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通过激活非NMDA离子型受体和I组代谢型谷氨酸受体刺激神经元中的钠-钾-2氯共转运体。

Stimulation of Na-K-2Cl cotransporter in neurons by activation of Non-NMDA ionotropic receptor and group-I mGluRs.

作者信息

Schomberg S L, Su G, Haworth R A, Sun D

机构信息

Department of Neurological Surgery, University of Wisconsin Medical School, Madison, Wisconsin 53792, USA.

出版信息

J Neurophysiol. 2001 Jun;85(6):2563-75. doi: 10.1152/jn.2001.85.6.2563.

Abstract

In a previous study, we found that Na(+)-K(+)-2Cl(-) cotransporter in immature cortical neurons was stimulated by activation of the ionotropic N-methyl-D-aspartate (NMDA) glutamate receptor in a Ca(2+)-dependent manner. In this report, we investigated whether the Na(+)-K(+)-2Cl(-) cotransporter in immature cortical neurons is stimulated by non-NMDA glutamate receptor-mediated signaling pathways. Expression of the Na(+)-K(+)-2Cl(-) cotransporter and metabotropic glutamate receptors (mGluR1 and 5) was detected in cortical neurons via immunoblotting and immunofluorescence staining. Significant stimulation of cotransporter activity was observed in the presence of both trans-(+/-)-1-aminocyclopentane-trans-1,3-dicarboxylic acid (trans-ACPD) (10 microM), a metabotropic glutamate receptor (mGluR) agonist, and (RS)-3,5-dihydroxyphenylglycine (DHPG) (20 microM), a selective group-I mGluR agonist. Both trans-ACPD and DHPG-mediated effects on the cotransporter were eradicated by bis-(o-aminophenoxy)-N,N,N',N'-tetraacetic acid-AM, a Ca(2+) chelator. In addition, DHPG-induced stimulation of the cotransporter activity was inhibited in the presence of mGluRs antagonist (RS)-1-aminoindan-1,5-dicarboxylic acid (AIDA) (1 mM) and also with selective mGluR1 antagonist 7-(hydroxyimino)cyclopropa[b]chromen-1a-carboxylate ethyl ester (CPCCOEt) (100 microM). A DHPG-induced rise in intracellular Ca(2+) in cortical neurons was detected with Fura-2. Moreover, DHPG-mediated stimulation of the cotransporter was abolished by inhibition of Ca(2+)/CaM kinase II. Interestingly, the cotransporter activity was increased by activation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor. These results suggest that the Na(+)-K(+)-2Cl(-) cotransporter in immature cortical neurons is stimulated by group-I mGluR- and AMPA-mediated signal transduction pathways. The effects are dependent on a rise of intracellular Ca(2+).

摘要

在之前的一项研究中,我们发现未成熟皮层神经元中的钠-钾-2氯协同转运体受离子型N-甲基-D-天冬氨酸(NMDA)谷氨酸受体激活的刺激,且呈钙依赖性。在本报告中,我们研究了未成熟皮层神经元中的钠-钾-2氯协同转运体是否受非NMDA谷氨酸受体介导的信号通路刺激。通过免疫印迹和免疫荧光染色在皮层神经元中检测钠-钾-2氯协同转运体和代谢型谷氨酸受体(mGluR1和5)的表达。在代谢型谷氨酸受体(mGluR)激动剂反式-(+/-)-1-氨基环戊烷-1,3-二羧酸(反式-ACPD)(10微摩尔)和选择性I组mGluR激动剂(RS)-3,5-二羟基苯甘氨酸(DHPG)(20微摩尔)存在的情况下,观察到协同转运体活性受到显著刺激。反式-ACPD和DHPG对协同转运体的作用均被钙螯合剂双-(邻氨基苯氧基)-N,N,N',N'-四乙酸-AM消除。此外,在代谢型谷氨酸受体拮抗剂(RS)-1-氨基茚满-1,5-二羧酸(AIDA)(1毫摩尔)以及选择性mGluR1拮抗剂7-(羟基亚氨基)环丙[b]色烯-1a-羧酸乙酯(CPCCOEt)(100微摩尔)存在的情况下,DHPG诱导的协同转运体活性刺激受到抑制。用Fura-2检测到DHPG诱导的皮层神经元细胞内钙升高。此外,钙/钙调蛋白激酶II的抑制消除了DHPG介导的协同转运体刺激。有趣的是,α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的激活增加了协同转运体活性。这些结果表明,未成熟皮层神经元中的钠-钾-2氯协同转运体受I组mGluR和AMPA介导的信号转导通路刺激。这些作用依赖于细胞内钙升高。

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