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Cardiac-Specific Overexpression of Diacylglycerol Kinase ζ Prevents Gq Protein-Coupled Receptor Agonist-Induced Cardiac Hypertrophy in Transgenic Mice
Author(s) -
Takanori Arimoto,
Yasuchika Takeishi,
Hiroki Takahashi,
Tetsuro Shishido,
Takeshi Niizeki,
Yo Koyama,
Ryoko Shiga,
Naoki Nozaki,
Osamu Nakajima,
Kazuhide Nishimaru,
Junichi Abe,
Masao Endoh,
Richard A. Walsh,
Kaoru Goto,
Isao Kubota
Publication year - 2005
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.560771
Subject(s) - diacylglycerol kinase , phenylephrine , endocrinology , medicine , angiotensin ii , protein kinase c , agonist , g protein coupled receptor , receptor , biology , signal transduction , microbiology and biotechnology , blood pressure
Diacylglycerol is a lipid second messenger that accumulates in cardiomyocytes when stimulated by Gqalpha protein-coupled receptor (GPCR) agonists such as angiotensin II, phenylephrine, and others. Diacylglycerol functions as a potent activator of protein kinase C (PKC) and is catalyzed by diacylglycerol kinase (DGK) to form phosphatidic acid and inactivated. However, the functional roles of DGK have not been previously examined in the heart. We hypothesized that DGK might prevent GPCR agonist-induced activation of diacylglycerol downstream signaling cascades and subsequent cardiac hypertrophy.

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