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Temporal analysis of the upregulation of GluR5 mRNA editing with age: regional evaluation.

作者信息

Paschen W, Schmitt J, Dux E, Djuricic B

机构信息

Max-Planck-Institut for Neurological Research, Department of Experimental Neurology, Köln, Germany.

出版信息

Brain Res Dev Brain Res. 1995 May 26;86(1-2):359-63. doi: 10.1016/0165-3806(95)00042-c.

DOI:10.1016/0165-3806(95)00042-c
PMID:7656430
Abstract

The extent of mRNA editing of the kainate receptor subunit GluR5 was evaluated in tissue samples taken from the cerebral cortex, hippocampus and cerebellum of rat brain and in cortical neurons held in tissue culture, by PCR amplification of GluR5 cDNA across the edited base and restriction analysis of the amplification product with Bbv 1. Samples were taken from embryonic brains of rats at day 21 of gestation and from brains 4 days, 25 days and 3 month after birth. Cortical neurons were isolated from the tissue at day 19 of gestation and kept for 2 or 8 days in culture. The extent of editing was sharply upregulated during development in all brain structures studied. In the cortex and hippocampus the extent of editing exhibited already the adult state 4 days after birth. In the cerebellum, in contrast, the extent of editing was still 42 +/- 11.4% 25 days after birth but 82 +/- 6.2% in the adult state. In neurons held in tissue culture for up to 8 days, upregulation of editing did not take place. It is concluded that GluR5 editing is differently regulated in different brain structures and that the developmental changes observed in vivo are blocked when cells are kept in vitro.

摘要

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引用本文的文献

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Kainate receptors expressed by a subpopulation of developing nociceptors rapidly switch from high to low Ca2+ permeability.发育中的伤害感受器亚群所表达的海人藻酸受体迅速从高钙离子通透性转变为低钙离子通透性。
J Neurosci. 2001 Jul 1;21(13):4572-81. doi: 10.1523/JNEUROSCI.21-13-04572.2001.
3
Glutamate receptor subunits GluR5 and KA-2 are coexpressed in rat trigeminal ganglion neurons.
谷氨酸受体亚基GluR5和KA-2在大鼠三叉神经节神经元中共同表达。
J Neurosci. 1997 Sep 1;17(17):6611-20. doi: 10.1523/JNEUROSCI.17-17-06611.1997.