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Effect of phosphodiesterase type 4 on circadian clock gene Per1 transcription
被引:8
|作者:
Masumoto, K
Fujioka, A
Nakahama, K
Inouye, SIT
Shigeyoshi, Y
[1
]
机构:
[1] Kinki Univ, Sch Med, Dept Anat & Neurobiol, Sayama, Osaka 5898511, Japan
[2] Yamaguchi Univ, Dept Phys Informat & Biol, Yamaguchi 7538512, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
关键词:
phosphodiesterase type 4;
rolipram;
forskolin;
Per1;
circadian rhythm;
cyclic AMP;
phosphorylated CREB;
rat-1;
D O I:
10.1016/S0006-291X(03)01048-9
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The induction of Per1 gene in the suprachiasmatic nucleus, the center of the circadian clock, is assumed to play significant roles in the adjustment of the internal clock. cAMP is one of the intracellular mediators which activates Per1 transcription. Here, we showed that the amount of the rat Per1 (rPer1) transcript induced by forskolin (FK) was significantly upregulated by the inhibition of phosphodiesterase type 4 (PDE4), a specific phosphodiesterase for cAMP, in rat-1 fibroblasts. Administration of rolipram, a specific inhibitor of PDE4, increased intracellular cAMP concentration, phosphorylation of cAMP response element binding protein (CREB) and enhanced rPer1 induction at their peaks. However, in the falling phase of rPer1 induction, the inhibition of PDE4 hardly affected the profile of rPerl expression. These findings suggest the involvement of PDE4 for the regulation of rPer1 expression via cAMP metabolism at peak of the induction but little or no participation of PDE4 in the decreasing phase of the gene expression. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:781 / 785
页数:5
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