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通过重组P2X受体在C6BU-1细胞中对钙离子内流的表征

Characterization of Ca2+ influx through recombinant P2X receptor in C6BU-1 cells.

作者信息

Ueno S, Koizumi S, Inoue K

机构信息

Division of Pharmacology, National Institute of Health Sciences, Tokyo, Japan.

出版信息

Br J Pharmacol. 1998 Aug;124(7):1484-90. doi: 10.1038/sj.bjp.0701963.

Abstract
  1. The effects of exogenous adenosine 5'-triphosphate (ATP) and alpha,beta-methylene ATP (alpha,beta meATP) on C6BU-1 cells transfected with P2X2 and P2X3 subtypes, separately or together (P2X2+3), were investigated using fura-2 fluorescence recording and whole-cell patch clamp recording methods. 2. Untransfected C6BU-1 cells showed no intracellular Ca2+ ([Ca2+]i) increase in response to depolarizing stimulation with high K+ or stimulation with ATP. There was no current induced by ATP under voltage clamp conditions in untransfected C6BU-1 cells. ATP caused Ca2+ influx only from extracellular sources in C6BU-1 cells transfected with the P2X subtypes, suggesting that the C6BU-1 cell line is suitable for the characterization of Ca2+ influx through the P2X subtypes. 3. In C6BU-1 cells transfected with the P2X2 subtype, ATP (more than 10 microM) but not alpha,beta meATP (up to 100 microM) evoked a rise in [Ca2+]i. 4. In the cells transfected with the P2X3 subtype, current responses under voltage clamp conditions were observed at ATP concentrations higher than 0.1 microM of alpha,beta meATP were required. This discrepancy in the concentration dependence of the agonist responses with respect to the [Ca2+]i rise and the current response was seen only with the P2X3 subtype. In addition, the agonist-induced rise in [Ca2+]i was observed only after the first application because of desensitization of this subtype. 5. In C6BU-1 cells co-transfected with P2X2 and P2X3, ATP at 1 microM evoked a [Ca2+]i rise. This responsiveness was higher than that of the other subtype combinations tested. The efficiency of expression was improved by co-transfection with P2X2 and P2X3, when compared to transfection with the P2X3 subtype alone. The desensitization of the P2X2+3 was apparently slower than that of the P2X3 subtype alone. Therefore, this combination could respond to the repeated application of agonists each time with a [Ca2+]i rise. 6. These results suggest that the P2X2 and P2X3 subtypes assemble a heteromultimer and that this heterogeneous expression acquires more effective Ca2+ dynamics than that by homogeneously expressed P2X2 or P2X3.
摘要
  1. 采用fura-2荧光记录法和全细胞膜片钳记录法,研究了外源性5'-三磷酸腺苷(ATP)和α,β-亚甲基ATP(α,β meATP)对单独或共同转染P2X2和P2X3亚型(P2X2 + 3)的C6BU - 1细胞的影响。2. 未转染的C6BU - 1细胞在高钾去极化刺激或ATP刺激下,细胞内钙离子浓度([Ca2+]i)无升高。在电压钳条件下,未转染的C6BU - 1细胞中ATP未诱导出电流。在转染P2X亚型的C6BU - 1细胞中,ATP仅引起细胞外钙离子内流,这表明C6BU - 1细胞系适用于通过P2X亚型来表征钙离子内流。3. 在转染P2X2亚型的C6BU - 1细胞中,ATP(大于10 microM)可引起[Ca2+]i升高,但α,β meATP(高达100 microM)则不能。4. 在转染P2X3亚型的细胞中,在电压钳条件下,ATP浓度高于0.1 microM时可观察到电流反应,而α,β meATP则需要更高浓度。激动剂反应在[Ca2+]i升高和电流反应方面的浓度依赖性差异仅在P2X3亚型中出现。此外,由于该亚型的脱敏作用,激动剂诱导的[Ca2+]i升高仅在首次应用后观察到。5. 在共同转染P2X2和P2X3的C6BU - 1细胞中,1 microM的ATP可引起[Ca2+]i升高。这种反应性高于测试的其他亚型组合。与单独转染P2X3亚型相比,P2X2和P2X3共同转染可提高表达效率。P2X2 + 3的脱敏明显慢于单独的P2X3亚型。因此,这种组合每次在激动剂重复应用时都能以[Ca2+]i升高做出反应。6. 这些结果表明,P2X2和P2X3亚型组装成异源多聚体,并且这种异源表达比同源表达的P2X2或P2X3获得更有效的钙离子动力学。

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