Role of regulator of G-protein signaling 2 (RGS2) in periodontal ligament cells under mechanical stress

被引:8
作者
de Araujo, Rui M. Santos
Oba, Yasuo
Moriyama, Keiji
机构
[1] Department of Orthodontics and Dentofacial Orthopedics, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima 770-8504
关键词
periodontal ligament; mechanical stress; cAMP; RGS2;
D O I
10.1002/cbf.1400
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
Mechanical stress is thought to regulate the expression of genes in the periodontal ligament (PDL) cells. Using a microarray approach, we recently identified a regulator of G-protein signaling 2 (RGS2) as an up-regulated gene in the PDL cells under compressive force. The RGS protein family is known to turn off G-protein signaling. G-protein signaling involves the production of cAMP, which is thought to be one of the biological mediators in response to mechanical stress. Here, we investigated the role of RGS2 in the PDL cells under mechanical stress. PDL cells derived from the ligament tissues of human premolar teeth were cultured in collagen gels and subjected to static compressive force. Compressive force application time-dependently enhanced RGS2 expression and intracellular cAMP levels. To examine the interrelationship between RGS2 and cAMP, the PDL cells were treated with 2',5'-dideoxyadenosine (DDA), an inhibitor of adenyl cyclase, or antisense S-oligonucleotide (S-ODN) to RGS2 under compressive force. DDA dose-dependently inhibited RGS2 stimulated by compressive force. Blockage of RGS2 by antisense S-ODN elevated the cAMP levels compared with controls. These results indicate that cAMP stimulates RGS2 expression, which in turn leads to a decrease in the cAMP production by inactivating the G-protein signaling in the mechanically stressed PDL cells. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:753 / 758
页数:6
相关论文
共 32 条
[1]   Orthodontic tooth movement and de novo synthesis of proinflammatory cytokines [J].
Alhashimi, N ;
Frithiof, L ;
Brudvik, P ;
Bakhiet, M .
AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 2001, 119 (03) :307-312
[2]   Functional genomic analysis of a commercial wine strain of Saccharomyces cerevisiae under differing nitrogen conditions [J].
Backhus, Leilah E. ;
DeRisi, Joseph ;
Brown, Patrick O. ;
Bisson, Linda F. .
FEMS YEAST RESEARCH, 2001, 1 (02) :111-125
[3]  
Beadling C, 1999, J IMMUNOL, V162, P2677
[4]   IMMUNO-HISTOCHEMICAL LOCALIZATION OF CYCLIC NUCLEOTIDES IN MINERALIZED TISSUES - MECHANICALLY-STRESSED OSTEOBLASTS INVIVO [J].
DAVIDOVITCH, Z ;
MONTGOMERY, PC ;
YOST, RW ;
SHANFELD, JL .
ANATOMICAL RECORD, 1978, 192 (03) :363-373
[5]  
DAVIDOVITCH Z, 1976, CALC TISS RES, V19, P317
[6]   CYCLIC-AMP LEVELS IN ALVEOLAR BONE OF ORTHODONTICALLY-TREATED CATS [J].
DAVIDOVITCH, Z ;
SHANFELD, JL .
ARCHIVES OF ORAL BIOLOGY, 1975, 20 (09) :567-&
[7]   Identification of genes related to mechanical stress in human periodontal ligament cells using microarray analysis [J].
de Araujo, R. M. S. ;
Oba, Y. ;
Moriyama, K. .
JOURNAL OF PERIODONTAL RESEARCH, 2007, 42 (01) :15-22
[8]   The G protein subunit gene families [J].
Downes, GB ;
Gautam, N .
GENOMICS, 1999, 62 (03) :544-552
[9]   Identification of genes differentially expressed in cultured human periodontal ligament fibroblasts vs. human gingival fibroblasts by DNA microarray analysis [J].
Han, X ;
Amar, S .
JOURNAL OF DENTAL RESEARCH, 2002, 81 (06) :399-405
[10]   G protein selectivity is a determinant of RGS2 function [J].
Heximer, SP ;
Srinivasa, SP ;
Bernstein, LS ;
Bernard, JL ;
Linder, ME ;
Hepler, JR ;
Blumer, KJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) :34253-34259