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Molecular Evidence of Organic Ion Transporters in the Rat Adrenal Cortex with Adrenocorticotropin-Regulated Zonal Expression

Abteilung Nephrologie und Rheumatologie (E.B., G.A.M., J.S.), Abteilung Pathologie (P.M.), Abteilung Vegetative Physiologie und Pathophysiologie (A.B., Y.H., G.B., J.S.) Universität Göttingen, 37073 Göttingen; Abteilung Endokrinologie (H.S.W., S.R.B.), Universität Düsseldorf, 40225 Düsseldorf; and Anatomisches Institut, Lehrstuhl I (H.K.), Universität Würzburg, 97070 Würzburg, Germany

Address all correspondence and requests for reprints to: Dr. Jürgen Steffgen, Abteilung Vegetative Physiologie und Pathophysiologie, Universität Göttingen, Humboldtallee 23, 37073 Göttingen, Germany. E-mail: jsteffgen{at}gmx.de.

Experimental evidence suggested that secretion of steroid hormones from adrenocortical cells involves carrier-mediated transport: Cortisol release from, and uptake of p-[³H]aminohippurate into, bovine adrenocortical cells showed properties of the renal p-[³H]aminohippurate/anion exchanger OAT1. Other poly-specific transporters such as organic anion-transporting polypeptides (oatps) and organic cation transporters (OCTs) could also be involved in steroid hormone release. A homology-cloning procedure was established to detect these transporters in rat adrenal gland cDNA. PCR revealed the presence of OAT1, oatp1, oatp2, and oatp3. In situ hybridization localized OAT1 in the outer zona fasciculata, oatp3 in the zona glomerulosa, and oatp1 and oatp2 in the inner zona fasciculata and outer zona reticularis. An OCT2-specific probe produced signals in the zona glomerulosa and outer zona fasciculata. Pretreatment of rats with ACTH increased the expression of OAT1 mRNA that spread to all zones, and hypophysectomy strongly decreased it. A less pronounced regulation was detected for OCT2 and oatp3. Specific antibodies confirmed the localization of OAT1 in the outer zona fasciculata, supporting a possible role of OAT1 in cortisol release. The zonated distribution of transporters furthermore suggest that oatp1–3 and OCT2 may be important for the endocrine function of rat adrenocortical cells.

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