RESUMO
Fragile X Mental Retardation Protein (FMRP) is a RNA-binding protein that modulates protein synthesis at the synapse and its function is regulated by glutamate. The retina is the first structure that participates in vision, and uses glutamate to transduce electromagnetic signals from light to electrochemical signals to neurons. FMRP has been previously detected in the retina, but its localization has not been studied yet. In this work, our objectives were to describe the localization of FMRP in the retina, to determine whether different exposure to dark or light stimulus alters FMRP expression in the retina, and to compare the pattern in two different species, the mouse and chick. We found that both FMRP mRNA and protein are expressed in the retina. By immunohistochemistry analysis we found that both mouse and chick present similar FMRP expression localized mainly in both plexiform layers and the inner retina. It was also observed that FMRP is down-regulated by 24 h dark adaptation compared to its expression in the retina of animals that were exposed to light for 1 h after 24 h in the dark. We conclude that FMRP is likely to participate in retinal physiology, since its expression changes with light exposure. In addition, the expression pattern and regulation by light of FMRP seems well conserved since it was similar in both mouse and chick.
Assuntos
Adaptação à Escuridão/fisiologia , Proteína do X Frágil da Deficiência Intelectual/genética , Regulação da Expressão Gênica , Luz , RNA/genética , Retina/metabolismo , Animais , Galinhas , Feminino , Proteína do X Frágil da Deficiência Intelectual/biossíntese , Proteína do X Frágil da Deficiência Intelectual/efeitos da radiação , Imuno-Histoquímica , Masculino , Camundongos , Camundongos Endogâmicos C57BLRESUMO
A new nicotinic acetylcholine receptor (nAChR) subunit, beta 4, was identified by screening a rat genomic library. In situ hybridization histochemistry revealed expression of the beta 4 gene in the medial habenula of adult rat brains. The primary structure of this subunit was deduced from a cDNA clone isolated from a PC12 cDNA library. Functional nAChRs were detected in Xenopus oocytes injected in pairwise combinations with in vitro synthesized RNAs encoding beta 4 and either the alpha 2, alpha 3, or alpha 4 subunit. Unlike the alpha 3 beta 2 receptor, the alpha 3 beta 4 receptor is not blocked by bungarotoxin 3.1, indicating that the beta subunit can affect the sensitivity of neuronal nAChRs to this toxin. These results extend the functional diversity of nicotinic receptors in the nervous system.
Assuntos
Neurônios/metabolismo , Receptores Nicotínicos/genética , Sequência de Aminoácidos , Animais , Fenômenos Químicos , Química , Regulação da Expressão Gênica , Dados de Sequência Molecular , Ratos/genética , Xenopus/genéticaRESUMO
To study the role of mGlu7 receptors (mGluR7), we used homologous recombination to generate mice lacking this metabotropic receptor subtype (mGluR7(-/-)). After the serendipitous discovery of a sensory stimulus-evoked epileptic phenotype, we tested two convulsant drugs, pentylenetetrazole (PTZ) and bicuculline. In animals aged 12 weeks and older, subthreshold doses of these drugs induced seizures in mGluR7(-/-), but not in mGluR7(+/-), mice. PTZ-induced seizures were inhibited by three standard anticonvulsant drugs, but not by the group III selective mGluR agonist (R,S)-4-phosphonophenylglycine (PPG). Consistent with the lack of signs of epileptic activity in the absence of specific stimuli, mGluR7(-/-) mice showed no major changes in synaptic properties in two slice preparations. However, slightly increased excitability was evident in hippocampal slices. In addition, there was slower recovery from frequency facilitation in cortical slices, suggesting a role for mGluR7 as a frequency-dependent regulator in presynaptic terminals. Our findings suggest that mGluR7 receptors have a unique role in regulating neuronal excitability and that these receptors may be a novel target for the development of anticonvulsant drugs.
Assuntos
Predisposição Genética para Doença , Glicina/análogos & derivados , Receptores de Glutamato Metabotrópico/deficiência , Convulsões/genética , Animais , Anticonvulsivantes/farmacologia , Bicuculina , Córtex Cerebral/efeitos dos fármacos , Córtex Cerebral/fisiopatologia , Convulsivantes , Resistência a Medicamentos/genética , Eletroencefalografia , Agonistas de Aminoácidos Excitatórios/farmacologia , Marcação de Genes , Glicina/farmacologia , Hipocampo/efeitos dos fármacos , Hipocampo/fisiopatologia , Homozigoto , Técnicas In Vitro , Camundongos , Camundongos Knockout , Pentilenotetrazol , Fenótipo , Mapeamento Físico do Cromossomo , Receptores de Glutamato Metabotrópico/genética , Convulsões/induzido quimicamente , Convulsões/fisiopatologia , Convulsões/prevenção & controleRESUMO
Angiostatin is an endogenous inhibitor of tumor neovascularization that inhibits the proliferation of endothelial cells. Production of sufficient quantities of biologically active angiostatin by the enzymatic cleavage of plasminogen has proven difficult in that it has delayed clinical testing. We have cloned, expressed, and purified a recombinant human angiostatin derivative (K1-3) using a mammalian expression system. Through the addition of a secretory signal and polyhistidine sequence tag, K1-3 can be purified from post-culture medium by simple column chromatography. Purified K1-3 protein is apparently folded in an active conformation, as evidenced by its ability to bind to lysine-Sepharose. In vitro, recombinant K1-3 significantly suppressed endothelial cell proliferation in a dose-dependent manner with an IC50 of 50 nM. Using an animal model of intracranial brain tumors in immune-competent rats, systemic administration of purified recombinant K1-3 resulted in up to 85% suppression of tumor growth (P = 0.011). Growth suppression was accompanied by a 32% decrease (P = 0.01) in tumor neovascularization. This study demonstrates a simple method to produce a biologically active recombinant angiostatin derivative. The ability to suppress intracerebral tumor growth after systemic administration suggests that K1-3 is likely to have therapeutic value in the treatment of malignant glial tumors.
Assuntos
Neoplasias Encefálicas/tratamento farmacológico , Endotélio Vascular/citologia , Glioma/tratamento farmacológico , Neovascularização Patológica/prevenção & controle , Fragmentos de Peptídeos/uso terapêutico , Plasminogênio/uso terapêutico , Animais , Neoplasias Encefálicas/irrigação sanguínea , Neoplasias Encefálicas/patologia , Divisão Celular/efeitos dos fármacos , Linhagem Celular , Células Cultivadas , Clonagem Molecular , Endotélio Vascular/efeitos dos fármacos , Feminino , Glioma/irrigação sanguínea , Glioma/patologia , Humanos , Microcirculação/efeitos dos fármacos , Microcirculação/patologia , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/toxicidade , Plasminogênio/genética , Plasminogênio/toxicidade , Ratos , Ratos Endogâmicos F344 , Proteínas Recombinantes/uso terapêutico , Proteínas Recombinantes/toxicidade , Transfecção , Veias UmbilicaisRESUMO
Two new expression vectors have been constructed to take advantage of several useful properties of bacteriophage T4-infected Escherichia coli. These plasmids, pRDB8 and pRDB9, contain the promoter region and start codon of T4 gene 32, a contiguous multiple cloning site (MCS), and translation and transcription termination signals. DNA fragments inserted into the MCS are transcribed and translated at a high level in both uninfected and phage T4-infected cells. Furthermore, the extreme stability of the hybrid mRNA after infection permits the specific biosynthetic labeling of the protein encoded by the cloned gene. In addition, the cloned gene product is stabilized, since the host-mediated degradation of foreign proteins is inhibited by phage infection. The properties of this expression system were demonstrated with the constant region of a rabbit immunoglobulin lambda light chain (C lambda) gene. Although proteolytic degradation of the C lambda fusion protein was rapid in uninfected cells, degradation was blocked in phage-infected cells and the protein accumulated in greater amounts.
Assuntos
Clonagem Molecular , Escherichia coli/genética , Genes Virais , Genes , Vetores Genéticos , Plasmídeos , RNA Mensageiro/genética , Fagos T/genética , Proteínas Virais/genética , Sequência de Bases , Replicação do DNA , Enzimas de Restrição do DNA , Mutação , Regiões Promotoras Genéticas , Biossíntese de Proteínas , Transcrição GênicaRESUMO
Mammalian cells are characterized by an endomembrane system. Nevertheless, some cells lose these membranes during their terminal differentiation, e.g. red blood cells and lens fiber cells of the eye. 15-Lipoxygenase is believed to be critical for this membrane degradation. Here we use cultivated rabbit reticulocytes in the presence or absence of a lipoxygenase inhibitor to provide further evidence for the importance of 15-lipoxygenase for the in vivo degradation of mitochondria. We find that inhibitor treatment retarded mitochondrial degradation, as shown by persistence of marker proteins and by direct visualization of mitochondria by electron microscopy.
Assuntos
Araquidonato 15-Lipoxigenase/metabolismo , Organelas/metabolismo , Reticulócitos/enzimologia , Animais , Ácidos Araquidônicos/farmacologia , Western Blotting , Tamanho Celular/efeitos dos fármacos , Citosol/enzimologia , Citosol/metabolismo , Retículo Endoplasmático/efeitos dos fármacos , Retículo Endoplasmático/metabolismo , Inibidores Enzimáticos/farmacologia , Eritrócitos/efeitos dos fármacos , Membranas Intracelulares/metabolismo , Inibidores de Lipoxigenase , Organelas/efeitos dos fármacos , Coelhos , Reticulócitos/efeitos dos fármacosRESUMO
Cyclic nucleotide-gated channels (CNGC) are ligand-gated ion channels that open and close in response to changes in the intracellular concentration of the second messengers, 3;,5;-cyclic adenosine monophosphate and 3;,5;-cyclic guanosine monophosphate. Most notably, they transduce the chemical signal produced by the absorption of light in photoreceptors into a membrane potential change, which is then transmitted to the ascending visual pathway. CNGCs have also been implicated in the signal transduction of other neurons downstream of the photoreceptors, in particular the ON-bipolar cells, as well as in other areas of the central nervous system. We therefore undertook a search for additional cyclic nucleotide-gated channels expressed in the retina. Following a degenerate reverse transcription polymerase chain reaction approach to amplify low-copy number messages, a cDNA encoding a new splice variant of CNGC alpha-subunit was isolated from mouse retina and classified as mCNG3. An antiserum raised against the carboxy-terminal sequence identified the retinal cell type expressing mCNG3 as cone photoreceptors. Preembedding immunoelectron microscopy demonstrated its membrane localization in the outer segments, consistent with its role in phototransduction. Double-labeling experiments with cone-specific markers indicated that all cone photoreceptors in the murid retina use the same or a highly conserved cyclic nucleotide-gated channel. Therefore, defects in this channel would be predicted to severely impair photopic vision.
Assuntos
Canais Iônicos/fisiologia , Retina/fisiologia , Células Fotorreceptoras Retinianas Cones/fisiologia , Sequência de Aminoácidos , Animais , Western Blotting , Clonagem Molecular , Canais de Cátion Regulados por Nucleotídeos Cíclicos , DNA Complementar/genética , DNA Complementar/fisiologia , Imuno-Histoquímica , Canais Iônicos/biossíntese , Canais Iônicos/ultraestrutura , Camundongos , Camundongos Endogâmicos C57BL , Microscopia Eletrônica , Dados de Sequência Molecular , Retina/citologia , Retina/ultraestrutura , Células Fotorreceptoras Retinianas Cones/metabolismo , Células Fotorreceptoras Retinianas Cones/ultraestrutura , Células Fotorreceptoras Retinianas Bastonetes/fisiologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Segmento Externo da Célula Bastonete/metabolismo , Segmento Externo da Célula Bastonete/ultraestrutura , Sistemas do Segundo Mensageiro/fisiologia , Especificidade da EspécieRESUMO
OBJECTIVE: To determine whether patients with antineuronal antibody-associated paraneoplastic cerebellar degeneration (PCD) harbor antibodies to non-N-methyl-D-aspartate glutamate receptors (GluRs) in their serum. BACKGROUND: A recent study identified antibodies to GluRs in the serum of patients with PCD. METHODS: Sera of 35 patients with PCD (20 anti-Yo, 5 anti-Ri, 5 anti-Tr, and 5 anti-Hu) were examined by immunohistochemistry and immunoblot techniques. The expression of GluRs was obtained after transfection of 293T cells with cDNA plasmids corresponding to GluR1, GluR2, GluR3, GluR4, GluR6, and GluR7. The tumors of four patients with anti-Yo-associated PCD and nine ovarian carcinomas from patients without PCD were examined for the expression of GluRs. RESULTS: The expression of each GluR subunit was confirmed using affinity-purified antibodies against the corresponding GluRs and with whole sera from two rabbits immunized with GluR3. Thirty-two sera from patients with PCD were negative and 3 showed equivocal reactivity with 293T cells expressing different GluRs. None of the 35 sera had a pattern of reactivity characteristic of any GluR antibody on immunohistochemistry of sections of rat brain. Eleven of 14 tumors did not express GluRs; only some cells of one paraneoplastic tumor expressed GluRs. CONCLUSIONS: That patients with antibody-associated PCD (anti-Yo, -Ri, -Tr, and -Hu) harbor GluR antibodies in their sera is unlikely. GluR antibodies cannot be used as markers of paraneoplastic neurologic disorders.
Assuntos
Doenças Cerebelares/patologia , Degeneração Neural/imunologia , Síndromes Paraneoplásicas/imunologia , Fragmentos de Peptídeos/imunologia , Receptores de Glutamato/imunologia , Animais , Anticorpos/sangue , Doenças Cerebelares/imunologia , Feminino , Immunoblotting , Imuno-Histoquímica , Neoplasias Ovarianas/patologia , Coelhos , Ratos , Receptores de Glutamato/química , Transfecção , Células Tumorais CultivadasRESUMO
Subtypes of nicotinic receptors previously reported to be unaffected by neuronal bungarotoxin (NBT), including alpha 3 beta 4-containing and muscle type (alpha 1 beta 1 gamma delta) receptors, are shown to be inhibited by this toxin, but with rapid kinetics of onset and recovery. This inhibition is in contrast to the slow and prolonged inhibition of alpha 3 beta 2-containing receptors, suggesting that the beta subunits determine the kinetics of NBT inhibition of alpha 3 receptors. We have coexpressed chimeric beta subunits with alpha 3, and our results show that the first 121 amino acids of the beta subunit extracellular domain are sufficient to regulate the kinetics of NBT inhibition. This domain is also an important determinant of whether cytisine will act as a full agonist or a partial agonist of nicotinic receptors formed with alpha 3.
Assuntos
Bungarotoxinas/farmacologia , Neurônios/fisiologia , Oócitos/fisiologia , Receptores Nicotínicos/fisiologia , Acetilcolina/farmacologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Feminino , Cinética , Substâncias Macromoleculares , Dados de Sequência Molecular , Antagonistas Nicotínicos , Oligodesoxirribonucleotídeos , Oligonucleotídeos Antissenso , Oócitos/efeitos dos fármacos , Receptores Nicotínicos/biossíntese , Proteínas Recombinantes de Fusão/antagonistas & inibidores , Proteínas Recombinantes de Fusão/biossíntese , Proteínas Recombinantes de Fusão/metabolismoRESUMO
A sensitive RNase protection assay was employed to determine the levels of mRNA encoding the GluR1 subunit flip and flop isoforms in the chick optic tectum and forebrain. We found that the flip GluR1 mRNA predominates in the forebrain, whereas the flop variant is more strongly expressed in the optic tectum. A temporal analysis of GluR1 variants in the embryonic and adult chick brain revealed that the flip isoform is more highly expressed at E12 than at P15-21, whereas mRNA levels of the flop isoform are higher at P15-21 than at E12. To study the effect of deafferentation on GluR1 expression, unilateral retinal lesions were performed. Two days later the mRNA levels of GluR1 flip and flop variants were decreased in the deafferented tectum, especially for the flop isoform. However, 7 days after the lesion, the mRNA levels of both GluR1 isoforms were increased, especially for the flip isoform. These results reveal an important control of the retinal input upon the expression of the different GluR1 isoforms. Furthermore, they indicate a differential spatial and temporal regulation of the flip and flop splice variants, suggesting the existence of a mechanism regulating differential splicing or possibly differential RNA stability.
Assuntos
Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Prosencéfalo/metabolismo , Receptores de AMPA/genética , Retina/fisiologia , Colículos Superiores/metabolismo , Envelhecimento , Animais , Embrião de Galinha , Galinhas , Lateralidade Funcional , Especificidade de Órgãos , Prosencéfalo/embriologia , Prosencéfalo/crescimento & desenvolvimento , Isoformas de Proteínas/genética , RNA Mensageiro/análise , Ribonucleases , Colículos Superiores/embriologia , Colículos Superiores/crescimento & desenvolvimentoRESUMO
The mRNA distribution of the two cloned GABA(B) receptor variants, GABA(B)R1a and -R1b, was analysed in the retina by non-radioactive in situ hybridization. GABA(B)R1a transcripts were found in the inner nuclear and ganglion cell layers, probably in horizontal, amacrine and ganglion cells, whereas GABA(B)R1b transcripts were detected in the ganglion cell layer only. Together with a recent immunohistochemical localization of GABA(B)R1 in the retina, this indicates a differential targeting of the receptor variants to pre- and postsynaptic sites with GABA(B)R1a and -R1b localized to axonal and dendritic compartments, respectively. In this way, inhibition of neurotransmitter release and slow postsynaptic inhibition could be provided by receptor variants derived from the same gene.
Assuntos
Dendritos/química , Receptores de GABA-B/genética , Células Ganglionares da Retina/química , Animais , Elementos Antissenso (Genética) , Clonagem Molecular , Hibridização In Situ , Camundongos , Camundongos Endogâmicos C57BL , Estrutura Terciária de Proteína , RNA Mensageiro/análise , Receptores de GABA-B/análise , Receptores de GABA-B/química , Células Ganglionares da Retina/ultraestruturaRESUMO
The distribution of expression during retinal differentiation of nine AMPA and kainate glutamate receptor subunit genes was studied by in situ hybridization. Transcripts encoding all subunits were detected in the inner nuclear and ganglion cell layers of the developing mouse retina, but their time courses of expression differed. The earliest expression was detected at embryonic day 14 (E14) for GluR1, GluR4 and KA-2; all the other subunits were first detected at E16. Most subunits were expressed at higher levels during development than in the adult. This suggests they play a role in the processes of neuronal differentiation and synaptogenesis that occur during the early postnatal days in the rodent retina.
Assuntos
Receptores de Glutamato/biossíntese , Retina/metabolismo , Animais , Animais Recém-Nascidos/fisiologia , Diferenciação Celular/fisiologia , Feminino , Expressão Gênica , Hibridização In Situ , Camundongos , Camundongos Endogâmicos C57BL , Gravidez , Receptores de AMPA/biossíntese , Receptores de AMPA/genética , Receptores de Glutamato/genética , Receptores de Ácido Caínico/biossíntese , Receptores de Ácido Caínico/genética , Células Ganglionares da Retina/metabolismoRESUMO
The effects of photoreceptor cell degeneration on the expression of nine alpha-amino-3-hydroxy-5-methyl-isoxasole-4-propionate (AMPA)/kainate glutamate receptor subunit genes were investigated in the rd mouse retina by in situ hybridization. All known AMPA/kainate receptor subunits were found to be expressed in normal mouse retina. Following retinal degeneration, the expression of KA-1 was reduced, that of the GluR7 subunit was greatly increased, and that of the other seven subunits were not significantly affected.
Assuntos
Receptores de Glutamato/classificação , Retina/patologia , Animais , Expressão Gênica , Hibridização In Situ , Ácido Caínico/farmacologia , Camundongos , Camundongos Endogâmicos C57BL , Degeneração Neural , Células Fotorreceptoras/patologia , Receptores de Glutamato/genética , Ácido alfa-Amino-3-hidroxi-5-metil-4-isoxazol Propiônico/farmacologiaRESUMO
1. In situ hybridization histochemistry has revealed that neuronal nicotinic acetylcholine receptor subunits are widely expressed in unique although overlapping patterns in the central and peripheral nervous systems. In addition, an intricate regulation of expression is apparent during development. This raises the question of the transcription control of these complex distributions. 2. An analysis of the transcription control elements of one nicotinic receptor subunit, alpha 3, which is expressed both in the central and peripheral nervous systems as well as in PC12 cells, is presented here. 3. Overlapping genomic clones containing the rat beta 4, alpha 3, and alpha 5 gene cluster were isolated and a restriction map of this region was constructed. 4. The transcription start sites of the alpha 3 gene were mapped by RNase protection experiments. Surprisingly, there is no consensus TATA box upstream of these sites. This is consistent with the finding of multiple initiation sites. 5. Functional assays were done in PC12 cells using the bacterial chloramphenicol acetyltransferase gene as a reporter gene. Several restriction fragments from the region located 5' and including the transcription start sites were shown to promote transcription of the reporter gene and thus contain at least part of the alpha 3 promoter. In addition, a region further upstream, within the beta 4 transcription unit, appears to reduce transcriptional activity and thus could be a silencer. 6. It is proposed that this putative silencer is a selective force in maintaining the tight linkage of these three genes.
Assuntos
Neurônios/química , Receptores Nicotínicos/análise , Transcrição Gênica , Animais , Sequência de Bases , Cloranfenicol O-Acetiltransferase/análise , Mapeamento Cromossômico , Dados de Sequência Molecular , Células PC12 , Ratos , Receptores Nicotínicos/química , Receptores Nicotínicos/genéticaRESUMO
Monitoring the effects of resuscitation efforts in a community emergency department are limited primarily to noninvasive techniques. Coronary perfusion pressure (CCP) has been used as a predictor for successful resuscitation. The authors investigated the feasibility of measuring the CPP in a community emergency department and incorporating the CPP into decisions for managing the resuscitation effort. During a 7-month period, the authors prospectively studied 77 nontraumatic, normothermic adults in cardiopulmonary arrest who were treated in the emergency department. Fifty-one patients underwent invasive monitoring and 26 patients entered a control (noninvasive monitoring) group. Successful CPP monitoring was accomplished in 84% of the patients; the average time to obtain an initial CPP was 12.1 +/- 7.3 minutes. Twenty patients had a return of spontaneous circulation, but no patient survived to hospital discharge. There was no significant difference in return of spontaneous circulation between patients in the invasively monitored and the noninvasively monitored group. Coronary perfusion pressure monitoring had a positive influence on the management of three patients. This study showed that CPP monitoring is feasible in a community hospital, but further studies are needed to better define the effects of CPP in resuscitation effort outcome.
Assuntos
Pressão Sanguínea , Reanimação Cardiopulmonar , Circulação Coronária , Idoso , Serviço Hospitalar de Emergência , Feminino , Hemodinâmica , Hospitais Comunitários , Humanos , Masculino , Michigan , Pessoa de Meia-Idade , Monitorização Fisiológica/métodos , Estudos Prospectivos , Resultado do TratamentoRESUMO
Extracellular and whole-cell light-evoked responses of mouse retinal ganglion cells were recorded in the presence of the mGluR8 selective agonist, (S)-3,4-dicarboxy-phenylglycine (DCPG). Off-light responses were reversibly reduced in the presence of DCPG in wild-type but not in mGluR8-deficient retinas. On-responses were only marginally modulated by DCPG. During Off-responses, DCPG suppressed both excitatory and inhibitory synaptic conductances suggesting that mGluR8 receptor activity reduces glutamate release from bipolar cell terminals and possibly also the release of an inhibitory neurotransmitter from amacrine cell processes.
Assuntos
Benzoatos/farmacologia , Glicina/análogos & derivados , Luz , Receptores de Glutamato Metabotrópico/agonistas , Células Ganglionares da Retina/efeitos da radiação , Animais , Potenciais Evocados , Glicina/farmacologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Técnicas de Patch-Clamp , Receptores de Glutamato Metabotrópico/genética , Receptores de Glutamato Metabotrópico/fisiologia , Células Ganglionares da Retina/fisiologia , Potenciais SinápticosRESUMO
Signaling by the metabotropic glutamate receptor 1alpha (mGluR1alpha) can lead to the accumulation of inositol 1,4, 5-trisphosphate (InsP(3)) and cAMP and to the modulation of K(+) and Ca(2+) channel opening. At present, very little is known about how these different actions are integrated and eventually turned off. Unraveling the molecular mechanisms underlying these functions is crucial for understanding mGluR-mediated regulation of synaptic transmission. It has been shown that receptor-induced activation of the InsP(3) pathway is subject to feedback inhibition mediated by protein kinase C (PKC). In this study, we provide evidence for a differential regulation by PKC and protein kinase A of two distinct mGluR1alpha-dependent signaling pathways. PKC activation selectively inhibits agonist-dependent stimulation of the InsP(3) pathway but does not affect receptor signaling via cAMP. In contrast, protein kinase A potentiates agonist-independent signaling of the receptor via InsP(3). Furthermore, we demonstrate that the selectivity of PKC action on receptor signaling rests on phosphorylation of a threonine residue located in the G protein-interacting domain of the receptor. Modification at Thr(695) selectively disrupts mGluR1alpha-G(q/11) interaction without affecting signaling through G(s). Together, these data provide insight on the mechanisms by which selective down-regulation of a specific receptor-dependent signaling pathway can be achieved and on how cross-talk between different second messenger cascades may contribute to fine-tune short- and long-term receptor activity.
Assuntos
Sinalização do Cálcio/fisiologia , Proteínas Quinases Dependentes de AMP Cíclico/fisiologia , Proteínas Heterotriméricas de Ligação ao GTP/metabolismo , Inositol 1,4,5-Trifosfato/fisiologia , Proteína Quinase C/fisiologia , Processamento de Proteína Pós-Traducional , Receptores de Glutamato Metabotrópico/fisiologia , Regulação Alostérica , Sequência de Aminoácidos , Animais , AMP Cíclico/fisiologia , Transporte de Íons , Dados de Sequência Molecular , Oócitos , Técnicas de Patch-Clamp , Fosforilação , Fosfotreonina/análise , Estrutura Terciária de Proteína , Receptores de Glutamato Metabotrópico/química , Proteínas Recombinantes de Fusão/metabolismo , Alinhamento de Sequência , Homologia de Sequência de Aminoácidos , Transfecção , Xenopus laevisRESUMO
On the basis of sequence homology and structural similarities, metabotropic glutamate receptors (mGluRs), extracellular Ca2+-sensing receptor, gamma-aminobutyric acid type B receptor, and pheromone receptors are enlisted in a distinct family within the larger G protein-coupled receptor superfamily. When expressed in heterologous systems, group I mGluRs can activate dual signal transduction pathways, phosphoinositides turnover and cAMP production. To investigate the structural basis of these coupling properties, we introduced single amino acid substitutions within the second and third intracellular loops (i2 and i3) of mGluR1alpha. Wild-type and mutant receptors were expressed in human embryonic kidney 293 cells and analyzed for their capacity to stimulate both signaling cascades. Each domain appeared to be critical for the coupling to phospholipase C and adenylyl cyclase. Within i2, Thr695, Lys697, and Ser702 were found to be selectively involved in the interaction with Gq class alpha subunit(s), whereas mutation of Pro698 and the deletion Cys694-Thr695 affected only Gs coupling. Furthermore, the mutation K690A profoundly altered mGluR1alpha signaling properties and imparted to the receptor the ability to couple to the inhibitory cAMP pathway. Within i3, we uncovered two residues, Arg775 and Phe781, that are crucial for coupling to both pathways, since their substitution leads to receptor inactivation.
Assuntos
Receptores de Glutamato Metabotrópico/química , Transdução de Sinais/fisiologia , Toxina Adenilato Ciclase , Adenilil Ciclases/metabolismo , Sequência de Aminoácidos , Linhagem Celular , AMP Cíclico/metabolismo , Proteínas de Ligação ao GTP/metabolismo , Regulação da Expressão Gênica/genética , Ácido Glutâmico/farmacologia , Humanos , Imuno-Histoquímica , Isoproterenol/farmacologia , Rim/metabolismo , Dados de Sequência Molecular , Mutagênese Sítio-Dirigida/genética , Receptores de Glutamato Metabotrópico/genética , Alinhamento de Sequência , Transfecção/genética , Fosfolipases Tipo C/metabolismo , Fatores de Virulência de Bordetella/farmacologiaRESUMO
Five cDNA clones designated pDH2, pDH8, pDH9, pDH31 and pDH101 encoding rabbit immunoglobulin lambda light chain sequences have been characterized. Comparison of the V lambda sequences suggests that, in addition to an increased divergence in all of the complementarity-determining regions (CDRs), variable-region diversity is amplified by the length heterogeneity of the CDR3, at the V lambda-J lambda junction. An insertion of four codons at positions 48a-d has been noted in three cDNA sequences. This insert, not found in lambda nor kappa light chains of other species, has a variable sequence, suggesting its possible implication in expanding variability of the CDR2. One of the cDNA clones was shown to encode a novel C lambda region which differs by four amino acid substitutions from the C lambda region common to all the other clones. Thus, the rabbit can use two different C lambda genes, which might correlate with the expression of the two known allotypes of lambda chains, C7 and C21. Southern blotting experiments indicate a small number of germ-line V lambda genes and the cDNA nucleotide sequence data reported here suggest that several of these genes can be expressed. The possibility of at least two V-J-C gene clusters is discussed.
Assuntos
DNA/genética , Cadeias lambda de Imunoglobulina/genética , Alelos , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Códon , Eletroforese em Gel de Ágar , CoelhosRESUMO
A novel metabotropic glutamate receptor, mGluR8, was identified by screening a mouse retina cDNA library. This receptor is most related to mGluR4, mGluR7, and mGluR6 (74%, 74%, and 70% identical amino acid residues, respectively). Similar to these receptors, stimulation by L-glutamate or L-2-amino-4-phosphonobutyrate (L-APB) of Chinese hamster ovary (CHO) cells stably transfected with mGluR8 result in the inhibition of forskolin-stimulated adenylyl cyclase. In situ hybridization studies revealed a strong expression of the mGluR8 gene in the olfactory bulb, accessory olfactory bulb, and mammillary body. A weaker expression was found in the retina, and in scattered cells in the cortex and hindbrain. During development, the distribution of mGluR8 expression was more widespread. These results extend the diversity of metabotropic glutamate receptors in the CNS. Because at least two APB receptors are expressed in the retina, the use of this drug to block selectively the ON pathway needs to be reconsidered. The pharmacology and expression of mGluR8 in mitral/tufted cells suggest it could be a presynaptic receptor modulating glutamate release by these cells at their axon terminals in the entorhinal cortex.