Lysophosphatidic acid (LPA) is a novel extracellular regulator of cortical neuroblast morphology

被引:145
作者
Fukushima, N [1 ]
Weiner, JA
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, Program Neurosci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Program Biomed Sci, La Jolla, CA 92093 USA
关键词
lysophosphatidic acid; LPA receptor; ventricular zone; neurogenesis; cerebral cortex; neuroblast; interkinetic nuclear migration; Rho;
D O I
10.1006/dbio.2000.9930
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During cerebral cortical neurogenesis, neuroblasts in the ventricular zone (VZ) undergo a shape change termed "interkinetic nuclear migration" whereby cells alternate between fusiform and rounded morphologies. We previously identified Ip(Ai) the first receptor gene for a signaling phospholipid called lysophosphatidic acid (LPA) and showed its enriched expression in the VZ. Here we report that LPA induces changes in neuroblast morphology from fusiform to round in primary culture, accompanied by nuclear movements, and formation of f-actin retraction fibers. These changes are mediated by the activation of the small GTPase, Rho. In explant cultures, where the cerebral cortical architecture remains intact, LPA not only induces cellular and nuclear rounding in the VZ, but also produces an accumulation of rounded nuclei at the ventricular surface. Consistent with a biological role for these responses, utilization of a sensitive and specific bioassay indicates that postmitotic neurons can produce extracellular LPA. These results implicate LPA as a novel factor in cortical neurogenesis and further implicate LPA as an extracellular signal from postmitotic neurons to proliferating neuroblasts. (C) 2000 Academic Press.
引用
收藏
页码:6 / 18
页数:13
相关论文
共 54 条
[1]   EMBRYONIC VERTEBRATE CENTRAL NERVOUS SYSTEM - REVISED TERMINOLOGY [J].
ANGEVINE, JB ;
BODIAN, D ;
COULOMBR.AJ ;
EDDS, MV ;
HAMBURGE.V ;
JACOBSON, M ;
LYSER, KM ;
PRESTIGE, MC ;
VARON, S ;
WEISS, PA .
ANATOMICAL RECORD, 1970, 166 (02) :257-&
[2]  
BERRY M, 1965, J ANAT, V99, P691
[3]  
Blaschke AJ, 1996, DEVELOPMENT, V122, P1165
[4]   Response diversity and the timing of progenitor cell maturation are regulated by developmental changes in EGFR expression in the cortex [J].
Burrows, RC ;
Wancio, D ;
Levitt, P ;
Lillien, L .
NEURON, 1997, 19 (02) :251-267
[5]   NUMBERS, TIME AND NEOCORTICAL NEURONOGENESIS - A GENERAL DEVELOPMENTAL AND EVOLUTIONARY MODEL [J].
CAVINESS, VS ;
TAKAHASHI, T ;
NOWAKOWSKI, RS .
TRENDS IN NEUROSCIENCES, 1995, 18 (09) :379-383
[6]   Clonal cell lines produced by infection of neocortical neuroblasts using multiple oncogenes transduced by retroviruses [J].
Chun, J ;
Jaenisch, R .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1996, 7 (04) :304-321
[7]  
CHUN J, 1999, CELL BIOCH BIOPHYS, V30, P243
[8]   TRANSIENT CELLS OF THE DEVELOPING MAMMALIAN TELENCEPHALON ARE PEPTIDE-IMMUNOREACTIVE NEURONS [J].
CHUN, JJM ;
NAKAMURA, MJ ;
SHATZ, CJ .
NATURE, 1987, 325 (6105) :617-620
[9]   Role of transactivation of the EGF receptor in signalling by G-protein-coupled receptors [J].
Daub, H ;
Weiss, FU ;
Wallasch, C ;
Ullrich, A .
NATURE, 1996, 379 (6565) :557-560
[10]  
Doe CQ, 1998, J NEUROBIOL, V36, P111, DOI 10.1002/(SICI)1097-4695(199808)36:2<111::AID-NEU2>3.0.CO