Cho Eun Sook, Yu Ja Heon, Kim Mi Sun, Yim Mijung
College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Yonsei Med J. 2005 Feb 28;46(1):149-54. doi: 10.3349/ymj.2005.46.1.149.
Phosphodiesterase (PDE) 4 inhibitors have been shown to induce the cAMP-mediated signaling pathway by inhibiting cAMP hydrolysis. This study investigated the effect of a PDE4 inhibitor on the expression of the inducible cAMP early repressor (ICER), which is an endogenous inhibitor of CRE- mediated transcription, in osteoblastic cells. RT-PCR analysis revealed that rolipram, a PDE4 inhibitor, stimulates the ICER mRNA in a dose dependent manner. The induction of ICER mRNA expression by rolipram was suppressed by the inhibitors of protein kinase A (PKA) and p38 MAPK, suggesting the involvement of PKA and p38 MAPK activation in ICER expression by rolipram. It was previously shown that rolipram induced the expression of TNF-related activation-induced cytokine (TRANCE, also known as RANKL, ODF, or OPGL) in osteoblasts. This paper provides evidences that a transcriptional repressor like ICER might modulate TRANCE mRNA expression by rolipram in osteoblasts.
磷酸二酯酶(PDE)4抑制剂已被证明可通过抑制环磷酸腺苷(cAMP)水解来诱导cAMP介导的信号通路。本研究调查了一种PDE4抑制剂对成骨细胞中诱导型cAMP早期阻遏物(ICER)表达的影响,ICER是一种CRE介导转录的内源性抑制剂。逆转录聚合酶链反应(RT-PCR)分析显示,PDE4抑制剂咯利普兰以剂量依赖的方式刺激ICER信使核糖核酸(mRNA)。蛋白激酶A(PKA)和p38丝裂原活化蛋白激酶(p38 MAPK)抑制剂可抑制咯利普兰对ICER mRNA表达的诱导作用,这表明PKA和p38 MAPK的激活参与了咯利普兰诱导的ICER表达。先前的研究表明,咯利普兰可诱导成骨细胞中肿瘤坏死因子相关激活诱导细胞因子(TRANCE,也称为核因子κB受体活化因子配体、骨保护素配体或破骨细胞分化因子)的表达。本文提供的证据表明,像ICER这样的转录阻遏物可能在成骨细胞中调节咯利普兰诱导的TRANCE mRNA表达。