Processing Temporal Growth Factor Patterns by an Epidermal Growth Factor Receptor Network Dynamically Established in Space

被引:20
作者
Koseska, Aneta [1 ]
Bastiaens, Philippe I. H. [2 ]
机构
[1] Ctr Adv European Studies & Res Caesar, Lise Meitner Grp Cellular Computat & Learning, D-53175 Bonn, Germany
[2] Max Planck Inst Mol Physiol, Dept Syst Cell Biol, D-44227 Dortmund, Germany
来源
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 36, 2020 | 2020年 / 36卷
关键词
spatially organized signaling; time-varying growth factors; receptor tyrosine kinases; nonlinear dynamics; spatial cycles; collective computing; PROTEIN-TYROSINE-PHOSPHATASE; UBIQUITIN LIGASE ACTIVITY; CLATHRIN-COATED PITS; EGF-RECEPTOR; NEGATIVE COOPERATIVITY; ENDOCYTIC TRAFFICKING; SIGNAL-TRANSDUCTION; EXTRACELLULAR DOMAIN; CRYSTAL-STRUCTURE; PLASMA-MEMBRANE;
D O I
10.1146/annurev-cellbio-013020-103810
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The proto-oncogenic epidermal growth factor (EGF) receptor (EGFR) is a tyrosine kinase whose sensitivity and response to growth factor signals that vary over time and space determine cellular behavior within a developing tissue. The molecular reorganization of the receptors on the plasma membrane and the enzyme-kinetic mechanisms of phosphorylation are key determinants that couple growth factor binding to EGFR signaling. To enable signal initiation and termination while simultaneously accounting for suppression of aberrant signaling, a coordinated coupling of EGFR kinase and protein tyrosine phosphatase activity is established through space by vesicular dynamics. The dynamical operation mode of this network enables not only time-varying growth factor sensing but also adaptation of the response depending on cellular context. By connecting spatially coupled enzymatic kinase/phosphatase processes and the corresponding dynamical systems description of the EGFR network, we elaborate on the general principles necessary for processing complex growth factor signals.
引用
收藏
页码:359 / 383
页数:25
相关论文
共 156 条
  • [61] Grb2 regulates internalization of EGF receptors through clathrin-coated pits
    Jiang, XJ
    Huang, FT
    Marusyk, A
    Sorkin, A
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (03) : 858 - 870
  • [62] Mechanism for Activation of the EGF Receptor Catalytic Domain by the Juxtamembrane Segment
    Jura, Natalia
    Endres, Nicholas F.
    Engel, Kate
    Deindl, Sebastian
    Das, Rahul
    Lamers, Meindert H.
    Wemmer, David E.
    Zhang, Xuewu
    Kuriyan, John
    [J]. CELL, 2009, 137 (07) : 1293 - 1307
  • [63] Temporal Resolution of Autophosphorylation for Normal and Oncogenic Forms of EGFR and Differential Effects of Gefitinib
    Kim, Youngjoo
    Li, Zhimin
    Apetri, Mihaela
    Luo, BeiBei
    Settleman, Jeffrey E.
    Anderson, Karen S.
    [J]. BIOCHEMISTRY, 2012, 51 (25) : 5212 - 5222
  • [64] Rapid Phospho-Turnover by Receptor Tyrosine Kinases Impacts Downstream Signaling and Drug Binding
    Kleiman, Laura B.
    Maiwald, Thomas
    Conzelmann, Holger
    Lauffenburger, Douglas A.
    Sorger, Peter K.
    [J]. MOLECULAR CELL, 2011, 43 (05) : 723 - 737
  • [65] DISTRIBUTION AND RELEASE OF EPIDERMAL GROWTH-FACTOR IN MAN
    KONTUREK, JW
    BIELANSKI, W
    KONTUREK, SJ
    BOGDAL, J
    OLEKSY, J
    [J]. GUT, 1989, 30 (09) : 1194 - 1200
  • [66] Cell signaling as a cognitive process
    Koseska, Aneta
    Bastiaens, Philippe I. H.
    [J]. EMBO JOURNAL, 2017, 36 (05) : 568 - 582
  • [67] Analysis of the Role of the C-Terminal Tail in the Regulation of the Epidermal Growth Factor Receptor
    Kovacs, Erika
    Das, Rahul
    Wang, Qi
    Collier, Timothy S.
    Cantor, Aaron
    Huang, Yongjian
    Wong, Kathryn
    Mirza, Amar
    Barros, Tiago
    Grob, Patricia
    Jura, Natalia
    Bose, Ron
    Kuriyan, John
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2015, 35 (17) : 3083 - 3102
  • [68] Cell surface organization by the membrane skeleton
    Kusumi, A
    Sako, Y
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (04) : 566 - 574
  • [69] Paradigm shift of the plasma membrane concept from the two-dimensional continuum fluid to the partitioned fluid: High-speed single-molecule tracking of membrane molecules
    Kusumi, A
    Nakada, C
    Ritchie, K
    Murase, K
    Suzuki, K
    Murakoshi, H
    Kasai, RS
    Kondo, J
    Fujiwara, T
    [J]. ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2005, 34 : 351 - U54
  • [70] PIP3 Induces the Recycling of Receptor Tyrosine Kinases
    Laketa, Vibor
    Zarbakhsh, Sirus
    Traynor-Kaplan, Alexis
    MacNamara, Aidan
    Subramanian, Devaraj
    Putyrski, Mateusz
    Mueller, Rainer
    Nadler, Andre
    Mentel, Matthias
    Saez-Rodriguez, Julio
    Pepperkok, Rainer
    Schultz, Carsten
    [J]. SCIENCE SIGNALING, 2014, 7 (308)