...
首页> 外文期刊>The journal of physiological sciences >Physiological significance of delayed rectifier KSuperscript+/Superscript channels (Kv1.3) expressed in T lymphocytes and their pathological significance in chronic kidney disease
【24h】

Physiological significance of delayed rectifier KSuperscript+/Superscript channels (Kv1.3) expressed in T lymphocytes and their pathological significance in chronic kidney disease

机译:T淋巴细胞表达的延迟整流K + 通道(Kv1.3)的生理意义及其在慢性肾脏病中的病理意义

获取原文
           

摘要

T lymphocytes predominantly express delayed rectifier K+ channels (Kv1.3) in their plasma membranes. More than 30??years ago, patch-clamp studies revealed that the channels play crucial roles in facilitating the calcium influx necessary to trigger lymphocyte activation and proliferation. In addition to selective channel inhibitors that have been developed, we recently showed physiological evidence that drugs such as nonsteroidal anti-inflammatory drugs, antibiotics, and anti-hypertensives effectively suppress the channel currents in lymphocytes, and thus exert immunosuppressive effects. Using experimental animal models, previous studies revealed the pathological relevance between the expression of ion channels and the progression of renal diseases. As an extension, we recently demonstrated that the overexpression of lymphocyte Kv1.3 channels contributed to the progression of chronic kidney disease (CKD) by promoting cellular proliferation and interstitial fibrosis. Together with our in-vitro results, the studies indicated the therapeutic potency of Kv1.3-channel inhibitors in the treatment or the prevention of CKD.
机译:T淋巴细胞主要在质膜上表达延迟的整流子K +通道(Kv1.3)。 30多年前,膜片钳研究表明,这些通道在促进触发淋巴细胞活化和增殖所必需的钙内流中起着关键作用。除了已开发的选择性通道抑制剂外,我们最近还显示了生理证据,如非甾体类抗炎药,抗生素和抗高血压药可有效抑制淋巴细胞中的通道电流,从而发挥免疫抑制作用。使用实验动物模型,先前的研究揭示了离子通道表达与肾脏疾病进展之间的病理相关性。作为扩展,我们最近证明了淋巴细胞Kv1.3通道的过表达通过促进细胞增殖和间质纤维化而促进了慢性肾脏疾病(CKD)的发展。连同我们的体外研究结果,研究表明Kv1.3通道抑制剂在CKD的治疗或预防中具有治疗作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号