Adaptor proteins: Flexible and dynamic modulators of immune cell signalling

被引:16
作者
Borowicz, Pawel [1 ]
Chan, Hanna [1 ]
Hauge, Anette [1 ]
Spurkland, Anne [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Mol Med, Oslo, Norway
基金
美国国家卫生研究院;
关键词
adaptor proteins; docking proteins; intracellular signalling; scaffold proteins; SH2; domain; TSAd; INTRINSICALLY DISORDERED PROTEINS; SHORT LINEAR MOTIFS; HOMOLOGY; DOMAINS; SH2; DOMAIN; SCAFFOLD PROTEINS; MICE LACKING; T-CELLS; STRUCTURAL DISORDER; POSTTRANSLATIONAL MODIFICATIONS; PEROXISOME BIOGENESIS;
D O I
10.1111/sji.12951
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To maintain homeostasis, all cells respond to environmental cues via a multitude of surface receptors. In order to act appropriately in their environment, cells are dependent on the transduction of the incoming signal through tightly regulated and interconnected signalling pathways to the cell nucleus. In particular, cells implicated in the immune system greatly depend on such systems to respond in a flexible and dynamic manner to environmental challenges. One major group of intracellular proteins that are involved in these signalling pathways are adaptor proteins. Although adaptor proteins are essential for normal immune cell operation, the functional role of this group of signalling proteins remains to be fully appreciated. So far, research on adaptor proteins has revealed their unique potential in building transient complexes in a reversible, dynamic and inducible manner. In this review, we explore the roles of adaptor proteins - in space and time of intracellular signalling - and their associations with human disease. Examples of adaptor proteins expressed in hematopoietic cells highlight their crucial role in the immune system. Lastly, we present challenges faced in elucidating roles of adaptor proteins, as illustrated by the T cell-specific adaptor (TSAd) protein encoded by the SH2D2A gene.
引用
收藏
页数:26
相关论文
共 257 条
  • [1] Abrahamsen G, 2018, SCI REP, V6, P1
  • [2] Agostinelli C, 2014, AM J SURG PATHOL, V38, P1349, DOI 10.1097/PAS.0000000000000309
  • [3] The SH3 domains of the protein kinases ITK and LCK compete for adjacent sites on T cell?specific adapter protein
    Andersen, Thorny Cecilie Bie
    Kristiansen, Per Eugen
    Huszenicza, Zsuzsa
    Johansson, Maria U.
    Gopalakrishnan, Ramakrishna Prabhu
    Kjelstrup, Hanna
    Boyken, Scott
    Sundvold-Gjerstad, Vibeke
    Granum, Stine
    Sorlie, Morten
    Backe, Paul Hoff
    Fulton, D. Bruce
    Karlsson, B. Goran
    Andreotti, Amy H.
    Spurkland, Anne
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2019, 294 (42) : 15480 - 15494
  • [4] SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system
    Arnaud, Estelle
    Zenker, Jennifer
    Charles, Anne-Sophie de Preux
    Stendel, Claudia
    Roos, Andreas
    Medard, Jean-Jacques
    Tricaud, Nicolas
    Weis, Joachim
    Suter, Ueli
    Senderek, Jan
    Chrast, Roman
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (41) : 17528 - 17533
  • [5] Systematic search for gastric cancer-specific genes based on SAGE data: melanoma inhibitory activity and matrix metalloproteinase-10 are novel prognostic factors in patients with gastric cancer
    Aung, PP
    Oue, N
    Mitani, Y
    Nakayama, H
    Yoshida, K
    Noguchi, T
    Bosserhoff, AK
    Yasui, W
    [J]. ONCOGENE, 2006, 25 (17) : 2546 - 2557
  • [6] Modulation of Intrinsically Disordered Protein Function by Post-translational Modifications
    Bah, Alaji
    Forman-Kay, Julie D.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (13) : 6696 - 6705
  • [7] Folding of an intrinsically disordered protein by phosphorylation as a regulatory switch
    Bah, Alaji
    Vernon, Robert M.
    Siddiqui, Zeba
    Krzeminski, Mickael
    Muhandiram, Ranjith
    Zhao, Charlie
    Sonenberg, Nahum
    Kay, Lewis E.
    Forman-Kay, Julie D.
    [J]. NATURE, 2015, 519 (7541) : 106 - U240
  • [8] Bypassing ubiquitination enables LAT recycling to the cell surface and enhanced signaling in T cells
    Balagopalan, Lakshmi
    Malik, Hiba
    McIntire, Katherine M.
    Garvey, Joseph A.
    Nguyen, Tiffany
    Rodriguez-Pena, Ana B.
    Samelson, Lawrence E.
    [J]. PLOS ONE, 2020, 15 (02):
  • [9] The Linker for Activation of T Cells (LAT) Signaling Hub: From Signaling Complexes to Microclusters
    Balagopalan, Lakshmi
    Kortum, Robert L.
    Coussens, Nathan P.
    Barr, Valarie A.
    Samelson, Lawrence E.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (44) : 26422 - 26429
  • [10] High levels of structural disorder in scaffold proteins as exemplified by a novel neuronal protein, CASK-interactive protein1
    Balazs, Annamaria
    Csizmok, Veronika
    Buday, Laszlo
    Rakacs, Marianna
    Kiss, Robert
    Bokor, Monika
    Udupa, Roopesh
    Tompa, Kalman
    Tompa, Peter
    [J]. FEBS JOURNAL, 2009, 276 (14) : 3744 - 3756