Time- and dose-related interactions between glucocorticoid and cyclic adenosine 3 ',5 '-monophosphate on CCAAT/enhancer-binding protein-dependent insulin-like growth factor I expression by osteoblasts

Glucocorticoid has complex effects on osteoblasts. Several of these changes appear to be related to steroid concentration, duration of exposure, or sp ecific effects on growth factor expression or activity within bone. One imp ortant bone growth factor, insulin-like growth factor I (IGF-I), is induced in osteoblasts by hormones such as PGE(2) that increase intracellular cAMP levels. In this way, PGE(2) activates transcription factor CCAAT/enhancer- binding protein-delta (C/EBP delta) and enhances its binding to a specific control element found in exon 1 in the IGF-I gene. Our current studies show that preexposure to glucocorticoid enhanced C/EBP delta and C/EBPP express ion by osteoblasts and thereby potentiated IGF-I gene promoter activation i n response to PGE(2). Importantly, this directly contrasts with inhibitory effects on IGF-I expression that result from sustained or pharmacologically high levels of glucocorticoid exposure: Consistent with the stimulatory ef fect of IGF-I on bone protein synthesis, pretreatment with glucocorticoid s ensitized osteoblasts to PGE(2), and in this context significantly enhanced new collagen and noncollagen protein synthesis. Therefore, pharmacological levels bf glucocorticoid may reduce IGF-I expression by osteoblasts and ca use osteopenic disease, whereas physiological transient increases in glucoc orticoid may permit or amplify the effectiveness of hormones that regulate skeletal tissue integrity. These events appear to converge on the important role of C/EBP delta and C/EBPP on IGF-I expression by osteoblasts.