Abstract
Expression of heat shock proteins (hsp) is a homeostatic mechanism induced in both prokaryotic and eukaryotic cells in response to metabolic and environmental insults. A growing body of evidence suggests that in mammals, the hsp response is integrated with physiological responses through neuroendocrine signaling. In the present study, we have examined the effect of noradrenaline (NA) on the hsp70 response in mollusc immune cells. Oyster and abalone hemocytes transfected with a gene construct containing a gastropod hsp70 gene promoter linked to the luciferase reporter-gene were exposed to physiological concentrations of NA, or to various alpha- and beta-adrenoceptor agonists and antagonists. Results show that NA and alpha-adrenergic stimulations induced the expression of luciferase in transfected mollusc immunocytes. Furthermore, exposure of hemocytes to NA or to the alpha-adrenoceptor agonist phenylephrine (PE) resulted in the expression of the inducible isoform of the hsp70 protein. Pertussis toxin (PTX), the phospholipase C (PLC) inhibitor U73122, the protein kinase C (PKC) inhibitor calphostin C, the Ca(2+)-dependent PKC inhibitor Gö 6976 and the phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor LY294002 blocked the PE-mediated induction of the hsp70 gene promoter. These results suggest that alpha-adrenergic signaling induces the transcriptionnal upregulation of hsp70 in mollusc hemocytes through a PTX-sensitive G-protein, PLC, Ca(2+)-dependent PKC and PI 3-kinase. Thus, a functional link exists between neuroendocrine signaling and the hsp70 response in mollusc immune cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adrenergic alpha-Agonists / pharmacology*
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Adrenergic alpha-Antagonists / pharmacology
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Adrenergic beta-Agonists / pharmacology
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Adrenergic beta-Antagonists / pharmacology
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Animals
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Carbazoles / pharmacology
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Chromones / pharmacology
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Enzyme Inhibitors / pharmacology
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Estrenes / pharmacology
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Flavonoids / pharmacology
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Gene Expression Regulation / physiology
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HSP70 Heat-Shock Proteins / genetics*
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Hemocytes / cytology
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Hemocytes / immunology*
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Indoles / pharmacology
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Isoproterenol / pharmacology
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Isoquinolines / pharmacology
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Luciferases / genetics
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Morpholines / pharmacology
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Naphthalenes / pharmacology
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Norepinephrine / pharmacology*
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Ostreidae
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Pertussis Toxin
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Phenylephrine / pharmacology
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Phosphodiesterase Inhibitors / pharmacology
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Prazosin / pharmacology
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Promoter Regions, Genetic / genetics*
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Propranolol / pharmacology
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Pyrrolidinones / pharmacology
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Signal Transduction / drug effects
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Signal Transduction / immunology
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Sulfonamides*
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Transfection
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Virulence Factors, Bordetella / pharmacology
Substances
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Adrenergic alpha-Agonists
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Adrenergic alpha-Antagonists
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Adrenergic beta-Agonists
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Adrenergic beta-Antagonists
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Carbazoles
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Chromones
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Enzyme Inhibitors
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Estrenes
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Flavonoids
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HSP70 Heat-Shock Proteins
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Indoles
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Isoquinolines
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Morpholines
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Naphthalenes
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Phosphodiesterase Inhibitors
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Pyrrolidinones
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Sulfonamides
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Virulence Factors, Bordetella
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1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione
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Go 6976
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Phenylephrine
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2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
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Propranolol
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Luciferases
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Pertussis Toxin
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calphostin C
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Isoproterenol
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N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide
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2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one
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Norepinephrine
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Prazosin