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   <subfield code="a">Induction of the C/EBPβ Gene by Dexamethasone and Glucagon in Primary-Cultured Rat Hepatocytes</subfield>
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   <subfield code="c">[Fumihiko Matsuno, Shoaib Chowdhury, Tomomi Gotoh, Katsuro Iwase, Hiromitsu Matsuzaki, Kiyoshi Takatsuki, Masataka Mori, Masaki Takiguchi]</subfield>
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   <subfield code="a">The synthetic glucocorticoid, dexamethasone, and glucagon cooperatively elevated the level of mRNA for the transcription factor CCAAT/enhancer binding protein β(c/EBPβ) in primary-cultured rat hepatocytes. In response to dexamethasone and/or glucagon, c/ EBPβ mRNA started to increase as early as at 30 min, reached a maximum within 2 h, and then gradually decreased. The administration of cycloheximide, a protein synthesis inhibitor, led rather to an increase in c/EBPβ mRNA, which suggested that a labile negative protein factor(s) is involved in regulation of the c/EBPβ mRNA level. Cycloheximide further augmented the increases in c/EBPβ mRNA by dexamethasone and/or glucagon. Therefore, c/EBPβ mRNA accumulation in response to these hormones is apparently independent of ongoing protein synthesis. The elevation of the c/EBPβ mRNA level by these hormones was accounted for by increases in the rate of transcription of the c/EBPβ gene, as deduced on nuclear run-on analysis. Gel mobility shift analysis revealed that the DNA-binding activity of C/EBPβ was increased cooperatively by dexamethasone and glucagon. These results suggest that the c/EBPβ gene is primarily induced by glucocorticoids and/or glucagon and that the accumulated c/EBPβ protein is then involved in secondary activation of target genes in response to these hormones in the liver</subfield>
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