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白细胞介素-13 增强气道平滑肌细胞中的 Ca2+ 振荡。

Interleukin-13 enhanced Ca2+ oscillations in airway smooth muscle cells.

机构信息

Department of Respiratory Medicine, Kyoto University, Kyoto, Japan.

出版信息

Cytokine. 2012 Jan;57(1):19-24. doi: 10.1016/j.cyto.2011.10.014. Epub 2011 Nov 9.

Abstract

Physiological mechanisms associated with interleukin-13 (IL-13), a key cytokine in asthma, in intracellular Ca(2+) signaling in airway smooth muscle cells (ASMCs) remain unclear. The aim of this study was to assess effects of IL-13 on Ca(2+) oscillations in response to leukotriene D4 (LTD4) in human cultured ASMCs. LTD4-induced Ca(2+) oscillations in ASMCs pretreated with IL-13 were imaged by confocal microscopy. mRNA expressions of cysteinyl leukotriene 1 receptors (CysLT1R), CD38, involved with the ryanodine receptors (RyR) system, and transient receptor potential canonical (TRPC), involved with store-operated Ca(2+) entry (SOCE), were determined by real-time PCR. In IL-13-pretreated ASMCs, frequency of LTD4-induced Ca(2+) oscillations and number of oscillating cells were significantly increased compared with untreated ASMCs. Both xestospongin C, a specific inhibitor of inositol 1,4,5-triphosphate receptors (IP(3)R), and ryanodine or ruthenium red, inhibitors of RyR, partially blocked LTD4-induced Ca(2+) oscillations. Ca(2+) oscillations were almost completely inhibited by 50 μM of 2-aminoethoxydiphenyl borate (2-APB), which dominantly blocks SOCE but not IP(3)R at this concentration. Pretreatment with IL-13 increased the mRNA expressions of CysLT1R and CD38, but not of TRPC1 and TRPC3. We conclude that IL-13 enhances frequency of LTD4-induced Ca(2+) oscillations in human ASMCs, which may be cooperatively modulated by IP(3)R, RyR systems and possibly by SOCE.

摘要

白细胞介素 13(IL-13)是哮喘的关键细胞因子,与它相关的细胞内钙离子信号转导在气道平滑肌细胞(ASMCs)中的机制尚不清楚。本研究旨在评估 IL-13 对人培养的 ASMCs 中白细胞三烯 D4(LTD4)诱导的 Ca2+振荡的影响。采用共聚焦显微镜对 IL-13 预处理后的 ASMCs 中 LTD4 诱导的 Ca2+振荡进行成像。通过实时 PCR 测定半胱氨酰白三烯 1 受体(CysLT1R)、与肌浆网 RyR 系统相关的 CD38、与储存操纵性 Ca2+内流(SOCE)相关的瞬时受体电位经典型(TRPC)的 mRNA 表达。与未经处理的 ASMCs 相比,在 IL-13 预处理的 ASMCs 中,LTD4 诱导的 Ca2+振荡的频率和振荡细胞的数量显著增加。特异性抑制肌醇 1,4,5-三磷酸受体(IP3R)的 Xestospongin C 以及肌浆网 RyR 的抑制剂钌红或 Ryanodine 部分阻断 LTD4 诱导的 Ca2+振荡。50 μM 的 2-氨基乙氧基二苯硼酸盐(2-APB)几乎完全抑制 Ca2+振荡,在该浓度下,2-APB 主要阻断 SOCE,但不阻断 IP3R。IL-13 预处理增加了 CysLT1R 和 CD38 的 mRNA 表达,但不增加 TRPC1 和 TRPC3 的表达。我们的结论是,IL-13 增强了人 ASMCs 中 LTD4 诱导的 Ca2+振荡的频率,这可能是由 IP3R、RyR 系统以及可能的 SOCE 协同调节的。

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