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海人酸诱导的细胞凋亡与培养的小脑颗粒细胞中c-Jun的激活相关。

Kainate-induced apoptosis correlates with c-Jun activation in cultured cerebellar granule cells.

作者信息

Cheung N S, Carroll F Y, Larm J A, Beart P M, Giardina S F

机构信息

Department of Pharmacology, Monash University, Clayton, Victoria, Australia.

出版信息

J Neurosci Res. 1998 Apr 1;52(1):69-82. doi: 10.1002/(SICI)1097-4547(19980401)52:1<69::AID-JNR7>3.0.CO;2-I.

Abstract

We have investigated the involvement of c-Jun in cell death induced by exposure of primary cultures of murine cerebellar granule cells to the glutamate receptor agonist kainate (KA) and evaluated its possible use as a marker for apoptosis. Using cerebellar granule cell neurones from postnatal day 7 mice, we found that 1 hr exposure to KA (1-1000 microM) induced a concentration-dependent neuronal cell death with characteristic apoptotic morphology, including cell shrinkage, neurite blebbing and DNA fragmentation. In addition KA-induced a concentration-dependent expression of c-Jun mRNA and protein as determined by in situ hybridization and immunocytochemistry respectively. DNA fragmentation was detected using terminal transferase-mediated nick-end (TUNEL) labelling and agarose gel electrophoresis. KA-induced cell death was significantly attenuated by the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX; 50 microM), which shifted the concentration-response curve significantly rightward. The number of apoptotic cell bodies, determined by TUNEL, was also reduced by CNQX (50 microM), with only 15-20% of neurones staining positive after exposure to 1mM KA. In addition, the number of positively stained cells for c-Jun protein and mRNA was substantially reduced by CNQX (50 microM) as determined by random and representative cell counts. These results show for the first time that KA induced apoptotic neuronal death in cultured murine cerebellar granule cells involves the induction of c-Jun mRNA and protein, suggesting the involvement of this immediate early gene in excitotoxic receptor-mediated apoptosis and its potential use as a marker for apoptotic cell death.

摘要

我们研究了c-Jun在小鼠小脑颗粒细胞原代培养物暴露于谷氨酸受体激动剂海藻酸(KA)诱导的细胞死亡中的作用,并评估了其作为细胞凋亡标志物的可能性。使用出生后第7天小鼠的小脑颗粒细胞神经元,我们发现暴露于KA(1-1000 microM)1小时会诱导浓度依赖性的神经元细胞死亡,并伴有特征性的凋亡形态,包括细胞收缩、神经突起泡和DNA片段化。此外,分别通过原位杂交和免疫细胞化学测定,KA诱导了c-Jun mRNA和蛋白质的浓度依赖性表达。使用末端转移酶介导的缺口末端(TUNEL)标记和琼脂糖凝胶电泳检测DNA片段化。非NMDA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX;50 microM)显著减弱了KA诱导的细胞死亡,使浓度-反应曲线明显右移。通过TUNEL测定的凋亡细胞体数量也因CNQX(50 microM)而减少,暴露于1mM KA后只有15-20%的神经元染色呈阳性。此外,通过随机和代表性细胞计数测定,CNQX(50 microM)使c-Jun蛋白和mRNA的阳性染色细胞数量大幅减少。这些结果首次表明,KA在培养的小鼠小脑颗粒细胞中诱导的凋亡神经元死亡涉及c-Jun mRNA和蛋白质的诱导,表明这个即刻早期基因参与了兴奋性毒性受体介导的细胞凋亡及其作为凋亡细胞死亡标志物的潜在用途。

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