ABSTRACT
BACKGROUND: The polymorphic enzyme cytochrome P450 2C19 affects omeprazole metabolism. This influence on metabolism might affect serum gastrin levels, and safety, during long-term treatment of reflux oesophagitis. AIM: To examine the relationship between cytochrome P450 2C19 genotype and the safety profile of long-term omeprazole treatment. METHODS: A total of 119 Japanese patients with recurrent reflux oesophagitis underwent cytochrome P450 2C19 genotyping prior to receiving daily omeprazole 10 mg or 20 mg for 6-12 months, during which adverse event frequency, serum gastrin levels and endoscopic findings were monitored. RESULTS: The incidences of adverse events, serious adverse events and adverse events leading to withdrawal did not differ between homozygous extensive metabolizer (n = 46), heterozygous extensive metabolizer (n = 53) or poor metabolizer (n = 20) groups. In all genotype groups, serum gastrin increased during the first 3 months of dosing but stabilized thereafter. No significant differences were seen either in the rate of reflux oesophagitis healing or symptom improvement among genotype groups. CONCLUSIONS: Long-term treatment with omeprazole was well-tolerated in Japanese patients, irrespective of their cytochrome P450 2C19 metabolic genotype, indicating that dose adjustment depending on metabolic genotype is not required during treatment with omeprazole.
Subject(s)
Anti-Ulcer Agents/administration & dosage , Aryl Hydrocarbon Hydroxylases/genetics , Esophagitis, Peptic/genetics , Gastroesophageal Reflux/genetics , Mixed Function Oxygenases/genetics , Omeprazole/administration & dosage , Polymorphism, Genetic/genetics , Adult , Aged , Anti-Ulcer Agents/adverse effects , Anti-Ulcer Agents/metabolism , Cytochrome P-450 CYP2C19 , Esophagitis, Peptic/drug therapy , Esophagitis, Peptic/metabolism , Female , Gastrins/blood , Gastroesophageal Reflux/drug therapy , Gastroesophageal Reflux/metabolism , Genotype , Heterozygote , Homozygote , Humans , Male , Middle Aged , Omeprazole/adverse effects , Omeprazole/metabolism , Recurrence , Treatment OutcomeABSTRACT
BACKGROUND: Gastrin is known to have stimulatory effects on gastric mucosa; however, long-term effect of gastrin stimulation is not well known. AIM AND METHODS: To investigate the long-term effect of hypergastrinaemia, we established hypergastrinaemic transgenic mice by introducing a mutated human gastrin gene. Homozygously transgene-expressing mice showed serum gastrin levels of more than 600 pg/mL. RESULTS: Neither progastrin nor glycine-extended gastrin titre elevation were observed in hypergastrinaemic transgenic mice. Stomachs from the 30-35-week-old transgenic mice were 30-50% heavier and their mucosa were markedly thicker than those of the controls. The hypertrophic gastric mucosa of hypergastrinaemic transgenic mice consisted of elongated pits with widespread proliferative zones, and comprised depleted glandular regions. In situ hybridization study indicated that expression of H, K-ATPase mRNA in parietal cells of hypergastrinaemic transgenic mice was markedly decreased. By gastrin binding assay in vivo, specific gastrin binding sites were observed in the mid-glandular region of hypergastrinaemic transgenic mice that consisted mainly of prepit cells. CONCLUSIONS: These results suggest that long-term stimulation of gastrin increases the expression of CCK-B/gastrin receptors in the less-differentiated pit cells that are the main component of elongated gastric units, and lessens the well-differentiated characteristics of parietal cells.
Subject(s)
Gastric Mucosa/pathology , Gastric Mucosa/physiology , Gastrins/physiology , Parietal Cells, Gastric/pathology , Animals , Cell Differentiation , Gastrins/blood , Gastrins/genetics , Gastrins/metabolism , Gene Expression , H(+)-K(+)-Exchanging ATPase/genetics , Hypertrophy , In Situ Hybridization , Mice , Mice, Inbred ICR , Mice, Transgenic , Parietal Cells, Gastric/metabolism , RNA, Messenger/analysisABSTRACT
Cis- and trans-5,8-dihydroxy-5,6,7,8-tetrahydro-1,4-naphthoquinone (1a, 1b) were for the first time synthesized from 5,8-dihydroxy-1,4-naphthoquinone (naphthazazine) (6) as a starting material and racemic triol (3) was first synthesized from 7. The configuration of 1a was determined by X-ray analysis.
Subject(s)
Naphthoquinones/chemical synthesis , Crystallography, X-Ray , Indicators and Reagents , Magnetic Resonance Spectroscopy , Methylation , Models, Molecular , StereoisomerismABSTRACT
BACKGROUND AND AIMS: Recently, some growth factors have been shown to play roles not only as growth factors but also as cell-surviving factors. Transforming growth factor (TGF)-alpha is expressed in normal gastric mucosa. In this study, we investigated the cell-surviving effect of TGF-alpha on gastric mucosal cells and its signaling mechanism. METHODS: We used a gastric mucosal cell line, GSM06, and gastric cancer cell line, AGS. Apoptosis was induced by serum depletion or exposure to sodium butyrate. Analysis of apoptosis was performed by DNA ladder assay, measuring the DNA fragmentation ratio (Burton method), and 4',6-diamidino-2-phenylindole staining. RESULTS: TGF-alpha protected gastric mucosal cells against apoptosis induced by serum depletion or sodium butyrate in a dose-dependent manner. This antiapoptotic effect of TGF-alpha was blocked by the pretreatment with reagents that can potentially inhibit NF-kappaB activation, whereas neither MEK inhibitor PD098059 nor PI-3-kinase inhibitor wortmannin abolished this effect. Electrophoretic mobility shift assay showed nuclear factor kappaB (NF-kappaB) activation by TGF-alpha stimulation. TGF-alpha also enhanced the expression of Bcl-2 family proteins in an NF-kappaB-dependent manner. CONCLUSIONS: TGF-alpha plays an antiapoptotic role in gastric mucosal cells via the NF-kappaB-dependent pathway.
Subject(s)
Apoptosis/drug effects , Gastric Mucosa/drug effects , MAP Kinase Kinase Kinase 1 , NF-kappa B/physiology , Transforming Growth Factors/pharmacology , Animals , Genes, bcl-2/drug effects , Mice , Mice, Transgenic , Mutagenesis , Protein Serine-Threonine Kinases/genetics , Reverse Transcriptase Polymerase Chain Reaction , Tumor Cells, CulturedABSTRACT
The structure and stereochemistry of a new terpenoid ester, nardostachysin (1), isolated from the rhizomes of Nardostachys jatamansi, were established as the 7',8'-dihydroxy-4'-methylene hexahydrocyclopenta[c]pyran-1'-one-8'-methyl ester of 7, 9-guaiadien-14-oic acid, by spectral and chemical studies.
Subject(s)
Plants, Medicinal/chemistry , Terpenes/chemistry , India , Magnetic Resonance Spectroscopy , Plant Extracts/analysis , Plant Roots/chemistry , Spectrophotometry, UltravioletABSTRACT
Stromal fibroblasts interact with invading cancer cells by secreting and activating matrix metalloproteinases (MMPs). To elucidate the mechanisms involved in the expression and activation patterns of MMPs, human colon-cancer cell lines Caco-2 and LoVo and colon-fibroblast cell line CCD18-Co were co-cultivated in non-contact and contact conditions which mimic in vivo interaction between cancer cells and fibroblasts before and after cancer invasion respectively. Gelatin zymography disclosed that MMP-2 was secreted from the fibroblasts but not from the cancer cells. The quantity of fibroblast-derived MMP-2 in conditioned medium was not significantly changed in either the contact or the non-contact co-cultures when compared with that of individual cultures of CCD18-Co fibroblasts. Cancer cells in non-contact co-cultures, however, enhanced the activation of fibroblast-derived MMP-2. Transcripts of membrane-type matrix metalloproteinase-1 (MT1-MMP), which is thought to be present on the cell surface and to work as a candidate activator of MMP-2, were detected in both cancer cell lines. Plasma membrane extracts of cancer cells also activated MMP-2 in conditioned media in cell-free conditions. This activation of MMP-2 may be caused by MT1-MMP of the cancer cells, since it was inhibited by a series of MMP inhibitors, including ethylenediaminetetraacetic acid (EDTA), the tissue inhibitor of metalloproteinase-2 (TIMP-2), and the MMP inhibitor CGS 27023A, but not by TIMP-1. Our data demonstrate that in non-contact co-cultures colon-cancer cells activate fibroblast-derived MMP-2 on their plasma membranes. These findings should help to elucidate the mechanism involved in the initial destruction of basement membrane by cancer cells.
Subject(s)
Colonic Neoplasms/metabolism , Fibroblasts/enzymology , Hydroxamic Acids , Matrix Metalloproteinase 2/metabolism , Pyrazines , Basement Membrane/metabolism , Blotting, Northern , Caco-2 Cells , Cell Line , Cell Membrane/metabolism , Chelating Agents/pharmacology , Coculture Techniques , Edetic Acid/pharmacology , Enzyme Activation/drug effects , Gelatin/metabolism , Humans , Matrix Metalloproteinases, Membrane-Associated , Metalloendopeptidases/metabolism , Protease Inhibitors/pharmacology , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Sulfonamides , Tissue Inhibitor of Metalloproteinase-2/pharmacology , Tumor Cells, CulturedABSTRACT
Gastrin stimulates the growth of gastric mucosa by increasing mostly its glandular region but is not known to induce the growth of a pit region where its major constituent cells, gastric surface mucous (GSM) cells, turn over rapidly. To investigate the effect of gastrin on GSM cells, we generated hypergastrinemic mice by expressing a human gastrin transgene. We obtained a hypergastrinemic mouse line whose average serum gastrin level is 671 +/- 252 pg/ml (normal level <150 pg/ml). Gastrin-positive cells were found in the fundic mucosa. The gastric mucosa exhibited hypertrophic growth, which was characterized by an elongated pit with an active proliferative zone, but the glandular region containing parietal cells was normal or reduced in size. The GSM cells contained fewer mucous granules than those of control littermates and lost reactivity to the GSM cell-specific cholera toxin beta-subunit lectin. GSM cells along the foveolar region and many mucous neck cells became Alcian blue positive, suggesting the appearance of sialomucin in these cells. We suggest that gastrin stimulates the growth of the proliferative zone of gastric glands, which results in the elongation of the pit region whose GSM cells exhibit less-differentiated features.
Subject(s)
Gastric Mucosa/growth & development , Gastrins/physiology , Animals , Base Sequence/genetics , Cell Differentiation , Endocrine Glands/pathology , Gastric Mucosa/pathology , Gastrins/blood , Gastrins/genetics , Gastrins/metabolism , Humans , Hypertrophy , Mice , Mice, Transgenic/genetics , Molecular Sequence DataABSTRACT
The proprotein-processing endoprotease furin is localized in the gastric epithelial cells of the pit region in the rat gastric gland. The gastric pit is composed of several cell types, including gastric surface mucosal (GSM) cells and parietal cells. Furin converts many growth- or differentiation-related proproteins to their active forms. We examined identification of furin-positive cells by immunostaining of rat gastric mucosa and regulators of the furin expression by measuring the furin promoter activity by luciferase assay. Furin-positive cells were stained for H(+)-K(+)-ATPase, indicating that they are parietal cells. Furin-positive parietal cells were not stained for transforming growth factor-alpha (TGF-alpha) but were surrounded by TGF-alpha-positive GSM cells. In contrast, parietal cells below the proliferative zone were positive for TGF-alpha but not for furin. Furin-positive parietal cells expressed a high level of epidermal growth factor receptor (EGFR). TGF-alpha stimulated the furin promoter activity highly in a mouse GSM cell line GSM06. Thus we suggest that the parietal cells of the pit region have furin-mediated functions that can be stimulated by EGFR signaling.
Subject(s)
Parietal Cells, Gastric/enzymology , Subtilisins/metabolism , Animals , Cell Line , Cells, Cultured , ErbB Receptors/metabolism , Furin , Immunohistochemistry , Male , Mice , Rats , Rats, Wistar , Stimulation, Chemical , Tissue Distribution/physiology , Transforming Growth Factor alpha/pharmacologyABSTRACT
Two new alkaloids, 9-carbethoxy-3-methylcarbazole and 9-formyl-3-methylcarbazole, and a known metabolite, 3-methyl-carbazole were isolated from the roots of Murraya koenigii. All three compounds were identified by detailed spectral analyses including 2D NMR studies and their structures confirmed by synthesis. Of the two new metabolites, the 9-formyl compound displayed weak cytotoxicity against both mouse melanoma B16 and adriamycin-resistant P388 mouse leukemia cell lines.
Subject(s)
Antineoplastic Agents, Phytogenic/isolation & purification , Carbazoles/isolation & purification , Plant Roots/chemistry , Animals , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Carbazoles/chemistry , Carbazoles/pharmacology , Leukemia P388/pathology , Magnetic Resonance Spectroscopy , Melanoma, Experimental/pathology , Mice , Molecular Structure , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Tumor Cells, CulturedABSTRACT
We have previously reported that in the well-differentiated beta-cell line MIN6 cells, the beta-cell-specific differentiated characteristics, such as insulin content, expression of prohormone convertases PC2 and PC3, and glucose-regulated insulin secretion, diminished when the proprotein-processing endoprotease furin was highly expressed. Since furin converts many growth-related protein precursors to their bioactive forms, we compared the four pancreatic islet cell lines RINm5F, betaTC3, betaHC9, and MIN6 with respect to cell growth rate, furin expression, endoprotease activity, and insulin content. RINm5F cells exhibited the strongest furin expression, higher furin-type endoprotease activity, and the fastest cell growth, but had the least insulin content. In contrast, MIN6 cells exhibited only a weak furin expression, little furin-type endoprotease activity, and the slowest cell growth, but had the highest insulin content. To test whether furin-expressing cells secrete growth-promoting factors cleaved by furin, we prepared conditioned media from RINm5F and furin cDNA-introduced MIN6 (MIN6-F) cells. The conditioned media from RINm5F and MIN6-F induced increased DNA synthesis and promoted the growth of normal MIN6 cells, compared with the medium from the empty vector-introduced MIN6-0 cells. We then examined the effect of the protease inhibitors alpha1-antitrypsin and its variants by infecting their vaccinia recombinants to the four cell lines. All conditioned media from each cell line expressing the furin-specific alpha1-antitrypsin variant exhibited the least DNA synthetic capacity on normal MIN6 cells. Furthermore, all three sublines of MIN6-F grew faster than MIN6-0 and MIN6. Thus, we suggest that the islet cells with higher furin expression may induce increased production of growth factors, which result in an increase in cell growth, through an autocrine/paracrine mechanism.
Subject(s)
Islets of Langerhans/cytology , Islets of Langerhans/enzymology , Serine Proteinase Inhibitors/pharmacology , Subtilisins/metabolism , alpha 1-Antitrypsin/pharmacology , Animals , Cell Count/drug effects , Cell Division/drug effects , Cell Division/physiology , Cell Line , Culture Media, Conditioned/metabolism , Cytoplasmic Granules/enzymology , Cytoplasmic Granules/ultrastructure , DNA/biosynthesis , Furin , Guinea Pigs , Hydrogen-Ion Concentration , Immune Sera/immunology , Immunohistochemistry , Insulin/analysis , Insulin/immunology , Islets of Langerhans/ultrastructure , Oligopeptides/metabolism , Radioimmunoassay , Subtilisins/analysis , Subtilisins/drug effects , Time FactorsABSTRACT
Gastric surface mucous cells originate from progenitor cells at the isthmus of the gastric gland, from where the cells migrate to the luminal surface. With migration they form secretory granules and express TGF alpha. We found that proprotein-processing endoprotease furin-positive cells were layered around the upper one fourth of the gastric glands of adult rats, whereas they were distributed along an outer epithelial layer in fetal rats. Because the furin-positive cell layer was localized from the upper cell proliferating zone to the less proliferating pit-cell region in the gastric gland unit, we examined the role of furin in the growth and differentiation of surface mucous cells by using the cell line, GSM06. This cell line is derived from the gastric surface mucous cells of transgenic mice harboring the temperature-sensitive simian virus 40 T antigen. At T antigen-active temperature (33 degrees C), the cells grew to confluency, whereas at T antigen-inactive temperature (39 degrees C), the cells ceased growing. At 33 degrees C, the cells exhibited a high level of furin expression with a negligible level of periodic acid Schiff (PAS)-positive materials and a low level of TGF alpha. In contrast, at 39 degrees C the cells produced a high level of PAS-positive materials, TGF alpha, and secretory granules, with a negligible level of furin expression. To further examine the role of furin, we established a GSM06 cell line introduced with either a sense or an antisense furin cDNA. The cells with sense furin expression produced fewer PAS-positive materials and a low level of TGF alpha even at 39 degrees C, whereas the cells with antisense furin expression exhibited more PAS-positive materials and TGF alpha even at 33 degrees C. When furin expression was suppressed by its antisense oligonucleotide, the cell growth was retarded with enhanced expression of the differentiated characteristics. Thus, we conclude that furin is instrumental in controlling the growth of the surface mucous cells.
Subject(s)
Gastric Mucosa/cytology , Gastric Mucosa/enzymology , Subtilisins/physiology , Animals , Antigens, Polyomavirus Transforming/genetics , Base Sequence , Cell Differentiation/physiology , Cell Division/physiology , Cell Line, Transformed , Culture Media, Conditioned , Female , Fetus/cytology , Fetus/enzymology , Furin , Gastric Mucosa/physiology , Gene Expression/drug effects , Mice , Microscopy, Electron , Oligonucleotides, Antisense/genetics , Oligonucleotides, Antisense/pharmacology , Pregnancy , Rats , Rats, Wistar , Stem Cells/cytology , Stem Cells/enzymology , Subtilisins/antagonists & inhibitors , Subtilisins/genetics , Transforming Growth Factor beta/metabolismABSTRACT
Furin, a member of the yeast Kex2 endoprotease family, converts a number of proproteins to their active forms. The liver produces a number of proproteins having a furin-cleavable site; thus, furin may be involved in growth and differentiation both in the partially hepatectomized liver and in primary cultured hepatocytes. Furin mRNA levels are elevated in tissues regenerated from partially hepatectomized rat liver. In primary culture of rat hepatocytes, furin expression increases gradually with time, and its expression is greatly enhanced by transforming growth factor beta1, whose processing from the precursor requires cleavage by furin. Thus, we suggest that the regeneration and differentiation of hepatocytes is dependent upon the co-elevation of furin and transforming growth factor beta1 mRNAs.
Subject(s)
Gene Expression Regulation, Developmental/physiology , Liver/physiology , Subtilisins/genetics , Transforming Growth Factor beta/genetics , Animals , Cell Differentiation , Cells, Cultured , Furin , Hepatectomy , Liver/cytology , Liver Regeneration , Male , Protein Precursors/genetics , Protein Processing, Post-Translational , RNA, Messenger/analysis , Rats , Rats, Wistar , Transforming Growth Factor beta/pharmacologyABSTRACT
The expression of furin in pancreatic beta-cells induces faster cell growth and a decrease in differentiated beta-cell-specific characteristics. During the development of rat pancreatic islets, the prohormone convertases, PC2 and PC3, appear during late gestation and are expressed long after birth. We investigated the developmental change in another yeast Kex2 family endoprotease, furin, in rat islets in relation to islet cell growth. Furin had appeared by gestational day 18 and was distributed in islets as well as exocrine tissues. The expression of furin in islets increased toward the neonatal stage. Bromodeoxyuridine (BrdU) incorporation was also elevated in the perinatal period. On postnatal days 10 and 20, staining characteristics were attenuated. On day 25, immediately after weaning, furin staining began to localize in the beta-cell region, and staining in the alpha-cell region became fainter. On day 270, the staining in the alpha-cell region disappeared, and staining in the beta-cell region remained positive, but was weaker. We conclude that furin expression was greatest during the perinatal period, when BrdU incorporation into islets was maximal. Furin expression continued, however, even after the BrdU incorporation decreased. Thus, furin appears to control the proliferation as well as differentiation of islet cells.
Subject(s)
Aging/metabolism , Gene Expression Regulation, Developmental , Islets of Langerhans/enzymology , Proprotein Convertases , Saccharomyces cerevisiae Proteins , Subtilisins/biosynthesis , Animals , Cell Differentiation , Embryo, Mammalian , Embryonic and Fetal Development , Furin , Insulin/analysis , Islets of Langerhans/cytology , Islets of Langerhans/growth & development , Rats , Rats, Wistar , Saccharomyces cerevisiae/enzymologyABSTRACT
Almost completely homogenous gastric mucous epithelial cells of guinea pigs were grown to confluence in the presence of 10% fetal calf serum (FCS). FCS, epidermal growth factor (EGF), and insulin significantly increased 5-bromo-2'-deoxyuridine (BrdU) uptake by the cells and EGF together with insulin increased the cells' [3H] thymidine uptake. Basic fibroblast growth factor (bFGF) enhanced EGF-induced DNA synthesis by the cells, but vasoactive intestinal peptide (VIP), secretin, prostaglandin E2 (PGE2), and dibutyryl cyclic AMP (dbcAMP) neither induced DNA synthesis nor enhanced the effect of EGF on DNA synthesis by the cells. Gastrin, cholecystokinin-octapeptide (CCK8), and carbamylcholine chloride (CCh) also did not enhance the effect of EGF on DNA synthesis. 125I-EGF, 125I-bFGF, and 125I-gastrin binding to the gastric mucous cells revealed the presence of high-affinity receptors for EGF and bFGF, but not for gastrin. Northern blot analysis showed the expression of EGF receptor mRNA, but not gastrin receptor mRNA. These results suggest that EGF, insulin, and bFGF may cooperatively regulate gastric mucous cell growth, but that gastrin and other gastrointestinal hormones do not have a direct stimulatory effect on mucous cell growth in the guinea pig.
Subject(s)
Gastric Mucosa/cytology , Gastrointestinal Hormones/pharmacology , Growth Substances/pharmacology , Animals , Blotting, Northern , Cell Division/drug effects , Cells, Cultured , ErbB Receptors/biosynthesis , ErbB Receptors/genetics , ErbB Receptors/physiology , Gastric Mucosa/drug effects , Gastrointestinal Hormones/physiology , Growth Substances/physiology , Guinea Pigs , Iodine Radioisotopes , RNA, Messenger/genetics , Receptors, Cholecystokinin/biosynthesis , Receptors, Cholecystokinin/genetics , Receptors, Cholecystokinin/physiologyABSTRACT
Prohormone convertases PC2 and PC3, yeast Kex2-family endoproteases specific to the regulated secretory pathway, cleave proinsulin to insulin in the secretory granules of pancreatic beta cells. The well-differentiated beta cell line MIN6 expresses PC2 and PC3 and another regulated secretory pathway-specific protein chromogranin A. Furin, another yeast Kex2 endoprotease, exists in the trans-Golgi networks of many cell types. The beta cell line RINm5F (a cell line that is less differentiated than the MIN6 cell line) does not express the regulated pathway-specific proteins, but strongly expresses furin. We suspected that furin expression may cause the decrement of regulated secretory pathway-specific proteins. To test this hypothesis, we expressed a furin cDNA with a metallothionein promoter in MIN6 cells. With Zn2+ stimulation of furin expression, the messages of PC2, PC3, and chromogranin A decreased, and the processing of proinsulin to mature insulin became less efficient. The furin-expressing MIN6 cells exhibited less insulin content and weakened insulin secretion in response to a high glucose concentration. The conditioned medium from furin-expressing MIN6 cells also exerted a decrease of PC2 and PC3 expression in unaltered MIN6 cells. Thus, proteins cleaved by furin inside the cells or by truncated furin shed into the culture medium appear to cause decreased PC2 and PC3 expression, insulin content, and glucose-responsive insulin secretion in MIN6 cells.
Subject(s)
Islets of Langerhans/metabolism , Proteins/metabolism , Subtilisins/metabolism , Amino Acid Sequence , Animals , Blotting, Northern , Cell Line , Culture Media, Conditioned , Furin , Immunohistochemistry , Insulin/metabolism , Metallothionein/genetics , Mice , Mice, Transgenic , Molecular Sequence Data , Proinsulin/metabolism , Promoter Regions, Genetic , Subtilisins/geneticsABSTRACT
We report the cloning of a novel human gene, CMKLR1, which encodes a protein that has notable sequence and structural homology to the seven transmembrane G-protein linked chemokine receptors. This gene has 55% nucleotide sequence homology to the IL-8 type 1 receptor and 53% to the N-formyl peptide related receptor 1 genes. The mRNA of this receptors is expressed in a broad array of tissues associated with hematopoietic and immune function including, spleen, thymus, appendix, lymph node, bone marrow, and fetal liver. Using fluorescence in situ hybridization the gene encoding CMLKR1 (chemokine-like receptor 1) was localized to human chromosome 12q24.1.
Subject(s)
Chromosomes, Human, Pair 12 , Cloning, Molecular , Receptors, Chemokine , Receptors, Cytokine/genetics , Amino Acid Sequence , Antigens, CD/chemistry , Antigens, CD/genetics , Chromosome Mapping , GTP-Binding Proteins/metabolism , Gene Expression , Humans , Molecular Sequence Data , Organ Specificity , Receptors, Cytokine/chemistry , Receptors, Formyl Peptide , Receptors, Immunologic/chemistry , Receptors, Immunologic/genetics , Receptors, Interleukin/chemistry , Receptors, Interleukin/genetics , Receptors, Interleukin-8A , Receptors, Peptide/chemistry , Receptors, Peptide/genetics , Sequence Alignment , Sequence Homology, Nucleic AcidABSTRACT
The present study was undertaken to investigate whether epidermal growth factor (EGF) could stimulate prostaglandin E2 release, and if so, by what mechanism EGF would exert such an effect in gastric mucosal cells. In cultured guinea pig gastric mucous cells, EGF dose-dependently stimulated prostaglandin E2 release, with maximal stimulation observed at 10 ng/ml. EGF stimulated an increase in cyclooxygenase activity, which was reduced by protein synthesis inhibitor, actinomycin D, and cycloheximide. EGF also stimulated the enzyme protein synthesis estimated by Western blot analysis, whereas EGF did not stimulate phospholipase A2 activity. These results suggest that such an effect of EGF of de novo synthesis of cyclooxygenase protein and prostaglandin E2 release may be involved at least in part in the mechanism of EGF-induced local regulation of gastric mucosal integrity.
Subject(s)
Dinoprostone/metabolism , Epidermal Growth Factor/physiology , Gastric Mucosa/metabolism , Prostaglandin-Endoperoxide Synthases/biosynthesis , Animals , Cell Division/drug effects , Cells, Cultured , Cycloheximide/pharmacology , Cyclooxygenase Inhibitors/pharmacology , Dactinomycin/pharmacology , Dose-Response Relationship, Drug , Enzyme Induction , Epidermal Growth Factor/pharmacology , Gastric Mucosa/cytology , Guinea Pigs , Male , Phospholipases A/metabolism , Phospholipases A2ABSTRACT
A high-performance liquid chromatographic method was established for the fractionation of oxidized choline glycerophospholipids (CGPs) that contain aldehyde residues, after their derivatization with a fluorescent reagent 4-(N,N-dimethylaminosulfonyl)-7-hydrazino-2,1,3-benzoxadiazole (DBD-H). DBD-H efficiently reacted with the aldehyde residues of phospholipids at room temperature. Fluorescent derivatives of aldehydic phospholipids were well separated into species that contained aldehyde groups at different sites. The relationship between the amount of each derivative and the signal was linear over a wide range and amounts as low as several picomoles of aldehydic CGP could be detected. This method is applicable to the quantitation of aldehydic phospholipids in peroxidized membranes of red blood cells. In the present study, formation of aldehydic choline glycerophospholipids was demonstrated for the first time in peroxidized red blood cell membranes and the compounds were quantitated.
Subject(s)
Aldehydes/chemistry , Chromatography, High Pressure Liquid , Phosphatidylcholines/analysis , Erythrocyte Membrane/chemistry , Fluorometry , Humans , Microchemistry , Oxidation-Reduction , Phosphatidylcholines/chemistry , Sensitivity and SpecificityABSTRACT
The melanocortins are peptide products of proopiomelanocortin post-translational processing that, among other functions, are thought to influence cognition. Recently, we isolated genes encoding two human melanocortin receptors, the melanocortin-3 receptor (hMC3R) and the melanocortin-4 receptor (hMC4R), which are expressed primarily in brain. We undertook the present studies to examine the structural features of melanocortins that determine activation of these two receptors. For our studies we expressed the coding regions of the hMC3R and hMC4R genes in Hepa cells using the eukaryotic expression vector CMVneo and examined the generation of intracellular cyclic 3',5'-adenosine monophosphate in response to stimulation with various melanocortins. Our findings indicate that the core heptapeptide sequence common to most of the melanocortins (amino acids 4-10 of adrenocorticotropic hormone [ACTH]) is the primary determinant for activation of hMC3R but, in addition, tyrosine2 is necessary for maximal response. Activity of hMC4R is heavily dependent on proline12, but full activity also requires a contribution by tyrosine2. These findings may provide insight into the development of targeted ligands for the brain melanocortin receptors.
Subject(s)
Adrenocorticotropic Hormone/pharmacology , Melanocyte-Stimulating Hormones/pharmacology , Receptors, Corticotropin/drug effects , Receptors, Peptide/drug effects , Adrenocorticotropic Hormone/chemistry , Amino Acid Sequence , Animals , Cyclic AMP/biosynthesis , Melanocyte-Stimulating Hormones/chemistry , Molecular Sequence Data , Rats , Receptor, Melanocortin, Type 3 , Receptor, Melanocortin, Type 4 , Structure-Activity RelationshipABSTRACT
BACKGROUND: H2-histamine receptors mediate a wide range of physiological functions extending from stimulation of gastric acid secretion to induction of human promyelocyte differentiation. We have previously cloned the H2-histamine receptor gene and noted that only three amino acids on the receptor were sufficient to define its specificity and selectivity. Despite only modest overall amino acid homology (34% amino acid identity and 57.5% similarity) between the H2-histamine receptor and the receptor for another monoamine, the beta 2-adrenergic receptor, there is remarkable similarity at their critical ligand binding sites. We hypothesized that, if the specificity and selectivity of both receptors are invested in just three amino acids, it should be possible to convert one of the receptors into one that recognizes the ligand of the other by simple mutations at only one or two sites. MATERIAL AND METHODS: We explored the effect of two single mutations in the fifth transmembrane domain of the H2-histamine receptor, which encompasses the sites that determine H2 selectivity. The canine H2 receptor gene was mutated at Asp186 and Gly187 (Asp186 to Ala186 and Gly187 to Ser187) by oligonuceotide directed mutagenesis. The coding region of both the wild-type and mutated H2 receptors was subcloned into the eukaryotic expression vector, CMVneo, and stably transfected into Hepa cells and L cells. The biological activity of histamine and epinephrine on the expressed receptor was examined by measurement of cellular cAMP production and inositol trisphosphate formation. RESULTS: Hepa cells transfected with the Ala186-Ser187 mutant H2 receptor demonstrated a biphasic rise in cAMP in response to epinephrine with an early phase (ED50 approximately 10(-11) M) that could be inhibited by both propranolol and cimetidine. Epinephrine also induced IP3 generation in the same cells, a biological response that is characteristic of activation of the wild-type H2 but not of the beta-adrenergic receptor. L cells transfected with the Ala186-Ser187 mutant H2 receptor also responded to epinephrine in a cimetidine and propranolol inhibitable manner. CONCLUSIONS: We converted the H2-histamine receptor into a bifunctional one that has characteristics of both histamine and adrenergic receptors by two simple mutations. These results support the hypothesis that ligand specificity is determined by only a few key points on a receptor regardless of the structure of the remainder of the molecule. Our studies have important implications on the design of pharmacological agents targeted for action at physiological receptors.