Adenylyl cyclase type VI increases Akt activity and phospholamban phosphorylation in cardiac myocytes. 2008

Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
Veterans Administration San Diego Healthcare System, University of California, San Diego, La Jolla, California 92093, USA.

Increased expression of adenylyl cyclase VI has beneficial effects on the heart, but strategies that increase cAMP production in cardiac myocytes usually are harmful. Might adenylyl cyclase VI have beneficial effects unrelated to increased beta-adrenergic receptor-mediated signaling? We previously reported that adenylyl cyclase VI reduces cardiac phospholamban expression. Our focus in the current studies is how adenylyl cyclase VI influences phospholamban phosphorylation. In cultured cardiac myocytes, increased expression of adenylyl cyclase VI activates Akt by phosphorylation at serine 473 and threonine 308 and is associated with increased nuclear phospho-Akt. Activated Akt phosphorylates phospholamban, a process that does not require beta-adrenergic receptor stimulation or protein kinase A activation. These previously unrecognized signaling events would be predicted to promote calcium handling and increase contractile function of the intact heart independently of beta-adrenergic receptor activation. We speculate that phospholamban phosphorylation, through activation of Akt, may be an important mechanism by which adenylyl cyclase VI increases the function of the failing heart.

UI MeSH Term Description Entries
D009206 Myocardium The muscle tissue of the HEART. It is composed of striated, involuntary muscle cells (MYOCYTES, CARDIAC) connected to form the contractile pump to generate blood flow. Muscle, Cardiac,Muscle, Heart,Cardiac Muscle,Myocardia,Cardiac Muscles,Heart Muscle,Heart Muscles,Muscles, Cardiac,Muscles, Heart
D010766 Phosphorylation The introduction of a phosphoryl group into a compound through the formation of an ester bond between the compound and a phosphorus moiety. Phosphorylations
D011943 Receptors, Adrenergic, beta One of two major pharmacologically defined classes of adrenergic receptors. The beta adrenergic receptors play an important role in regulating CARDIAC MUSCLE contraction, SMOOTH MUSCLE relaxation, and GLYCOGENOLYSIS. Adrenergic beta-Receptor,Adrenergic beta-Receptors,Receptors, beta-Adrenergic,beta Adrenergic Receptor,beta-Adrenergic Receptor,beta-Adrenergic Receptors,Receptor, Adrenergic, beta,Adrenergic Receptor, beta,Adrenergic beta Receptor,Adrenergic beta Receptors,Receptor, beta Adrenergic,Receptor, beta-Adrenergic,Receptors, beta Adrenergic,beta Adrenergic Receptors,beta-Receptor, Adrenergic,beta-Receptors, Adrenergic
D002135 Calcium-Binding Proteins Proteins to which calcium ions are bound. They can act as transport proteins, regulator proteins, or activator proteins. They typically contain EF HAND MOTIFS. Calcium Binding Protein,Calcium-Binding Protein,Calcium Binding Proteins,Binding Protein, Calcium,Binding Proteins, Calcium,Protein, Calcium Binding,Protein, Calcium-Binding
D002467 Cell Nucleus Within a eukaryotic cell, a membrane-limited body which contains chromosomes and one or more nucleoli (CELL NUCLEOLUS). The nuclear membrane consists of a double unit-type membrane which is perforated by a number of pores; the outermost membrane is continuous with the ENDOPLASMIC RETICULUM. A cell may contain more than one nucleus. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed) Cell Nuclei,Nuclei, Cell,Nucleus, Cell
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D004789 Enzyme Activation Conversion of an inactive form of an enzyme to one possessing metabolic activity. It includes 1, activation by ions (activators); 2, activation by cofactors (coenzymes); and 3, conversion of an enzyme precursor (proenzyme or zymogen) to an active enzyme. Activation, Enzyme,Activations, Enzyme,Enzyme Activations
D006333 Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. Cardiac Failure,Heart Decompensation,Congestive Heart Failure,Heart Failure, Congestive,Heart Failure, Left-Sided,Heart Failure, Right-Sided,Left-Sided Heart Failure,Myocardial Failure,Right-Sided Heart Failure,Decompensation, Heart,Heart Failure, Left Sided,Heart Failure, Right Sided,Left Sided Heart Failure,Right Sided Heart Failure
D000242 Cyclic AMP An adenine nucleotide containing one phosphate group which is esterified to both the 3'- and 5'-positions of the sugar moiety. It is a second messenger and a key intracellular regulator, functioning as a mediator of activity for a number of hormones, including epinephrine, glucagon, and ACTH. Adenosine Cyclic 3',5'-Monophosphate,Adenosine Cyclic 3,5 Monophosphate,Adenosine Cyclic Monophosphate,Adenosine Cyclic-3',5'-Monophosphate,Cyclic AMP, (R)-Isomer,Cyclic AMP, Disodium Salt,Cyclic AMP, Monoammonium Salt,Cyclic AMP, Monopotassium Salt,Cyclic AMP, Monosodium Salt,Cyclic AMP, Sodium Salt,3',5'-Monophosphate, Adenosine Cyclic,AMP, Cyclic,Adenosine Cyclic 3',5' Monophosphate,Cyclic 3',5'-Monophosphate, Adenosine,Cyclic Monophosphate, Adenosine,Cyclic-3',5'-Monophosphate, Adenosine,Monophosphate, Adenosine Cyclic
D000262 Adenylyl Cyclases Enzymes of the lyase class that catalyze the formation of CYCLIC AMP and pyrophosphate from ATP. Adenyl Cyclase,Adenylate Cyclase,3',5'-cyclic AMP Synthetase,Adenylyl Cyclase,3',5' cyclic AMP Synthetase,AMP Synthetase, 3',5'-cyclic,Cyclase, Adenyl,Cyclase, Adenylate,Cyclase, Adenylyl,Cyclases, Adenylyl,Synthetase, 3',5'-cyclic AMP

Related Publications

Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
February 2013, Journal of the American Society of Nephrology : JASN,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
July 2000, The Journal of biological chemistry,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
January 1999, European journal of pharmacology,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
September 1995, Journal of molecular and cellular cardiology,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
January 2019, PloS one,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
May 2000, Molecular pharmacology,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
March 2015, Biochemical and biophysical research communications,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
August 2009, The Journal of biological chemistry,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
August 1997, The Journal of biological chemistry,
Mei Hua Gao, and Tong Tang, and Tracy Guo, and Atsushi Miyanohara, and Toshitaka Yajima, and Kersi Pestonjamasp, and James R Feramisco, and H Kirk Hammond
August 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology,
Copied contents to your clipboard!