An Emerging Role for Voltage-Gated Na+ Channels in Cellular Migration: Regulation of Central Nervous System Development and Potentiation of Invasive Cancers

被引:86
作者
Brackenbury, William J. [1 ]
Djamgoz, Mustafa B. A. [2 ]
Isom, Lori L. [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[2] Univ London Imperial Coll Sci Technol & Med, Div Cell & Mol Biol, Neurosci Solut Canc Res Grp, London, England
关键词
Cancer; Development; Migration; Signaling; Voltage-gated Na+ channel;
D O I
10.1177/1073858408320293
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Voltage-gated Na+ channels (VGSCs) exist as macromolecular complexes containing a pore-forming alpha subunit and one or more beta subunits. The VGSC alpha subunit gene family consists of 10 members, which have distinct tissue-specific and developmental expression profiles. So far, four beta subunits (beta 1-beta 4) and one splice variant of beta 1 (beta 1A, also called beta 1B) have been identified. VGSC beta subunits are multifunctional, serving as modulators of channel activity, regulators of channel cell surface expression, and as members of the immunoglobulin superfamily, cell adhesion molecules (CAMs) beta subunits are substrates of beta amyloid precursor protein-cleaving enzyme (BACE1) and gamma-secretase, yielding intracellular domains (ICDs) that may further modulate cellular activity via transcription. Recent evidence shows that beta 1 regulates migration and pathfinding in the developing postnatal CNS in vivo. The alpha and beta subunits, together with other components of the VGSC signaling complex, may have dynamic interactive roles depending on cell/tissue type, developmental stage, and pathophysiology. In addition to excitable cells like nerve and muscle, VGSC alpha and beta subunits are functionally expressed in cells that are traditionally considered nonexcitable, including glia, vascular endothelial cells, and cancer cells. In particular, the alpha subunits are up-regulated in line with metastatic potential and are proposed to enhance cellular migration and invasion. In contrast to the alpha subunits, beta 1 is more highly expressed in weakly metastatic cancer cells, and evidence suggests that its expression enhances cellular adhesion. Thus, novel roles are emerging for VGSC alpha and beta subunits in regulating migration during normal postnatal development of the CNS as well as during cancer metastasis. NEUROSCIENTIST 14(6):571-583, 2008. DOI: 10.1177/1073858408320293
引用
收藏
页码:571 / 583
页数:13
相关论文
共 144 条
  • [1] Abdul M, 2002, ANTICANCER RES, V22, P1727
  • [2] Abdul M, 2001, ANTICANCER RES, V21, P2045
  • [3] Neuroendocrine cells in tumour growth of the prostate
    Abrahamsson, PA
    [J]. ENDOCRINE-RELATED CANCER, 1999, 6 (04) : 503 - 519
  • [4] Identification of SCN3B as a novel p53-inducible proapoptotic gene
    Adachi, K
    Toyota, M
    Sasaki, Y
    Yamashita, T
    Ishida, S
    Ohe-Toyota, M
    Maruyama, R
    Hinoda, Y
    Saito, T
    Imai, K
    Kudo, R
    Tokino, T
    [J]. ONCOGENE, 2004, 23 (47) : 7791 - 7798
  • [5] Ion channel phenotype of melanoma cell lines
    Allen, DH
    LeppleWienhues, A
    Cahalan, MD
    [J]. JOURNAL OF MEMBRANE BIOLOGY, 1997, 155 (01) : 27 - 34
  • [6] [Anonymous], 1992, Ionic Channels of Excitable Membranes Sunderland
  • [7] [Anonymous], MOL CANC
  • [8] Armisén R, 2002, J NEUROSCI, V22, P8347
  • [9] A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy
    Audenaert, D
    Claes, L
    Ceulemans, B
    Löfgren, A
    Van Broeckhoven, C
    De Jonghe, P
    [J]. NEUROLOGY, 2003, 61 (06) : 854 - 856
  • [10] BARRES BA, 1990, ANNU REV NEUROSCI, V13, P441, DOI 10.1146/annurev.ne.13.030190.002301