Gebremedhin Debebe, Yamaura Ken, Zhang Chenyang, Bylund Johan, Koehler Raymond C, Harder David R
Department of Physiology and Cardiovascular Research Center, Medical College of Wisconsin, Milwaukee 53226, USA.
J Neurosci. 2003 Mar 1;23(5):1678-87. doi: 10.1523/JNEUROSCI.23-05-01678.2003.
The influence of activation of glutamate receptor (GluR) on outward K(+) current in cultured neonate rat hippocampal astrocytes was investigated. Patch-clamp analysis of K(+) channel currents in cultured astrocytes identified the existence of 71 +/- 6 and 161 +/- 11 pS single-channel K(+) currents that were sensitive to changes in voltage and Ca(2+) and blocked by external TEA but not by charybdotoxin, iberiotoxin, apamin, or 4-aminopyridine. Reverse transcriptase (RT)-PCR and Northern blot analysis revealed transcripts of the Ca(2+)-activated K(+) channel (K(Ca)) beta(4)-subunit (beta4) (KCNMB4) in cultured astrocytes. Expression of the metabotropic glutamate receptor (mGluR) subtypes mGluR1 and mGluR5 and the ionotropic glutamate receptor (iGluR) subtypes iGluR1 and iGluR4 were detected by RT-PCR and immunofluorescence analysis in cultured astrocytes. The mGluR agonists L-glutamate and quisqualate increased the open state probability (NP(o)) of the 71 and 161 pS K(+) channel currents that were prevented by the mGluR receptor antagonists 1-aminoindan-1,5-dicarboxylic acid or L-(+)-2-amino-3-phosphonopropionic acid and not by the iGluR antagonists (+)-5-methyl-10,11-dihydro-5H-dibenzo [a,d] cyclohepten-5,10-imine maleate or CNQX. Activation of the two types of K(+) channel currents by mGluR agonists was attenuated by pertussis toxin and by inhibition of phospholipase C (PLC) or cytochrome P450 arachidonate epoxygenase. These results indicate that brain astrocytes contain the KCNMB4 transcript and express two novel types of K(Ca) channels that are gated by activation of a G-protein coupled metabotropic glutamate receptor functionally linked to PLC and cytochrome P450 arachidonate epoxygenase activity.
研究了谷氨酸受体(GluR)激活对新生大鼠海马培养星形胶质细胞外向钾离子电流的影响。对培养星形胶质细胞中钾离子通道电流进行膜片钳分析,确定存在71±6和161±11 pS的单通道钾离子电流,这些电流对电压和细胞内钙离子浓度变化敏感,可被细胞外四乙铵阻断,但不被蝎毒素、iberiotoxin、蜂毒明肽或4-氨基吡啶阻断。逆转录酶(RT)-PCR和Northern印迹分析显示,培养星形胶质细胞中存在钙激活钾离子通道(KCa)β4亚基(β4)(KCNMB4)的转录本。通过RT-PCR和免疫荧光分析在培养星形胶质细胞中检测到代谢型谷氨酸受体(mGluR)亚型mGluR1和mGluR5以及离子型谷氨酸受体(iGluR)亚型iGluR1和iGluR4的表达。mGluR激动剂L-谷氨酸和quisqualate增加了71和161 pS钾离子通道电流的开放概率(NP(o)),这被mGluR受体拮抗剂1-氨基茚满-1,5-二羧酸或L-(+)-2-氨基-3-膦酰丙酸阻断,而不被iGluR拮抗剂(+)-5-甲基-10,11-二氢-5H-二苯并[a,d]环庚烯-5,10-亚胺马来酸盐或CNQX阻断。百日咳毒素以及磷脂酶C(PLC)或细胞色素P450花生四烯酸环氧化酶的抑制作用减弱了mGluR激动剂对两种类型钾离子通道电流的激活。这些结果表明,脑星形胶质细胞含有KCNMB4转录本,并表达两种新型的KCa通道,这些通道通过与PLC和细胞色素P450花生四烯酸环氧化酶活性功能相关的G蛋白偶联代谢型谷氨酸受体的激活而门控。