• 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

氯离子通道、交换体及调节剂在慢性炎症性气道疾病中的新作用

Novel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway Diseases.

作者信息

Sala-Rabanal Monica, Yurtsever Zeynep, Berry Kayla N, Brett Tom J

机构信息

Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA ; Center for the Investigation of Membrane Excitability Diseases, Washington University School of Medicine, St. Louis, MO 63110, USA.

Center for the Investigation of Membrane Excitability Diseases, Washington University School of Medicine, St. Louis, MO 63110, USA ; Biochemistry Program, Washington University School of Medicine, St. Louis, MO 63110, USA ; Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA ; Drug Discovery Program in Pulmonary and Critical Care Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Mediators Inflamm. 2015;2015:497387. doi: 10.1155/2015/497387. Epub 2015 Nov 3.

DOI:10.1155/2015/497387
PMID:26612971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4647060/
Abstract

Chloride transport proteins play critical roles in inflammatory airway diseases, contributing to the detrimental aspects of mucus overproduction, mucus secretion, and airway constriction. However, they also play crucial roles in contributing to the innate immune properties of mucus and mucociliary clearance. In this review, we focus on the emerging novel roles for a chloride channel regulator (CLCA1), a calcium-activated chloride channel (TMEM16A), and two chloride exchangers (SLC26A4/pendrin and SLC26A9) in chronic inflammatory airway diseases.

摘要

氯离子转运蛋白在炎性气道疾病中发挥着关键作用,导致黏液过度产生、黏液分泌和气道收缩等有害影响。然而,它们在黏液的固有免疫特性和黏液纤毛清除中也起着至关重要的作用。在本综述中,我们聚焦于氯离子通道调节蛋白(CLCA1)、钙激活氯离子通道(TMEM16A)以及两种氯离子交换体(SLC26A4/ Pendrin和SLC26A9)在慢性炎性气道疾病中的新出现的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/09593e139cfc/MI2015-497387.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/fbea82275273/MI2015-497387.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/f7af7998d1fa/MI2015-497387.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/489e349dc739/MI2015-497387.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/830742c1137d/MI2015-497387.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/09593e139cfc/MI2015-497387.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/fbea82275273/MI2015-497387.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/f7af7998d1fa/MI2015-497387.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/489e349dc739/MI2015-497387.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/830742c1137d/MI2015-497387.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b694/4647060/09593e139cfc/MI2015-497387.005.jpg

相似文献

1
Novel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway Diseases.氯离子通道、交换体及调节剂在慢性炎症性气道疾病中的新作用
Mediators Inflamm. 2015;2015:497387. doi: 10.1155/2015/497387. Epub 2015 Nov 3.
2
Calcium-activated chloride channel regulator 1 (CLCA1): More than a regulator of chloride transport and mucus production.钙激活氯离子通道调节因子1(CLCA1):不止是氯离子转运和黏液分泌的调节因子。
World Allergy Organ J. 2019 Nov 29;12(11):100077. doi: 10.1016/j.waojou.2019.100077. eCollection 2019 Nov.
3
SLC26A9-mediated chloride secretion prevents mucus obstruction in airway inflammation.SLC26A9 介导的氯离子分泌可防止气道炎症中的黏液阻塞。
J Clin Invest. 2012 Oct;122(10):3629-34. doi: 10.1172/JCI60429. Epub 2012 Sep 4.
4
CLCA1 and TMEM16A: the link towards a potential cure for airway diseases.CLCA1和TMEM16A:通向气道疾病潜在治愈方法的纽带。
Expert Rev Respir Med. 2015 Oct;9(5):503-6. doi: 10.1586/17476348.2015.1081064. Epub 2015 Aug 20.
5
Secreted CLCA1 modulates TMEM16A to activate Ca(2+)-dependent chloride currents in human cells.分泌型CLCA1调节TMEM16A以激活人类细胞中钙依赖性氯电流。
Elife. 2015 Mar 17;4:e05875. doi: 10.7554/eLife.05875.
6
TMEM16A in Cystic Fibrosis: Activating or Inhibiting?囊性纤维化中的TMEM16A:激活还是抑制?
Front Pharmacol. 2019 Jan 29;10:3. doi: 10.3389/fphar.2019.00003. eCollection 2019.
7
[CFTR as cAMP-dependent chloride channels and as cAMP-dependent regulator of sodium channels].[囊性纤维化跨膜传导调节因子作为环磷酸腺苷依赖性氯离子通道及作为钠离子通道的环磷酸腺苷依赖性调节因子]
Nihon Rinsho. 1996 Feb;54(2):429-33.
8
STAT6 links IL-4/IL-13 stimulation with pendrin expression in asthma and chronic obstructive pulmonary disease.STAT6 将 IL-4/IL-13 刺激与哮喘和慢性阻塞性肺疾病中的 pendrin 表达联系起来。
Clin Pharmacol Ther. 2011 Sep;90(3):399-405. doi: 10.1038/clpt.2011.128. Epub 2011 Aug 3.
9
Pendrin and anoctamin as mediators of apical iodide efflux in thyroid cells.作为甲状腺细胞顶端碘流出介质的pendrin和anoctamin
Curr Opin Endocrinol Diabetes Obes. 2015 Oct;22(5):374-80. doi: 10.1097/MED.0000000000000188.
10
Increased expression of human calcium-activated chloride channel 1 gene is correlated with mucus overproduction in Chinese asthmatic airway.人钙激活氯离子通道1基因表达增加与中国哮喘患者气道黏液过度分泌相关。
Cell Biol Int. 2007 Nov;31(11):1388-95. doi: 10.1016/j.cellbi.2007.06.004. Epub 2007 Jun 29.

引用本文的文献

1
ANO1: central role and clinical significance in non-neoplastic and neoplastic diseases.ANO1:在非肿瘤性和肿瘤性疾病中的核心作用及临床意义
Front Immunol. 2025 Apr 28;16:1570333. doi: 10.3389/fimmu.2025.1570333. eCollection 2025.
2
Availability of Receptors for Advanced Glycation End-Products (RAGE) Influences Differential Transcriptome Expression in Lungs from Mice Exposed to Chronic Secondhand Smoke (SHS).晚期糖基化终产物受体(RAGE)的可及性影响暴露于慢性二手烟(SHS)的小鼠肺部差异转录组表达。
Int J Mol Sci. 2024 Apr 30;25(9):4940. doi: 10.3390/ijms25094940.
3
Engineering the ChlorON Series: Turn-On Fluorescent Protein Sensors for Imaging Labile Chloride in Living Cells.

本文引用的文献

1
Structure of a prokaryotic fumarate transporter reveals the architecture of the SLC26 family.原核延胡索酸转运蛋白的结构揭示了 SLC26 家族的结构。
Nat Struct Mol Biol. 2015 Oct;22(10):803-8. doi: 10.1038/nsmb.3091. Epub 2015 Sep 14.
2
Increased expression of the epithelial anion transporter pendrin/SLC26A4 in nasal polyps of patients with chronic rhinosinusitis.慢性鼻窦炎患者鼻息肉中上皮阴离子转运体pendrin/SLC26A4的表达增加。
J Allergy Clin Immunol. 2015 Dec;136(6):1548-1558.e7. doi: 10.1016/j.jaci.2015.05.024. Epub 2015 Jul 2.
3
Targeting ion channels in cystic fibrosis.
设计氯ON系列:用于活细胞中不稳定氯离子成像的开启型荧光蛋白传感器。
ACS Cent Sci. 2023 Dec 18;10(1):77-86. doi: 10.1021/acscentsci.3c01088. eCollection 2024 Jan 24.
4
Chloride channel accessory 1 gene deficiency causes selective loss of mucus production in a new pig model.氯离子通道辅助蛋白 1 基因缺失导致新型猪模型中黏液产生的选择性丧失。
Am J Physiol Lung Cell Mol Physiol. 2022 Jun 1;322(6):L842-L852. doi: 10.1152/ajplung.00443.2021. Epub 2022 Apr 19.
5
The Ca-activated chloride channel ANO1/TMEM16A: An emerging therapeutic target for epithelium-originated diseases?钙激活氯离子通道ANO1/TMEM16A:上皮源性疾病的新兴治疗靶点?
Acta Pharm Sin B. 2021 Jun;11(6):1412-1433. doi: 10.1016/j.apsb.2020.12.003. Epub 2020 Dec 9.
6
Effects of cannabis oil extract on immune response gene expression in human small airway epithelial cells (HSAEpC): implications for chronic obstructive pulmonary disease (COPD).大麻油提取物对人小气道上皮细胞(HSAEpC)免疫反应基因表达的影响:对慢性阻塞性肺疾病(COPD)的意义。
J Cannabis Res. 2020 Jan 31;2(1):5. doi: 10.1186/s42238-019-0014-9.
7
Inhibition of Pendrin by a small molecule reduces Lipopolysaccharide-induced acute Lung Injury.小分子抑制 Pendrin 可减轻脂多糖诱导的急性肺损伤。
Theranostics. 2020 Aug 7;10(22):9913-9922. doi: 10.7150/thno.46417. eCollection 2020.
8
Tiotropium and Fluticasone Inhibit Rhinovirus-Induced Mucin Production via Multiple Mechanisms in Differentiated Airway Epithelial Cells.噻托溴铵和氟替卡松通过多种机制抑制分化气道上皮细胞中鼻病毒诱导的粘蛋白产生。
Front Cell Infect Microbiol. 2020 Jun 19;10:278. doi: 10.3389/fcimb.2020.00278. eCollection 2020.
9
Structural and Biophysical Analysis of the CLCA1 VWA Domain Suggests Mode of TMEM16A Engagement.CLCA1 VWA 结构域的结构和生物物理分析提示 TMEM16A 的结合模式。
Cell Rep. 2020 Jan 28;30(4):1141-1151.e3. doi: 10.1016/j.celrep.2019.12.059.
10
TMEM16A chloride channel does not drive mucus production.跨膜蛋白 16A 氯离子通道不会驱动黏液产生。
Life Sci Alliance. 2019 Nov 15;2(6). doi: 10.26508/lsa.201900462. Print 2019 Dec.
靶向囊性纤维化中的离子通道。
J Cyst Fibros. 2015 Sep;14(5):561-70. doi: 10.1016/j.jcf.2015.06.002. Epub 2015 Jun 23.
4
Airway hydration and COPD.气道水化与慢性阻塞性肺疾病
Cell Mol Life Sci. 2015 Oct;72(19):3637-52. doi: 10.1007/s00018-015-1946-7. Epub 2015 Jun 12.
5
New selective inhibitors of calcium-activated chloride channels - T16A(inh) -A01, CaCC(inh) -A01 and MONNA - what do they inhibit?新型钙激活氯离子通道选择性抑制剂——T16A(inh)-A01、CaCC(inh)-A01和莫娜——它们抑制的是什么?
Br J Pharmacol. 2015 Aug;172(16):4158-72. doi: 10.1111/bph.13201. Epub 2015 Jul 8.
6
Secreted CLCA1 modulates TMEM16A to activate Ca(2+)-dependent chloride currents in human cells.分泌型CLCA1调节TMEM16A以激活人类细胞中钙依赖性氯电流。
Elife. 2015 Mar 17;4:e05875. doi: 10.7554/eLife.05875.
7
Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis.溶质载体SLC26A9基因变异可改变囊性纤维化患者的产前外分泌胰腺损伤。
J Pediatr. 2015 May;166(5):1152-1157.e6. doi: 10.1016/j.jpeds.2015.01.044. Epub 2015 Mar 11.
8
TMEM16A mediates the hypersecretion of mucus induced by Interleukin-13.跨膜蛋白16A(TMEM16A)介导白细胞介素-13诱导的黏液过度分泌。
Exp Cell Res. 2015 Jun 10;334(2):260-9. doi: 10.1016/j.yexcr.2015.02.026. Epub 2015 Mar 10.
9
TMEM16A-Mediated Mucin Secretion in IL-13-Induced Nasal Epithelial Cells From Chronic Rhinosinusitis Patients.TMEM16A 介导的白细胞介素 13 诱导的慢性鼻-鼻窦炎患者鼻黏膜上皮细胞黏蛋白分泌
Allergy Asthma Immunol Res. 2015 Jul;7(4):367-75. doi: 10.4168/aair.2015.7.4.367. Epub 2015 Mar 5.
10
Four basic residues critical for the ion selectivity and pore blocker sensitivity of TMEM16A calcium-activated chloride channels.四个对TMEM16A钙激活氯离子通道的离子选择性和孔道阻滞剂敏感性至关重要的碱性残基。
Proc Natl Acad Sci U S A. 2015 Mar 17;112(11):3547-52. doi: 10.1073/pnas.1502291112. Epub 2015 Mar 2.