RESUMO
AIM: To analyse the performance of arterial spin labelling (ASL) in predicting surgical bleeding in a paediatric cohort of optic pathway glioma (OPG). MATERIALS AND METHODS: Preoperative ASL data were obtained for 51 OPG in 40 patients, aged from 9 months to 16 years. The relative cerebral blood flow (rCBF) in the tumour areas with the highest CBF (maximum rCBF) was measured and then correlated with qualitative local bleeding (graded no, moderate, and major by the neurosurgeon) and quantitative global surgical bleeding (assessed in millilitres using haematocrit data). RESULTS: Intratumoural maximum rCBF was significantly higher when qualitative local bleeding was high (median value in the no, moderate, and major bleeding groups equal to 0.81, 1.39 and 4.22, respectively, p=0.004), but there was no difference in global quantitative bleeding (p=0.7 for the total blood loss). The maximum tumour rCBF cut-off value of 1.1 yielded a sensitivity of 73%, a specificity of 78%, and an accuracy of 76% (39/51 tumours) in detecting haemorrhagic OPG. Choosing a maximum tumour rCBF cut-off value > 1.7 improved the specificity in diagnosing tumours with high bleeding risk with a specificity of 94%, a sensitivity of 53%, and an accuracy of 82% (42/51 tumours). CONCLUSION: ASL tumoural rCBF is a useful and simple diagnostic tool to help predict high intraoperative tumoural bleeding risk in paediatric OPG.
Assuntos
Neoplasias Encefálicas , Glioma , Humanos , Criança , Neoplasias Encefálicas/complicações , Neoplasias Encefálicas/diagnóstico por imagem , Neoplasias Encefálicas/cirurgia , Marcadores de Spin , Glioma/complicações , Glioma/diagnóstico por imagem , Glioma/cirurgia , Perda Sanguínea Cirúrgica , Circulação Cerebrovascular/fisiologia , Imageamento por Ressonância MagnéticaRESUMO
Heterotrimeric guanosine triphosphate (GTP)-binding proteins (G proteins) may participate in membrane traffic events. A complementary DNA (cDNA) was isolated from a mouse pituitary cDNA library that corresponded to an alternatively spliced form of the gene encoding the G protein alpha subunit G alpha i2. The cDNA was identical to that encoding G alpha i2 except that the region encoding for the carboxyl-terminal 24 amino acids was replaced by a longer region encoding 35 amino acids that have no sequence similarity with G alpha i2 or other members of the G protein family. This alternative spliced product and the corresponding protein (sGi2) were present in several tissues. Specific antibodies revealed that sGi2 was localized in the Golgi apparatus, suggesting a role in membrane transport. Thus, alternative splicing may generate from a single gene two G protein alpha subunits with differential cellular localization and function.
Assuntos
Processamento Alternativo , Subunidades alfa Gi-Go de Proteínas de Ligação ao GTP , Proteínas de Ligação ao GTP/metabolismo , Complexo de Golgi/metabolismo , Proteínas Oncogênicas/metabolismo , Proteínas Proto-Oncogênicas , Sequência de Aminoácidos , Animais , Sequência de Bases , Linhagem Celular , Membrana Celular/metabolismo , Proteína Coatomer , DNA Complementar/genética , Subunidade alfa Gi2 de Proteína de Ligação ao GTP , Proteínas de Ligação ao GTP/análise , Proteínas de Ligação ao GTP/química , Proteínas de Ligação ao GTP/genética , Complexo de Golgi/química , Camundongos , Proteínas Associadas aos Microtúbulos/análise , Dados de Sequência Molecular , Proteínas Oncogênicas/análise , Proteínas Oncogênicas/química , Proteínas Oncogênicas/genéticaRESUMO
The mechanisms underlying sweet taste in mammals have been elusive. Although numerous studies have implicated G proteins in sweet taste detection, the expected G protein-coupled receptors have not been found. Here we describe a candidate taste receptor gene, T1r3, that is located at or near the mouse Sac locus, a genetic locus that controls the detection of certain sweet tastants. T1R3 differs in amino acid sequence in mouse strains with different Sac phenotypes ('tasters' versus 'nontasters'). In addition, a perfect correlation exists between two different T1r3 alleles and Sac phenotypes in recombinant inbred mouse strains. The T1r3 gene is expressed in a subset of taste cells in circumvallate, foliate and fungiform taste papillae. In circumvallate and foliate papillae, most T1r3-expressing cells also express a gene encoding a related receptor, T1R2, raising the possibility that these cells recognize more than one ligand, or that the two receptors function as heterodimers.
Assuntos
Células Quimiorreceptoras/fisiologia , Genes/fisiologia , Paladar/genética , Alelos , Sequência de Aminoácidos , Animais , Mapeamento Cromossômico , Clonagem Molecular , DNA/genética , Hibridização In Situ , Camundongos , Camundongos Endogâmicos , Dados de Sequência Molecular , Fenótipo , Polimorfismo Genético/genética , Papilas Gustativas/metabolismoRESUMO
The mechanisms governing neuronal differentiation, including the signals underlying the induction of voltage-dependent sodium (Na+) channel expression by neurotrophic factors, which occurs independent of Ras activity, are not well understood. Therefore, Na+ channel induction was analyzed in sublines of PC12 cells stably expressing platelet-derived growth factor (PDGF) beta receptors with mutations that eliminate activation of specific signalling molecules. Mutations eliminating activation of phosphatidylinositol 3-kinase (PI3K), phospholipase C gamma (PLC gamma), the GTPase-activating protein (GAP), and Syp phosphatase failed to diminish the induction of type II Na+ channel alpha-subunit mRNA and functional Na+ channel expression by PDGF, as determined by RNase protection assays and whole-cell patch clamp recording. However, mutation of juxtamembrane tyrosines that bind members of the Src family of kinases upon receptor activation inhibited the induction of functional Na+ channels while leaving the induction of type II alpha-subunit mRNA intact. Mutation of juxtamembrane tyrosines in combination with mutations eliminating activation of PI3K, PLC gamma, GAP, and Syp abolished the induction of type II alpha-subunit mRNA, suggesting that at least partially redundant signaling mechanisms mediate this induction. The differential effects of the receptor mutations on Na+ channel expression did not reflect global changes in receptor signaling capabilities, as in all of the mutant receptors analyzed, the induction of c-fos and transin mRNAs still occurred. The results reveal an important role for the Src family in the induction of Na+ channel expression and highlight the multiplicity and combinatorial nature of the signaling mechanisms governing neuronal differentiation.
Assuntos
Mutação , Neurônios/citologia , Receptores do Fator de Crescimento Derivado de Plaquetas/genética , Transdução de Sinais/fisiologia , Canais de Sódio/fisiologia , Animais , Becaplermina , Diferenciação Celular , Proteínas Ativadoras de GTPase , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Isoenzimas/metabolismo , Metaloproteinase 3 da Matriz/genética , Fatores de Crescimento Neural/farmacologia , Neuritos/metabolismo , Neurônios/metabolismo , Células PC12 , Técnicas de Patch-Clamp , Fosfatidilinositol 3-Quinases , Fosfolipase C gama , Fosfotransferases (Aceptor do Grupo Álcool)/metabolismo , Fator de Crescimento Derivado de Plaquetas/farmacologia , Proteína Tirosina Fosfatase não Receptora Tipo 11 , Proteína Tirosina Fosfatase não Receptora Tipo 6 , Proteínas Tirosina Fosfatases/metabolismo , Proteínas/metabolismo , Proteínas Proto-Oncogênicas c-fos/genética , Proteínas Proto-Oncogênicas c-sis , RNA Mensageiro/biossíntese , Ratos , Receptores Proteína Tirosina Quinases/metabolismo , Receptor beta de Fator de Crescimento Derivado de Plaquetas , Receptores do Fator de Crescimento Derivado de Plaquetas/fisiologia , Canais de Sódio/genética , Fosfolipases Tipo C/metabolismo , Tirosina/metabolismo , Proteínas Ativadoras de ras GTPaseRESUMO
The D2 dopamine receptor, an inhibitor of adenylyl cyclase, belongs to the family of seven transmembrane domain G-protein-coupled receptors. This receptor is encoded by two mRNAs produced from the same gene by alternative splicing, here referred to as D2L and D2S. The resultant proteins are identical except for an insertion of 29 amino acids in the putative third intracytoplasmic domain. This domain has been shown to be important for the coupling of this family of receptors to G-proteins. We have previously shown that there is differential inhibition of the adenylyl cyclase activity when these two receptors are produced in JEG3 cells; D2S is more efficient than D2L. To understand the molecular basis of such differential activity, we analyzed the G-proteins expressed in these cells. Here we show that G alpha i2 is absent in this cell line. Moreover, it is possible to restore the same inhibitory activity obtained by D2S when an expression vector encoding this alpha-subunit is cotransfected with D2L. In addition, transfections of the two receptors in a recipient cell line containing the three G alpha i subtypes confirm that the two receptors behave similarly. We conclude that the 29-amino acid insertion present in D2L allows it to interact specifically with G alpha i2. These data suggest that in vivo the function of activated D2 receptors is exerted by specific interactions with Gi-protein subtypes.
Assuntos
Inibidores de Adenilil Ciclases , Dopamina/farmacologia , Proteínas de Ligação ao GTP/metabolismo , Receptores Dopaminérgicos/metabolismo , Transdução de Sinais , 1-Metil-3-Isobutilxantina/farmacologia , Colforsina/farmacologia , Humanos , Splicing de RNA , RNA Mensageiro/metabolismo , Receptores Dopaminérgicos/classificação , Receptores Dopaminérgicos/genética , Espiperona/metabolismo , Transfecção , Células Tumorais CultivadasRESUMO
We have identified and characterized the cDNAs corresponding to the mouse D2 dopamine receptors. We show that in the mouse the D2 dopamine receptor is found in two forms, generated by alternative splicing of the same gene, mRNA distribution analysis of areas expressing the D2 receptors shows that the larger form is the most abundant, except in the brain stem where the shorter form is predominant. Membranes of mammalian cells transiently transfected with both forms of D2 receptor bind [3H]spiperone with a high affinity.
Assuntos
Encéfalo/fisiologia , Receptores Dopaminérgicos/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Southern Blotting , Mapeamento Encefálico , Bromocriptina/metabolismo , Clonagem Molecular , DNA/genética , Camundongos , Dados de Sequência Molecular , RNA Mensageiro/genética , Receptores Dopaminérgicos/metabolismo , Proteínas Recombinantes/metabolismo , Espiperona/metabolismoRESUMO
Dopaminergic D2 receptors mediate the effect of dopamine on cellular effector systems by means of guanine nucleotide-binding proteins (G proteins). The major biochemical effect evoked by these receptors is the inhibition of adenylyl cyclase. As a consequence, the activation of D2 receptors lowers the intracellular cAMP level. Two cDNAs, originated by alternative splicing of the same gene, have been isolated: D2A and D2B. They code for two proteins of 444 and 415 amino acids. These proteins display high affinity for selective D2 dopamine ligands. D2A differs from D2B by an insertion of 87 nucleotides in its cDNA, which is located in a region of the protein considered important for the coupling to G proteins. To investigate functional differences between the two dopamine D2 receptor isoforms, we transiently expressed them in cultured cells. To do so we developed an assay to study membrane receptors that are coupled to the adenylyl cyclase. Using this assay, we were able to show that the stimulation of the adenylyl cyclase induced by the activation of the beta 2-adrenergic receptor is inhibited more efficiently by D2B than D2A. The effects elicited by the D2 receptors are mediated by pertussis toxin-sensitive G proteins. Treatment of transfected cells with pertussis toxin abolishes the inhibitory effects in a dose- and receptor isoform-dependent manner. Our results suggest that the two dopamine receptor isoforms are differentially coupled to G proteins.
Assuntos
AMP Cíclico/fisiologia , Proteínas de Ligação ao GTP/fisiologia , Regiões Promotoras Genéticas , Receptores de AMP Cíclico/fisiologia , Receptores Dopaminérgicos/fisiologia , Transcrição Gênica , Toxina Adenilato Ciclase , Animais , Northern Blotting , Linhagem Celular , Colforsina/farmacologia , Proteínas de Ligação ao GTP/genética , Regulação da Expressão Gênica , Humanos , Técnicas In Vitro , Camundongos , Toxina Pertussis , Receptores Adrenérgicos beta/fisiologia , Sequências Reguladoras de Ácido Nucleico , Transdução de Sinais , Fatores de Virulência de Bordetella/farmacologiaRESUMO
The gustatory system of mammals can sense four basic taste qualities, bitter, sweet, salty and sour, as well as umami, the taste of glutamate. Previous studies suggested that the detection of bitter and sweet tastants by taste receptor cells in the mouth is likely to involve G-protein-coupled receptors. Although two putative G-protein-coupled bitter/sweet taste receptors have been identified, the chemical diversity of bitter and sweet compounds leads one to expect that there is a larger number of different receptors. Here we report the identification of a family of candidate taste receptors (the TRBs) that are members of the G-protein-coupled receptor superfamily and that are specifically expressed by taste receptor cells. A cluster of genes encoding human TRBs is located adjacent to a Prp gene locus, which in mouse is tightly linked to the SOA genetic locus that is involved in detecting the bitter compound sucrose octaacetate. Another TRB gene is found on a human contig assigned to chromosome 5p15, the location of a genetic locus (PROP) that controls the detection of the bitter compound 6-n-propyl-2-thiouracil in humans.
Assuntos
Receptores de Superfície Celular/fisiologia , Papilas Gustativas/fisiologia , Sequência de Aminoácidos , Animais , Mapeamento Cromossômico , Cromossomos Humanos Par 12 , Cromossomos Humanos Par 5 , Proteínas de Ligação ao GTP/metabolismo , Expressão Gênica , Humanos , Camundongos , Dados de Sequência Molecular , Receptores de Superfície Celular/análise , Receptores de Superfície Celular/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , PaladarRESUMO
Stimulation of the platelet-derived growth factor beta receptor (betaPDGFR) activates enzymes such as phosphatidylinositol 3-kinase (PI3K) and phospholipase Cgamma1 (PLCgamma), which ultimately initiate nuclear responses such as enhanced expression of immediate early genes. In an attempt to compare the signaling cascades initiated by PI3K and PLCgamma, we examined the activation of a panel of immediate early genes by betaPDGFR mutants, which preferentially engage PI3K or PLCgamma. When expressed in A431 cells, the wild type receptor and to a lesser extent the mutant receptor that associates with PLCgamma (Y1021) was able to up-regulate c-fos, junB, and KC mRNA expression. In contrast, the receptor mutant that engages PI3K (Y740/51) poorly stimulated c-fos mRNA expression and did not significantly stimulate expression of either JunB or KC. Receptor mutants that did not associate with either PI3K or PLCgamma were dramatically compromised or unable to increase expression of any of these immediate early genes. The differential ability of the Y1021 and Y740/51 receptors to activate c-fos correlated well with an apparent difference in their ability to engage distinct protein kinase C family members. However there did appear to be a degree of redundancy in the cytoplasmic signaling pathways initiated by PI3K and PLCgamma, since both the Y1021 and Y740/51 receptors were able to activate an AP-1-responsive element. We conclude that recruitment of signal relay enzymes to the betaPDGFR is necessary for PDGF-dependent activation of at least some immediate early genes. In addition, whereas the betaPDGFR activates multiple signaling enzymes capable of activating the same nuclear response (activation of c-fos), these signaling cascades do not appear to converge in the cytoplasm but arrive at the nucleus as distinguishable inputs.
Assuntos
Núcleo Celular/metabolismo , Citoplasma/metabolismo , Receptores do Fator de Crescimento Derivado de Plaquetas/metabolismo , Transdução de Sinais , Genes Precoces , Humanos , Fosfatidilinositol 3-Quinases/metabolismo , Fosforilação , Receptor beta de Fator de Crescimento Derivado de Plaquetas , Fator de Transcrição AP-1/metabolismo , Células Tumorais CultivadasRESUMO
The transcriptional activity of a gene can be regulated by a multitude of trans-acting factors that interact with specific cis-acting elements, mostly located in the promoter regions. The function of transcription factors is modulated by intracellular signal transduction pathways, which are activated by specific ligands binding to the appropriate membrane receptors. Here we discuss the links between the activation of the adenylyl cyclase pathway and the transcriptional response of cAMP-inducible genes that is achieved by the interplay of a multitude of nuclear transcription factors such as CREB and CREM.
Assuntos
AMP Cíclico/fisiologia , Regulação da Expressão Gênica/fisiologia , Transdução de Sinais/fisiologia , Adenilil Ciclases/fisiologia , Sequência de Aminoácidos , Animais , Comunicação Celular/fisiologia , Proteínas de Ligação ao GTP/fisiologia , Humanos , Dados de Sequência Molecular , Regiões Promotoras Genéticas/fisiologia , Proteínas Quinases/fisiologia , Receptores de AMP Cíclico/fisiologia , Homologia de Sequência , Fatores de Transcrição/genética , Fatores de Transcrição/fisiologia , Transcrição Gênica/fisiologiaRESUMO
The olfactory system translates myriad chemical structures into diverse odour perceptions. To gain insight into how this is accomplished, we prepared mice that coexpressed a transneuronal tracer with only one of about 1,000 different odorant receptors. The tracer travelled from nasal neurons expressing that receptor to the olfactory bulb and then to the olfactory cortex, allowing visualization of cortical neurons that receive input from a particular odorant receptor. These studies revealed a stereotyped sensory map in the olfactory cortex in which signals from a particular receptor are targeted to specific clusters of neurons. Inputs from different receptors overlap spatially and could be combined in single neurons, potentially allowing for an integration of the components of an odorant's combinatorial receptor code. Signals from the same receptor are targeted to multiple olfactory cortical areas, permitting the parallel, and perhaps differential, processing of inputs from a single receptor before delivery to the neocortex and limbic system.
Assuntos
Condutos Olfatórios/fisiologia , Lectinas de Plantas , Olfato/fisiologia , Animais , Mapeamento Encefálico , Marcação de Genes , Lectinas , Camundongos , Vias Neurais , Neurônios/fisiologia , Bulbo Olfatório/fisiologia , Neurônios Receptores Olfatórios/fisiologia , Olfato/genéticaRESUMO
Two isoforms of the dopamine D2 receptor have been characterized, D2L (long) and D2S (short), generated by alternative splicing from the same gene. They differ by an in-frame insert of 29 amino acids specific to D2L within the putative third intracytoplasmic loop of the receptor. We have previously demonstrated (Montmayeur, J.-P., Guiramand, J., and Borelli, E. (1993) Mol. Endocrinol. 7, 161-170) that D2S and D2L, although presenting very similar pharmacological profiles, couple differently to the alpha-subunit of guanine nucleotide-binding regulatory proteins (G-proteins). In particular, D2L, but not D2S, requires the presence of the alpha-subunit of the inhibitory G-protein (G alpha i2) to elicit greater inhibition of adenylyl cyclase activity. The insert present in D2L must therefore confer the specificity of interaction with G alpha i2. Thus, we introduced substitution mutations within the D2L insert. These mutant receptors were expressed in JEG3 cells, a G alpha i2-deficient cell line, scoring for those presenting an increased inhibition of adenylyl cyclase by dopamine. Our analysis identified two mutants, S259/262A and D249V, with these properties. These results clearly show that the insert present in D2L plays a critical role in the selectivity for the G-proteins interacting with the receptor.
Assuntos
Processamento Alternativo , Proteínas de Ligação ao GTP/metabolismo , Receptores de Dopamina D2/biossíntese , Inibidores de Adenilil Ciclases , Sequência de Aminoácidos , Animais , Apomorfina/análogos & derivados , Apomorfina/metabolismo , Sequência de Bases , Linhagem Celular , Clonagem Molecular , AMP Cíclico/metabolismo , Dopamina/farmacologia , Agonistas de Dopamina/metabolismo , Humanos , Isoproterenol/metabolismo , Cinética , Camundongos , Dados de Sequência Molecular , Mutagênese Insercional , Receptores Adrenérgicos beta 2/biossíntese , Receptores Adrenérgicos beta 2/metabolismo , Receptores de Dopamina D2/metabolismo , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/metabolismo , Espiperona/metabolismo , TransfecçãoRESUMO
Mammalian nervous system function involves billions of neurons which are interconnected in a multitude of neural circuits. Here we describe a genetic approach to chart neural circuits. By using an olfactory-specific promoter, we selectively expressed barley lectin in sensory neurons in the olfactory epithelium and vomeronasal organ of transgenic mice. The lectin was transported through the axons of those neurons to the olfactory bulb, transferred to the bulb neurons with which they synapse, and transported through the axons of bulb neurons to the olfactory cortex. The lectin also was retrogradely transported from the bulb to neuromodulatory brain areas. No evidence could be obtained for adverse effects of the lectin on odorant receptor gene expression, sensory axon targeting in the bulb, or the generation or transmission of signals by olfactory sensory neurons. Transneuronal transfer was detected prenatally in the odor-sensing pathway, but only postnatally in the pheromone-sensing pathway, suggesting that odors, but not pheromones, may be sensed in utero. Our studies demonstrate that a plant lectin can serve as a transneuronal tracer when its expression is genetically targeted to a subset of neurons. This technology can potentially be applied to a variety of vertebrate and invertebrate neural systems and may be particularly valuable for mapping connections formed by small subsets of neurons and for studying the development of connectivity as it occurs in utero.