A Phosphodiesterase 2A Isoform Localized to Mitochondria Regulates Respiration

被引:114
作者
Acin-Perez, Rebeca [2 ]
Russwurm, Michael [4 ]
Guennewig, Kathrin [5 ]
Gertz, Melanie [1 ,5 ]
Zoidl, Georg [3 ]
Ramos, Lavoisier [6 ]
Buck, Jochen [6 ]
Levin, Lonny R. [6 ]
Rassow, Joachim [1 ]
Manfredi, Giovanni [2 ]
Steegborn, Clemens [1 ]
机构
[1] Univ Bayreuth, Dept Biochem, D-95447 Bayreuth, Germany
[2] Cornell Univ, Weill Med Coll, Dept Neurol & Neurosci, New York, NY 10065 USA
[3] Ruhr Univ Bochum, Dept Neuroanat & Mol Brain Res, D-44780 Bochum, Germany
[4] Ruhr Univ Bochum, Dept Pharmacol & Toxicol, D-44780 Bochum, Germany
[5] Ruhr Univ Bochum, Dept Physiol Chem, D-44780 Bochum, Germany
[6] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
SOLUBLE ADENYLYL-CYCLASE; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE; GUANYLYL CYCLASE; RAT-BRAIN; STIMULATED PHOSPHODIESTERASE; CRYSTAL-STRUCTURE; GAF DOMAINS; CAMP; PROTEIN; CGMP;
D O I
10.1074/jbc.M111.266379
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Mitochondria are central organelles in cellular energy metabolism, apoptosis, and aging processes. A signaling network regulating these functions was recently shown to include soluble adenylyl cyclase as a local source of the second messenger cAMP in the mitochondrial matrix. However, a mitochondrial cAMP degrading phosphodiesterase (PDE) necessary for switching off this cAMP signal has not yet been identified. Here, we describe the identification and characterization of a PDE2A isoform in mitochondria from rodent liver and brain. We find that mitochondrial PDE2A is located in the matrix and that the unique N terminus of PDE2A isoform 2 specifically leads to mitochondrial localization of this isoform. Functional assays show that mitochondrial PDE2A forms a local signaling system with soluble adenylyl cyclase in the matrix, which regulates the activity of the respiratory chain. Our findings complete a cAMP signaling cascade in mitochondria and have implications for understanding the regulation of mitochondrial processes and for their pharmacological modulation.
引用
收藏
页码:30423 / 30432
页数:10
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