Termination of immediate-early gene expression after stimulation by parathyroid hormone or isoproterenol

被引:11
作者
Chen, X
Dai, JC
Greenfield, EM
机构
[1] Case Western Reserve Univ, Dept Orthopaed, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA
[4] Univ Hosp Cleveland, Cleveland, OH 44106 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2002年 / 283卷 / 05期
关键词
receptor desensitization; cAMP degradation; IL-6; c-fos; osteoblast;
D O I
10.1152/ajpcell.00221.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
cAMP/PKA signaling transiently stimulates mRNA expression of immediate-early genes, including IL-6 and c-fos. We confirmed that these mRNAs are transiently stimulated by parathyroid hormone (PTH) in ROS 17/2.8 osteoblastic cells. Consistent with the role for cAMP/PKA signaling in this response, PTH induces transient cAMP elevation, PKA activation, and cAMP-responsive element-binding protein (CREB) phosphorylation. Our goal was to determine whether termination of immediate-early gene expression is due to receptor desensitization or cAMP degradation. The approaches used were 1) inhibition of PTH receptor desensitization with G protein-coupled receptor kinase 2 (GRK2) antisense oligonucleotides or antisense plasmids, 2) sustained activation of adenyl cyclase with forskolin, and 3) inhibition of cAMP degradation with 3-isobutyl-1-methylxanthine. These experiments show that mechanisms downstream of receptor desensitization and cAMP degradation are primarily responsible for termination of PKA activity, CREB phosphorylation, and immediate-early gene expression. Similar conclusions were also obtained in response to PTH in a second osteoblastic cell line (MC3T3-E1) and in response to isoproterenol in NIH3T3 fibroblasts. This conclusion may therefore reflect a general mechanism for termination of immediate-early gene expression after induction by cAMP/PKA.
引用
收藏
页码:C1432 / C1440
页数:9
相关论文
共 58 条
[41]  
Penn RB, 1998, HANDBK PHYS, V1, P125
[42]   Classical and new roles of β-arrestins in the regulation of G-protein-coupled receptors [J].
Pierce, KL ;
Lefkowitz, RJ .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (10) :727-733
[43]   G protein-coupled receptor kinases [J].
Pitcher, JA ;
Freedman, NJ ;
Lefkowitz, RJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :653-692
[44]  
Pollock JH, 1996, J BONE MINER RES, V11, P754
[45]   Measurement and removal of adherent endotoxin from titanium particles and implant surfaces [J].
Ragab, AA ;
Van de Motter, R ;
Lavish, SA ;
Goldberg, VM ;
Ninomiya, JT ;
Carlin, CR ;
Greenfield, EM .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1999, 17 (06) :803-809
[46]  
Segre Gino V., 1996, P377
[47]   Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families [J].
Suda, T ;
Takahashi, N ;
Udagawa, N ;
Jimi, E ;
Gillespie, MT ;
Martin, TJ .
ENDOCRINE REVIEWS, 1999, 20 (03) :345-357
[48]   INVITRO DIFFERENTIATION AND CALCIFICATION IN A NEW CLONAL OSTEOGENIC CELL-LINE DERIVED FROM NEWBORN MOUSE CALVARIA [J].
SUDO, H ;
KODAMA, HA ;
AMAGAI, Y ;
YAMAMOTO, S ;
KASAI, S .
JOURNAL OF CELL BIOLOGY, 1983, 96 (01) :191-198
[49]  
TASH JS, 1979, J BIOL CHEM, V254, P1241
[50]   Phosphorylation of the receptor for PTH and PTHrP is required for internalization and regulates receptor signaling [J].
Tawfeek, HAW ;
Qian, F ;
Abou-Samra, AB .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (01) :1-13