Lysophosphatidic acid influences the morphology and motility of young, postmitotic cortical neurons

被引:118
作者
Fukushima, N [1 ]
Weiner, JA
Kaushal, D
Contos, JJA
Rehen, SK
Kingsbury, MA
Kim, KY
Chun, J
机构
[1] Univ Calif San Diego, Sch Med, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Neurosci Program, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Biomed Sci Program, La Jolla, CA 92093 USA
[4] Hokkaido Univ, Grad Sch Med, Dept Biochem, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[5] Merck Res Labs, Dept Mol Neurosci, San Diego, CA 92121 USA
基金
美国国家科学基金会;
关键词
D O I
10.1006/mcne.2002.1123
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Lysophosphatidic acid (LPA) is a bioactive lysophospholipid that produces process retraction and cell rounding through its cognate receptors in neuroblastoma cell lines. Although the expression profile of LPA receptors in developing brains suggests a role for LPA in central nervous system (CNS) development, how LPA influences the morphology of postmitotic CNS neurons remains to be determined. Here we have investigated the effects of exogenous LPA on the morphology of young, postmitotic neurons in primary culture. When treated with LPA, these neurons responded by not only retracting processes but also producing retraction fiber "caps" characterized by fine actin filaments emanating from a dense core. Retraction fiber caps gradually vanished due to the outward spread of regrowing membranes along the fibers, suggesting a role for caps as scaffolds for regrowth of retracted processes. Furthermore, LPA also affects neuronal migration in vitro and in vivo. Taken together, these results implicate LPA as an extracellular lipid signal affecting process outgrowth and migration of early postmitotic neurons during development.
引用
收藏
页码:271 / 282
页数:12
相关论文
共 48 条
  • [1] Characterization of a novel subtype of human G protein-coupled receptor for lysophosphatidic acid
    An, SZ
    Bleu, T
    Hallmark, OG
    Goetzl, EJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (14) : 7906 - 7910
  • [2] Molecular cloning and characterization of a novel human G-protein-coupled receptor, EDG7, for lysophosphatidic acid
    Bandoh, K
    Aoki, J
    Hosono, H
    Kobayashi, S
    Kobayashi, T
    Murakami-Murofushi, K
    Tsujimoto, M
    Arai, H
    Inoue, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) : 27776 - 27785
  • [3] Slit proteins: key regulators of axon guidance, axonal branching, and cell migration
    Brose, K
    Tessier-Lavigne, M
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) : 95 - 102
  • [4] Rho-stimulated contractility drives the formation of stress fibers and focal adhesions
    ChrzanowskaWodnicka, M
    Burridge, K
    [J]. JOURNAL OF CELL BIOLOGY, 1996, 133 (06) : 1403 - 1415
  • [5] Lysophospholipid receptors: Implications for neural signaling
    Chun, J
    [J]. CRITICAL REVIEWS IN NEUROBIOLOGY, 1999, 13 (02): : 151 - 168
  • [6] Clonal cell lines produced by infection of neocortical neuroblasts using multiple oncogenes transduced by retroviruses
    Chun, J
    Jaenisch, R
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 1996, 7 (04) : 304 - 321
  • [7] A Growing Family of Receptor Genes for Lysophosphatidic Acid (LPA) and other Lysophospholipids (LPs)
    Chun J.
    Contos J.J.A.
    Munroe D.
    [J]. Cell Biochemistry and Biophysics, 1999, 30 (2) : 213 - 242
  • [8] Lysophosphatidic acid receptors
    Contos, JJA
    Ishii, I
    Chun, J
    [J]. MOLECULAR PHARMACOLOGY, 2000, 58 (06) : 1188 - 1196
  • [9] Requirement for the IpA1 lysophosphatidic acid receptor gene in normal suckling behavior
    Contos, JJA
    Fukushima, N
    Weiner, JA
    Kaushal, D
    Chun, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (24) : 13384 - 13389
  • [10] Genomic characterization of the lysophosphatidic acid receptor gene, IpA2/Edg4, and identification of a frameshift mutation in a previously characterized cDNA
    Contos, JJA
    Chun, J
    [J]. GENOMICS, 2000, 64 (02) : 155 - 169