Retinoic acid signaling in the nervous system of adult vertebrates

被引:110
作者
Mey, J
McCaffery, P
机构
[1] Rhein Westfal TH Aachen, Inst Biol 2, D-52074 Aachen, Germany
[2] UMMS EK Shriver Ctr, Waltham, MA USA
[3] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01605 USA
关键词
retinoic acid; plasticity; learning; Parkinson's disease; depression; regeneration;
D O I
10.1177/1073858404263520
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The majority of the functions of vitamin A are carried out by its metabolite, retinoic acid (RA), a potent transcriptional activator acting through members of the nuclear receptor family of transcription factors. In the CNS, RA was first recognized to be essential for the control of patterning and differentiation in the developing embryo. It has recently come to light, however, that many of the same functions that RA directs in the embryo are involved in the regulation of plasticity and regeneration in the adult brain. The same intricate metabolic control system of synthetic and catabolic enzymes, combined with cytoplasmic binding proteins, is used in both embryo and adult to create regions of high and low RA to modulate gene transcription. This review summarizes some of the discoveries in the new field of retinoid neurobiology including its functions in neural plasticity and LTP in the hippocampus; its possible role in motor disorders such as Parkinson's disease, motoneuron disease, and Huntington's disease; its role in regeneration after sciatic nerve and spinal cord injury; and its possible involvement in psychiatric diseases such as depression.
引用
收藏
页码:409 / 421
页数:13
相关论文
共 110 条
  • [1] The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures
    Abu-Abed, S
    Dollé, P
    Metzger, D
    Beckett, B
    Chambon, P
    Petkovich, M
    [J]. GENES & DEVELOPMENT, 2001, 15 (02) : 226 - 240
  • [2] Differential expression of the retinoic acid-metabolizing enzymes CYP26A1 and CYP26B1 during murine organogenesis
    Abu-Abed, S
    MacLean, G
    Fraulob, V
    Chambon, P
    Petkovich, M
    Dollé, P
    [J]. MECHANISMS OF DEVELOPMENT, 2002, 110 (1-2) : 173 - 177
  • [3] A retinoic acid receptor antagonist suppresses brain retinoic acid receptor overexpression and reverses a working memory deficit induced by chronic ethanol consumption in mice
    Alfos, S
    Boucheron, C
    Pallet, W
    Higueret, D
    Enderlin, V
    Béracochéa, D
    Jaffard, R
    Higueret, P
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2001, 25 (10) : 1506 - 1514
  • [4] AlvarezBuylla A, 1997, J NEUROBIOL, V33, P585, DOI 10.1002/(SICI)1097-4695(19971105)33:5<585::AID-NEU7>3.0.CO
  • [5] 2-0
  • [6] DIFFERENT PATTERNS OF GLYCOLIPID ANTIGENS ARE EXPRESSED FOLLOWING DIFFERENTIATION OF TERA-2 HUMAN EMBRYONAL CARCINOMA-CELLS INDUCED BY RETINOIC ACID, HEXAMETHYLENE BISACETAMIDE (HMBA) OR BROMODEOXYURIDINE (BUDR)
    ANDREWS, PW
    NUDELMAN, E
    HAKOMORI, SI
    FENDERSON, BA
    [J]. DIFFERENTIATION, 1990, 43 (02) : 131 - 138
  • [7] Acne drug depression warnings highlight need for expert care
    不详
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (14): : 1057 - 1057
  • [8] EMBRYONIC STEM-CELLS EXPRESS NEURONAL PROPERTIES IN-VITRO
    BAIN, G
    KITCHENS, D
    YAO, M
    HUETTNER, JE
    GOTTLIEB, DI
    [J]. DEVELOPMENTAL BIOLOGY, 1995, 168 (02) : 342 - 357
  • [9] EFFICIENT CLONING OF CDNAS OF RETINOIC ACID-RESPONSIVE GENES IN P19 EMBRYONAL CARCINOMA-CELLS AND CHARACTERIZATION OF A NOVEL MOUSE GENE, STRA1 (MOUSE LERK-2/EPLG2)
    BOUILLET, P
    OULADABDELGHANI, M
    VICAIRE, S
    GARNIER, JM
    SCHUHBAUR, B
    DOLLE, P
    CHAMBON, P
    [J]. DEVELOPMENTAL BIOLOGY, 1995, 170 (02) : 420 - 433
  • [10] BOYLAN JF, 1992, J BIOL CHEM, V267, P21486