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ARTICLES |
Department of Internal Medicine III, University of Leipzig (A.H., S.R.B., A.G., K.U., M.E.-B.), 04103 Leipzig; and Research Institute of Molecular Pharmacology (C.L.), 10315 Berlin, Germany; and the National Institute of Child Health and Human Development, National Institutes of Health (S.R.B.), Bethesda, Maryland 20892
Address all correspondence and requests for reprints to: A. Haidan, Medizinische Klinik und Poliklinik III der Universität Leipzig, Philipp Rosenthal Strasse 27, 04103 Leipzig, Germany.
Historically, catecholamine-producing chromaffin cells and steroid-producing adrenocortical cells have been regarded as two independent endocrine systems that are united under a common capsule to form the adrenal gland. There is increasing evidence for bidirectional interactions, with regulatory influences of adrenocortical secretory products on adrenomedullary functions and vice versa. However, the direct involvement of chromaffin cells on the regulation and maintenance of cortical function has not yet been demonstrated. Therefore, we analyzed glucocorticoid secretion and P450 messenger RNA (mRNA) expression in bovine adrenocortical cells in cocultures with chromaffin cells compared with those in pure cortical cell cultures.
Cortisol release from cortical cells in coculture with chromaffin cells
was 10 times as high (mean ± SEM, 1035 ± 119%)
as that from the same number of isolated cortical cells (100 ±
11%). By a [3H]thymidine incorporation assay, it was
demonstrated that this effect was not due to a higher proliferation
rate. Northern analysis revealed an increasing expression of
P45017
mRNA in the coculture from days 15, whereas in
isolated cortical cells, P45017
mRNA decreased, leading
to a 6-fold difference on day 5. Inhibitors of protein (cycloheximide)
or RNA (actinomycin D) synthesis completely annulled the observed
increase in cortisol release, indicating that de novo
protein synthesis is required for this activation of adrenocortical
steroidogenesis. Addition of the cyclooxygenase inhibitor indomethacin
reduced the stimulatory effect, suggesting that this stimulation is in
part mediated by PGs. Locally produced ACTH, catecholamines, and
interleukin-1 accounted for 43% of the effect. Secretory products of
chromaffin cells that act in concert are believed to be responsible for
the stimulation of steroidogenesis in the coculture.
The coculture system is an in vitro model that corresponds to the in vivo situation in the intact adrenal gland, where both endocrine cell systems are in close contact. Our data demonstrate the requirement of intraadrenal cellular communication for the full strength of the adrenocortical hormonal response.
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