Regulation and cellular functions of class II phosphoinositide 3-kinases

被引:122
作者
Falasca, Marco [1 ]
Maffucci, Tania [1 ]
机构
[1] Queen Mary Univ London, Baits & London Sch Med & Dent, Blizard Inst, Inositide Signalling Grp,Ctr Diabet, 4 Newark St, London E1 2AT, England
关键词
cell migration; glucose transport; insulin secretion; phosphoinositide; phosphoinositide 3-kinase (PI3K); PHOSPHATIDYLINOSITOL 3-PHOSPHATE PTDINS(3)P; STIMULATED GLUCOSE-UPTAKE; ALPHA-ISOFORM; MYOSIN PHOSPHATASE; C2; DOMAIN; INSULIN-SECRETION; SIGNALING PATHWAY; KINASE-ACTIVITY; MYOTUBULARIN; ACTIVATION;
D O I
10.1042/BJ20120008
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
Class II isoforms of PI3K (phosphoinositide 3-kinase) are still the least investigated and characterized of all PI3Ks. In the last few years, an increased interest in these enzymes has improved our understanding of their cellular functions. However, several questions still remain unanswered on their mechanisms of activation, their specific downstream effectors and their contribution to physiological processes and pathological conditions. Emerging evidence suggests that distinct PI3Ks activate different signalling pathways, indicating that their functional roles are probably not redundant. In the present review, we discuss the recent advances in our understanding of mammalian class II PI3Ks and the evidence suggesting their involvement in human diseases.
引用
收藏
页码:587 / 601
页数:15
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[31]   The role of phosphoinositide 3-kinase C2α in insulin signaling [J].
Falasca, Marco ;
Hughes, William E. ;
Dominguez, Veronica ;
Sala, Gianluca ;
Fostira, Florentia ;
Fang, Michelle Q. ;
Cazzolli, Rosanna ;
Shepherd, Peter R. ;
James, David E. ;
Maffucci, Tania .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (38) :28226-28236
[32]   PI3K/Akt Signalling Pathway Specific Inhibitors: A Novel Strategy to Sensitize Cancer Cells to Anti-Cancer Drugs [J].
Falasca, Marco .
CURRENT PHARMACEUTICAL DESIGN, 2010, 16 (12) :1410-1416
[33]   Rethinking phosphatidylinositol 3-monophosphate [J].
Falasca, Marco ;
Maffucci, Tania .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2009, 1793 (12) :1795-1803
[34]   Phosphoinositide Signalling Pathways in Metabolic Regulation [J].
Foukas, Lazaros C. ;
Withers, Dominic J. .
PHOSPHOINOSITIDE 3-KINASE IN HEALTH AND DISEASE, VOL 1, 2010, 346 :115-141
[35]   The class II phosphoinositide 3-kinase C2α is activated by clathrin and regulates clathrin-mediated membrane trafficking [J].
Gaidarov, I ;
Smith, MEK ;
Domin, J ;
Keen, JH .
MOLECULAR CELL, 2001, 7 (02) :443-449
[36]   The p110β isoform of phosphoinositide 3-kinase signals downstream of G protein-coupled receptors and is functionally redundant with p110γ [J].
Guillermet-Guibert, Julie ;
Bjorklof, Katja ;
Salpekar, Ashreena ;
Gonella, Cristiano ;
Ramadani, Faruk ;
Bilancio, Antonio ;
Meek, Stephen ;
Smith, Andrew J. H. ;
Okkenhaug, Klaus ;
Vanhaesebroeck, Bart .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (24) :8292-8297
[37]   The class II phosphoinositide 3-kinase C2β is not essential for epidermal differentiation [J].
Harada, K ;
Truong, AB ;
Cai, T ;
Khavari, PA .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (24) :11122-11130
[38]   Requirement for Class II Phosphoinositide 3-Kinase C2α in Maintenance of Glomerular Structure and Function [J].
Harris, David P. ;
Vogel, Peter ;
Wims, Marie ;
Moberg, Karen ;
Humphries, Juliane ;
Jhaver, Kanchan G. ;
DaCosta, Christopher M. ;
Shadoan, Melanie K. ;
Xu, Nianhua ;
Hansen, Gwenn M. ;
Balakrishnan, Sanjeevi ;
Domin, Jan ;
Powell, David R. ;
Oravecz, Tamas .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (01) :63-80
[39]   Parallel RNAi and compound screens identify the PDK1 pathway as a target for tamoxifen sensitization [J].
Iorns, Elizabeth ;
Lord, Christopher J. ;
Ashworth, Alan .
BIOCHEMICAL JOURNAL, 2009, 417 :361-370
[40]   Insulin regulates the membrane arrival, fusion, and C-terminal unmasking of glucose transporter-4 via distinct phosphoinositides [J].
Ishiki, M ;
Randhawa, VK ;
Poon, V ;
JeBailey, L ;
Klip, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (31) :28792-28802