Phosphoinositides in cell regulation and membrane dynamics

被引:2106
作者
Di Paolo, Gilbert
De Camilli, Pietro [1 ]
机构
[1] Yale Univ, Sch Med, Dept Cell Biol, Program Cellular Neurosci,Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, Dept Neurobiol,Program Cellular Neurosci, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Kavli Inst Neurosci, New Haven, CT 06510 USA
[4] Columbia Univ, Med Ctr, Taub Inst Res Alzheimers Dis & Aging Brain, Dept Pathol & Cell Biol, New York, NY 10032 USA
关键词
D O I
10.1038/nature05185
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Inositol phospholipids have long been known to have an important regulatory role in cell physiology. The repertoire of cellular processes known to be directly or indirectly controlled by this class of lipids has now dramatically expanded. Through interactions mediated by their headgroups, which can be reversibly phosphorylated to generate seven species, phosphoinositides play a fundamental part in controlling membrane-cytosol interfaces. These lipids mediate acute responses, but also act as constitutive signals that help define organelle identity. Their functions, besides classical signal transduction at the cell surface, include regulation of membrane traffic, the cytoskeleton, nuclear events and the permeability and transport functions of membranes. © 2006 Nature Publishing Group.
引用
收藏
页码:651 / 657
页数:7
相关论文
共 75 条
  • [1] THE LOWE OCULOCEREBRORENAL SYNDROME GENE ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO INOSITOL POLYPHOSPHATE-5-PHOSPHATASE
    ATTREE, O
    OLIVOS, IM
    OKABE, I
    BAILEY, LC
    NELSON, DL
    LEWIS, RA
    MCINNES, RR
    NUSSBAUM, RL
    [J]. NATURE, 1992, 358 (6383) : 239 - 242
  • [2] PDGF-DEPENDENT TYROSINE PHOSPHORYLATION STIMULATES PRODUCTION OF NOVEL POLYPHOSPHOINOSITIDES IN INTACT-CELLS
    AUGER, KR
    SERUNIAN, LA
    SOLTOFF, SP
    LIBBY, P
    CANTLEY, LC
    [J]. CELL, 1989, 57 (01) : 167 - 175
  • [3] Oncogenic PI3K deregulates transcription and translation
    Bader, AG
    Kang, SY
    Zhao, L
    Vogt, PK
    [J]. NATURE REVIEWS CANCER, 2005, 5 (12) : 921 - 929
  • [4] PIP2 increases the speed of response of synaptotagmin and steers its membrane-penetration activity toward the plasma membrane
    Bai, JH
    Tucker, WC
    Chapman, ER
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (01) : 36 - 44
  • [5] Inositol-lipid binding motifs: signal integrators through protein-lipid and protein-protein interactions
    Balla, T
    [J]. JOURNAL OF CELL SCIENCE, 2005, 118 (10) : 2093 - 2104
  • [6] Organelle identity and the signposts for membrane traffic
    Behnia, R
    Munro, S
    [J]. NATURE, 2005, 438 (7068) : 597 - 604
  • [7] INOSITOL PHOSPHATES AND CELL SIGNALING
    BERRIDGE, MJ
    IRVINE, RF
    [J]. NATURE, 1989, 341 (6239) : 197 - 205
  • [8] Birkeland HCG, 2004, CURR TOP MICROBIOL, V282, P89
  • [9] Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
    Bolino, A
    Muglia, M
    Conforti, FL
    LeGuern, E
    Salih, MAM
    Georgiou, DM
    Christodoulou, K
    Hausmanowa-Petrusewicz, I
    Mandich, P
    Schenone, A
    Gambardella, A
    Bono, F
    Quattrone, A
    Devoto, M
    Monaco, AP
    [J]. NATURE GENETICS, 2000, 25 (01) : 17 - 19
  • [10] Botelho RJ, 2004, CURR TOP MICROBIOL, V282, P1