Mechanical stress-dependent transcriptional regulation of sarcolipin gene in the rodent atrium

被引:17
作者
Shimura, M
Minamisawa, S [1 ]
Yokoyama, U
Umemura, S
Ishikawa, Y
机构
[1] Yokohama City Univ, Grad Sch Med, Dept Physiol, Yokohama, Kanagawa 232, Japan
[2] Yokohama City Univ, Grad Sch Med, Dept Internal Med, Yokohama, Kanagawa 232, Japan
[3] Univ Med & Dent New Jersey, Dept Med Cardiol, Cardiovasc Res Inst, New Jersey Med Sch, Newark, NJ 07103 USA
关键词
excitation-contraction; calcium; remodeling; mechanical stress; hypertrophy; gene expression; pulmonary hypertension; sarcoplaslnic reticulum; atrium; rodent;
D O I
10.1016/j.bbrc.2005.06.186
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
Sarcolipin. a homologue of phospholamban, regulates Ca2+ uptake through the interaction with sarcoplasmic reticulum Ca2+ ATPase (SERCA) and is predominantly expressed in the atrial muscle. Although the atria] chamber-specific expression of sarcolipin could be primarily regulated at the transcriptional level, the transcriptional regulation remains poorly understood. Since mechanical stress plays all important role in transcriptional regulation of a gene involved in cardiac hypertrophy and remodeling, we generated left-sided or right-sided pressure-overload models by transverse aortic constriction (TAC) in ddY mice or by monocrotaline administration in Wistar rats. respectively. TAC significantly decreased the expression of sarcolipin, SERCA2a, and phospholamban ,RNAs in the left atrium (LA) than those in the right atrium (RA). By contrast, monocrotaline administration significantly decreased the expression of sarcolipin. SERCA2a. and phospholamban mRNAs in the RA than those in the LA. The two independent complementary experiments unequivocally demonstrated that mechanical stress down-regulates the transcription of the sarcolipin gene. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:861 / 866
页数:6
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