Progesterone synthesis and myelin formation in peripheral nerves

被引:105
作者
Schumacher, M
Guennoun, R
Mercier, G
Désarnaud, F
Lacor, P
Bénavides, J
Ferzaz, B
Robert, F
Baulieu, EE
机构
[1] INSERM, U488, F-94276 Le Kremlin Bicetre, France
[2] Sanofi Synthelabo, Bagneux, France
关键词
progesterone; neurosteroid; myelin; Schwann cell; sciatic nerve;
D O I
10.1016/S0165-0173(01)00139-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Progesterone is synthesized in the nervous system by neurons and glial cells. Because of their simple structure, plasticity and capacity of regeneration, peripheral nerves are particularly well suited for studying the biosynthesis, mechanisms of action and effects of the hormone. Schwann cells, the myelinating glial cells in the peripheral nervous system, synthesize progesterone in response to a diffusible neuronal signal. In peripheral nerves, the local synthesis of progesterone plays an important role in the formation of myelin sheaths. This has been shown in vivo, after cryolesion of the mouse sciatic nerve, and in vitro, in cocultures of Schwann cells and sensory neurons. Schwann cells also express an intracellular receptor for progesterone, which thus functions as an autocrine signalling molecule. Progesterone may promote myelination by activating the expression of genes coding for transcription factors (Krox-20) and/or for myelin proteins (P0, PMP22). Recently, it has been proposed that progesterone may indirectly regulate myelin formation by influencing gene expression in neurons. Steroid hormones also influence the proliferation of Schwann cells: estradiol becomes a potent mitogen for Schwann cells when levels of cAMP are elevated and glucocorticosteroids have been shown to increase the mitogenic effects of peptide growth factors. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:343 / 359
页数:17
相关论文
共 161 条
[1]  
AKWA Y, 1993, CR ACAD SCI III-VIE, V316, P410
[2]   DEXAMETHASONE STIMULATES THE BIOCHEMICAL DIFFERENTIATION OF FETAL FOREBRAIN CELLS IN REAGGREGATING CULTURES [J].
ALMAZAN, G ;
HONEGGER, P ;
DUPASQUIER, P ;
MATTHIEU, JM .
DEVELOPMENTAL NEUROSCIENCE, 1986, 8 (01) :14-23
[3]   Correlation between sex hormones and magnetic resonance imaging lesions in multiple sclerosis [J].
Bansil, S ;
Lee, HJ ;
Jindal, S ;
Holtz, CR ;
Cook, SD .
ACTA NEUROLOGICA SCANDINAVICA, 1999, 99 (02) :91-94
[4]  
BAULIEU EE, 1999, NEUROSTEROIDS NEW RE, P378
[5]   Steroid hormone receptors: an update [J].
Beato, M ;
Klug, J .
HUMAN REPRODUCTION UPDATE, 2000, 6 (03) :225-236
[6]   A RANDOMIZED, CONTROLLED TRIAL OF CORTICOSTEROIDS IN THE TREATMENT OF ACUTE OPTIC NEURITIS [J].
BECK, RW ;
CLEARY, PA ;
ANDERSON, MM ;
KELTNER, JL ;
SHULTS, WT ;
KAUFMAN, DI ;
BUCKLEY, EG ;
CORBETT, JJ ;
KUPERSMITH, MJ ;
MILLER, NR ;
SAVINO, PJ ;
GUY, JR ;
TROBE, JD ;
MCCRARY, JA ;
SMITH, CH ;
CHROUSOS, GA ;
THOMPSON, HS ;
KATZ, BJ ;
BRODSKY, MC ;
GOODWIN, JA ;
ATWELL, CW .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (09) :581-588
[7]  
Bellone E, 1999, Hum Mutat, V14, P353, DOI 10.1002/(SICI)1098-1004(199910)14:4<353::AID-HUMU17>3.0.CO
[8]  
2-4
[9]   IDENTIFICATION OF DES-(GLY-ILE)-ENDOZEPINE AS AN EFFECTOR OF CORTICOTROPIN-DEPENDENT ADRENAL STEROIDOGENESIS - STIMULATION OF CHOLESTEROL DELIVERY IS MEDIATED BY THE PERIPHERAL BENZODIAZEPINE RECEPTOR [J].
BESMAN, MJ ;
YANAGIBASHI, K ;
LEE, TD ;
KAWAMURA, M ;
HALL, PF ;
SHIVELY, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :4897-4901
[10]   NEURONS REGULATE SCHWANN-CELL GENES BY DIFFUSIBLE MOLECULES [J].
BOLIN, LM ;
SHOOTER, EM .
JOURNAL OF CELL BIOLOGY, 1993, 123 (01) :237-243