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s-Subunit of the Gs Protein with Microfilaments and Microtubules: Implication during Adrenocorticotropin Stimulation in Rat Adrenal Glomerulosa Cells1
Service of Endocrinology, Departments of Medicine (M.C., N.G.-P.), Anatomy and Cell Biology (M.C., N.G.-P.), and Physiology and Biophysics (M.D.P.), Faculty of Medicine, University of Sherbrooke, Sherbrooke, Quebec, Canada J1H 5N4
Address all correspondence and requests for reprints to: Dr. Nicole Gallo-Payet, Service of Endocrinology, Department of Medicine, Faculty of Medicine, University of Sherbrooke, 3001 12th Avenue North, Sherbrooke, Quebec, Canada J1H 5N4. E-mail: n.gallo{at}courrier.usherb.ca
The aim of the present study was to investigate if and how
microfilaments and microtubules could be involved in the early events
of ACTH action. In primary cultures of rat glomerulosa cells, a 30-min
preincubation with either 10 µM colchicine (a
microtubule-disrupting agent) or 10 µM cytochalasin
B (a microfilament-disrupting agent) decreased ACTH-induced cAMP
production. Moreover, colchicine decreased cAMP production induced by
fluoroaluminate (a nonspecific activator of all G proteins), but not of
forskolin (which directly activates adenylyl cyclase). These results
indicate that microtubules appear to be essential for the
Gs protein activation. In contrast, cytochalasin B
decreased the stimulating effect of both fluoroaluminate and forskolin,
indicating that microfilaments may be involved in both Gs
and adenylyl cyclase activations. Analyses of microfilament- and
microtubule-enriched fractions and immunoprecipitation of actin and
tubulin indicated that the
s-subunit of the
Gs protein was associated with both structures. Stimulation
of cells with ACTH induced a rapid increase (within 1 min) in the
levels of microfilaments, microtubules, and
s associated
with the membrane. In addition, ACTH stimulation of cAMP production was
very sensitive to Ca2+, without any stimulation in
Ca2+-free medium. Under these conditions, actin filaments
were short and formed a dense network. These observations suggest that
the Ca2+-free medium stabilized the actin fibers in such a
way that activation by ACTH failed, further documenting the importance
of microfilaments in cAMP production.
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