Back to Search
Start Over
Ca 2+ -dependent down-regulation of human histamine H 1 receptors in Chinese hamster ovary cells.
- Source :
-
Journal of neurochemistry [J Neurochem] 2018 Jan; Vol. 144 (1), pp. 68-80. Date of Electronic Publication: 2017 Nov 21. - Publication Year :
- 2018
-
Abstract
- G <subscript>q/11</subscript> protein-coupled human histamine H <subscript>1</subscript> receptors in Chinese hamster ovary cells stimulated with histamine undergo clathrin-dependent endocytosis followed by proteasome/lysosome-mediated down-regulation. In this study, we evaluated the effects of a sustained increase in intracellular Ca <superscript>2+</superscript> concentrations induced by a receptor-bypassed stimulation with ionomycin, a Ca <superscript>2+</superscript> ionophore, on the endocytosis and down-regulation of H <subscript>1</subscript> receptors in Chinese hamster ovary cells. All cellular and cell-surface H <subscript>1</subscript> receptors were detected by the binding of [ <superscript>3</superscript> H]mepyramine to intact cells sensitive to the hydrophobic and hydrophilic H <subscript>1</subscript> receptor ligands, mepyramine and pirdonium, respectively. The pretreatment of cells with ionomycin markedly reduced the mepyramine- and pirdonium-sensitive binding sites of [ <superscript>3</superscript> H]mepyramine, which were completely abrogated by the deprivation of extracellular Ca <superscript>2+</superscript> and partially by a ubiquitin-activating enzyme inhibitor (UBEI-41), but were not affected by inhibitors of calmodulin (W-7 or calmidazolium) and protein kinase C (chelerythrine or GF109203X). These ionomycin-induced changes were also not affected by inhibitors of receptor endocytosis via clathrin (hypertonic sucrose) and caveolae/lipid rafts (filipin or nystatin) or by inhibitors of lysosomes (E-64, leupeptin, chloroquine, or NH <subscript>4</subscript> Cl), proteasomes (lactacystin or MG-132), and a Ca <superscript>2+</superscript> -dependent non-lysosomal cysteine protease (calpain) (MDL28170). Since H <subscript>1</subscript> receptors were normally detected by confocal immunofluorescence microscopy with an antibody against H <subscript>1</subscript> receptors, even after the ionomycin treatment, H <subscript>1</subscript> receptors appeared to exist in a form to which [ <superscript>3</superscript> H]mepyramine was unable to bind. These results suggest that H <subscript>1</subscript> receptors are apparently down-regulated by a sustained increase in intracellular Ca <superscript>2+</superscript> concentrations with no process of endocytosis and lysosomal/proteasomal degradation of receptors.<br /> (© 2017 International Society for Neurochemistry.)
- Subjects :
- Animals
Astrocytoma
CHO Cells
Calcium Ionophores pharmacology
Calcium Signaling drug effects
Calmodulin antagonists & inhibitors
Calpain antagonists & inhibitors
Cell Line, Tumor
Cricetinae
Cricetulus
Down-Regulation drug effects
Endocytosis drug effects
Histamine pharmacology
Humans
Inositol Phosphates metabolism
Ionomycin pharmacology
Lysosomes drug effects
Membrane Microdomains drug effects
Proteasome Endopeptidase Complex drug effects
Protein Kinase Inhibitors pharmacology
Pyrilamine metabolism
Receptors, Histamine H1 genetics
Recombinant Proteins biosynthesis
Calcium pharmacology
Calcium Signaling physiology
Receptors, Histamine H1 biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1471-4159
- Volume :
- 144
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of neurochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29063596
- Full Text :
- https://doi.org/10.1111/jnc.14245