Bisaggio R D, Nihei O K, Persechini P M, Savino W, Alves L A
Laboratório de Pesquisas sobre o Timo, Departamento de Imunologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Cell Mol Biol (Noisy-le-grand). 2001 Feb;47(1):19-31.
The presence of P2 receptors was investigated in three distinct preparations of murine thymic epithelial cells (TEC): 2BH4 murine cell line, IT45-R1 rat cell line, and a primary murine cell derived from the Nurse cell lympho-epithelial complex. In all preparations, application of ATP to the extracellular milieu triggered intracellular calcium signals indicating the presence of P2 receptor(s) in these cells. After an initial peak of calcium concentration, a plateau phase that could last more than 10 min was frequently observed. Ion replacement and channel blockage experiments indicated that the initial peak was associated with the release of calcium from intracellular stores, while the plateau phase was associated with an influx from the extracellular medium. ATP and UTP induced similar calcium signals, suggesting the presence of P2Y2 receptors in all three cell types. The murine 2BH4 cells also expressed P2X7/P2Z receptor, since under exposure to millimolar concentrations of ATP, a continuous rise in intracellular calcium concentration was observed and their plasma membranes became permeabilized to the fluorescent dyes Lucifer yellow and ethidium bromide. In addition, this permeabilization phenomenon was blocked by the P2Z-specific antagonist, oxidized ATP. RT-PCR assays confirmed the presence of mRNAs for the P2Y2 molecule in all TEC, while mRNA for the P2X7 molecule was detected only in 2BH4 cells. Our data indicate that P2Y2 purinergic receptors are widely expressed by thymic epithelial cells, whereas the expression of the P2X7 receptor appears to be more restricted, raising the possibility that its expression is related only to a particular epithelial microenvironment within/the thymus.
在三种不同的小鼠胸腺上皮细胞(TEC)制剂中研究了P2受体的存在情况:2BH4小鼠细胞系、IT45-R1大鼠细胞系以及源自滋养细胞淋巴细胞上皮复合体的原代小鼠细胞。在所有制剂中,向细胞外环境施加ATP会触发细胞内钙信号,表明这些细胞中存在P2受体。在钙浓度出现初始峰值后,经常观察到一个可持续超过10分钟的平台期。离子置换和通道阻断实验表明,初始峰值与细胞内钙库中钙的释放有关,而平台期与细胞外介质中钙的内流有关。ATP和UTP诱导了相似的钙信号,表明在所有三种细胞类型中都存在P2Y2受体。小鼠2BH4细胞还表达P2X7/P2Z受体,因为在暴露于毫摩尔浓度的ATP时,观察到细胞内钙浓度持续升高,并且它们的质膜对荧光染料路西法黄和溴化乙锭变得通透。此外,这种通透现象被P2Z特异性拮抗剂氧化ATP所阻断。逆转录聚合酶链反应(RT-PCR)分析证实了所有TEC中都存在P2Y2分子的mRNA,而仅在2BH4细胞中检测到P2X7分子的mRNA。我们的数据表明,P2Y2嘌呤能受体在胸腺上皮细胞中广泛表达,而P2X7受体的表达似乎更受限制,这增加了其表达仅与胸腺内特定的上皮微环境相关的可能性。