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P2X嘌呤受体在胸腺细胞凋亡中并不重要。

P2x purinoceptor is not important in thymocyte apoptosis.

作者信息

Jiang S, Kull B, Fredholm B B, Orrenius S

机构信息

Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

Immunol Lett. 1996 Mar;49(3):197-201. doi: 10.1016/0165-2478(96)02507-2.

Abstract

Since the P2X purinoceptor has been shown to be homologous with RP-2, a gene activated in thymocytes undergoing apoptosis after glucocorticoid treatment, we have investigated the possible role of P2X purinoceptors in thymocyte apoptosis. We report that P2X purinoceptor mRNA is expressed both in untreated rat thymocytes and thymocytes treated with the synthetic glucocorticoid, 6 alpha-methylprednisolone, in a dose that can induce apoptosis. Furthermore, the P2X receptor agonist, extracellular ATP, was unable to trigger apoptosis in rat thymocytes and had no effect on methylprednisolone-induced DNA fragmentation. Finally, the P2X purinoceptor antagonist, suramin and pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid, had no inhibitory effects on DNA fragmentation caused by methylprednisolone. Thus, our data demonstrate that P2X purinoceptors are not directly involved in glucocorticoid-mediated thymocyte apoptosis.

摘要

由于已证明P2X嘌呤受体与RP-2同源,RP-2是一种在糖皮质激素处理后经历凋亡的胸腺细胞中被激活的基因,我们研究了P2X嘌呤受体在胸腺细胞凋亡中的可能作用。我们报告,P2X嘌呤受体mRNA在未处理的大鼠胸腺细胞以及用合成糖皮质激素6α-甲基泼尼松龙处理的胸腺细胞中均有表达,该剂量可诱导凋亡。此外,P2X受体激动剂细胞外ATP无法触发大鼠胸腺细胞凋亡,且对甲基泼尼松龙诱导的DNA片段化没有影响。最后,P2X嘌呤受体拮抗剂苏拉明和磷酸吡哆醛-6-偶氮苯基-2',4'-二磺酸对甲基泼尼松龙引起的DNA片段化没有抑制作用。因此,我们的数据表明P2X嘌呤受体不直接参与糖皮质激素介导的胸腺细胞凋亡。

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