• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

钾离子通道α亚基和β亚基在牛肺动脉循环中的差异表达。

Differential expression of K(V) channel alpha- and beta-subunits in the bovine pulmonary arterial circulation.

作者信息

Coppock E A, Tamkun M M

机构信息

Department of Physiology, Colorado State University, Fort Collins, Colorado 80523, USA.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2001 Dec;281(6):L1350-60. doi: 10.1152/ajplung.2001.281.6.L1350.

DOI:10.1152/ajplung.2001.281.6.L1350
PMID:11704530
Abstract

Resistance pulmonary arteries constrict in response to hypoxia, whereas conduit pulmonary arteries typically do not respond or dilate slightly. One proposed mechanism for this differential response is the variable expression of pulmonary arterial smooth muscle cell voltage-gated K(+) (K(V)) channel subunits (Kv1.2, Kv2.1, Kv1.5, and Kv3.1b) shown to be O(2) sensitive in heterologous expression systems. In this study, immunoblotting and immunohistochemistry were used to examine the expression of K(V) channel alpha- and beta-subunits in the bovine pulmonary arterial circulation to determine whether differential K(V) channel subunit distribution is responsible for the distinct sensitivities of pulmonary arteries to hypoxia. Surprisingly, there was little difference in the expression levels of Kv1.2, Kv1.5, and Kv2.1 between conduit and resistance pulmonary arteries. In contrast, expression of the Kv3.1b alpha-subunit and Kv beta.1, Kv beta 1.2, and Kv beta 1.3 accessory subunits dramatically increased along the pulmonary arterial tree. The differential expression of all the beta-subunits but of only one of the putative O(2)-sensitive alpha-subunits suggests that the alpha-subunits alone are not the O(2) sensors but further implicates the auxiliary beta-subunits in pulmonary arterial O(2) sensing.

摘要

阻力性肺动脉会对低氧作出收缩反应,而传导性肺动脉通常无反应或仅有轻微扩张。对于这种差异反应,一种提出的机制是肺动脉平滑肌细胞电压门控钾离子(K(+))通道亚基(Kv1.2、Kv2.1、Kv1.5和Kv3.1b)的表达存在差异,这些亚基在异源表达系统中显示对氧气敏感。在本研究中,采用免疫印迹和免疫组织化学方法检测牛肺动脉循环中K(V)通道α亚基和β亚基的表达,以确定K(V)通道亚基的差异分布是否导致肺动脉对低氧的不同敏感性。令人惊讶的是,传导性肺动脉和阻力性肺动脉之间Kv1.2、Kv1.5和Kv2.1的表达水平几乎没有差异。相比之下,Kv3.1bα亚基以及Kvβ.1、Kvβ1.2和Kvβ1.3辅助亚基的表达沿肺动脉树显著增加。所有β亚基的差异表达,但只有一个假定的对氧气敏感的α亚基存在差异,这表明仅α亚基不是氧气传感器,而是进一步暗示辅助β亚基参与了肺动脉的氧气感知。

相似文献

1
Differential expression of K(V) channel alpha- and beta-subunits in the bovine pulmonary arterial circulation.钾离子通道α亚基和β亚基在牛肺动脉循环中的差异表达。
Am J Physiol Lung Cell Mol Physiol. 2001 Dec;281(6):L1350-60. doi: 10.1152/ajplung.2001.281.6.L1350.
2
Preferential expression and function of voltage-gated, O2-sensitive K+ channels in resistance pulmonary arteries explains regional heterogeneity in hypoxic pulmonary vasoconstriction: ionic diversity in smooth muscle cells.电压门控、氧敏感钾通道在肺阻力动脉中的优先表达及功能解释了缺氧性肺血管收缩中的区域异质性:平滑肌细胞中的离子多样性。
Circ Res. 2004 Aug 6;95(3):308-18. doi: 10.1161/01.RES.0000137173.42723.fb. Epub 2004 Jun 24.
3
Potential role for kv3.1b channels as oxygen sensors.Kv3.1b通道作为氧传感器的潜在作用。
Circ Res. 2000 Mar 17;86(5):534-40. doi: 10.1161/01.res.86.5.534.
4
Molecular basis and function of voltage-gated K+ channels in pulmonary arterial smooth muscle cells.肺动脉平滑肌细胞中电压门控钾通道的分子基础与功能
Am J Physiol. 1998 Apr;274(4):L621-35. doi: 10.1152/ajplung.1998.274.4.L621.
5
Molecular identification of the role of voltage-gated K+ channels, Kv1.5 and Kv2.1, in hypoxic pulmonary vasoconstriction and control of resting membrane potential in rat pulmonary artery myocytes.电压门控钾通道Kv1.5和Kv2.1在大鼠肺动脉肌细胞缺氧性肺血管收缩及静息膜电位调控中作用的分子鉴定
J Clin Invest. 1998 Jun 1;101(11):2319-30. doi: 10.1172/JCI333.
6
Expression of voltage-dependent K(+) channel genes in mesenteric artery smooth muscle cells.肠系膜动脉平滑肌细胞中电压依赖性钾通道基因的表达
Am J Physiol. 1999 Nov;277(5):G1055-63. doi: 10.1152/ajpgi.1999.277.5.G1055.
7
Regulation of Shaker-type potassium channels by hypoxia. Oxygen-sensitive K+ channels in PC12 cells.缺氧对震荡器型钾通道的调节。PC12细胞中的氧敏感钾通道。
Adv Exp Med Biol. 2000;475:265-74. doi: 10.1007/0-306-46825-5_25.
8
Generation and characterization of subtype-specific monoclonal antibodies to K+ channel alpha- and beta-subunit polypeptides.钾离子通道α亚基和β亚基多肽亚型特异性单克隆抗体的产生与特性分析
Neuropharmacology. 1996;35(7):851-65. doi: 10.1016/0028-3908(96)00128-1.
9
A new K+ channel beta subunit to specifically enhance Kv2.2 (CDRK) expression.一种新的钾离子通道β亚基,可特异性增强Kv2.2(CDRK)的表达。
J Biol Chem. 1996 Oct 18;271(42):26341-8. doi: 10.1074/jbc.271.42.26341.
10
Contributions of Kv1.2, Kv1.5 and Kv2.1 subunits to the native delayed rectifier K(+) current in rat mesenteric artery smooth muscle cells.Kv1.2、Kv1.5和Kv2.1亚基对大鼠肠系膜动脉平滑肌细胞中天然延迟整流钾电流的作用
Life Sci. 2002 Aug 9;71(12):1465-73. doi: 10.1016/s0024-3205(02)01922-7.

引用本文的文献

1
HO Sensitivity of K Channels in Hypoxic Pulmonary Vasoconstriction: Experimental Conditions Matter.缺氧性肺血管收缩中钾通道的HO敏感性:实验条件很重要。
Int J Mol Sci. 2025 Jul 17;26(14):6857. doi: 10.3390/ijms26146857.
2
Biochemical and physiological properties of K channel-associated AKR6A (Kvβ) proteins.K 通道相关 AKR6A(Kvβ)蛋白的生化和生理特性。
Chem Biol Interact. 2019 May 25;305:21-27. doi: 10.1016/j.cbi.2019.03.023. Epub 2019 Mar 26.
3
Coronary microvascular Kv1 channels as regulatory sensors of intracellular pyridine nucleotide redox potential.
冠状动脉微血管Kv1通道作为细胞内吡啶核苷酸氧化还原电位的调节传感器。
Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12426.
4
Perpetual change: autophagy, the endothelium, and response to vascular injury.持续变化:自噬、内皮细胞与对血管损伤的反应
J Leukoc Biol. 2017 Aug;102(2):221-235. doi: 10.1189/jlb.3RU1116-484RR. Epub 2017 Jun 16.
5
Heteromeric complexes of aldo-keto reductase auxiliary Kβ subunits (AKR6A) regulate sarcolemmal localization of K1.5 in coronary arterial myocytes.醛糖酮还原酶辅助Kβ亚基(AKR6A)的异源复合物调节冠状动脉心肌细胞中K1.5的肌膜定位。
Chem Biol Interact. 2017 Oct 1;276:210-217. doi: 10.1016/j.cbi.2017.03.011. Epub 2017 Mar 22.
6
Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1.抑制15-脂氧合酶(15-LOX)可逆转缺氧诱导的钾通道Kv1.5和Kv2.1下调。抑制15-脂氧合酶(15-LOX)可逆转缺氧诱导的钾通道Kv1.5和Kv2.1下调。
Int J Clin Exp Med. 2014 Nov 15;7(11):4147-53. eCollection 2014.
7
Protein kinase A-phosphorylated KV1 channels in PSD95 signaling complex contribute to the resting membrane potential and diameter of cerebral arteries.PSD95信号复合物中蛋白激酶A磷酸化的KV1通道有助于脑动脉的静息膜电位和管径。
Circ Res. 2014 Apr 11;114(8):1258-67. doi: 10.1161/CIRCRESAHA.114.303167. Epub 2014 Feb 28.
8
Role of voltage-gated potassium channels in pathogenesis of chronic pulmonary heart disease.电压门控钾通道在慢性肺源性心脏病发病机制中的作用
J Huazhong Univ Sci Technolog Med Sci. 2013 Oct;33(5):644-649. doi: 10.1007/s11596-013-1174-z. Epub 2013 Oct 20.
9
Regulation of ion channels by pyridine nucleotides.烟酰胺核苷酸对离子通道的调节。
Circ Res. 2013 Feb 15;112(4):721-41. doi: 10.1161/CIRCRESAHA.111.247940.
10
Regulation of Kv2.1 K(+) conductance by cell surface channel density.通过细胞膜通道密度调节 Kv2.1 K(+) 电导。
J Neurosci. 2013 Jan 16;33(3):1259-70. doi: 10.1523/JNEUROSCI.3008-12.2013.