基础医学与临床 ›› 2017, Vol. 37 ›› Issue (12): 1674-1680.

• 研究论文 • 上一篇    下一篇

酸环境对过敏性紫癜患儿血清IgA1诱导血管内皮细胞ASIC1a表达的影响及机制

闫波1,袁丽萍2,彭启迪3,房功思1,戴寒晶1   

  1. 1. 安徽医学高等专科学校
    2. 安徽医科大学第一附属医院儿科一病区
    3. 安徽医科大学第一附属医院儿科
  • 收稿日期:2017-01-16 修回日期:2017-08-13 出版日期:2017-12-05 发布日期:2017-11-29
  • 通讯作者: 袁丽萍 E-mail:yuanliping3986@163.com
  • 基金资助:
    国家自然科学基金面上项目;安徽省高校自然科学重点科研项目

Effect of low pH on acid-sensing ion channel1a expression in vascular endothelial cell injury induced by serum IgA1 from Henoch-Schonlein purpura children and its mechanism

  • Received:2017-01-16 Revised:2017-08-13 Online:2017-12-05 Published:2017-11-29
  • Contact: Li-ping Yuan E-mail:yuanliping3986@163.com

摘要: 目的:初步探讨酸性环境对过敏性紫癜(Henoch-Sch?nlein Purpura, HSP)患儿血清IgA1诱导血管内皮细胞ASIC1a (Acid-sensing ion channels1a, ASIC1a)表达的影响及在其中的调控作用。方法:体外培养的人皮肤微血管内皮细胞经过处理后,荧光定量PCR检测血管内皮细胞ASIC1a,destrin及α-SM mRNA表达的影响。ELISA法测定血管内皮细胞细胞分泌因子的变化。同时采用荧光定量PCR和Western blot法检测细胞骨架destrin及α-SM蛋白表达。结果:酸化环境中HSP患儿血清IgA1作用血管内皮细胞后,ASIC1amRNA表达明显上调,细胞因子IL-8,NO和TM分泌明显增加,ASICs阻滞剂可以显著降低酸化诱导的细胞因子的分泌;细胞外酸化下,HSP患儿血清IgA1导致细胞骨架蛋白destrin及α-SM mRNA和蛋白表达明显下调,而ASICs阻断剂组destrin及α-SM和蛋白表达明显上调。结论:ASICs在HSP患儿血管炎的发生中起着重要作用,阻断细胞外ASICs能显著改善HSP患儿血管内皮细胞损伤。

关键词: 过敏性紫癜(HSP), 酸敏感离子通道(ASICs), 血管内皮细胞

Abstract: Objective To investigate the effect of low pH on acid-sensing ion channel 1a(ASIC1a) expression in vascular endothelial cell injury induced by serum IgA1 from Henoch-Schonlein purpura (HSP) children and regulatory role of ASIC1a in it. Methods Human dermal microvascular endothelial cells (HDMECs) treated by serum IgA1 from HSP patients were incubated in different pH medium. ASIC1a, destrin and α-SM mRNA expressions in HDMECs were evaluated by real-time quantitative polymerase chain reaction (qPCR). The level of inflammatory cytokines release assay was detected by ELISA method. Moreover destrin and α-SM protein expression in HDMECs was evaluated by western blot. Results The results showed that extracellular acid could induce the upregulation of ASIC1a mRNA expression, stimulate IL-8, NO,TM release and decrease , destrin and α-SM mRNA expression in HDMECs of HSP patients. Furthermore, pharmacological blockade of ASICs attenuated the inflammation response and inhibited the loss of cytoskeletal protein in vascular endothelial cells of HSP patients. Conclusions These findings showed that activation of ASIC1a could involve in the vascular endothelial cell injury of HSP patients. Blocking ASIC1a may have a significant protective effect on the inflammatory injury of vascular endothelial cells.

Key words: Henoch-schonlein purpura(HSP), Acid-sensing ion channels (ASICs), Vascular endothelium cells

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