Abstract
Stimulation of mas-oncogene transfected 401L-C3 cells by angiotensins leads to the production of inositol phosphates. This response shows dose dependence, and has an apparent rank order of potency angiotensin III greater than or equal to angiotensin II much greater than angiotensin I. Preincubation with 12-O-tetradecanoylphorbol 13-acetate, for 5 min, significantly diminishes both inositol phosphate and intracellular [Ca2+] responses to angiotensins, without affecting those stimulated by the endogenous bradykinin receptor. Incubation of 401L-C3 cells with either phorbol ester or angiotensins leads to elevation of intracellular pH, implying that mas/angiotensin receptor stimulation itself leads to protein kinase C activation. These results suggest the operation of a negative feedback loop specific for the mas/angiotensin receptor signalling pathway, and which may be essential in defining the final biological output response to this receptor stimulation.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Angiotensin I / pharmacology
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Angiotensin II / pharmacology
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Angiotensin III / pharmacology
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Angiotensins / pharmacology*
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Bradykinin / pharmacology
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Calcium / metabolism*
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Cell Line
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Enzyme Activation
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Hydrogen-Ion Concentration
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Inositol Phosphates / metabolism*
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Neoplasm Proteins / genetics*
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Neoplasm Proteins / physiology
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Neurons / drug effects
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Neurons / metabolism*
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Protein Kinase C / metabolism
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Proto-Oncogene Mas
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Proto-Oncogene Proteins / genetics*
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Proto-Oncogene Proteins / physiology
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Proto-Oncogenes*
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Receptors, Angiotensin / physiology*
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Receptors, G-Protein-Coupled
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Spectrometry, Fluorescence
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Sugar Phosphates / metabolism*
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Tetradecanoylphorbol Acetate / pharmacology*
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Transfection
Substances
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Angiotensins
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Inositol Phosphates
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Neoplasm Proteins
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Proto-Oncogene Mas
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Proto-Oncogene Proteins
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Receptors, Angiotensin
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Receptors, G-Protein-Coupled
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Sugar Phosphates
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Angiotensin II
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Angiotensin III
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Angiotensin I
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Protein Kinase C
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Tetradecanoylphorbol Acetate
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Bradykinin
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Calcium