New Horizons in Cellular Regulation by Inositol Polyphosphates: Insights from the Pancreatic β-Cell

被引:26
作者
Barker, Christopher J. [1 ]
Berggren, Per-Olof [1 ]
机构
[1] Karolinska Inst, Rolf Luft Res Ctr Diabet & Endocrinol, S-17176 Stockholm, Sweden
基金
瑞典研究理事会; 新加坡国家研究基金会;
关键词
PHOSPHOLIPASE-C BETA-1; CA2+ CHANNEL ACTIVITY; HEXAKISPHOSPHATE KINASE; INSULIN-SECRETION; GLUCOSE-HOMEOSTASIS; PHYTIC ACID; IN-VIVO; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; DIPHOSPHOINOSITOL PENTAKISPHOSPHATE; MYOINOSITOL HEXAKISPHOSPHATE;
D O I
10.1124/pr.112.006775
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies of inositol polyphosphates in the pancreatic beta-cell have led to an exciting synergism between new discoveries regarding their cellular roles and new insights into beta-cell function. Because the loss or malfunction of the beta-cell is central to diabetes, these studies open the possibility of new pharmacological interventions in a disease that has reached epidemic proportions worldwide. Using the beta-cell as our prime but not exclusive example, we examine the inositol polyphosphates in three main groups: 1) inositol 1,4,5-trisphosphate and its influence on Ca2+ signaling, specifically in a cell in which cytoplasmic-free Ca2+ concentration is principally increased by plasma membrane standing voltage-gated Ca2+ channels; 2) higher inositol polyphosphates including a novel second messenger inositol 3,4,5,6-tetrakisphosphate and a regulatory role for inositol hexakisphosphate in beta-cell Ca2+ homeostasis and exo- and endocytosis; and 3) inositol pyrophosphates and their role in beta-cell exocytosis, together with the exciting possibility of being novel targets for therapy in diabetes. We conclude with some of the new perspectives that are likely to become apparent in the next few years.
引用
收藏
页码:641 / 669
页数:29
相关论文
共 204 条
[1]  
ABDULLAH M, 1992, J BIOL CHEM, V267, P22340
[2]   Type 2 diabetes, insulin secretion and β-cell mass [J].
Ahrén, B .
CURRENT MOLECULAR MEDICINE, 2005, 5 (03) :275-286
[3]   Control of mRNA Export and Translation Termination by Inositol Hexakisphosphate Requires Specific Interaction with Gle1 [J].
Alcazar-Roman, Abel R. ;
Bolger, Timothy A. ;
Wente, Susan R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (22) :16683-16692
[4]  
ALI N, 1993, J BIOL CHEM, V268, P6161
[5]   INOSITOL TRISPHOSPHATE-DEPENDENT PERIODIC ACTIVATION OF A CA2+ - ACTIVATED K+ CONDUCTANCE IN GLUCOSE-STIMULATED PANCREATIC BETA-CELLS [J].
AMMALA, C ;
LARSSON, O ;
BERGGREN, PO ;
BOKVIST, K ;
JUNTTIBERGGREN, L ;
KINDMARK, H ;
RORSMAN, P .
NATURE, 1991, 353 (6347) :849-852
[6]   ATP-SENSITIVE K+ CHANNELS - A LINK BETWEEN B-CELL METABOLISM AND INSULIN-SECRETION [J].
ASHCROFT, FM ;
RORSMAN, P .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (01) :109-111
[7]  
Azevedo C, 2010, METHODS MOL BIOL, V645, P73, DOI 10.1007/978-1-60327-175-2_5
[8]   Inositol pyrophosphate mediated pyrophosphorylation of AP3B1 regulates HIV-1 Gag release [J].
Azevedo, Cristina ;
Burton, Adam ;
Ruiz-Mateos, Ezequiel ;
Marsh, Mark ;
Saiardi, Adolfo .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (50) :21161-21166
[9]   mTORC1 Activation Regulates β-Cell Mass and Proliferation by Modulation of Cyclin D2 Synthesis and Stability [J].
Balcazar, Norman ;
Sathyamurthy, Aruna ;
Elghazi, Lynda ;
Gould, Aaron ;
Weiss, Aaron ;
Shiojima, Ichiro ;
Walsh, Kenneth ;
Bernal-Mizrachi, Ernesto .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (12) :7832-7842
[10]  
Barker CJ, 2010, METHODS MOL BIOL, V645, P1, DOI 10.1007/978-1-60327-175-2_1