PKD at the crossroads of DAG and PKC signaling

被引:274
作者
Wang, Qiming J. [1 ]
机构
[1] Univ Pittsburgh, Dept Pharmacol, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tips.2006.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diacylglycerol (DAG) and its primary target protein kinase C (PKC) regulate many important cellular responses, yet the molecular mechanisms that control the specificity of DAG and PKC signaling are not fully understood. As such, targeting the PKC pathway for therapeutic purposes has been challenging. Protein kinase D (PKD), a novel DAG receptor, has been the subject of intense investigation in recent years. DAG regulates the intracellular localization of PKD and also activates PKD through PKC by phosphorylation. The PKC-PKD signaling cascade is crucial to PKD function in cells. Important discoveries have been made regarding the roles of PKD in cell growth, gene expression, survival, motility, protein trafficking and lymphocyte biology. This kinase is implicated in pathological processes such as cardiac hypertrophy, tumor cell proliferation and metastasis. Thus, PKD represents a novel therapeutic target for the DAG-PKC signaling network.
引用
收藏
页码:317 / 323
页数:7
相关论文
共 63 条
[1]   PKCη is required for β1γ2/β3γ2- and PKD-mediated transport to the cell surface and the organization of the Golgi apparatus [J].
Añel, AMD ;
Malhotra, V .
JOURNAL OF CELL BIOLOGY, 2005, 169 (01) :83-91
[2]   Role of the regulatory domain of protein kinase D2 in phorbol ester binding, catalytic activity, and nucleocytoplasmic shuttling [J].
Auer, A ;
von Blume, J ;
Sturany, S ;
von Wichert, G ;
Van Lint, J ;
Vandenheede, J ;
Adler, G ;
Seufferlein, T .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (09) :4375-4385
[3]   Cell-type specific phosphorylation of threonines T654 and T669 by PKD defines the signal capacity of the EGF receptor [J].
Bagowski, CP ;
Stein-Gerlach, M ;
Choidas, A ;
Ullrich, A .
EMBO JOURNAL, 1999, 18 (20) :5567-5576
[4]   Role of diacylglycerol in PKD recruitment to the TGN and protein transport to the plasma membrane [J].
Baron, CL ;
Malhotra, V .
SCIENCE, 2002, 295 (5553) :325-328
[5]   Protein kinase D and keratinocyte proliferation [J].
Bollag, WB ;
Dodd, ME ;
Shapiro, BA .
DRUG NEWS & PERSPECTIVES, 2004, 17 (02) :117-126
[6]   An invasion-related complex of cortactin, paxillin and PKCμ associates with invadopodia at sites of extracellular matrix degradation [J].
Bowden, ET ;
Barth, M ;
Thomas, D ;
Glazer, RI ;
Mueller, SC .
ONCOGENE, 1999, 18 (31) :4440-4449
[7]   BMP-2 and insulin-like growth factor-I mediate osterix (Osx) expression in human mesenchymal stem cells via the MAPK and protein kinase D signaling pathways [J].
Celil, AB ;
Campbell, PG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (36) :31353-31359
[8]   Phosphorylation of histone deacetylase 7 by protein kinase D mediates T cell receptor-induced Nur77 expression and apoptosis [J].
Dequiedt, F ;
Van Lint, J ;
Lecomte, E ;
Van Duppen, V ;
Seufferlein, T ;
Vandenheede, JR ;
Wattiez, R ;
Kettmann, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (05) :793-804
[9]   A phosphorylation state-specific antibody recognizes Hsp27, a novel substrate of protein kinase D [J].
Döppler, H ;
Storz, P ;
Li, J ;
Comb, MJ ;
Toker, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (15) :15013-15019
[10]   Inhibition of protein kinase C mu by various inhibitors. Differentiation from protein kinase c isoenzymes [J].
Gschwendt, M ;
Dieterich, S ;
Rennecke, J ;
Kittstein, W ;
Mueller, HJ ;
Johannes, FJ .
FEBS LETTERS, 1996, 392 (02) :77-80