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1.
J Am Soc Nephrol ; 30(11): 2159-2176, 2019 11.
Article in English | MEDLINE | ID: mdl-31462402

ABSTRACT

BACKGROUND: Having a comprehensive map of the cellular anatomy of the normal human bladder is vital to understanding the cellular origins of benign bladder disease and bladder cancer. METHODS: We used single-cell RNA sequencing (scRNA-seq) of 12,423 cells from healthy human bladder tissue samples taken from patients with bladder cancer and 12,884 cells from mouse bladders to classify bladder cell types and their underlying functions. RESULTS: We created a single-cell transcriptomic map of human and mouse bladders, including 16 clusters of human bladder cells and 15 clusters of mouse bladder cells. The homology and heterogeneity of human and mouse bladder cell types were compared and both conservative and heterogeneous aspects of human and mouse bladder evolution were identified. We also discovered two novel types of human bladder cells. One type is ADRA2A+ and HRH2+ interstitial cells which may be associated with nerve conduction and allergic reactions. The other type is TNNT1+ epithelial cells that may be involved with bladder emptying. We verify these TNNT1+ epithelial cells also occur in rat and mouse bladders. CONCLUSIONS: This transcriptomic map provides a resource for studying bladder cell types, specific cell markers, signaling receptors, and genes that will help us to learn more about the relationship between bladder cell types and diseases.


Subject(s)
Single-Cell Analysis , Transcriptome , Urinary Bladder/cytology , Urinary Bladder/metabolism , Animals , Female , Humans , Male , Mice , Mice, Inbred C57BL , Rats , Rats, Sprague-Dawley , Receptors, Adrenergic, alpha-2/analysis , Receptors, Histamine H2/analysis , Sequence Analysis, RNA , Troponin T/analysis
2.
Cytometry A ; 87(1): 23-31, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25212523

ABSTRACT

Flow cytometry is one of the most widely used methods for the qualitative and quantitative analysis of cell surface expressed proteins by making use of fluorescent specific antibodies. Lacking an antibody validated for flow cytometry, an alternative approach for labeling cell surface receptors is the use of fluorescently tagged ligands. In this study, histamine H4 receptor transfected Chinese hamster ovary cells and murine bone marrow-derived mast cells (mBMMCs) were selected for studying the possibility of staining individual histamine receptors using BODIPY(®) FL histamine and selective antagonists. Flow cytometric measurements and supporting calculations showed that BODIPY FL histamine is suitable tool for quantitating cell surface histamine receptors. The binding, and competitive inhibition of this fluorescent ligand were characterized, which were in good agreement with a semi-empirical model constructed from fundamental protein-binding relationships. Using this method it was shown for the first time that even though mature mBMMCs express H2R and H4R to the same extent, immunoglobulin E sensitization results in H4R upregulation only, while the surface expression of H2R remains unchanged.


Subject(s)
Bone Marrow Cells/metabolism , Boron Compounds , Flow Cytometry/methods , Fluorescent Dyes , Mast Cells/metabolism , Receptors, G-Protein-Coupled/analysis , Receptors, Histamine/analysis , Animals , Binding, Competitive , Bone Marrow Cells/cytology , Bone Marrow Cells/drug effects , Boron Compounds/chemistry , CHO Cells , Cricetulus , Fluorescent Dyes/chemistry , Gene Expression , Histamine/chemistry , Histamine/metabolism , Humans , Immunoglobulin E/pharmacology , Male , Mast Cells/cytology , Mast Cells/drug effects , Mice , Mice, Inbred BALB C , Primary Cell Culture , Protein Binding , Receptors, G-Protein-Coupled/genetics , Receptors, G-Protein-Coupled/metabolism , Receptors, Histamine/genetics , Receptors, Histamine/metabolism , Receptors, Histamine H2/analysis , Receptors, Histamine H2/genetics , Receptors, Histamine H2/metabolism , Receptors, Histamine H4 , Transfection
3.
Inflamm Res ; 56(8): 339-44, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17687518

ABSTRACT

OBJECTIVES: Histamine is a known inducer of cAMP-responsive element binding protein (CREB), which plays a key role in initiation of adipogenesis. Our present goal was to study how histamine deficiency impacts CREB signalling and adipogenesis. METHODS: We used a histidine-decarboxylase gene-targeted (HDC KO) mice model lacking endogenous histamine. We measured CREB activity and expression by EMSA, Western blot and real-time RT-PCR, as well as cAMP levels by ELISA in primary embryonic fibroblasts derived from WT and HDC KO mice. The ability of these cells to form adipocytes was also tested in preliminary experiments. RESULTS: We found that in the absence of the histamine, cells show higher constitutive CREB activity and greatly increased intracellular cAMP levels, as well as that in contrast to WT cells, HDC KO fibroblasts are more prone to differentiate into adipocytes. CONCLUSION: These data suggest a newly recognised inhibitory role for histamine in CREB activity and draws attention to the potential role of histamine in adipocyte differentiation.


Subject(s)
Adipogenesis , Cyclic AMP Response Element-Binding Protein/metabolism , Histamine/physiology , Adipocytes/cytology , Animals , Blotting, Western , Cell Differentiation , Cell Nucleus/metabolism , Cyclic AMP/biosynthesis , Fibroblasts/cytology , Histamine H1 Antagonists/analysis , Histidine Decarboxylase/physiology , Mice , Phosphorylation , Receptors, Histamine H2/analysis
4.
Eur J Pharmacol ; 546(1-3): 161-70, 2006 Sep 28.
Article in English | MEDLINE | ID: mdl-16919622

ABSTRACT

The aim of the present study was to investigate the effect of histamine, a product of e.g. mast cells, on short-circuit current (I(sc)) across rat distal colon. Histamine concentration-dependently stimulated an increase in I(sc), which often was preceded by a transient negative current. Neither a release of neurotransmitters nor a release of prostaglandins contributed to the histamine response. The histamine-induced increase in I(sc) was blocked by the histamine H(1) antagonist, pyrilamine, but was resistant against the histamine H(2) antagonist, cimetidine. Conversely, the histamine H(1) agonist, TMPH (2-(3-trifluoromethylphenyl)histamine), exclusively evoked an increase in I(sc), whereas the histamine H(2) agonist, amthamine, evoked only a decrease in I(sc) suggesting that stimulation of different types of histamine receptors is responsible for the two phases of the response evoked by native histamine. Histamine induces the opening of glibenclamide-sensitive Cl(-) channels and of charybdotoxin-sensitive K(+) channels in the apical membrane as demonstrated by experiments at basolaterally depolarized epithelia. A further action site is the basolateral membrane, because histamine stimulates a charybdotoxin- and tetrapentylammonium-sensitive K(+) conductance in this membrane as observed in tissues, in which the apical membrane was permeabilized with an ionophore, nystatin. The increase in I(sc) evoked by histamine was blocked after depletion of intracellular Ca(2+) stores with cyclopiazonic acid and after blockade of inositol 1,4,5-trisphosphate (IP(3)) receptors, suggesting a release of stored Ca(2+). This was confirmed by the observation that the histamine H(1) agonist TMPH induced an increase in the fura-2 ratio signal of epithelial cells within isolated colonic crypts. Consequently, the mediator histamine seems to stimulate both histamine H(1) and H(2) receptors, from which the former seems to be prominently involved in the induction of epithelial chloride secretion.


Subject(s)
Chlorides/metabolism , Colon/drug effects , Histamine/pharmacology , Potassium/metabolism , Receptors, Histamine H1/drug effects , Receptors, Histamine H2/drug effects , Animals , Calcium/metabolism , Calcium Channel Blockers/pharmacology , Calcium Signaling/drug effects , Colon/chemistry , Colon/metabolism , Cyclic AMP/metabolism , Cystic Fibrosis Transmembrane Conductance Regulator/drug effects , Cystic Fibrosis Transmembrane Conductance Regulator/metabolism , Dose-Response Relationship, Drug , Histamine Agonists/pharmacology , Histamine Antagonists/pharmacology , In Vitro Techniques , Intestinal Mucosa/chemistry , Intestinal Mucosa/drug effects , Intestinal Mucosa/metabolism , Membrane Potentials/drug effects , Potassium Channel Blockers/pharmacology , Potassium Channels, Calcium-Activated/drug effects , Potassium Channels, Calcium-Activated/metabolism , Rats , Rats, Wistar , Receptors, Histamine H1/analysis , Receptors, Histamine H2/analysis , Ryanodine Receptor Calcium Release Channel/drug effects , Ryanodine Receptor Calcium Release Channel/metabolism
6.
Gut ; 55(4): 498-504, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16299042

ABSTRACT

BACKGROUND AND AIMS: Histamine is known as a regulator of gastrointestinal functions, such as gastric acid production, intestinal motility, and mucosal ion secretion. Most of this knowledge has been obtained from animal studies. In contrast, in humans, expression and distribution of histamine receptors (HR) within the human gastrointestinal tract are unclear. METHODS: We analysed HR expression in human gastrointestinal tissue specimens by quantitative reverse transcription-polymerase chain reaction and immunostaining. RESULTS: We found that H1R, H2R, and H4R mRNA were expressed throughout the gastrointestinal tract, while H3R mRNA was absent. No significant differences in the distribution of HR were found between different anatomical sites (duodenum, ileum, colon, sigma, and rectum). Immunostaining of neurones and nerve fibres revealed that H3R was absent in the human enteric nervous system; however, H1R and H2R were found on ganglion cells of the myenteric plexus. Epithelial cells also expressed H1R, H2R and, to some extent, H4R. Intestinal fibroblasts exclusively expressed H1R while the muscular layers of human intestine stained positive for both H1R and H2R. Immune cells expressed mRNA and protein for H1R, H2R, and low levels of H4R. Analysis of endoscopic biopsies from patients with food allergy and irritable bowel syndrome revealed significantly elevated H1R and H2R mRNA levels compared with controls. CONCLUSIONS: We have demonstrated that H1R, H2R and, to some extent, H4R, are expressed in the human gastrointestinal tract, while H3R is absent, and we found that HR expression was altered in patients with gastrointestinal diseases.


Subject(s)
Intestines/chemistry , Receptors, Histamine/analysis , Cells, Cultured , Fluorescent Antibody Technique/methods , Food Hypersensitivity/metabolism , Humans , Immunohistochemistry/methods , Intestinal Mucosa/chemistry , Intestines/innervation , Irritable Bowel Syndrome/metabolism , Mast Cells/immunology , RNA, Messenger/analysis , Receptors, G-Protein-Coupled/analysis , Receptors, Histamine H1/analysis , Receptors, Histamine H2/analysis , Receptors, Histamine H3/analysis , Receptors, Histamine H4
7.
Laryngoscope ; 114(12): 2249-51, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15564855

ABSTRACT

OBJECTIVE: Histamine may have physiologic functions in the inner ear. The locations of histamine receptors, however, have not yet been identified in the mammalian cochlea. The aim of this study was to investigate the localization of histamine receptor subtypes (H1, H2, and H3 receptors) in rat cochlea. METHODS: Immunohistochemistry was performed with antibodies specific for each of the histamine receptors (H1, H2, and H3). To identify the type I and II spiral ganglion cells in the cochlea, some cryostat sections were double stained with antibodies to both a histamine receptor and neurofilament 200 kD, which predominantly stains type II spiral ganglion cells in the cochlea. RESULTS: All H1, H2, and H3 receptor immunoreactive staining was limited to the spiral ganglion cells of the cochlea. Spiral ganglion cells with positive immunoreactivity to the neurofilament 200 kD antibody were stained only slightly by histamine H1, H2, and H3 receptor antibodies, indicating that histamine receptor immunoreactivity is specific to type I ganglion cells. CONCLUSIONS: These findings indicate that histamine receptors are present in the cochlea and support the hypothesis that histamine plays a physiologic role in the cochlea.


Subject(s)
Cochlea/anatomy & histology , Cochlea/ultrastructure , Receptors, Histamine/analysis , Animals , Female , Immunohistochemistry , Microscopy, Confocal , Models, Animal , Rats , Rats, Wistar , Receptors, Histamine H1/analysis , Receptors, Histamine H2/analysis , Receptors, Histamine H3/analysis , Sensitivity and Specificity
8.
Curr Allergy Asthma Rep ; 3(3): 227-31, 2003 May.
Article in English | MEDLINE | ID: mdl-12662472

ABSTRACT

Histamine and antihistamines are so deeply woven into the fabric of allergic diseases that it is sometimes difficult to see how this field could advance beyond our current, potent histamine H1-receptor drugs. Investigations of other actions of histamine and the identification of H2, H3, and now H4 receptors have suddenly reignited the search for new mono- and multi-receptor-specific agonists and antagonists. There is great excitement due to preliminary findings that H3 receptors act as neural inhibitory autoreceptors, and H4 receptors might modulate immune cell functions.


Subject(s)
Receptors, G-Protein-Coupled , Receptors, Histamine/physiology , Animals , Humans , Receptors, Histamine/analysis , Receptors, Histamine/genetics , Receptors, Histamine H1/analysis , Receptors, Histamine H1/genetics , Receptors, Histamine H1/physiology , Receptors, Histamine H2/analysis , Receptors, Histamine H2/genetics , Receptors, Histamine H2/physiology , Receptors, Histamine H3/analysis , Receptors, Histamine H3/genetics , Receptors, Histamine H3/physiology , Receptors, Histamine H4
9.
J Invest Dermatol ; 121(5): 1073-9, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14708609

ABSTRACT

Human monocyte-derived dendritic cells (MoDC) have both histamine H1 and H2 receptors and can induce CD86 expression by histamine. Nevertheless, it has not been reported whether human epidermal Langerhans cells (LC) have histamine receptors or not. In this study, using RT-PCR, we investigated the expression of H1 and H2 receptor mRNA on DC with the features of LC (LC-like DC) that were generated in vitro from peripheral blood monocytes, LC derived from CD34+ hematopoietic progenitor cells, and LC obtained from human epidermis. We compared the histamine-induced CD86 expression among these cells. In contrast to MoDC, LC and LC-like DC did not express H1 or H2 receptors. In addition, they could not augment the CD86 expression by histamine. Interestingly, when transforming growth factor-beta1 (TGF-beta1) was added to the culture of MoDC, the expression of H1 and H2 receptors and the histamine-induced CD86 expression were abrogated in a concentration-dependent fashion. Finally, in the assessment of the cell surface expression of histamine receptors using fluorescence-labeled histamine, histamine could bind to MoDC and dermal dendritic cells obtained from the skin, whereas there was no specific binding of histamine to LC-like DC or LC obtained from the skin. These data suggest that LC do not express either H1 or H2 receptors, mainly because of the effect of TGF-beta1. This made a striking contrast with the expression of the functional H1 and H2 receptors on MoDC and dermal dendritic cells.


Subject(s)
Dendritic Cells/chemistry , Langerhans Cells/chemistry , Receptors, Histamine H1/analysis , Receptors, Histamine H2/analysis , Skin/chemistry , Cells, Cultured , Histamine/metabolism , Humans , RNA, Messenger/analysis , Receptors, Histamine H1/genetics , Receptors, Histamine H2/genetics , Transforming Growth Factor beta/physiology , Transforming Growth Factor beta1
10.
Synapse ; 38(3): 343-54, 2000 Dec 01.
Article in English | MEDLINE | ID: mdl-11020238

ABSTRACT

The distribution of histamine H(2) receptor mRNA was determined by in situ hybridization histochemistry in human and monkey brain. In the case of monkey brain, we combined this technique with receptor ligand autoradiography to compare the distribution of mRNA and receptor binding sites. [(125)I]Iodoaminopotentidine ([(125)I]-APT), a reversible, high specific activity antagonist with high affinity and selectivity for the H(2) receptor, was used for receptor autoradiography. Radiolabeled oligonucleotides derived from the human mRNA sequence encoding this receptor were used as hybridization probes. The highest density of the H(2) receptor mRNA in human and monkey brain was found in caudate and putamen nuclei and external layers of cerebral cortex. Moderate levels were seen in the hippocampal formation and lower densities in the dentate nucleus of cerebellum. Areas such as globus pallidus, amygdaloid complex, cerebellar cortex, and substantia nigra were devoid of hybridization signal. The distribution of H(2) receptor mRNA in monkey brain is generally in good agreement with that of the corresponding binding sites: prominent in caudate, putamen, accumbens nuclei, and cortical areas. The hippocampus showed lower densities of receptors and low levels were detected in the globus pallidus pars lateralis. No binding sites were seen in amygdaloid complex and substantia nigra. The distribution of histaminergic innervation is in good correlation with the areas of high density for H(2) receptors: caudate, putamen, and external layers of cerebral cortex in monkey and human brain. The presence of mRNA in caudate and putamen nuclei, together with its absence from substantia nigra, suggests that the H(2) receptors found in the striatum are synthesized by intrinsic cells and not by nigral dopaminergic cells. These striatal H(2) receptors may be located on short circuit striatal interneurons or somatodendritically on striatal projection neurons which project to the globus pallidus pars lateralis. In conclusion, the present results, which constitute, to our knowledge, the first report of the regional distribution of mRNA encoding H(2) receptors detected by in situ hybridization, define the sites of synthesis of H(2) receptors and are the basis for future, more detailed studies that should result in a better understanding of H(2) receptor function.


Subject(s)
Brain Chemistry , Neurons/chemistry , RNA, Messenger/analysis , Receptors, Histamine H2/analysis , Adult , Aged , Aged, 80 and over , Animals , Female , Humans , In Situ Hybridization , Macaca fascicularis , Male , Middle Aged
12.
Acta Otolaryngol ; 119(5): 588-91, 1999.
Article in English | MEDLINE | ID: mdl-10478601

ABSTRACT

mRNA encoding histamine H1 and H2 receptors were detected in the human nasal mucosa using reverse transcriptase-polymerase chain reaction. The possibility of local release in connection with specific target receptors suggests a role for histamine in the regulation of vascular tone, glandular secretion and epithelial functions.


Subject(s)
Nasal Mucosa/metabolism , Receptors, Histamine H1/analysis , Receptors, Histamine H2/analysis , Adult , DNA Primers , DNA, Complementary , Electrophoresis, Agar Gel , Epithelium/physiology , Gene Expression Regulation , Histamine/physiology , Humans , Nasal Mucosa/blood supply , Polymerase Chain Reaction , RNA, Messenger/analysis , RNA, Ribosomal, 28S/analysis , RNA-Directed DNA Polymerase , Receptors, Histamine H1/genetics , Receptors, Histamine H2/genetics , Rhinitis/metabolism , Rhinitis/pathology , Sequence Analysis, DNA , Vasomotor System/physiology
13.
Diabetes ; 47(1): 104-12, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9421382

ABSTRACT

[Ca2+]i and whole-cell membrane current were measured in microvascular endothelial cells from bovine brain. The effects of histamine on [Ca2+]i were examined, and the acute effect of changing extracellular glucose concentration on Ca2+ homeostasis was investigated. Application of 10 micromol/l histamine evoked an initially transient and then sustained increase in [Ca2+]i in normal Krebs solution, but only the transient component in Ca2+-free solution, thereby indicating that histamine mobilizes Ca2+ both from intracellular store sites and extracellular space. The effects of histamine on [Ca2+]i were inhibited by the H2 antagonists, ranitidine and cimetidine, but not by the H1 antagonist, pyrilamine. Incubation of the cells for 2 h in solutions containing low (1.1 and 2.3 mmol/l) or high (23 mmol/l) concentrations of glucose did not influence the resting level of [Ca2+]i. Treatment with low concentrations of glucose did not impair histamine-induced Ca2+ mobilization. On the other hand, when histamine was applied to the cells pretreated with 23 mmol/l glucose, it failed to mobilize Ca2+ from both intracellular store sites and extracellular space. The effect of histamine was mimicked by dibutyryl cyclic AMP, but glucose overload failed to inhibit this, suggesting that glucose overload inhibits H2 receptor-mediated cyclic AMP production. Glucose overload-induced impairment of histamine action was reversed by pretreatment with staurosporine and calphostin C and mimicked by phorbol-12,13-dibutyrate, thereby suggesting the involvement of protein kinase C in the high glucose-induced inhibition of Ca2+ mobilization. Whole-cell membrane current measurement showed that there was no difference in the membrane currents between control and high glucose-treated cells. These results indicate that in bovine brain microvascular endothelial cells, histamine induces Ca2+ release from intracellular store sites and subsequent entry from the extracellular space through the activation of H2 receptors. Glucose overload acutely inhibits histamine-induced Ca2+ mobilization by the activation of protein kinase C.


Subject(s)
Brain/blood supply , Calcium/metabolism , Endothelium, Vascular/metabolism , Glucose/pharmacology , Receptors, Histamine H2/physiology , Animals , Bradykinin/pharmacology , Bucladesine/pharmacology , Cattle , Cells, Cultured , Cimetidine/pharmacology , Cyclic AMP/pharmacology , Dose-Response Relationship, Drug , Endothelium, Vascular/chemistry , Endothelium, Vascular/cytology , Histamine/pharmacology , Histamine Antagonists/pharmacology , Homeostasis , Microcirculation , Neomycin/pharmacology , Neurotransmitter Agents/pharmacology , Protein Kinase C/physiology , Pyrilamine/pharmacology , Ranitidine/pharmacology , Receptors, Histamine H2/analysis , Staurosporine/pharmacology
14.
Biochem Biophys Res Commun ; 214(3): 1138-45, 1995 Sep 25.
Article in English | MEDLINE | ID: mdl-7575521

ABSTRACT

Histamine H2 receptors were tagged at the N-terminus with the eight amino acid Flag epitope to allow the immunological identification of the receptor peptide with the monoclonal anti-Flag M2 antibody. The introduction of the epitope did not modify the binding of several H2 ligands to the H2 receptor, nor the ability of histamine to stimulate the H2 receptor mediated cAMP production in HEK-293 cells. Western blots revealed a major protein band of 57 +/- 1 kDa, whereas a second band of 31 +/- 1 kDa was probably the result of a proteolytic breakdown of the 57 kDa band. Immunofluorescence measurements of stably transfected HEK-293 cells revealed the presence of anti-Flag-immunoreactivity in the plasma membrane. This immunoreactivity completely disappeared after a one hour treatment with histamine. The receptor internalization was reversible and blocked by the endocytosis inhibitor phenylarsine oxide. Forskolin did not induce H2 receptor internalization, indicating that histamine causes H2 receptor internalization via a cAMP-independent pathway.


Subject(s)
Histamine Agonists/pharmacology , Histamine/pharmacology , Receptors, Histamine H2/metabolism , Amino Acid Sequence , Animals , Base Sequence , Blotting, Western , Cell Line , DNA Primers , Epitopes/analysis , Fluorescent Antibody Technique , Humans , Kidney , Kinetics , Molecular Sequence Data , Polymerase Chain Reaction , Radioligand Assay , Rats , Receptors, Histamine H2/analysis , Receptors, Histamine H2/immunology , Recombinant Proteins/analysis , Recombinant Proteins/immunology , Recombinant Proteins/metabolism , Transfection
15.
Vestn Otorinolaringol ; (3): 35-9, 1995.
Article in Russian | MEDLINE | ID: mdl-7631468

ABSTRACT

Classic physiological and pharmacological experiments were made on 33 rabbits under hexenal anesthesia to determine the presence, topical concentration and activity of H2 and B2-receptors. These parameters were inferred by edema and other vascular responses of the mucosa to local application of histamine and bradykinin prior to and after usage of specific blocker of each receptor type. Both mediators and receptor blockers were applied to laryngeal and tracheal mucosa for 10 min (histamine 10(-4) and 10(-3) g/ml, H2-receptor blocker metiamide 0.1 and 1 mmol, bradykinin 10(-5) and 10(-4) g/ml, B2-receptor blocker pyridinolcarbamate 10(-2) and 10(-1) g/ml). The larynx and trachea were found to contain H2- and B2-receptors the concentrations of which were greater in the subvocal part of the larynx than in the vestibular part and trachea. B2-receptor activity and concentrations in the subvocal part of the larynx were 10 times while in the trachea 1.5-2 times greater than those of H2-receptors. These regularities were not influenced by individual varieties of receptor topical concentrations. The blocker density in the receptors and the duration of their binding were not universally proportional. This is also true for the relations mediator-receptor. Concentrations and activity of H2- and B2-receptors are thought important in pathogenesis and location of acute inflammatory and allergic conditions in the upper respiratory tract.


Subject(s)
Larynx/metabolism , Receptors, Bradykinin/analysis , Receptors, Histamine H2/analysis , Trachea/metabolism , Animals , Bradykinin/pharmacology , Bradykinin Receptor Antagonists , Histamine/pharmacology , Histamine Antagonists/pharmacology , In Vitro Techniques , Larynx/drug effects , Larynx/physiology , Metiamide/pharmacology , Mucous Membrane/drug effects , Mucous Membrane/metabolism , Pyridinolcarbamate/pharmacology , Rabbits , Receptors, Bradykinin/physiology , Receptors, Histamine H2/physiology , Trachea/drug effects , Trachea/physiology
19.
J Leukoc Biol ; 55(3): 392-7, 1994 Mar.
Article in English | MEDLINE | ID: mdl-8120456

ABSTRACT

We investigated effects of the biogenic diamine histamine on antibody-dependent cellular cytotoxicity (ADCC) against autologous anti-D-coated red blood cells mediated by human granulocytes, monocytes, and natural killer (NK) cells. Effector cells were separated from peripheral blood by countercurrent centrifugal elutriation. ADCC of monocytes and neutrophilic granulocytes was suppressed by histamine. ADCC of enriched CD3-/56+ NK cells was unchanged by histamine. ADCC of NK cells was effectively inhibited by elutriated monocytes or neutrophils. Histamine completely reversed the inhibition of NK cell-mediated ADCC induced by monocytes and partly reversed the inhibition induced by neutrophils; thereby, histamine augmented ADCC of NK cells in the presence of monocytes or neutrophils. The indirect effect of histamine on ADCC of NK cells and the effect of histamine on ADCC of monocytes/neutrophils were completely antagonized by the specific H2 receptor (H2R) blocker ranitidine. We conclude that activation of H2R suppresses ADCC reactivity of monocytes/neutrophils and, concomitantly, promotes ADCC reactivity of NK cells by abrogating a phagocyte-derived, suppressive signal.


Subject(s)
Antibody-Dependent Cell Cytotoxicity/physiology , Granulocytes/cytology , Granulocytes/physiology , Histamine/physiology , Killer Cells, Natural/cytology , Killer Cells, Natural/physiology , Monocytes/cytology , Monocytes/physiology , Cell Communication , Cells, Cultured , Flow Cytometry , Granulocytes/ultrastructure , Humans , Killer Cells, Natural/ultrastructure , Monocytes/ultrastructure , Ranitidine/pharmacology , Receptors, Histamine H2/analysis , Receptors, Histamine H2/drug effects , Receptors, Histamine H2/physiology
20.
Biochem Biophys Res Commun ; 198(3): 1195-202, 1994 Feb 15.
Article in English | MEDLINE | ID: mdl-8117277

ABSTRACT

In contrast with many physiological studies suggesting that histamine H2 receptors are present on acid-secreting parietal cells of the gastric epithelium, it was recently shown that immune cells in the lamina propria are the only cells expressing H2-receptor mRNAs (Mezey and Palkovits, Science, 1992, 258, 1662-1665). We have reinvestigated the cellular localization of H2 receptors in the rat stomach by visualizing both the H2 receptor mRNA and the H2-receptor protein itself. In situ hybridization histochemistry performed with an antisense riboprobe for the rat H2 receptor, and autoradiographic distribution of 125I-aminopotentidine binding sites, a highly selective H2-receptor ligand, did not show any labeling of the lamina propria. Signals were clearly and solely detected in the gastric epithelium, the strongest being observed in the upper part of the glands where the H2 receptor gene transcripts were only detected within parietal cells. In situ hybridization performed with an antisense riboprobe for L-histidine decarboxylase mRNA confirmed the basal localization of the histamine-synthetizing cells in the rat gastric gland, at some distance from parietal histamine-sensitive cells.


Subject(s)
Gastric Mucosa/metabolism , Parietal Cells, Gastric/metabolism , RNA, Messenger/biosynthesis , Receptors, Histamine H2/analysis , Receptors, Histamine H2/biosynthesis , Animals , Autoradiography , Epithelial Cells , Epithelium/metabolism , Gene Expression , Guanidines/metabolism , Guinea Pigs , Histidine Decarboxylase/analysis , Histidine Decarboxylase/biosynthesis , In Situ Hybridization , Iodine Radioisotopes , Male , Parietal Cells, Gastric/cytology , RNA, Messenger/analysis , Rats , Rats, Wistar , Receptors, Histamine H2/metabolism , Stomach/cytology , Transcription, Genetic
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