Effects of 18β-Glycyrrhetinic acid on the junctional complex and steroidogenesis in rat adrenocortical cells

✍ Scribed by Shih-Horng Huang; Jiahn-Chun Wu; Ra-Der Hwang; Hui-Lin Yeo; Seu-Mei Wang

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 302 KB
• Volume: 90
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.10610

✦ Synopsis

Abstract

Cellular junctions play important roles in cell differentiation, signal transduction, and cell function. This study investigated their function in steroid secretion by adrenal cells. Immunofluorescence staining revealed the presence of gap junctions and adherens junctions between adrenal cells. The major gap junction protein, connexin43, was seen as a linear dotted pattern of the typical gap junction plaques, in contrast to α‐, β‐, and γ‐catenin, which were seen as continuous, linear staining of cell–cell adherens junction. Treatment with 18β‐glycyrrhetinic acid, a gap junction inhibitor, reduced the immunoreactivity of these proteins in a time‐ and dose‐dependent manner, and caused the gap junction and adherens junction to separate longitudinally from the cell–cell contact sites, indicating the structural interdependency of these two junctions. Interestingly, 18β‐glycyrrhetinic acid stimulated a two‐ to three–fold increase in steroid production in these adrenal cells lacking intact cell junctions. These data raise the question of the necessity for cell communication for the endocrine function of adrenal cells. Pharmacological analyses indicated that the steroidogenic effect of 18β‐glycyrrhetinic acid was partially mediated by extracellular signal‐related kinase and calcium/calmodulin‐dependent kinase, a pathway distinct from the protein kinase A signaling pathway already known to mediate steroidogenesis in adrenal cells. J. Cell. Biochem. 90: 33–41, 2003. © 2003 Wiley‐Liss, Inc.