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MODULATION OF INTERFERON γ INDUCED INCREASES IN CATHEPSIN B IN THP‐1 CELLS BY ADRENERGIC AGONISTS AND ANTAGONISTS
Author(s) -
LI QINGDI,
BEVER CHRISTOPHER T.
Publication year - 1998
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1006/cbir.1997.0209
Subject(s) - endocrinology , medicine , phentolamine , receptor , agonist , phorbol , antagonist , receptor antagonist , biology , chemistry , protein kinase c , propranolol , signal transduction , microbiology and biotechnology
In order to investigate the possible modulation of macrophage function by the autonomic nervous system, the effect of adrenergic agonists and antagonists on interferon (IFN)‐γ‐induced increases in cathepsin B (CB) in a macrophage‐like cell line was studied. It has been shown previously that IFN‐γ induces increased CB activity in phorbol myristate acetate (PMA)‐primed THP‐1 cells. Isoproterenol (ISO) (10μ m ), a mixed β‐receptor agonist, increased the induction of CB activity in the cells but norepinephrine (10μ m ) and epinephrine (10μ m ), the α and β receptor agonists, had little effect. The addition of the mixed α‐receptor antagonist phentolamine (10μ m ) had no effect on ISO induced increases but the mixed β‐receptor antagonist propranolol (10μ m ) and the selective β 1 ‐receptor antagonist atenolol produced significant inhibition. These results suggest that the activation of β‐receptors could be involved in the induction of CB activity in macrophages and provide a possible mechanism for the regulation of macrophage effector function by the autonomic nervous system. Dibutyryl cAMP (1m m ) alone also induced increases in CB in THP‐1 cells, and H‐89 or HA1004 abrogated the effect of dibutyryl cAMP, suggesting that the effect of ISO on CB could be through the elevation of cAMP and the activation of cAMP‐dependent protein kinases.