in the maturation and function of the salivary glands and the kidney. CRTR-1 has also recently been identified as a component of the complex transcriptional network that maintains pluripotency in embryonic stem (ES) cells. CRTR-1 was previously shown to be a repressor of transcription. We examine the activity of CRTR-1 in ES and other cells and show that CRTR-1 is generally an activator of transcription and that it modulates the activity of other family members, CP2, NF2d9 and altNF2d9, in a cell specific manner. We also demonstrate that CRTR-1 activity is regulated by sumoylation at a single major site, residue K30. These findings imply that functional redundancy with other family members may mask important roles for CRTR-1 in other tissues, including the blastocyst stage embryo and embryonic stem cells.


Assuntos
Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/metabolismo , Proteínas Repressoras/metabolismo , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Animais , Western Blotting , Células COS , Linhagem Celular , Chlorocebus aethiops , Ensaio de Desvio de Mobilidade Eletroforética , Humanos , Imunoprecipitação , Ligação Proteica , Proteínas Repressoras/genética
16.
Cell Transplant ; 19(8): 985-98, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20350350

RESUMO

Pluripotent stem cells, including human embryonic stem cells and induced pluripotent stem cells, have generated much excitement about their prospects for use in cell transplantation therapies. This is largely attributable to their virtually unlimited growth potential, their ability to be precisely genetically altered in culture, and their utility for forming differentiated cell populations with potential clinical applications. Lysosomal storage diseases such as Sanfilippo syndrome (MPS-IIIA) represent ideal candidate diseases for the evaluation of cell therapies in the central nervous system (CNS). These diseases exhibit widespread pathology yet result from a single gene deficiency, in the case of Sanfilippo syndrome the lysosomal enzyme sulfamidase. The aim of this study was to investigate mouse embryonic stem (ES) cell-derived glial precursor cells as a vehicle for sulfamidase delivery in the MPS-IIIA mouse brain. In this study we have created a mouse ES cell line genetically modified to stably express and secrete high levels of human sulfamidase and a protocol for the in vitro derivation of large numbers glial precursors from ES cells. Differentiation of sulfamidase-expressing ES cells resulted in cell populations with sustained secretion of high levels of sulfamidase, comprised primarily of glial precursor cells with minor contaminants of other neural cell phenotypes but not residual pluripotent cells. CNS implantation studies demonstrated that ES cell-derived glial precursor cells formed using this differentiation method were able to engraft and survive for at least 12 weeks following implantation. The percentage of engraftment was quantified in different regions of the brain in 2-, 4-, and 8-week-old normal and MPS-IIIA mice. No teratomas were observed in any of the cell-transplanted animals. The results of this study support the further investigation of sulfamidase-expressing glial precursor cells as a vehicle for delivery of deficient enzyme into the CNS of MPS-IIIA mice.


Assuntos
Encéfalo/enzimologia , Células-Tronco Embrionárias/citologia , Hidrolases/metabolismo , Mucopolissacaridose III/enzimologia , Neuroglia/enzimologia , Animais , Células-Tronco Embrionárias/transplante , Humanos , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Mucopolissacaridose III/patologia , Mucopolissacaridose III/terapia , Neuroglia/metabolismo , Fatores de Tempo
18.
PLoS One ; 4(5): e5579, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19440553

RESUMO

In the mammal, the pluripotent cells of embryo differentiate and commit to either the mesoderm/endoderm lineages or the ectoderm lineage during gastrulation. In culture, the ability to direct lineage choice from pluripotent cells into the mesoderm/endoderm or ectoderm lineages will enable the development of technologies for the formation of highly enriched or homogenous populations of cells. Here we show that manipulation of cell:cell contact and a mesoderm suppressing activity in culture affects the outcome of pluripotent cell differentiation and when both variables are manipulated appropriately they can direct differentiation to either the mesoderm or ectoderm lineage. The disruption of cell:cell contacts and removal of a mesoderm suppressor activity results in the differentiation of pluripotent, primitive ectoderm-like cells to the mesoderm lineage, while maintenance of cell:cell contacts and inclusion, within the culture medium, of a mesoderm suppressing activity results in the formation of near homogenous populations of ectoderm. Understanding the contribution of these variables in lineage choice provides a framework for the development of directed differentiation protocols that result in the formation of specific cell populations from pluripotent cells in culture.


Assuntos
Comunicação Celular/fisiologia , Linhagem da Célula , Ectoderma/citologia , Mesoderma/citologia , Células-Tronco/citologia , Animais , Comunicação Celular/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Linhagem Celular , Meios de Cultura/farmacologia , Ectoderma/metabolismo , Citometria de Fluxo , Mesoderma/metabolismo , Camundongos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Ultrafiltração
19.
J Neurosci Res ; 76(2): 184-92, 2004 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-15048916

RESUMO

The many and varied proposed applications of cell replacement therapies in the treatment of human disease states, particularly those arising from cell loss or dysfunction, have been discussed widely in both the scientific and popular press. Although an attractive concept, cell therapies require the development of a readily available source of donor cells suitable for transplantation. Embryonic stem (ES) cells, with proven ability to differentiate to all cell populations of the embryo and adult in vitro, provide a potential source of therapeutic cells. The differentiation capability of mouse ES cells in vitro has been studied extensively over the last 20 years and the formation of neural precursors and neural cell lineages from mouse ES cells is well established. Cell populations highly enriched/homogenous in neural precursors have been achieved using a variety of chemical or biological inducing agents coupled with selective growth conditions. Preliminary reports suggest that similar neural enrichment is seen when these methodologies are applied to primate and human ES cells. ES cell-derived neural precursors have been analyzed in vitro and in vivo and found to be functionally normal and, after introduction into rodent models of human neurodegenerative diseases, capable of effecting measurable disease recovery. We review progress in the formation of neural precursors from mouse ES cells, particularly the recent reports of directed differentiation of ES in response to biological inductive factors, and assess the transfer of these approaches to human ES cells.


Assuntos
Diferenciação Celular/fisiologia , Sistema Nervoso/citologia , Neurônios/fisiologia , Células-Tronco/fisiologia , Animais , Linhagem da Célula/fisiologia , Células Cultivadas/citologia , Células Cultivadas/metabolismo , Células Cultivadas/transplante , Embrião de Mamíferos , Substâncias de Crescimento/metabolismo , Humanos , Neurônios/transplante , Transplante de Células-Tronco/métodos
20.
Biol Reprod ; 69(6): 1863-71, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12904310

RESUMO

Pluripotent cell development in the mammalian embryo results in the sequential formation of several developmentally distinct populations, inner cell mass, primitive ectoderm, and the primordial germ lineage. Factors within medium conditioned by HepG2 cells (MEDII) have been implicated in the formation and maintenance of primitive ectoderm from inner cell mass cells both in vitro and in vivo. Here we demonstrate that MEDII, but not LIF, is able to support the maintenance and proliferation in culture of pluripotent cells derived from primitive ectoderm formed in vitro or during embryonic development. This distinguishes primitive ectoderm and inner cell mass (ICM) on the basis of cytokine responsiveness and validates the biological activity proposed for factors within MEDII in primitive ectoderm establishment and maintenance. Further, it potentially provides an alternative technology for the isolation of pluripotent cells from the mammalian embryo.


Assuntos
Fatores Biológicos/farmacologia , Ectoderma/citologia , Células-Tronco Pluripotentes/citologia , Animais , Blastocisto/citologia , Blastocisto/efeitos dos fármacos , Carcinoma Hepatocelular , Divisão Celular/efeitos dos fármacos , Divisão Celular/fisiologia , Células Cultivadas , Meios de Cultivo Condicionados/farmacologia , Ectoderma/efeitos dos fármacos , Matriz Extracelular/fisiologia , Feminino , Interleucina-6/farmacologia , Fator Inibidor de Leucemia , Camundongos , Camundongos Endogâmicos CBA , Células-Tronco Pluripotentes/efeitos dos fármacos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA