Effect of 17β-estradiol on gene expression in lumbar spinal cord following sciatic nerve crush injury in ovariectomized mice

被引:46
作者
Islamov, RR [1 ]
Hendricks, WA [1 ]
Katwa, LC [1 ]
McMurray, RJ [1 ]
Pak, ES [1 ]
Spanier, NS [1 ]
Murashov, AK [1 ]
机构
[1] E Carolina Univ, Brody Sch Med, Dept Physiol, Greenville, NC 27858 USA
关键词
spinal cord; sciatic nerve; motor neurom; estrogen; estrogen receptor; gene expression; regeneration;
D O I
10.1016/S0006-8993(02)04191-4
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Previously, we observed that estrogen treatment enhances regeneration of the sciatic nerve after crush injury [Brain Res. 943 (2002) 283]. In this research, we studied expression of estrogen receptors and effects of estrogen on gene expression in the lumbar spinal cord, following sciatic nerve crush injury. Using the Atlas Mouse 1.2 Array, changes in the expression of 267 of 1176 genes were registered 4 days after nerve injury. Those genes that exhibited a change in signal intensity ratios of 2-fold or greater were selected as up-regulated (42) or down-regulated (21). In estrogen treated mice, we have observed up-regulation of the genes known to control apoptosis, cell proliferation, and growth, which might account for the positive effects of estrogen on the regeneration of motor neurons. Immunohistochemical staining revealed estrogen receptor-a and estrogen receptor-P localized in the nucleus and cytoplasm of lumbar motor neurons, and in the regenerating neurites of the sciatic nerve. Expression of estrogen receptor-a and estrogen receptor-P mRNA in lumbar spinal cord was shown by traditional RT-PCR. Using real-time quantitative RT-PCR, we demonstrated increased expression of estrogen receptors-alpha and -beta mRNA on the injured side of the lumbar spinal cord. Western blot analysis showed the accumulation of ERs in regenerating sciatic nerve, and revealed a 40% increase of activated ERK1/2 in estrogen treated mice, compared to placebo. Our findings indicate that: (i) axotomized motor neurons increase expression of estrogen receptors-alpha and -beta mRNA, (ii) estrogen mediates the expression of genes which accelerate the growth and maturation of axons, and (iii) estrogen receptors are transported from the perikaryon into regenerating neurites, and estrogen promotes regeneration locally through the non-genomic ERK-activated signaling pathway. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:65 / 75
页数:11
相关论文
共 50 条
[1]
Colocalization of oestrogen receptor immunoreactivity and preproenkephalin mRNA expression to neurons in the superficial laminae of the spinal and medullary dorsal horn of rats [J].
Amandusson, A ;
Hermanson, O ;
Blomqvist, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (11) :2440-2445
[2]
SEX-DIFFERENCES IN THE PATTERN OF STEROID ACCUMULATION BY MOTONEURONS OF THE RAT LUMBAR SPINAL-CORD [J].
BREEDLOVE, SM ;
ARNOLD, AP .
JOURNAL OF COMPARATIVE NEUROLOGY, 1983, 215 (02) :211-216
[3]
Burke KA, 2000, J NEUROSCI RES, V61, P329, DOI 10.1002/1097-4547(20000801)61:3<329::AID-JNR11>3.0.CO
[4]
2-A
[5]
Interactions of estrogens and insulin-like growth factor-I in the brain:: implications for neuroprotection [J].
Cardona-Gómez, GP ;
Mendez, P ;
DonCarlos, LL ;
Azcoitia, I ;
Garcia-Segura, LM .
BRAIN RESEARCH REVIEWS, 2001, 37 (1-3) :320-334
[6]
PI3-kinase in concert with Src promotes the S-phase entry of oestradiol-stimulated MCF-7 cells [J].
Castoria, G ;
Migliaccio, A ;
Bilancio, A ;
Di Domenico, M ;
de Falco, A ;
Lombardi, M ;
Fiorentino, R ;
Varricchio, L ;
Barone, MV ;
Auricchio, F .
EMBO JOURNAL, 2001, 20 (21) :6050-6059
[7]
Cato A.C., 2002, SCI STKE, V2002, pre9, DOI [DOI 10.1126/STKE.2002.138.RE9, 10.1126/stke.2002.138.re9]
[8]
Green PS, 1997, J NEUROSCI, V17, P511
[9]
Estradiol-induced nongenomic calcium signaling regulates genotropic signaling in macrophages [J].
Guo, ZY ;
Krücken, J ;
Benten, WPM ;
Wunderlich, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (09) :7044-7050
[10]
Histochemical and electrophysiological evidence for estrogen receptors on cultured astrocytes:: colocalization with cholinergic receptors [J].
Hösli, E ;
Rühl, W ;
Hösli, L .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2000, 18 (01) :101-111