Asunto(s)
Artritis , Endopeptidasas , Proteínas de la Matriz Extracelular , Metaloendopeptidasas , Proteínas ADAM , Proteína ADAM17 , Agrecanos , Animales , Artritis/tratamiento farmacológico , Artritis/etiología , Endopeptidasas/fisiología , Humanos , Lectinas Tipo C , Metaloendopeptidasas/antagonistas & inhibidores , Metaloendopeptidasas/fisiología , Inhibidores de Proteasas/farmacología , Inhibidores de Proteasas/uso terapéutico , Proteoglicanos/metabolismo , Inhibidor Tisular de Metaloproteinasa-3/farmacología , Inhibidor Tisular de Metaloproteinasa-3/uso terapéuticoRESUMEN
ADAMTS4 (aggrecanase-1) is considered to play a key role in the degradation of aggrecan in arthritides. The inhibitory activity of tissue inhibitors of metalloproteinases (TIMPs) to ADAMTS4 was examined in an assay using aggrecan substrate. Among the four TIMPs, TIMP-3 inhibited the activity most efficiently with an IC(50) value of 7.9 nM, which was at least 44-fold lower than that of TIMP-1 (350 nM) and TIMP-2 (420 nM) and >250-fold less than that of TIMP-4 (2 microM for 35% inhibition). These results suggest that TIMP-3 is a potent inhibitor against the aggrecanase activity of ADAMTS4 in vivo.
Asunto(s)
Proteínas de la Matriz Extracelular , Metaloendopeptidasas/antagonistas & inhibidores , Inhibidores Tisulares de Metaloproteinasas/farmacología , Proteínas ADAM , Proteína ADAMTS4 , Agrecanos , Humanos , Concentración 50 Inhibidora , Lectinas Tipo C , Metaloendopeptidasas/metabolismo , Fragmentos de Péptidos/química , Fragmentos de Péptidos/metabolismo , Procolágeno N-Endopeptidasa , Procesamiento Proteico-Postraduccional , Proteoglicanos/química , Proteoglicanos/metabolismo , Proteínas Recombinantes/antagonistas & inhibidores , Proteínas Recombinantes/metabolismo , Inhibidor Tisular de Metaloproteinasa-1/farmacología , Inhibidor Tisular de Metaloproteinasa-2/farmacología , Inhibidor Tisular de Metaloproteinasa-3/farmacología , Inhibidor Tisular de Metaloproteinasa-4RESUMEN
During carcinogenesis of pancreatic islets in transgenic mice, an angiogenic switch activates the quiescent vasculature. Paradoxically, vascular endothelial growth factor (VEGF) and its receptors are expressed constitutively. Nevertheless, a synthetic inhibitor (SU5416) of VEGF signalling impairs angiogenic switching and tumour growth. Two metalloproteinases, MMP-2/gelatinase-A and MMP-9/gelatinase-B, are upregulated in angiogenic lesions. MMP-9 can render normal islets angiogenic, releasing VEGF. MMP inhibitors reduce angiogenic switching, and tumour number and growth, as does genetic ablation of MMP-9. Absence of MMP-2 does not impair induction of angiogenesis, but retards tumour growth, whereas lack of urokinase has no effect. Our results show that MMP-9 is a component of the angiogenic switch.
Asunto(s)
Transformación Celular Neoplásica , Islotes Pancreáticos/patología , Metaloproteinasa 9 de la Matriz/metabolismo , Neovascularización Patológica , Neoplasias Pancreáticas/irrigación sanguínea , Acetamidas/farmacología , Animales , Factores de Crecimiento Endotelial/aislamiento & purificación , Genes de Cambio , Linfocinas/aislamiento & purificación , Ratones , Ratones Transgénicos , Proteínas Tirosina Quinasas Receptoras/aislamiento & purificación , Receptores de Factores de Crecimiento/aislamiento & purificación , Receptores de Factores de Crecimiento Endotelial Vascular , Transducción de Señal , Distribución Tisular , Factor A de Crecimiento Endotelial Vascular , Factores de Crecimiento Endotelial VascularRESUMEN
Brevican is a member of the lectican family of chondroitin sulfate proteoglycans that is predominantly expressed in the central nervous system. The susceptibility of brevican to digestion by matrix metalloproteinases (MMP-1, -2, -3, -7, -8, -9, -10, and -13 and membrane type 1 and 3 MMPs) and aggrecanase-1 (ADAMTS4) was examined. MMP-1, -2, -3, -7, -8, -10, and -13 degraded brevican into a few fragments with similar molecular masses, whereas the degradation products of aggrecanase-1 had apparently different sizes. NH(2)-terminal sequence analyses of the digestion fragments revealed that cleavages of the brevican core protein by these metalloproteinases occurred commonly within the central non-homologous domain. MMP-1, -2, -3, -7, -8, -10, and -13 preferentially attacked the Ala(360)-Phe(361) bond, whereas aggrecanase-1 cleaved the Glu(395)-Ser(396) bond, which are similar to the cleavage sites observed with cartilage proteoglycan (aggrecan) for the MMPs and aggrecanase-1, respectively. These data demonstrate that MMP-1, -2, -3, -7, -8, -10, and -13 and aggrecanase-1 digest brevican in a similar pattern to aggrecan and suggest that they may be responsible for the physiological turnover and pathological degradation of brevican.
Asunto(s)
Proteoglicanos Tipo Condroitín Sulfato/química , Proteoglicanos Tipo Condroitín Sulfato/metabolismo , Metaloendopeptidasas/metabolismo , Proteínas del Tejido Nervioso/química , Proteínas del Tejido Nervioso/metabolismo , Proteínas ADAM , Proteína ADAMTS4 , Secuencia de Aminoácidos , Animales , Sitios de Unión , Brevicano , Células CHO , Cricetinae , Humanos , Cinética , Lectinas Tipo C , Datos de Secuencia Molecular , Fragmentos de Péptidos/química , Procolágeno N-Endopeptidasa , Ratas , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Especificidad por Sustrato , TransfecciónRESUMEN
We have determined the nucleotide sequence of the clone pAL2 obtained from Porphyromonas gingivalis 381 in the previous study [Ansai et al. (1995) Microbiology 141, 2047-20521. The DNA sequence analysis of this fragment revealed one complete ORF and one incomplete ORF. The ORF encoded a protein (PgPepO) of 690 amino acids with a calculated molecular weight of 78796. The deduced amino acid sequence exhibited a significant homology with human endothelin-converting enzyme (ECE)-1. Recombinant PgPepO was purified to homogeneity and characterized. The purified enzyme was strongly inhibited by phosphoramidon, and converted big endothelin-1 to endothelin-1. Furthermore, the purified PgPepO strongly cross-reacted with a monoclonal antibody against rat ECE-1. These results indicate that PgPepO has striking similarity to mammalian ECE in structure and function.
Asunto(s)
Ácido Aspártico Endopeptidasas/genética , Proteínas Bacterianas , Genes Bacterianos , Metaloendopeptidasas/genética , Porphyromonas gingivalis/genética , Secuencia de Aminoácidos , Ácido Aspártico Endopeptidasas/química , Secuencia de Bases , Southern Blotting , Clonación Molecular , Endotelina-1 , Enzimas Convertidoras de Endotelina , Endotelinas/metabolismo , Inhibidores Enzimáticos/farmacología , Glicopéptidos/farmacología , Humanos , Cinética , Metaloendopeptidasas/química , Datos de Secuencia Molecular , Porphyromonas gingivalis/química , Porphyromonas gingivalis/enzimología , Precursores de Proteínas/metabolismo , Proteínas Recombinantes/química , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Especificidad por SustratoRESUMEN
Mammalian fertilization is characterized by the presence of long-lasting intracellular calcium ([Ca2+]i) oscillations that are required to induce oocyte activation. One of the Ca2+ channels that may mediate this Ca2+ release is the inositol 1,4, 5-trisphosphate receptor (IP(3)R). Three isoforms of the receptor have been described, but their expression in oocytes and possible roles in mammalian fertilization are not well known. Using isoform-specific antibodies against IP(3)R types 1, 2, and 3 and Western analysis, we determined the isoforms that are expressed in bovine metaphase II oocytes and ovaries. In oocytes, all isoforms are expressed, but type 1 is present in overwhelmingly larger amounts and is likely responsible for the majority of Ca2+ release at fertilization. In ovarian microsomes, all three isoforms appear well expressed, suggesting the participation of all IP(3)R isoforms in ovarian Ca2+ signaling. We then investigated whether the reported cessation/reduction in amplitude of fertilization-associated [Ca2+]i oscillations, which is observed as pronuclear formation approaches, corresponded with down-regulation of the IP(3)R-1 isoform. Fertilization resulted in approximately 40% reduction in the amount of receptor by 16 h postinsemination. In addition, injection of adenophostin A, a potent IP(3)R agonist that elicits high-frequency [Ca2+]i oscillations in mammalian oocytes, induced similar reduction in receptor numbers. Together, these data show that 1) the three IP(3)R isoforms are expressed in bovine oocytes; 2) IP(3)R-1 is likely to mediate most of the Ca2+ release during fertilization; 3) its down-regulation may explain the decline in amplitude of sperm-induced [Ca2+]i rises as fertilization progresses toward pronuclear formation; and 4) agonists of the IP(3)R induce down-regulation of the type-1 receptor in oocytes similar to that evoked by fertilization.
Asunto(s)
Adenosina/análogos & derivados , Canales de Calcio/biosíntesis , Regulación hacia Abajo , Fertilización , Inositol 1,4,5-Trifosfato/metabolismo , Receptores Citoplasmáticos y Nucleares/biosíntesis , Adenosina/farmacología , Animales , Western Blotting/veterinaria , Calcio/metabolismo , Canales de Calcio/química , Bovinos , Femenino , Receptores de Inositol 1,4,5-Trifosfato , Oocitos/química , Ovario/química , Receptores Citoplasmáticos y Nucleares/químicaRESUMEN
Erosion of cartilage is a major feature of joint diseases, i.e., osteoarthritis and rheumatoid arthritis, which leads with time to a loss of joint function. Proteolytic cleavage of the aggrecan core protein is a key event in the progress of these joint diseases. Aggrecan degradation has been believed to be mediated by a putative proteinase, aggrecanase. We identified aggrecanase activity in conditioned medium from explant culture of bovine nasal cartilage stimulated by retinoic acid. The activity was partially purified more than 10,000-fold. The enzyme cleaves at the aggrecanase site (Glu(373)-Ala(374)) but not at the MMP site (Asn(341)-Phe(342)) in the interglobular domain of the aggrecan. It also cleaves at Glu(1971)-Leu(1972), which is located in the gap region in the chondroitin sulfate attachment region prior to the aggrecanase site. The enzyme is a typical Ca(2+)-dependent metalloproteinase with a unique salt-dependency and is inhibited by several hydroxamate-based inhibitors for matrix metalloproteinases. Heparin and chondroitin sulfate inhibited the enzyme in a dose-dependent manner, suggesting that the large carbohydorate in aggrecan is important for substrate recognition by aggrecanase.
Asunto(s)
Cartílago/enzimología , Endopeptidasas/metabolismo , Inhibidores de la Metaloproteinasa de la Matriz , Animales , Calcio/metabolismo , Cartílago/efectos de los fármacos , Bovinos , Relación Dosis-Respuesta a Droga , Electroforesis en Gel de Poliacrilamida , Endopeptidasas/aislamiento & purificación , Glicosaminoglicanos/metabolismo , Concentración de Iones de Hidrógeno , Metaloproteinasas de la Matriz/metabolismo , Modelos Biológicos , Tabique Nasal , Técnicas de Cultivo de Órganos , Cloruro de Sodio/farmacologíaRESUMEN
The recognition mode of adenophostin A at the D-myo-inositol 1,4, 5-trisphosphate [Ins(1,4,5)P(3)] receptor was investigated. Comparison of conformations of Ins(1,4,5)P(3) and adenophostin A by using the combination of NMR and molecular mechanics (MM) calculations demonstrated that adenophostin A adopted a moderately extended conformation regarding the distance between the 2'-phosphoryl group and the 3' ',4' '-bisphosphate motif, as suggested previously [Wilcox, R. A. et al. (1995) Mol. Pharmacol. 47, 1204-1211]. Based on the nuclear Overhauser effect (NOE) observed between 3'-H and 1' '-H and on MM calculations, the molecular shape of adenophostin A proved to be an extended form at least in solution, in contrast to Wilcox's compactly folded, preliminary hairpin model. GlcdR(2,3',4')P(3), an adenophostin analogue without adenine moiety, was found to be less potent than adenophostin A and almost equipotent to Ins(1,4,5)P(3). We propose the possibility that (i) the optimal spatial arrangement of the three phosphoryl groups and/or (ii) the interaction of the adenine moiety of adenophostin A with the putative binding site, if it exists in the vicinity of the Ins(1,4,5)P(3)-binding site, might account for the exceptional potency of adenophostin A.
Asunto(s)
Adenosina/análogos & derivados , Canales de Calcio/metabolismo , Calcio/metabolismo , Inositol 1,4,5-Trifosfato/metabolismo , Receptores Citoplasmáticos y Nucleares/metabolismo , Adenosina/síntesis química , Adenosina/química , Adenosina/metabolismo , Animales , Sitios de Unión , Canales de Calcio/química , Cerebelo/metabolismo , Glucósidos/metabolismo , Inositol 1,4,5-Trifosfato/agonistas , Inositol 1,4,5-Trifosfato/química , Receptores de Inositol 1,4,5-Trifosfato , Microsomas/metabolismo , Modelos Moleculares , Resonancia Magnética Nuclear Biomolecular , Conformación de Ácido Nucleico , Penicillium/química , Ratas , Receptores Citoplasmáticos y Nucleares/químicaRESUMEN
The activation of intracellular calcium release and calcium entry across the plasmalemma in response to intracellular application of inositol 2,4,5-trisphosphate and adenophostin A, two metabolically stable agonists for inositol 1,4,5-trisphosphate receptors, was investigated using Xenopus laevis oocytes and confocal imaging. Intracellular injection of inositol 2,4,5-trisphosphate induced a rapidly spreading calcium signal associated with regenerative calcium waves; the calcium signal filled the peripheral regions of the cell in 1-5 min. Injection of high concentrations of adenophostin A (250 nM) similarly induced rapidly spreading calcium signals. Injection of low concentrations of adenophostin A resulted in calcium signals that spread slowly (>1 h). With extremely low concentrations of adenophostin A (approximately 10 pM), stable regions of Ca2+ release were observed that did not expand to peripheral regions. When the adenophostin A-induced calcium signal was restricted to central regions, compartmentalized calcium oscillations were sometimes observed. Restoration of extracellular calcium caused a rise in cytoplasmic calcium restricted to the region of adenophostin A-induced calcium mobilization. The limited diffusion of adenophostin A provides an opportunity to examine calcium signaling processes under spatially restricted conditions and provides insights into mechanisms of intracellular calcium oscillations and capacitative calcium entry.
Asunto(s)
Adenosina/análogos & derivados , Señalización del Calcio/efectos de los fármacos , Adenosina/farmacología , Animales , Femenino , Cinética , Microscopía Confocal , Microscopía Fluorescente , Oocitos/efectos de los fármacos , Oocitos/metabolismo , Xenopus laevisRESUMEN
R-94138, a matrix metalloproteinase inhibitor, was examined for the ability to prevent peritoneal dissemination of a human gastric cancer xenograft, TMK-1. When the supernatant of a co-culture of TMK-1 cells and human normal fibroblast cells was subjected to gelatin zymography, it was clear that the protein expression of MMP-2 had been inhibited by R-94138. When TMK-1 was injected intraperitoneally (i.p.) into nude mice at 5 x 10(5) cells/body, the resulting peritoneal dissemination mimicked clinical carcinomatous peritonitis. When the maximum tolerated dose of mitomycin C (MMC) or cisplatin (DDP) was given 12 h after the tumor inoculation, peritoneal dissemination was completely inhibited, while the effect of R-94138 was limited when it was given i.p. at a dose of 20 mg/kg in a schedule of q.d. x 5 starting 12 h after tumor injection. MMC and DDP also suppressed peritoneal dissemination when they were administered 1 week after the tumor inoculation at a single dose of 2 and 3 mg/kg i.p., respectively. R-94138 inhibited peritoneal dissemination when it was administered i.p. at a dose of 30 mg/kg in a schedule of q.d. x 5 starting from 1 week after tumor injection. The combination of MMC and R-94138 increased the preventive effect on peritoneal dissemination. R-94138 seems to be a promising candidate to prevent peritoneal dissemination of gastric cancer.
Asunto(s)
Acetamidas/uso terapéutico , Antineoplásicos/uso terapéutico , Cisplatino/uso terapéutico , Gelatinasas/antagonistas & inhibidores , Metaloendopeptidasas/antagonistas & inhibidores , Mitomicina/uso terapéutico , Metástasis de la Neoplasia/prevención & control , Neoplasias Peritoneales/secundario , Neoplasias Gástricas/secundario , Animales , Humanos , Masculino , Metaloproteinasa 2 de la Matriz , Ratones , Ratones Desnudos , Neoplasias Peritoneales/prevención & control , Neoplasias Gástricas/tratamiento farmacológico , Neoplasias Gástricas/patología , Trasplante Heterólogo , Células Tumorales CultivadasRESUMEN
Endothelin-1 (ET-1) is thought to play a significant role in acute renal failure induced by cyclosporin A (CsA). The cDNA sequence encoding endothelin-converting enzyme-1 (ECE-1), which produces the active form of ET-1 from big ET-1, was recently reported. To elicit the role of ECE-1 in the glomerular and tubular dysfunction induced by CsA, the effects of CsA on mRNA and protein expression of ECE-1 in rat kidney and on mRNA expression of prepro-ET-1 and ET A- and B-type receptors in glomeruli were studied. ECE-1 mRNA was detected in glomeruli and in whole nephron segments. ECE-1 mRNA expression was downregulated in all nephron segments at 24 h after CsA injection. Protein levels were also downregulated in glomeruli and in the outer and inner medulla. CsA rapidly increased prepro-ET-1 mRNA expression in glomeruli at 30 to 60 min after injection; this rapid increase was followed by an increase in plasma ET-1 levels. These increases were followed by decreased expression of ECE-1, ET A-type receptor, and ET B-type receptor mRNA at 6 h after injection, and serum creatinine levels were increased at 24 h after CsA injection. It is suggested that downregulation of glomerular and tubular ECE-1 expression may be caused by increased ET-1 synthesis in CsA-induced acute renal failure.
Asunto(s)
Lesión Renal Aguda/enzimología , Ácido Aspártico Endopeptidasas/metabolismo , Nefronas/enzimología , Animales , Ácido Aspártico Endopeptidasas/genética , Secuencia de Bases , Western Blotting , Creatinina/sangre , Técnicas de Cultivo , Ciclosporina/sangre , Modelos Animales de Enfermedad , Enzimas Convertidoras de Endotelina , Glomérulos Renales/efectos de los fármacos , Glomérulos Renales/enzimología , Masculino , Metaloendopeptidasas , Datos de Secuencia Molecular , Nefronas/efectos de los fármacos , Reacción en Cadena de la Polimerasa , ARN Mensajero/análisis , Ratas , Ratas Sprague-Dawley , Valores de ReferenciaRESUMEN
In most non-excitable cells, calcium influx is signaled by depletion of intracellular calcium stores, a process known as capacitative calcium entry. Adenophostin A, a potent activator of the inositol 1, 4,5-trisphosphate receptor, has been reported to activate Ca2+ entry in Xenopus oocytes to a greater extent than expected on the basis of its ability to release calcium stores. In this study, we compared the abilities of adenophostin A and inositol 2,4,5-trisphosphate ((2, 4,5)IP3) to release Ca2+ from intracellular stores, to activate Ca2+ entry, and to activate calcium release-activated calcium current (Icrac) in rat basophilic leukemia cells. Under conditions of low intracellular Ca2+ buffering (0.1 mM BAPTA), adenophostin A-induced Ca2+ release and activation of Icrac could be monitored simultaneously. However, other reagents that would be expected to deplete Ca2+ stores ((2,4,5)IP3, 3-fluoro-inositol 1,4, 5-trisphosphate, thapsigargin, and ionomycin) were unable to activate Icrac under this low Ca2+ buffering condition. Adenophostin A activated Icrac after a significant delay, longer than the delay for Ca2+ release. Thus, adenophostin A activates Icrac as a consequence of release of intracellular Ca2+, rather than directly acting on store-operated channels. The unique ability of adenophostin A to activate Icrac under conditions of low intracellular Ca2+ buffering suggests an additional site of action, perhaps in preventing or reducing rapid Ca2+-dependent inactivation of store-operated Ca2+ channels.
Asunto(s)
Adenosina/análogos & derivados , Canales de Calcio/fisiología , Calcio/metabolismo , Adenosina/farmacología , Animales , Bario/metabolismo , Canales de Calcio/efectos de los fármacos , Ácido Egtácico/análogos & derivados , Ácido Egtácico/farmacología , Inositol 1,4,5-Trifosfato/metabolismo , Fosfatos de Inositol/metabolismo , Cinética , Leucemia Basofílica Aguda , Ratas , Factores de Tiempo , Células Tumorales CultivadasRESUMEN
The cell-surface activation of pro-matrix metalloproteinase 2 (pro-MMP-2) is considered to be critical for cell migration and invasion. Treatment of human uterine cervical fibroblasts with concanavalin A activates pro-MMP-2 on the cell surface by converting it to the 65-kDa form with a minor form of 45 kDa. However, the 65-kDa MMP-2 was inactivated by tissue inhibitor of metalloproteinases (TIMP)-2 that was bound to the plasma membrane upon concanavalin A treatment. TIMP-2 binds to the plasma membrane through its N-terminal domain by two different modes of interaction as follows: one is sensitive to a hydroxamate (HXM) inhibitor of MMPs and the other is HXM-insensitive. TIMP-2 bound to the membrane in a HXM-insensitive manner, comprising about 40-50% of TIMP-2 on the membrane, is the inhibitor of the cell surface-activated MMP-2. It, however, does not inhibit MMP-3, MMP-9, and the 45-kDa MMP-2 lacking the C-terminal domain. The inhibition of the 65-kDa MMP-2 by TIMP-2 is initiated by the interaction of their C-terminal domains. Subsequently, the MMP-2.TIMP-2 complex is released from the membrane, and the activity of MMP-2 is blocked by TIMP-2. In the presence of collagen types I, II, III, V, or gelatin, the rate of inhibition of the 65-kDa MMP-2 by the membrane-bound TIMP-2 decreased considerably. These results suggest that the pericellular activity of MMP-2 is tightly regulated by membrane-bound TIMP-2 and surrounding extracellular matrix components.
Asunto(s)
Gelatinasas/metabolismo , Metaloendopeptidasas/metabolismo , Inhibidor Tisular de Metaloproteinasa-2/metabolismo , Animales , Células CHO , Membrana Celular/metabolismo , Células Cultivadas , Colagenasas/metabolismo , Concanavalina A/farmacología , Cricetinae , Activación Enzimática , Femenino , Fibroblastos/citología , Fibroblastos/enzimología , Gelatinasas/antagonistas & inhibidores , Humanos , Ácidos Hidroxámicos/farmacología , Cinética , Metaloproteinasa 2 de la Matriz , Metaloproteinasa 3 de la Matriz/metabolismo , Metaloproteinasa 9 de la Matriz , Metaloendopeptidasas/antagonistas & inhibidores , Peso Molecular , Proteínas Recombinantes/metabolismo , Transfección , Útero/citología , Útero/enzimologíaRESUMEN
The type-3 inositol 1,4,5-trisphosphate (InsP3) receptor is the major isoform expressed in 16HBE14o- cells from bronchial mucosa, representing 93% at the mRNA level as determined by ratio reverse transcription-polymerase chain reaction and about 81% at the protein level as determined with isoform-specific antibodies (Sienaert, I., Huyghe, S., Parys, J. B., Malfait, M., Kunzelmann, K., De Smedt, H., Verleden, G. M., and Missiaen, L., Pflügers Arch. Eur. Y. Physiol., in press). The present 45Ca2+ efflux experiments indicate that these InsP3 receptors were 3 times less sensitive to InsP3 and 11 times less sensitive to ATP than those in A7r5 cells, where the type-1 InsP3 receptor is the main isoform. ATP did not increase the cooperativity of the InsP3-induced Ca2+ release in 16HBE14o- cells, in contrast to its effect in A7r5 cells. The sulfhydryl reagent thimerosal also did not stimulate InsP3-induced Ca2+ release in 16HBE14o- cells, again in contrast to its effect in A7r5 cells. Adenophostin A was more potent than InsP3 in stimulating the release in both cell types. The biphasic activation of the InsP3 receptor by cytosolic Ca2+ occurred in both cell types. We conclude that Ca2+ release mediated by the type-3 InsP3 receptor mainly differs from that mediated by the type-1 InsP3 receptor by its lack of stimulation by sulfhydryl oxidation and its lower ATP and InsP3 sensitivity. The predominant expression of the type-3 InsP3 receptor in the bronchial mucosa may be part of a mechanism coping with oxidative stress in that tissue.
Asunto(s)
Canales de Calcio/fisiología , Calcio/metabolismo , Inositol 1,4,5-Trifosfato/farmacología , Receptores Citoplasmáticos y Nucleares/fisiología , Timerosal/farmacología , Adenosina/análogos & derivados , Adenosina/farmacología , Adenosina Trifosfato/farmacología , Animales , Aorta , Bronquios , Canales de Calcio/biosíntesis , Canales de Calcio/clasificación , Línea Celular , Permeabilidad de la Membrana Celular , Citosol/metabolismo , Receptores de Inositol 1,4,5-Trifosfato , Cinética , Membrana Mucosa/metabolismo , Reacción en Cadena de la Polimerasa , ARN Mensajero/biosíntesis , Ratas , Receptores Citoplasmáticos y Nucleares/biosíntesis , Receptores Citoplasmáticos y Nucleares/clasificación , Transcripción GenéticaRESUMEN
The purpose of this study was to determine the effect of mutation of rat endothelin-converting enzyme-1 (ECE-1) on the potencies of various inhibitors. The two amino acids mutated were Cys(412), which was shown to link the two monomeric enzymes to form a dimer, and Glu(752), postulated to be involved in substrate and inhibitor binding. No significant effects were noted when Glu(752) was replaced by an acidic (E752D) or uncharged (E752Q) residue. Replacing Glu(752) by a basic residue (E752R) slightly weakened the potencies of the inhibitors. In contrast, a significant decrease in the potencies was observed with the monomeric enzyme C412S. Phosphoramidon inhibited the wild-type ECE-1 with an IC50 of 1.5 microM, but it was about sixfold weaker for the C412S mutant. CGS 31447, an aminophosphonic acid, inhibited the wild-type and C412S enzymes with IC50 values of 5.8 and 76 nM, respectively. A similar degree of change in the potencies was also seen with CGS 25015, a thiol-containing compound, which inhibited the respective enzymes with IC50 values of 17 and 190 microM. These results suggest that the charge in Glu(752) may not be important for inhibitor binding and that the dimeric ECE-1 is more susceptible to inhibition than the monomeric enzyme.
Asunto(s)
Ácido Aspártico Endopeptidasas/antagonistas & inhibidores , Metaloendopeptidasas/antagonistas & inhibidores , Mutación/fisiología , Animales , Ácido Aspártico Endopeptidasas/genética , Enzimas Convertidoras de Endotelina , Humanos , Metaloendopeptidasas/genética , Mutagénesis Sitio-Dirigida , Inhibidores de Proteasas/farmacología , Ratas , Relación Estructura-ActividadRESUMEN
The expression and immunoreactivity of endothelin-converting enzyme (ECE) were examined in the renal tissue of rats with experimental congestive heart failure (CHF). Reverse transcriptase polymerase chain reaction (RT-PCR) revealed that ECE mRNA was more abundant (about twofold) in the renal medulla than in the cortex. Induction of heart failure caused a significant enhancement in the expression of this key enzyme in the renal cortex of rats with compensated CHF (delta + 28%) and in animals with decompensated heart failure (delta + 58%). An identical trend was also observed in the renal medulla, although these increases were moderate compared to those in the cortex. Similar findings were observed with Western blot techniques applying two monoclonal antibodies to rat ECE (AEC32-236 and AEC27-121). Taken together, these data suggest that upregulation of ECE is an important component in the activated renal ET system in CHF.
Asunto(s)
Ácido Aspártico Endopeptidasas/metabolismo , Insuficiencia Cardíaca/enzimología , Riñón/enzimología , Metaloendopeptidasas/metabolismo , Animales , Western Blotting , Enzimas Convertidoras de Endotelina , Corteza Renal/enzimología , Médula Renal/enzimología , Masculino , Reacción en Cadena de la Polimerasa , ARN Mensajero/biosíntesis , Ratas , Ratas WistarRESUMEN
Abnormal renal handling of water and sodium is implicated in the pathogenesis of hypertension in spontaneously hypertensive rats (SHR). Alteration of renal endothelin-1 synthesis is also reported in SHR. Endothelin-1, a potent vasoconstrictor and regulator of sodium reabsorption in the nephron, has a pathophysiological potential in the development of hypertension. Because synthesis of bioactive endothelin-1 requires endothelin converting enzyme-1 (ECE-1), we investigated whether renal ECE-1 gene expression is altered in the kidney of SHR. Kidneys from both 4- and 12-week-old SHR and age-matched Wistar-Kyoto rats (WKY) were studied. ECE-1 mRNA in microdissected nephron segments was assessed by reverse transcription-competitive polymerase chain reaction, and ECE-1 protein level by Western blot. In 4-week-old SHR, ECE-1 mRNA was significantly increased in the proximal straight tubule, medullary thick ascending limb, cortical thick ascending limb, and inner medullary collecting duct. ECE-1 protein level was increased in both the outer and inner medulla. In 12-week-old SHR, ECE-1 gene expression was significantly increased in the proximal straight tubule, medullary thick ascending limb, and also in the glomeruli. Glomerular preproendothelin-1 mRNA expression was not different between the two strains at both 4 and 12 weeks. We conclude that high ECE-1 gene expression in the nephron, via increase of endothelin-1 synthesis, may promote sodium retention that contributes to the development and/or maintenance of hypertension in SHR.
Asunto(s)
Ácido Aspártico Endopeptidasas/biosíntesis , Regulación Enzimológica de la Expresión Génica , Hipertensión/enzimología , Riñón/enzimología , Envejecimiento , Animales , Cartilla de ADN , Enzimas Convertidoras de Endotelina , Regulación del Desarrollo de la Expresión Génica , Hipertensión/genética , Riñón/crecimiento & desarrollo , Corteza Renal/enzimología , Médula Renal/enzimología , Túbulos Renales/enzimología , Masculino , Metaloendopeptidasas , Reacción en Cadena de la Polimerasa , Ratas , Ratas Endogámicas SHR , Ratas Endogámicas WKY , Especificidad de la EspecieRESUMEN
Adenophostin A possesses the highest known affinity for the inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) receptor (InsP3R). The compound shares with Ins(1,4,5)P3 those structural elements essential for binding to the InsP3R. However, its adenosine 2'-phosphate moiety has no counterpart in the Ins(1,4,5)P3 molecule. To determine whether its unique structure conferred a distinctive biological activity, we characterized the adenophostin-induced Ca2+ signal in Xenopus oocytes using the Ca2+-gated Cl- current assay. In high concentrations, adenophostin A released Ca2+ from Ins(1,4, 5)P3-sensitive stores and stimulated a Cl- current that depended upon the presence of extracellular Ca2+. We used this Cl- current as a marker of Ca2+ influx. In low concentrations, however, adenophostin A stimulated Ca2+ influx exclusively. In contrast, Ins(1,4,5)P3 and (2-hydroxyethyl)-alpha-D-glucopyranoside 2',3, 4-trisphosphate, an adenophostin A mimic lacking most of the adenosine moiety, always released intracellular Ca2+ before causing Ca2+ influx. Ins(1,4,5)P3 could still release Ca2+ during adenophostin A-induced Ca2+ influx, confirming that the Ins(1,4, 5)P3-sensitive intracellular Ca2+ stores had not been emptied. Adenophostin- and Ins(1,4,5)P3-induced Ca2+ influx were not additive, suggesting that both agonists stimulated a common Ca2+ entry pathway. Heparin, which blocks binding to the InsP3R, prevented adenophostin-induced Ca2+ influx. These data indicate that adenophostin A can stimulate the influx of Ca2+ across the plasma membrane without inevitably emptying the Ins(1,4,5)P3-sensitive intracellular Ca2+ stores.
Asunto(s)
Adenosina/análogos & derivados , Calcio/metabolismo , Inositol 1,4,5-Trifosfato/metabolismo , Oocitos/metabolismo , Adenosina/farmacología , Animales , Compartimento Celular , Femenino , Manganeso/metabolismo , Oocitos/efectos de los fármacos , XenopusRESUMEN
Mammalian cell-surface peptidases participate in the postsecretory processing and metabolism of neuropeptides and peptide hormones. Neutral endopeptidase-24.11 (NEP) is the prototype of a family of zinc metallopeptidases that also includes the endothelin-converting enzymes (ECE) and which are structurally related to the bacterial enzymes thermolysin and lactococcal endopeptidase. Two other mammalian gene products exhibit strong homology with NEP: the erythrocyte cell-surface antigen, KELL; and the putative product of the PEX gene, which has been associated with X-linked hypophosphatemic rickets. No enzymic activity has yet been attributed to KELL and PEX proteins, and they remain peptidases in search of a substrate. A wide range of biologically active peptide substrates has been described for NEP, of which the enkephalins and the atrial natriuretic peptide family have assumed greatest significance. Endothelin-converting enzyme catalyses the final step in the biosynthesis of the vasoconstrictor peptide, endothelin (ET). Like NEP, it is a type II integral membrane protein, but is expressed predominantly in endothelial cells. Isoforms of ECE (ECE-1alpha, ECE-1beta, and ECE-2) exist that differ in a number of characteristics. In particular, ECE-1, through the paracrine effects of ET-1, may contribute to the proliferation of smooth muscle after angioplasty and to the development of human atherosclerosis. Inhibitors of ECE and NEP may have important therapeutic applications in cardiovascular and renal medicine.