Regulated expression of dual specificity protein phosphatases in rat brain

被引:29
作者
Boschert, U [1 ]
Dickinson, R
Muda, M
Camps, M
Arkinstall, S
机构
[1] Serono Int SA, Serono Pharmaceut Res Inst, CH-1228 Geneva, Switzerland
[2] Univ Oxford, Dept Anat, Oxford OX1 3QX, England
关键词
B23; development; dual specificity phosphatases; ERK; JNK/SAPK; MAP kinase; MKP-1; MKP-3; MKP-X; p38; seizures;
D O I
10.1097/00001756-199812210-00014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
ACTIVATED mitogen-activated protein (MAP) kinases play an essential role controlling many neuronal functions. Dual specificity protein phosphatases (DS-PTPs) elicit selective inactivation of MAP kinases and are under tight transcriptional control. We have studied expression of four DS-PTPs (MKP-1, MKP-X, MKP-3 and B23) in rat brain and examined changes during post-natal development and following kainic acid induced seizure activity. In normal adult brain these DS-PTPs exhibit a strikingly different expression pattern. Only MKP-1 was regulated during development with levels increased transiently (P15-P21) within the thalamus and somatosensory cortex. Following kainate treatment, MKP-1, MKP-3 and B23 all exhibit striking changes in expression within hippocampal subfields CA1-3 and dentate gyrus. Regulated transcription of DS-PTPs may play a critical role controlling MAP kinase dependent processes including synaptic remodeling and neuronal death. (C) 1998 Lippincott Williams & Wilkins.
引用
收藏
页码:4081 / 4086
页数:6
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