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The transcription factor CREB, but not immediate-early gene encoded proteins, is expressed in activated microglia of lumbar spinal cord following sciatic nerve transection in the rat.

作者信息

Herdegen T, Fiallos-Estrada C, Schmid W, Bravo R, Zimmermann M

机构信息

II. Physiologisches Institut, Universität Heidelberg, FRG.

出版信息

Neurosci Lett. 1992 Aug 3;142(1):57-61. doi: 10.1016/0304-3940(92)90619-i.

DOI:10.1016/0304-3940(92)90619-i
PMID:1407719
Abstract

Expression of CREB, JUN, FOS and KROX-24 proteins was investigated in glial cells of the lumbar spinal cord. In untreated rats, CREB, c-JUN and JUN D were present in glial cells of the ventral and dorsal horn. Following sciatic nerve transection, the number of CREB immunoreactive glial cells increased in both the ipsilateral ventral and dorsal horns between 24 h and 48 h, reached a maximum after 5 days and returned to control levels after 20 days. Counterstaining with Cresyl violet, a general stain of cells, revealed that the increase of CREB positive glial cells was congruent with the increase of the number of glial cells. Staining with GFAP, a marker for astrocytes, showed an increase in intensity of labelling but no change in number of GFAP labelled cells. This indicates a constitutive expression of CREB in activated microglia. The number of glial cells labelled by c-JUN and JUN D did not change, and glial cells were not labelled by FOS and KROX-24 proteins following sciatic nerve transection. These findings demonstrate that proliferation and differentiation of glial cells in vivo can occur in absence of JUN, FOS and KROX proteins.

摘要

相似文献

1
The transcription factor CREB, but not immediate-early gene encoded proteins, is expressed in activated microglia of lumbar spinal cord following sciatic nerve transection in the rat.
Neurosci Lett. 1992 Aug 3;142(1):57-61. doi: 10.1016/0304-3940(92)90619-i.
2
The transcription factors c-JUN, JUN D and CREB, but not FOS and KROX-24, are differentially regulated in axotomized neurons following transection of rat sciatic nerve.转录因子c-JUN、JUN D和CREB,而非FOS和KROX-24,在大鼠坐骨神经横断后被切断的轴突损伤神经元中受到差异调节。
Brain Res Mol Brain Res. 1992 Jul;14(3):155-65. doi: 10.1016/0169-328x(92)90170-g.
3
Specific temporal and spatial distribution of JUN, FOS, and KROX-24 proteins in spinal neurons following noxious transsynaptic stimulation.伤害性经突触刺激后脊髓神经元中JUN、FOS和KROX-24蛋白的特定时空分布。
J Comp Neurol. 1991 Nov 1;313(1):178-91. doi: 10.1002/cne.903130113.
4
Expression of nitric oxide synthase and colocalisation with Jun, Fos and Krox transcription factors in spinal cord neurons following noxious stimulation of the rat hindpaw.大鼠后爪受到伤害性刺激后脊髓神经元中一氧化氮合酶的表达及其与Jun、Fos和Krox转录因子的共定位
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5
JUN, FOS, KROX, and CREB transcription factor proteins in the rat cortex: basal expression and induction by spreading depression and epileptic seizures.大鼠皮层中的JUN、FOS、KROX和CREB转录因子蛋白:基础表达以及扩散性抑制和癫痫发作诱导情况
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6
Expression of JUN, KROX, and CREB transcription factors in goldfish and rat retinal ganglion cells following optic nerve lesion is related to axonal sprouting.视神经损伤后金鱼和大鼠视网膜神经节细胞中JUN、KROX和CREB转录因子的表达与轴突发芽有关。
J Neurobiol. 1993 Apr;24(4):528-43. doi: 10.1002/neu.480240410.
7
Differential time course and spatial expression of Fos, Jun, and Krox-24 proteins in spinal cord of rats undergoing subacute or chronic somatic inflammation.亚急性或慢性躯体炎症大鼠脊髓中Fos、Jun和Krox-24蛋白的差异时程和空间表达。
J Comp Neurol. 1993 Jul 8;333(2):223-35. doi: 10.1002/cne.903330208.
8
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Brain Res Mol Brain Res. 1994 Oct;26(1-2):259-70. doi: 10.1016/0169-328x(94)90098-1.
9
Expression of activating transcription factor-2, serum response factor and cAMP/Ca response element binding protein in the adult rat brain following generalized seizures, nerve fibre lesion and ultraviolet irradiation.全身性癫痫发作、神经纤维损伤及紫外线照射后成年大鼠脑中激活转录因子2、血清反应因子和cAMP/Ca反应元件结合蛋白的表达
Neuroscience. 1997 Nov;81(1):199-212. doi: 10.1016/s0306-4522(97)00170-x.
10
Induction of c-Jun and suppression of CREB transcription factor proteins in axotomized neurons of substantia nigra and covariation with tyrosine hydroxylase.黑质轴突切断神经元中c-Jun的诱导及CREB转录因子蛋白的抑制与酪氨酸羟化酶的共变关系
Mol Cell Neurosci. 1994 Oct;5(5):431-41. doi: 10.1006/mcne.1994.1053.

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