RESUMO
AIMS: G protein-coupled receptor/free fatty acid receptor 1 (GPR40/FFAR1 ) regulates free fatty acid-induced insulin secretion. This study has been performed to clarify whether or not loss of GPR40/FFAR1 function exacerbates diabetes, that is, whether GPR40 has an essential physiological role in the development of diabetes or not. METHODS: We generated GPR40/FFAR1 knockout (KO) mice and analysed their phenotypes in vitro and in vivo under the condition of dietary or genetically induced insulin resistance. RESULTS: GPR40/FFAR1 KO mice kept on a high-fat diet became obese, developed glucose intolerance to a similar degree as GPR40/FFAR1 wild-type (WT) mice. In addition, the phenotype of KO mice harbouring diabetogenic KK background genes showed glucose intolerance at a level similar to level for control KK mice. In both mouse models with insulin resistance, insulin secretion after oral glucose load and homeostasis model assessment-insulin resistance (HOMA-IR) did not change between GPR40/FFAR1 KO and WT mice. Although glucose-induced insulin secretion under high palmitate concentration was significantly lower in KO than in WT islets, pancreatic insulin content and insulin secretion stimulated with glucose alone were not different between KO and WT mice. CONCLUSIONS: GPR40/FFAR1 has a major role in regulating fatty-acid-mediated insulin secretion, but the lack of GPR40/FFAR1 does not exacerbate glucose intolerance and insulin resistance induced by high-fat diet or diabetogenic KK gene. Our findings indicate that loss of GPR40/FFAR1 function does not play an important role in inducing or exacerbating diabetes.
Assuntos
Diabetes Mellitus Experimental/patologia , Insulina/metabolismo , Pâncreas/patologia , Receptores Acoplados a Proteínas G/deficiência , Animais , Glicemia/metabolismo , Diabetes Mellitus Experimental/genética , Teste de Tolerância a Glucose , Homeostase , Imuno-Histoquímica , Resistência à Insulina/genética , Secreção de Insulina , Ilhotas Pancreáticas , Camundongos , Camundongos Knockout , Fenótipo , Receptores Acoplados a Proteínas G/genéticaRESUMO
We have recently identified RFamide-related peptide (RFRP) gene that would encode three peptides (i.e., RFRP-1, -2, and -3) in human and bovine, and demonstrated that synthetic RFRP-1 and -3 act as specific agonists for a G protein-coupled receptor OT7T022. However, molecular characteristics and tissue distribution of endogenous RFRPs have not been determined yet. In this study, we prepared a monoclonal antibody for the C-terminal portion of rat RFRP-1. As this antibody could recognize a consensus sequence among the C-terminal portions of rat, human, and bovine RFRP-1, we purified endogenous RFRP-1 from bovine hypothalamus on the basis of immunoreactivity to the antibody. The purified bovine endogenous RFRP-1 was found to have 35-amino-acid length that corresponds to 37-amino-acid length in human and rat. We subsequently constructed a sandwich enzyme immunoassay using the monoclonal antibody and a polyclonal antibody for the N-terminal portion of rat RFRP-1, and analyzed the tissue distribution of endogenous RFRP-1 in rats. Significant levels of RFRP-1 were detected only in the central nervous system, and the highest concentration of RFRP-1 was detected in the hypothalamus. RFRP-1-positive nerve cells were detected in the rat hypothalamus by immunohistochemical analyses using the monoclonal antibody. In culture, RFRP-1 lowered cAMP production in Chinese hamster ovary cells expressing OT7T022 and it was abolished by pre-treatment with pertussis toxin, suggesting that OT7T022 couples G(i)/G(o) in the signal transduction pathway.
Assuntos
Hipotálamo/metabolismo , Neuropeptídeos/metabolismo , Receptores Acoplados a Proteínas G , Proteínas de Saccharomyces cerevisiae , Sequência de Aminoácidos , Animais , Encéfalo/metabolismo , Células CHO , Bovinos , Cromatografia em Gel , Cricetinae , Técnicas Imunoenzimáticas , Imuno-Histoquímica , Dados de Sequência Molecular , Neuropeptídeos/análise , Neuropeptídeos/isolamento & purificação , Ratos , Receptores de Superfície Celular/metabolismo , Alinhamento de SequênciaRESUMO
The present study examined a novel function of PRL-releasing peptide (PrRP) on the neuroendocrine. PrRP-immunoreactive nerve fibers and nerve terminals were located in the vicinity of the somatostatin (SOM)-neurons in the hypothalamic periventricular nucleus (PerVN). Immuno-electron microscopy revealed that PrRP-immunoreactive nerve terminals made synaptic contacts with nonimmunoreactive neuronal elements in the PerVN. Intracerebroventricular (icv) administration of PrRP induced immediate early gene, NGFI-A, in SOM-neurons in the PerVN. Double-labeling in situ hybridization showed that some parts of SOM-neurons in the PerVN expressed PrRP receptor messenger RNA. Therefore, some parts of SOM-neurons in the PerVN are considered to be directly innervated by PrRP via PrRP receptor. In addition to the above morphological characteristics, icv administration of PrRP decreased plasma GH levels. Such inhibitory effects of PrRP on the secretion of GH from the anterior pituitary were diminished by depletion or neutralization of SOM. From these findings it was strongly suggested that SOM-neurons respond to PrRP and secrete SOM into the portal vessels and thus inhibit GH secretion from the anterior pituitary.
Assuntos
Hormônio do Crescimento/metabolismo , Hipotálamo/metabolismo , Somatostatina/metabolismo , Hormônio Liberador de Tireotropina/fisiologia , Animais , Cisteamina/farmacologia , Hormônio do Crescimento/sangue , Hormônio Liberador de Hormônio do Crescimento/farmacologia , Hormônios Hipotalâmicos/farmacologia , Imuno-Histoquímica , Injeções Intraventriculares , Masculino , Terminações Nervosas/metabolismo , Neurônios/efeitos dos fármacos , Neuropeptídeos/farmacologia , Núcleo Hipotalâmico Paraventricular/metabolismo , Hormônio Liberador de Prolactina , Ratos , Ratos Wistar , Receptores de Neuropeptídeos/fisiologia , Hormônio Liberador de Tireotropina/metabolismo , Hormônio Liberador de Tireotropina/farmacologiaRESUMO
Prolactin releasing peptide (PrRP) was recently identified as the stimulator of prolactin release from the anterior pituitary. PrRP mRNA is expressed in the medulla oblongata and the hypothalamus in the rat brain. The fibers containing PrRP are widely distributed in the brain, therefore, it was postulated that PrRP may act as a neurotransmitter or neuromodulator as well as an endocrine substance. To clarify the developmental changes in the expression of PrRP during brain development, we examined PrRP in rat fetuses and neonates using in situ hybridization and immunohistochemistry. The PrRP mRNA was expressed in the nucleus of the solitary tract (NTS) at embryonic day 18 (E18) and in the ventral and lateral reticular nucleus (VLRN) of the caudal medulla oblongata at E20. The PrRP mRNA in the hypothalamus was first expressed at postnatal day 13 (P13). Reverse transcription-polymerase chain reaction analysis (RT-PCR) for PrRP revealed that PCR product, a 268 bp band, was detected from either E18 in the medulla or P13 in the hypothalamus. Immunodetection with monoclonal antibody against prepro-PrRP revealed intensive staining of cells in the NTS at E18, in the VLRN at E20 or in the dorsomedial hypothalamus at P13. Immunohistochemistry using monoclonal antibody against mature PrRP at P6 showed PrRP fibers to be distributed in the paraventricular hypothalamic nucleus, periventricular hypothalamic nucleus, medial preoptic area, basolateral amygdaloid nucleus, dorsomedial hypothalamus, ventromedial hypothalamus, periventricular nucleus of the thalamus and bed nucleus of the stria terminalis as previously shown in the adult rat. PrRP fibers were also found in the optic chiasm, dorsal endopiriform nucleus, cingulum, intermediate reticular nucleus, and caudal ventrolateral reticular nucleus at P6 and P9. However, PrRP fibers were never found in the above regions in the adult animal. These findings suggest that PrRP fibers originating in the medulla oblongata have been widely distributed in the rat brain during the early postnatal day and PrRP may play various roles in the brain development.
Assuntos
Química Encefálica/fisiologia , Regulação da Expressão Gênica no Desenvolvimento , Neurônios/fisiologia , Hormônio Liberador de Tireotropina/genética , Animais , Animais Recém-Nascidos , Feminino , Hipotálamo/química , Hipotálamo/citologia , Hipotálamo/embriologia , Imuno-Histoquímica , Hibridização In Situ , Masculino , Neurônios/química , Gravidez , RNA Mensageiro/análise , Ratos , Ratos Sprague-Dawley , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Núcleo Solitário/química , Núcleo Solitário/citologia , Núcleo Solitário/embriologia , Hormônio Liberador de Tireotropina/análise , Hormônio Liberador de Tireotropina/imunologia , Tirosina 3-Mono-Oxigenase/análise , Tirosina 3-Mono-Oxigenase/imunologiaRESUMO
We analyzed the tissue distribution of apelin mRNA in rats by a quantitative reverse transcription-polymerase chain reaction and that of immunoreactive apelin (ir-apelin) by an enzyme immunoassay (EIA) using a monoclonal antibody. The expression levels of apelin mRNA and ir-apelin seemed to be consistent among tissues: they were highly expressed in the lung and mammary gland. By the combination of gel filtration and EIA, we found that the molecular forms of apelin differ among respective tissues: apelin molecules with sizes close to apelin-36 (long forms) were major components in the lung, testis, and uterus, but both long and short (whose sizes were close to [Assuntos
Proteínas de Transporte/análise
, Receptores Acoplados a Proteínas G
, Sequência de Aminoácidos
, Animais
, Apelina
, Receptores de Apelina
, Proteínas de Transporte/síntese química
, Proteínas de Transporte/metabolismo
, Cromatografia em Gel
, Feminino
, Técnicas Imunoenzimáticas
, Peptídeos e Proteínas de Sinalização Intercelular
, Pulmão/metabolismo
, Masculino
, Glândulas Mamárias Animais/metabolismo
, Dados de Sequência Molecular
, Peso Molecular
, RNA Mensageiro/análise
, Ratos
, Ratos Wistar
, Receptores de Dopamina D2
, Reação em Cadeia da Polimerase Via Transcriptase Reversa
, Testículo/metabolismo
, Útero/metabolismo
RESUMO
We investigated the prolactin-releasing peptide (PrRP) gene expression quantitatively in the rat brain and the involvement of estrogen and progesterone using in situ hybridization. The strongest signals were observed in the nucleus tractus solitarius (NTS), which showed approximately 70% of total PrRP mRNA in the brain. Moderate expression was observed in the ventral and lateral reticular nuclei (VLRN) of the medulla oblongata. PrRP mRNA signals in the hypothalamic ventromedial- and dorsomedial nuclei showed only 5% of total signals. The PrRP mRNA expression among female rats showing normal gonadal cycle and male rats showed that the highest levels were in female rats in proestrus. Administration of estrogen or progesterone after ovariectomy induced an increase in PrRP mRNA expression in the NTS. PrRP mRNA content in the NTS increased with the progress of the pregnancy and reached a peak on the 14th day, the mid-period of pregnancy, when plasma progesterone increases. We also observed the colocalization of PrRP and estrogen receptor alpha in the neurons distributed in the NTS by double labeling immunocytochemistry. These findings indicate that PrRP gene expression is regulated by gonadal steroid hormones in the medulla oblongata, and parts of PrRP synthesizing neurons are considered to be directly influenced by estrogen in the NTS.
Assuntos
Hormônios Hipotalâmicos/genética , Neuropeptídeos/genética , Formação Reticular/fisiologia , Núcleo Solitário/fisiologia , Animais , Diestro/fisiologia , Receptor alfa de Estrogênio , Estrogênios/fisiologia , Feminino , Expressão Gênica/fisiologia , Hibridização In Situ , Lactação/fisiologia , Masculino , Neurônios/química , Neurônios/fisiologia , Ovariectomia , Gravidez , Proestro/fisiologia , Progesterona/fisiologia , Hormônio Liberador de Prolactina , RNA Mensageiro/análise , Ratos , Ratos Sprague-Dawley , Receptores de Estrogênio/análise , Formação Reticular/citologia , Núcleo Solitário/citologiaRESUMO
In addition to the CCR5 and CXCR4 chemokine receptors, a subset of primary human immunodeficiency virus type 1 (HIV-1) isolates can also use the seven-transmembrane-domain receptor APJ as a coreceptor. A previously identified ligand of APJ, apelin, specifically inhibited the entry of primary T-tropic and dualtropic HIV-1 isolates from different clades into cells expressing CD4 and APJ. Analysis of apelin analogues demonstrated that potent and specific antiviral activity was retained by a 13-residue, arginine-rich peptide. Antiviral potency was influenced by the integrity of methionine 75, which contributes to APJ-binding affinity, and by the retention of apelin residues 63 to 65. These studies demonstrate the ability of a small peptide ligand to block the function of APJ as an HIV-1 coreceptor, identify apelin sequences important for the inhibition, and provide new reagents for the investigation of the significance of APJ to HIV-1 infection and pathogenesis.
Assuntos
Síndrome da Imunodeficiência Adquirida/virologia , Proteínas de Transporte/fisiologia , HIV-1/fisiologia , Receptores de Dopamina D2/fisiologia , Receptores Acoplados a Proteínas G , Sequência de Aminoácidos , Apelina , Receptores de Apelina , Humanos , Peptídeos e Proteínas de Sinalização Intercelular , Ligantes , Dados de Sequência Molecular , Receptores Virais/fisiologia , Replicação ViralRESUMO
The gene of prolactin-releasing peptide (PrRP) was first cloned in 1998 and preproproteins encoded by cDNAs produced at least two isoforms of PrRP with different lengths; PrRP31 and PrRP20. PrRP has been shown to release prolactin from the anterior pituitary at least in vitro (Hinuma, Y.S., Habata, Y., Fuji, R., Hosoya, M., Fukusumi, S., Kitada, C., Masuo, Y., Asano, T., Matsumoto, H., Sekiguchi, M., Kurokawa, T., Nishimura, O., Onda, H., and Fujino, A., 1998. A prolactin-releasing peptide in the brain. Nature 393, 272-6). PrRP receptor has also been detected by quantitive reverse transcription polymerase chain reaction, and in situ hybridization histochernistry revealed that expression of PrRP receptor mRNA was found in the broad areas of the brain and in the anterior pituitary of the rat. This review surveys morphological studies on PrRP, PrRP mRNA and PrRP receptor mRNA in the rat brain and discusses the possible functional significance of PrRP in the brain. PrRP immunoreactive neuronal perikarya showed a similar distributional pattern to those with PrRP mRNA signals. However, distribution of nerve processes and terminals with PrRP immunoreactivity was broadly expanded in the forebrain and brainstem. They were hardly detected in the median eminence particularly in its external layer. PrRP receptor mRNA signals were distributed in the preoptic area, and the hypothalamic area, where PrRP immunoreactive nerve processes and terminals were also detected. The strongest signal of PrRP receptor mRNA was detected in the reticular nucleus of the thalamus where neither PrRP immunoreactive nerve processes nor axon terminals were distributed. From the distribution pattern of PrRP and its receptor, it is suggested that PrRP is involved in control of secretion of oxytocin, corticotropin releasing hormone and somatostatin.
Assuntos
Encéfalo/metabolismo , Hormônios Hipotalâmicos/fisiologia , Neuropeptídeos/fisiologia , Receptores de Neuropeptídeos/fisiologia , Animais , Hormônios Hipotalâmicos/genética , Hormônios Hipotalâmicos/metabolismo , Neuropeptídeos/genética , Neuropeptídeos/metabolismo , Hormônio Liberador de Prolactina , RNA Mensageiro/metabolismo , Ratos/fisiologia , Receptores de Neuropeptídeos/genética , Receptores de Neuropeptídeos/metabolismo , Distribuição TecidualRESUMO
Only a few RFamide peptides have been identified in mammals, although they have been abundantly found in invertebrates. Here we report the identification of a human gene that encodes at least three RFamide-related peptides, hRFRP-1-3. Cells transfected with a seven-transmembrane-domain receptor, OT7T022, specifically respond to synthetic hRFRP-1 and hRFRP-3 but not to hRFRP-2. RFRP and OT7T022 mRNAs are expressed in particular regions of the rat hypothalamus, and intracerebroventricular administration of hRFRP-1 increases prolactin secretion in rats. Our results indicate that a variety of RFamide-related peptides may exist and function in mammals.
Assuntos
Neuropeptídeos/isolamento & purificação , Receptores de Neuropeptídeos/isolamento & purificação , Sequência de Aminoácidos , Animais , Bovinos , Clonagem Molecular , Humanos , Camundongos , Dados de Sequência Molecular , Neuropeptídeos/química , Neuropeptídeos/genética , Ratos , Receptores de Neuropeptídeos/genética , Homologia de Sequência de Aminoácidos , Especificidade da EspécieRESUMO
Recently a novel peptide which specifically stimulates the secretion of prolactin (PRL) was found and named PRL-releasing peptide (PrRP). To evaluate the regulation of human (h) PrRP-receptor (PrRP-R) gene expression, we cloned the 5'-flanking region of the hPrRP-R gene and determined the nucleotide sequence of 4.0 kilobase pairs (kb) upstream from the translation start site. Analysis of the hPrRP-R transcripts by means of 5'-rapid amplification of cDNA ends suggested that the hPrRP-R gene had multiple transcription start sites between -429 and -365 from the translation start site. There is no typical TATA or CAAT but a GC box and putative binding sites for several transcription factors including Pit-1 and pituitary homeobox 1 (Ptx1). However, transient transfection studies using a luciferase reporter gene demonstrated that 5'-flanking region exerts promoter activity in several non-pituitary cell lines as well as in GH(3) cells. The GC box located from -467 to -457 was identified as an important region for the basal expression of the hPrRP-R gene. Knowledge of the promoter region of the hPrRP-R gene, which was obtained in the present study, will facilitate the clarification of its transcriptional regulation.
Assuntos
Regulação da Expressão Gênica , Regiões Promotoras Genéticas/genética , Receptores de Neuropeptídeos/genética , Animais , Sequência de Bases , Células Cultivadas , Clonagem Molecular , DNA/análise , Humanos , Dados de Sequência Molecular , RatosRESUMO
We validated the effect of prolactin-releasing peptide (PrRP) on prolactin (PRL) secretion from rat anterior pituitary cells in in vitro culture. We found that culture conditions considerably influenced the response of the anterior pituitary cells to PrRP. Longer culture term (4 d) was required to obtain better responses of the anterior pituitary cells to PrRP in comparison to thyrotropin-releasing hormone (TRH). Under the culture conditions employed here, PrRP was comparable to TRH in the potency promoting PRL secretion, and the action of PrRP was very specific for PRL secretion. The susceptibility of the anterior pituitary cells to PrRP varied in female rats depending on the process of reproduction: the cells prepared from lactating rats were the most sensitive to PrRP compared with those from random-cycle and pregnant rats. Because the expression levels of PrRP receptor mRNA in the pituitary varied during the reproductive process, we speculated that the susceptibility of the anterior pituitary cells would reflect cellular changes including the expression level of PrRP receptors. In addition, treatment with estrogen in vivo enhanced the susceptibility of the cultured anterior pituitary cells in male rats. Our results indicate that the susceptibility of the rat anterior pituitary cells to PrRP is regulated by physiological mechanisms.
Assuntos
Hormônios Hipotalâmicos/farmacologia , Neuropeptídeos/farmacologia , Adeno-Hipófise/efeitos dos fármacos , Prolactina/metabolismo , Animais , Células Cultivadas , Hormônio Liberador da Corticotropina/farmacologia , Feminino , Expressão Gênica , Hormônio Liberador de Gonadotropina/farmacologia , Hormônio Liberador de Hormônio do Crescimento/farmacologia , Cinética , Lactação , Masculino , Adeno-Hipófise/química , Adeno-Hipófise/metabolismo , Gravidez , Hormônio Liberador de Prolactina , RNA Mensageiro/análise , Ratos , Ratos Endogâmicos F344 , Receptores de Neuropeptídeos/genética , Receptores de Neuropeptídeos/fisiologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Hormônio Liberador de Tireotropina/farmacologia , Fatores de TempoRESUMO
Neuromedin U is a bioactive peptide isolated originally from the porcine spinal cord. We recently identified neuromedin U as the cognate ligand for the orphan G protein-coupled receptor FM-3. In this study, we isolated cDNA coding for a novel G protein-coupled receptor, TGR-1, which was highly homologous with FM-3. We found that neuromedin U specifically and clearly elevated the extracellular acidification rates, arachidonic acid metabolite release, and intracellular Ca(2+) mobilization in Chinese hamster ovary cells expressing TGR-1. Radiolabeled neuromedin U specifically bound with high affinity to membrane fractions prepared from these cells. These results show that TGR-1, like FM-3, is a specific and functional receptor for neuromedin U. We analyzed TGR-1 mRNA tissue distribution in rats using quantitative reverse transcription-polymerase chain reaction and found it to considerably differ from that of FM-3 mRNA. TGR-1 mRNA was primarily expressed in the uterus, suggesting that TGR-1 mediates the contractile activity of neuromedin U in this tissue. The identification of specific and functional receptor subtypes for neuromedin U will facilitate the study of their physiological roles and the search for their specific agonists and antagonists.
Assuntos
Proteínas de Membrana , Neuropeptídeos/metabolismo , Receptores de Neurotransmissores/genética , Receptores de Neurotransmissores/metabolismo , Transdução de Sinais , Sequência de Aminoácidos , Animais , Clonagem Molecular , Cricetinae , Proteínas de Ligação ao GTP/metabolismo , Humanos , Dados de Sequência Molecular , Ratos , Alinhamento de SequênciaRESUMO
Prolactin-releasing peptide (PrRP) is a recently isolated hypothalamic peptide which is an endogenous ligand to an orphan receptor. We previously demonstrated that PrRP neurons are widely distributed throughout the rat brain and suggested that PrRP may have important functions in the central nervous system. To analyze the function of PrRP, we studied the effect of intracerebroventricular (i.c.v.) PrRP administration on c-Fos protein accumulation in the rat brain. The results clearly indicated that c-Fos protein accumulation was dramatically increased in the nuclei of corticotropin-releasing hormone (CRH)-positive parvocellular neurosecretory cells in the paraventricular nucleus (PVN). We also demonstrated synapse-like contact between PrRP neurons and CRH cell bodies in the PVN, which suggests that PrRP31 has some effect on CRH secretion. We therefore investigated the effect of i.c.v. administration of PrRP31 on the CRH-mediated increase in adrenocorticotropin (ACTH) levels, and found that plasma ACTH levels were indeed increased by i.c.v. PrRP31. In addition, animals pre-treated with intravenous alpha-helical CRH, a potent CRH antagonist, showed attenuated plasma ACTH responses after i.c.v. PrRP31 administration. These results strongly suggest that PrRP affects the hypothalamic-pituitary-adrenal axis.
Assuntos
Hormônio Adrenocorticotrópico/efeitos dos fármacos , Hormônio Liberador da Corticotropina/farmacologia , Antagonistas de Hormônios/farmacologia , Hormônios Hipotalâmicos/farmacologia , Neuropeptídeos/farmacologia , Prolactina/farmacologia , Hormônio Adrenocorticotrópico/sangue , Animais , Hormônio Liberador da Corticotropina/efeitos dos fármacos , Hormônio Liberador da Corticotropina/metabolismo , Masculino , Núcleo Hipotalâmico Paraventricular/efeitos dos fármacos , Núcleo Hipotalâmico Paraventricular/metabolismo , Hormônio Liberador de Prolactina , Ratos , Ratos WistarRESUMO
Neuromedin U is a bioactive peptide first isolated from porcine spinal cord. In this paper, we demonstrate that neuromedin U is the cognate ligand for the orphan G protein-coupled receptor, FM-3, isolated originally as a homologue of neurotensin and growth hormone secretogogue receptors. Neuromedin U induced specific and evident elevation of extracellular acidification rates, arachidonic acid metabolite release, and intracellular Ca(2+) mobilization in Chinese hamster ovary cells expressing human FM-3. In addition, radiolabeled neuromedin U specifically bound to membrane fractions prepared from these cells with high affinity. We subsequently analyzed the tissue distribution of neuromedin U and FM-3 mRNAs in rats using quantitative reverse transcription-polymerase chain reaction. Neuromedin U mRNA was highly expressed in the gastrointestinal tract, and the highest expression was detected in the pituitary gland. On the other hand, FM-3 mRNA was highly expressed in the small intestine and lung, suggesting that neuromedin U plays important roles in these tissues. The identification of a specific and functional receptor for neuromedin U will facilitate studies on their physiological roles and the search for receptor agonists and antagonists.
Assuntos
Proteínas de Membrana , Neuropeptídeos/genética , Neuropeptídeos/metabolismo , Receptores de Superfície Celular/genética , Receptores de Superfície Celular/metabolismo , Receptores de Neurotransmissores , Sequência de Aminoácidos , Animais , Ácido Araquidônico/metabolismo , Sequência de Bases , Encéfalo/metabolismo , Células CHO , Cálcio/metabolismo , Sinalização do Cálcio/fisiologia , Cricetinae , Feminino , Humanos , Concentração de Íons de Hidrogênio , Ligantes , Masculino , Dados de Sequência Molecular , Neuropeptídeos/farmacologia , Especificidade de Órgãos , RNA Mensageiro/genética , Ratos , Receptores de Superfície Celular/química , Proteínas Recombinantes/metabolismo , Alinhamento de Sequência , Homologia de Sequência de Aminoácidos , Transcrição Gênica , TransfecçãoRESUMO
We have recently identified apelin as the endogenous ligand for human APJ. In rats, the highest expression of APJ mRNA was detected in the lung, suggesting that APJ and its ligand play an important role in the pulmonary system. When apelin-36 and its pyroglutamylated C-terminal peptide, [Assuntos
Encéfalo/metabolismo
, Proteínas de Transporte/metabolismo
, Receptores de Dopamina D2/genética
, Receptores de Dopamina D2/metabolismo
, Receptores Acoplados a Proteínas G
, Sequência de Aminoácidos
, Animais
, Apelina
, Receptores de Apelina
, Células CHO
, Bovinos
, Membrana Celular/metabolismo
, Cricetinae
, Feminino
, Humanos
, Peptídeos e Proteínas de Sinalização Intercelular
, Cinética
, Ligantes
, Masculino
, Dados de Sequência Molecular
, Especificidade de Órgãos
, Gravidez
, RNA Mensageiro/metabolismo
, Ratos
, Receptores de Dopamina D2/química
, Proteínas Recombinantes/química
, Proteínas Recombinantes/metabolismo
, Reação em Cadeia da Polimerase Via Transcriptase Reversa
, Alinhamento de Sequência
, Homologia de Sequência de Aminoácidos
, Transfecção
, Fatores de Virulência de Bordetella/farmacologia
RESUMO
Prolactin release from the anterior pituitary is regulated principally by inhibitory influences imparted by the tuberoinfundibular dopamine system. Stimulatory control is provided by several hypothalamic, peripheral and local factors. Recently a new peptide, prolactin releasing peptide (PrRP), showing prolactin-secretagogue effects was discovered, synthesized and found to be expressed in brain. We have used histochemical and axonal transport methods to characterize the distribution of PrRP mRNA in the rat brain, and to identify possible pathways through which this factor might be delivered to the anterior lobe of the pituitary and thereby participate in the regulation of prolactin secretion. Analysis of histochemical preparations indicated that apart from a small population of cells in a non-neurosecretory portion of the hypothalamus, PrRP mRNA is expressed exclusively in the caudal part of the nucleus of the solitary tract and in the caudal ventrolateral medulla. All medullary PrRP expressing cells could be immunolabeled for tyrosine hydroxylase, and none were found to stain for glucagon-like peptide-1, identifying them as comprising subsets of A2 and A1 noradrenergic neurones, respectively. Numerous PrRP-expressing cells were retrogradely labelled following tracer injections in the paraventricular nucleus, while only a handful were backfilled following intravenous injections of tracer, indicating that this population issues substantial projections to the endocrine hypothalamus and meager ones to the median eminence and/or posterior pituitary. This conclusion was supported by the results of experiments in which the anterograde tracer, biotinylated dextran-amine, was injected into the PrRP cell group in the nucleus of the solitary tract. These findings suggest that PrRP expressing neurones display a highly restricted distribution, and are in a position to regulate the output of particular cell types in the endocrine hypothalamus. Whether and how PrRP might be delivered to the anterior pituitary remains to be determined.
Assuntos
Hormônios Hipotalâmicos/genética , Neurônios Aferentes/química , Neuropeptídeos/genética , Núcleo Hipotalâmico Paraventricular/citologia , Núcleo Solitário/citologia , Amidinas/farmacocinética , Animais , Barreira Hematoencefálica/fisiologia , Catecolaminas/fisiologia , Feminino , Corantes Fluorescentes/farmacocinética , Expressão Gênica/fisiologia , Hibridização In Situ , Masculino , Neurônios Aferentes/enzimologia , Sistemas Neurossecretores/citologia , Sistemas Neurossecretores/fisiologia , Núcleo Hipotalâmico Paraventricular/química , Núcleo Hipotalâmico Paraventricular/fisiologia , Gravidez , Hormônio Liberador de Prolactina , RNA Mensageiro/análise , Ratos , Ratos Sprague-Dawley , Núcleo Solitário/química , Estresse Fisiológico/metabolismo , Núcleo Supraóptico/química , Núcleo Supraóptico/citologia , Núcleo Supraóptico/fisiologia , Tirosina 3-Mono-Oxigenase/análiseRESUMO
Regulation of the mitogen-activated protein kinase (MAPK) family by prolactin-releasing peptide (PrRP) in both GH3 rat pituitary tumor cells and primary cultures of rat anterior pituitary cells was investigated. PrRP rapidly and transiently activated extracellular signal-regulated protein kinase (ERK) in both types of cells. Both pertussis toxin, which inactivates G(i)/G(o) proteins, and exogenous expression of a peptide derived from the carboxyl terminus of the beta-adrenergic receptor kinase I, which specifically blocks signaling mediated by the betagamma subunits of G proteins, completely blocked the PrRP-induced ERK activation, suggesting the involvement of G(i)/G(o) proteins in the PrRP-induced ERK activation. Down-regulation of cellular protein kinase C did not significantly inhibit the PrRP-induced ERK activation, suggesting that a protein kinase C-independent pathway is mainly involved. PrRP-induced ERK activation was not dependent on either extracellular Ca(2+) or intracellular Ca(2+). However, the ERK cascade was not the only route by which PrRP communicated with the nucleus. JNK was also shown to be significantly activated in response to PrRP. JNK activation in response to PrRP was slower than ERK activation. Moreover, to determine whether a MAPK family cascade regulates rat prolactin (rPRL) promoter activity, we transfected the intact rPRL promoter ligated to the firefly luciferase reporter gene into GH3 cells. PrRP activated the rPRL promoter activity in a time-dependent manner. Co-transfection with a catalytically inactive form of a MAPK construct or a dominant negative JNK, partially but significantly inhibited the induction of the rPRL promoter by PrRP. Furthermore, co-transfection with a dominant negative Ets completely abolished the response of the rPRL promoter to PrRP. These results suggest that PrRP differentially activates ERK and JNK, and both cascades are necessary to elicit rPRL promoter activity in an Ets-dependent mechanism.
Assuntos
Regulação da Expressão Gênica , Hormônios Hipotalâmicos/metabolismo , Proteínas Quinases Ativadas por Mitógeno/metabolismo , Neuropeptídeos/metabolismo , Prolactina/metabolismo , Transdução de Sinais , Animais , Hormônios Hipotalâmicos/genética , Proteínas Quinases JNK Ativadas por Mitógeno , Sistema de Sinalização das MAP Quinases , Neuropeptídeos/genética , Prolactina/genética , Hormônio Liberador de Prolactina , Regiões Promotoras Genéticas , Ratos , Células Tumorais CultivadasRESUMO
The prolactin-releasing peptide (PrRP) is a novel hypothalamic peptide that has been purified as a ligand of an orphan receptor which is expressed in pituitary cells, and is known to stimulate prolactin release both in vitro and in vivo. We previously determined the immunocytochemical localization of PrRP neurons in the rat brain and our results suggest that PrRP takes part in a variety of brain functions. Additionally, in rats we have demonstrated the synaptic contact of PrRP neurons with oxytocin cell bodies in the paraventricular hypothalamic nucleus (PVH) and supraoptic nucleus (SON). This observation indicates that PrRP may regulate oxytocin secretion. In the present study, we performed intra-cerebroventricular administration of PrRP to conscious rats, and examined the effect of PrRP on the plasma levels of oxytocin and vasopressin. Our results show that central administration of PrRP increased the plasma oxytocin and vasopressin levels in female rats, but in male rats only oxytocin was increased. These results suggest that the PrRP acts as a neuro-modulator of the function of magnocellular neurons, especially oxytocin neurons, in the brain.
Assuntos
Encéfalo/fisiologia , Hormônios Hipotalâmicos/administração & dosagem , Neuropeptídeos/administração & dosagem , Ocitocina/metabolismo , Animais , Feminino , Hormônios Hipotalâmicos/farmacologia , Injeções Intraventriculares , Masculino , Neuropeptídeos/farmacologia , Ocitocina/sangue , Hormônio Liberador de Prolactina , Ratos , Ratos Wistar , Caracteres Sexuais , Vasopressinas/sangueRESUMO
By using a strategy that we have developed to search for the ligands of orphan seven-transmembrane-domain receptors [S. Hinuma et al., Nature 393 (1998) 272-276], we have recently identified a natural ligand, apelin, for the orphan 7TMR, APJ [K. Tatemoto et al., Biochem. Biophys. Res. Commun. 251 (1998) 471-476]. In this paper, we isolated rat and mouse apelin cDNAs, and analyzed the tissue distribution of apelin mRNA in rats. Although apelin mRNA was widely detected in a variety of tissues, the highest expression of apelin mRNA was detected in the mammary gland of pregnant rats. In the mammary gland, biologically active apelin and its mRNA considerably increased during pregnancy and lactation, and reached a maximal level around parturition. Moreover, a large amount of apelin (14-93 pmol/ml) was found to be secreted in the bovine colostrum, and it was still detectable even in commercial bovine milk. Since apelin partially suppressed cytokine production by mouse spleen cells in response to T cell receptor/CD3 cross-linking, the oral intake of apelin in the colostrum and milk might modulate immune responses in neonates.
Assuntos
Proteínas de Transporte/metabolismo , Colostro/metabolismo , Receptores Acoplados a Proteínas G , Adipocinas , Sequência de Aminoácidos , Animais , Apelina , Receptores de Apelina , Células CHO , Proteínas de Transporte/síntese química , Proteínas de Transporte/genética , Bovinos , Colforsina , Cricetinae , AMP Cíclico/metabolismo , DNA Complementar/isolamento & purificação , Feminino , Peptídeos e Proteínas de Sinalização Intercelular , Lactação/metabolismo , Ligantes , Masculino , Glândulas Mamárias Animais/metabolismo , Camundongos , Leite/química , Dados de Sequência Molecular , Gravidez/metabolismo , RNA Mensageiro/análise , Ratos , Ratos Wistar , Receptores de Dopamina D2/química , Receptores de Dopamina D2/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase ReversaRESUMO
Various sorts of bioactive molecules including hormones, neurotransmitters, and chemokines transmit signals into cells by binding to so-called seven-transmembrane-domain receptors (7TMRs). The recent progress in cDNA and genome DNA analyses has brought the discovery of numerous genes encoding ligand-unknown "orphan" 7TMRs. We have developed a strategy to identify the ligands of orphan 7TMRs by monitoring specific signal transductions induced in cells expressing orphan 7TMRs. Employing this method, we succeeded in identifying the natural ligands of the orphan 7TMRs, hGR3, and APJ. The ligand peptide identified for hGR3 was found to show a specific prolactin release promoting activity in rat anterior pituitary cells in in vitro culture and was therefore named "prolactin-releasing peptide." We named another novel bioactive peptide "apelin," for "APJ endogenous ligand." Although the biological functions of apelin are still under investigation, APJ reportedly acts as a coreceptor in the process of human immunodeficiency virus infection. We believe that the identification of orphan 7TMR ligands will provide clues to reveal the unknown regulatory mechanisms of various physiological phenomena and opportunities for novel drug discovery in the future.