RESUMO
Platelet-derived growth factors (PDGFs) are soluble proteins that mediate intercellular signaling via receptor tyrosine kinases. The patterns of PDGF and PDGF receptor expression during embryogenesis are complex and dynamic and suggest that signaling can be autocrine or paracrine, depending on the particular tissue and the stage of development. Mesenchymal cells throughout the embryo and within some developing organs produce PDGF receptors, whereas their ligands are often produced by adjacent epithelial or endothelial cells. Disruption of PDGF signaling in the embryo leads to morphogenetic defects and embryonic or perinatal lethality. Tissues that are particularly susceptible to the absence of PDGF signaling are migrating mesoderm cells during gastrulation, nonneuronal neural crest cell derivatives, and kidney mesangial cells. These tissues share the common feature of undergoing epithelial-mesenchymal transitions. We review current knowledge of the distribution of PDGF ligands and receptors and discuss how this distribution may relate to several roles for PDGF during embryogenesis, particularly the regulation of mesenchymal cell behavior.
Assuntos
Embrião de Mamíferos/metabolismo , Desenvolvimento Embrionário e Fetal , Feto/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Fator de Crescimento Derivado de Plaquetas/metabolismo , Receptores do Fator de Crescimento Derivado de Plaquetas/metabolismo , Animais , Diferenciação Celular , Movimento Celular , Feminino , Humanos , Camundongos , Fator de Crescimento Derivado de Plaquetas/análise , Gravidez , Ratos , Receptores do Fator de Crescimento Derivado de Plaquetas/análiseRESUMO
Cartilage formation in the chick limb follows rapid proliferation, condensation and differentiation of limb mesenchyme. The control of these early events is poorly understood. Platelet-derived growth factor receptor alpha (PDGFR-alpha) is present throughout the mesenchyme of early chick limb buds, while its ligand, PDGF-A, is expressed in the surrounding epithelium. PDGFR-alpha is down-regulated in areas that will not give rise to cartilage and is then lost from cartilage forming areas after they begin to differentiate. PDGF-A increases chondrogenesis in micromass cultures of stage-20-24 limb buds, but not stage 25, where it inhibits chondrogenesis. Ectopic PDGF-A in the chick wing can lead to either a localized increase in cartilage formation, or an inhibition. Inhibition of PDGF signalling in the chick limb results in the loss of cartilage. These data demonstrate that PDGF-A functions to promote chondrogenesis at early stages of limb development and suggest that it inhibits chondrogenesis at later stages.
Assuntos
Cartilagem/embriologia , Condrogênese/genética , Extremidades/embriologia , Fator de Crescimento Derivado de Plaquetas/genética , Animais , Apoptose/genética , Embrião de Galinha , DNA/biossíntese , Regulação da Expressão Gênica no Desenvolvimento , Botões de Extremidades/fisiologia , Técnicas de Cultura de Órgãos , Fator de Crescimento Derivado de Plaquetas/metabolismo , Receptor alfa de Fator de Crescimento Derivado de Plaquetas/genética , Transdução de SinaisRESUMO
SnR, twist and Fgf10 are expressed in presumptive limb territories of early chick embryos. When FGF-2/FGF-8 beads are implanted in chick flank, an ectopic limb develops and SnR is irreversibly activated as early as 1 h. Ectopic Fgf10 and twist expression are activated much later at 17 and 20 h, respectively. FGF-10 can also induce SnR, but much later, and in this case activation occurs simultaneously with that of twist and Fgf10 via the Fgf8- expressing ridge. Tbx-4 and Tbx-5 are expressed in leg and wing forming regions, respectively, in a similar pattern to SnR and twist. FGF-2 leads to ectopic expression of Tbx-4 and Tbx-5 as rapidly as ectopic expression of SnR, but the patterns of ectopic transcripts suggest that induction of SnR and Tbx gene expression occur via different pathways.
Assuntos
Proteínas Aviárias , Proteínas de Ligação a DNA/genética , Fatores de Crescimento de Fibroblastos/genética , Regulação da Expressão Gênica no Desenvolvimento , Proteínas com Domínio T/genética , Fatores de Transcrição/genética , Animais , Sequência de Bases , Embrião de Galinha , DNA Complementar , Extremidades/embriologia , Fator 10 de Crescimento de Fibroblastos , Fator 2 de Crescimento de Fibroblastos/farmacologia , Fator 8 de Crescimento de Fibroblasto , Fatores de Crescimento de Fibroblastos/farmacologia , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Dados de Sequência Molecular , Fatores de Transcrição da Família Snail , Proteína 1 Relacionada a TwistRESUMO
Despite the central importance of cell lines in contemporary studies in cellular and molecular biology, many areas of potential investigation remain impeded by the limited number of lines available and by the difficulty in generating new lines of interest. Thus, there has been a constant pressure to develop improved methods for obtaining cell lines of particular interest. This review examines some of the problems associated with in vitro approaches to cell line generation. In addition, two different ways in which transgenic animals can be used to overcome the limitations of in vitro production of cell lines are discussed. In the first approach, specific promoters are utilized to target expression of immortalizing genes to cells of interest. The second approach is concerned with development of a strain of transgenic animals (the H-2KbtsA58 transgenic mouse) designed to obviate the need for identification of cell-type specific promoters, and in which it is theoretically possible to directly generate conditionally immortal cell lines from any tissue of the body by simple dissection and growth of cells in appropriate tissue culture conditions. Finally, approaches are also discussed in which investigations on the control of precursor differentiation have been applied so as to bypass the need for expression of activated immortalizing oncogenes in the generation of large quantities of conditionally immortalized cells with the capacity to undergo normal differentiation in vitro and in vivo.
Assuntos
Técnicas de Cultura/métodos , Neurônios/citologia , Animais , Animais Geneticamente Modificados , Antígenos Transformantes de Poliomavirus/biossíntese , Antígenos Transformantes de Poliomavirus/genética , Diferenciação Celular , Divisão Celular/efeitos dos fármacos , Linhagem Celular , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Genes MHC Classe I , Antígenos H-2/biossíntese , Antígenos H-2/genética , Interferon gama/farmacologia , Camundongos , Camundongos Transgênicos , Regiões Promotoras Genéticas , Pele/citologiaAssuntos
Neoplasias do Sistema Nervoso Central/fisiopatologia , Sistema Nervoso Central/fisiologia , Regeneração Nervosa , Neuroglia/fisiologia , Animais , Sistema Nervoso Central/citologia , Neoplasias do Sistema Nervoso Central/patologia , Glioma/fisiopatologia , Humanos , Camundongos , Camundongos Transgênicos , Esclerose Múltipla/fisiopatologia , Bainha de Mielina/fisiologia , Neuroglia/citologia , Oligodendroglia/citologia , Células-Tronco/fisiologiaRESUMO
Intestinal mucosal cells have proved difficult to culture in vitro. Many attempts have been made to develop long-term cultures of these cells either by direct culturing or by attempting to immortalize these cells by using a range of transforming viral genes, but with little success. The recent development of a transgenic mouse bearing a temperature-sensitive mutation of the simian virus 40 large tumor antigen gene (tsA58) has enabled us to initiate conditionally immortalized cultures of epithelial cells from both small intestinal and colonic mucosa of adult mice. Crypts were isolated from either the small intestines or colons of young adult mice and cultured at the permissive temperature (33 degrees C) in medium containing conditioned medium from a human colon carcinoma cell line, LIM1863. Crypts from both tissues yielded cultures of epithelial cells that have now been in culture for more than 12 months with regular passaging. The epithelial nature of the cells has been confirmed by staining with anti-keratin antibodies. The intestinal origin of the cells was demonstrated by the ability of the cells to synthesize low levels of both brush border peptidases and a disaccharidase. The levels of expression of these enzymes were modulated by the addition of sodium butyrate or phorbol myristate acetate to the medium, which resulted in an increase in the synthesis of the peptidases and a decrease in the synthesis of the disaccharidase. The cells proliferate continuously at the permissive temperature (33 degrees C), but proliferation ceases at the nonpermissive temperature (39.5 degrees C). To our knowledge, this is the first description of the establishment of epithelial cell lines from both small intestine and colon of the same mouse strain. The success reported here indicates that this transgenic mouse will be a useful source of tissue for the study of the mechanisms that control the proliferation and eventual differentiation and senescence of the cells of the intestinal mucosa. These mice will also be a useful source of cells for attempts to culture cells from other tissues that have proved difficult to culture in vitro.
Assuntos
Linhagem Celular , Colo/citologia , Mucosa Intestinal/citologia , Intestino Delgado/citologia , Camundongos Transgênicos , Animais , Antígenos Virais de Tumores/genética , Divisão Celular , Colo/ultraestrutura , Técnicas de Cultura/métodos , Fator de Crescimento Epidérmico/farmacologia , Células Epiteliais , Epitélio/ultraestrutura , Fatores de Crescimento de Fibroblastos/farmacologia , Antígenos H-2/genética , Imuno-Histoquímica , Mucosa Intestinal/ultraestrutura , Intestino Delgado/ultraestrutura , Queratinas/imunologia , Queratinas/isolamento & purificação , Camundongos , Microvilosidades/enzimologia , Vírus 40 dos Símios/genética , Fator de Crescimento Transformador beta/farmacologiaRESUMO
During Xenopus gastrulation, platelet-derived growth factor (PDGF) receptor-alpha is expressed in involuting marginal zone cells which migrate over ectodermal cells expressing PDGF-A. To investigate the role of PDGF signalling during this process, we have generated a novel point mutant of PDGF receptor-alpha analogous to the W37 mutation of c-kit. This molecule is a specific, potent, dominant inhibitor of PDGF signalling in vivo. Injection of RNA encoding this protein into Xenopus embryos prevents closure of the blastopore, leads to abnormal gastrulation and a loss of anterior structures. Convergent extension is not inhibited in these embryos, but rather, involuting mesodermal cells fail to adhere to the overlying ectoderm. PDGF may therefore be required for mesodermal cell-substratum interaction.
Assuntos
Gástrula/fisiologia , Fator de Crescimento Derivado de Plaquetas/fisiologia , Transdução de Sinais/fisiologia , Xenopus laevis/embriologia , Animais , Gástrula/ultraestrutura , Hibridização In Situ , Mesoderma/fisiologia , Morfogênese/fisiologia , Mutagênese Sítio-Dirigida , Reação em Cadeia da Polimerase , Receptores do Fator de Crescimento Derivado de PlaquetasRESUMO
The ability to generate expanded populations of individual cell types able to undergo normal differentiation in vitro and in vivo is of critical importance in the investigation of the mechanisms that underly differentiation and in studies on the use of cell transplantation to repair damaged tissues. This review discusses the development of a strain of transgenic mice that allows the direct derivation of conditionally immortal cell lines from a variety of tissues, simply by dissociation of the tissue of interest and growth of cells in appropriate conditions. In these mice the tsA58 mutant of SV40 large T antigen is controlled by the interferon-inducible Class I antigen promoter. Cells can be grown for extended periods in vitro simply by growing them at 33 degrees C in the presence of interferon, while still retaining the capacity to undergo normal differentiation in vivo and in vitro. In addition, it appears that cell lines expressing mutant phenotypes can readily be generated by preparing cultures from appropriate offspring of matings between H-2KbtsA58 transgenic mice and mutant mice of interest.
Assuntos
Linhagem Celular , Antígenos H-2 , Camundongos Transgênicos/fisiologia , Animais , Antígenos Transformantes de Poliomavirus/genética , Antígenos Transformantes de Poliomavirus/metabolismo , Astrócitos/fisiologia , Diferenciação Celular , Transformação Celular Viral , Interferon gama/farmacologia , Camundongos , Camundongos Mutantes , Camundongos Transgênicos/genética , Músculo Esquelético/citologia , Músculo Esquelético/fisiologia , Osteoclastos/fisiologia , Regiões Promotoras Genéticas , Mapeamento por Restrição , Vírus 40 dos Símios/genéticaRESUMO
Studies on cell lines have greatly improved our understanding of many important biological questions. Generation of cell lines is facilitated by the introduction of immortalizing oncogenes into cell types of interest. One gene known to immortalize many different cell types in vitro encodes the simian virus 40 (SV40) large tumor (T) antigen (TAg). To circumvent the need for gene insertion in vitro to generate cell lines, we created transgenic mice harboring the SV40 TAg gene. Since previous studies have shown that TAg expression in transgenic mice is associated with tumorigenesis and aberrant development, we utilized a thermolabile TAg [from a SV40 strain, tsA58, temperature sensitive (ts) for transformation] to reduce the levels of functional TAg present in vivo. To direct expression to a broad range of tissues, we used the mouse major histocompatibility complex H-2Kb promoter, which is both widely active and can be further induced by interferons. tsA58 TAg mRNA was expressed in tissues of all animals harboring the hybrid construct. Development of all tissues was macroscopically normal except for thymus, which consistently showed hyperplasia. Fibroblast and cytokeratin+ thymic epithelial cultures from these mice were readily established without undergoing crisis and were conditionally immortal in their growth; the degree of conditionality was correlated with the levels of tsA58 TAg detected. One strain of H-2Kb-tsA58 mice has been bred through several generations to homozygosity and transmits a functional copy of the transgene.
Assuntos
Linhagem Celular , Animais , Northern Blotting , Western Blotting , Transformação Celular Viral , Clonagem Molecular , Epitélio/patologia , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Imunofluorescência , Hiperplasia , Interferon gama/farmacologia , Queratinas/metabolismo , Camundongos , Camundongos Transgênicos , Hibridização de Ácido Nucleico , Regiões Promotoras Genéticas , RNA/genética , Vírus 40 dos Símios , Pele/citologia , Timo/patologiaRESUMO
The platelet-derived growth factor alpha-receptor (PDGFRalpha) plays a vital role in the development of vertebrate embryos, since mice lacking PDGFRalpha die in mid-gestation. PDGFRalpha is expressed in several types of migratory progenitor cells in the embryo including cranial neural crest cells, lung smooth muscle progenitors and oligodendrocyte progenitors. To study PDGFRalpha gene regulation and function during development, we generated transgenic mice by pronuclear injection of a 380 kb yeast artificial chromosome (YAC) containing the human PDGFRalpha gene. The YAC transgene was expressed in neural crest cells, rescued the profound craniofacial abnormalities and spina bifida observed in PDGFRalpha knockout mice and prolonged survival until birth. The ultimate cause of death was respiratory failure due to a defect in lung growth, stemming from failure of the transgene to be expressed correctly in lung smooth muscle progenitors. However, the YAC transgene was expressed faithfully in oligodendrocyte progenitors, which was not previously observed with plasmid-based transgenes containing only upstream PDGFRalpha control sequences. Our data illustrate the complexity of PDGFRalpha genetic control, provide clues to the location of critical regulatory elements and reveal a requirement for PDGF signalling in prenatal lung growth, which is distinct from the known requirement in postnatal alveogenesis. In addition, we found that the YAC transgene did not prolong survival of Patch mutant mice, indicating that genetic defects outside the PDGFRalpha locus contribute to the early embryonic lethality of Patch mice.
Assuntos
Anormalidades Craniofaciais/genética , Pulmão/embriologia , Crista Neural/fisiologia , Receptor alfa de Fator de Crescimento Derivado de Plaquetas/fisiologia , Disrafismo Espinal/genética , Animais , Osso e Ossos/embriologia , Células Cultivadas , Cromossomos Artificiais de Levedura , Anormalidades Craniofaciais/embriologia , Anormalidades Craniofaciais/prevenção & controle , Desenvolvimento Embrionário e Fetal , Feminino , Homozigoto , Humanos , Camundongos , Camundongos Knockout , Camundongos Transgênicos , Neurônios/citologia , Neurônios/fisiologia , Gravidez , Receptor alfa de Fator de Crescimento Derivado de Plaquetas/deficiência , Receptor alfa de Fator de Crescimento Derivado de Plaquetas/genética , Medula Espinal/embriologia , Disrafismo Espinal/embriologia , Disrafismo Espinal/prevenção & controleRESUMO
Following our study in Balb/c 3T3 cells and other cultured fibroblasts of the changes in myosin light chain phosphorylation associated with alterations in cell shape, attachment, and receptor patching, we have now determined the corresponding changes in cytoskeletal myosin distribution, and in the cellular calcium concentration, since this might, in part, mediate such responses. Immunofluorescence microscopy showed that myosin assembly into ordered forms such as actomyosin bundles and myosin sheath almost always correlated with previously shown high phosphorylation levels of myosin regulatory light chain, whereas diffuse distributions usually correlated with low or undetectable levels. An exception was observed in treatment to alter cellular cAMP levels when, in a biphasic response, assembly was correlated inversely with the phosphorylation states shown previously. Fluorescent indicators for intracellular calcium concentration, [Ca++]i, showed that myosin disassembly by trypsin or EGTA acting externally on the cells was preceded by a transient increase in [Ca++]i. For EGTA this was associated with transient recruitment of myosin into dorsal sheath structure as well as the transient enhancement of phosphorylation shown earlier. Blockage of EGTA-induced disassembly could be achieved by azide, which also caused an immediate increase in [Ca++]i and inhibited its subsequent decline. Trypsin-induced dephosphorylation did not appear to involve an eventual reduction of [Ca++]i. Therefore, in many but not all of the systems studied, correlated changes were observed in myosin assembly, [Ca++]i, and the myosin phosphorylation levels shown earlier.
Assuntos
Cálcio/metabolismo , Fibroblastos/citologia , Miosinas/metabolismo , Animais , Bucladesina/farmacologia , Adesão Celular/efeitos dos fármacos , Concanavalina A/farmacologia , Metabolismo Energético/efeitos dos fármacos , Fibroblastos/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos BALB C , Microscopia de Fluorescência , Agregação de Receptores/efeitos dos fármacosRESUMO
We have cloned the human genes coding for desmosomal glycoproteins DGII and DGIII, found in desmosomal cell junctions, and sequencing shows that they are related to the cadherin family of cell adhesion molecules. Thus a new super family of cadherin-like molecules exists which also includes the other major desmosomal glycoprotein, DGI (Wheeler, G. N., Parker, A. E., Thomas, C. L., Ataliotis, P., Poynter, D., Arnemann, J., Rutman, A. J., Pidsley, S. C., Watt, F. M., Rees, D. A., Buxton, R. S., and Magee, A. I. (1991) Proc. Natl. Acad. Sci. U.S.A., in press). DGIII differs from DGII by the addition of a 46-base pair exon containing an in-frame stop codon resulting in mature protein molecular weights of 84,633 for DGII and 78,447 for DGIII. The unique carboxyl-terminal region of DGII contains a potential serine phosphorylation site explaining why only DGII is phosphorylated on serine. The cadherin cell adhesion recognition sequence (His-Ala-Val) is replaced by Phe-Ala-Thr, suggesting that DGII/III may be adhesive molecules using a different mechanism.
Assuntos
Caderinas/genética , Desmossomos/metabolismo , Glicoproteínas/genética , Splicing de RNA , Sequência de Aminoácidos , Animais , Sequência de Bases , Northern Blotting , Southern Blotting , Caderinas/metabolismo , Clonagem Molecular , DNA/genética , Eletroforese em Gel de Ágar , Eletroforese em Gel de Poliacrilamida , Feminino , Glicoproteínas/metabolismo , Humanos , Masculino , Camundongos , Dados de Sequência Molecular , Fosforilação , Reação em Cadeia da Polimerase , Alinhamento de Sequência , Homologia de Sequência do Ácido NucleicoRESUMO
Skeletal myoblasts cloned from limb muscles of H-2Kb-tsA58 transgenic mice remained proliferative through at least 80 generations under conditions permissive for expression and function of the tsA58 gene product. When switched to nonpermissive conditions or implanted into muscles of nude mdx mice they underwent differentiation but, in one clonal cell line, a small proportion appeared to become quiescent muscle precursors in vivo. H-2Kb-tsA58 X mdx/mdx F1 male mice yielded dystrophin-deficient myoblasts. By such simple genetic crosses, H-2Kb-tsA58 transgenic mice provide a valuable tool for the rapid isolation of cell lines, myogenic or otherwise, bearing mutations of interest.
Assuntos
Antígenos Transformantes de Poliomavirus/genética , Antígenos H-2/genética , Músculos/citologia , Animais , Diferenciação Celular , Linhagem Celular , Transplante de Células , Células Clonais , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Camundongos Transgênicos , Mutação , Especificidade de Órgãos , Vírus 40 dos Símios/imunologiaRESUMO
Among the variety of specialized intercellular junctions, those of the adherens type have the most obvious association with cytoskeletal elements. This may be with the actin microfilament system as in the zonula adherens or with intermediate filaments as in the macula adherens, or desmosome. In the former case, it is clear that transmembrane glycoproteins of the cadherin family are important adhesive components of the molecular assembly. We now show for desmosomes that a major glycoprotein component (desmosomal glycoprotein DGI) has extensive homology with the cadherins, defining an extended family, but also has unique features in its cytoplasmic domain that are likely to be relevant to the association with intermediate rather than actin filaments. A novel 282-residue extension contains repeats of approximately 29 amino acid residues predicted to have an antiparallel beta-sheet structure, followed by a glycine-rich sequence. As in the cadherins, the extracellular domain contains possible Ca2(+)-binding sequences and a potential protease processing site. The cell adhesion recognition region (His-Ala-Val) of the cadherins is modified to Arg-Ala-Leu.