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本文引用的文献

1
An endogenous ribonuclease inhibitor regulates the antimicrobial activity of ribonuclease 7 in the human urinary tract.一种内源性核糖核酸酶抑制剂调节人泌尿道中核糖核酸酶7的抗菌活性。
Kidney Int. 2014 May;85(5):1179-91. doi: 10.1038/ki.2013.395. Epub 2013 Oct 9.
2
Diagnostic and prognostic stratification in the emergency department using urinary biomarkers of nephron damage: a multicenter prospective cohort study.使用肾单位损伤的尿生物标志物进行急诊科的诊断和预后分层:一项多中心前瞻性队列研究。
J Am Coll Cardiol. 2012 Jan 17;59(3):246-55. doi: 10.1016/j.jacc.2011.10.854.
3
Contribution of siderophore systems to growth and urinary tract colonization of asymptomatic bacteriuria Escherichia coli.铁载体系统对无症状菌尿大肠埃希菌生长和尿路定植的贡献。
Infect Immun. 2012 Jan;80(1):333-44. doi: 10.1128/IAI.05594-11. Epub 2011 Sep 19.
4
Urinary tract infection: clinical practice guideline for the diagnosis and management of the initial UTI in febrile infants and children 2 to 24 months.尿路感染:发热婴儿和儿童(2 至 24 个月)初始尿路感染的诊断和管理临床实践指南。
Pediatrics. 2011 Sep;128(3):595-610. doi: 10.1542/peds.2011-1330. Epub 2011 Aug 28.
5
Ribonuclease 7 is a potent antimicrobial peptide within the human urinary tract.核糖核酸酶 7 是人体泌尿道中一种有效的抗菌肽。
Kidney Int. 2011 Jul;80(2):174-80. doi: 10.1038/ki.2011.109. Epub 2011 Apr 27.
6
Vesico-ureteric reflux: using mouse models to understand a common congenital urinary tract defect.膀胱输尿管反流:利用小鼠模型了解常见的先天性泌尿道缺陷。
Pediatr Nephrol. 2011 Sep;26(9):1513-22. doi: 10.1007/s00467-011-1821-1. Epub 2011 Mar 20.
7
International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases.国际临床实践指南:女性急性单纯性膀胱炎和肾盂肾炎的治疗(2010 年更新):美国传染病学会和欧洲临床微生物学和传染病学会。
Clin Infect Dis. 2011 Mar 1;52(5):e103-20. doi: 10.1093/cid/ciq257.
8
The Ngal reporter mouse detects the response of the kidney to injury in real time.Ngal 报告鼠实时检测肾脏对损伤的反应。
Nat Med. 2011 Feb;17(2):216-22. doi: 10.1038/nm.2290. Epub 2011 Jan 16.
9
Redundancy and specificity of Escherichia coli iron acquisition systems during urinary tract infection.大肠埃希菌尿路感染中铁摄取系统的冗余性和特异性。
Infect Immun. 2011 Mar;79(3):1225-35. doi: 10.1128/IAI.01222-10. Epub 2011 Jan 10.
10
Host-pathogen interactions in urinary tract infection.尿路感染中的宿主-病原体相互作用。
Nat Rev Urol. 2010 Aug;7(8):430-41. doi: 10.1038/nrurol.2010.101. Epub 2010 Jul 20.

α-闰细胞保护泌尿系统免受细菌感染。

α-Intercalated cells defend the urinary system from bacterial infection.

作者信息

Paragas Neal, Kulkarni Ritwij, Werth Max, Schmidt-Ott Kai M, Forster Catherine, Deng Rong, Zhang Qingyin, Singer Eugenia, Klose Alexander D, Shen Tian Huai, Francis Kevin P, Ray Sunetra, Vijayakumar Soundarapandian, Seward Samuel, Bovino Mary E, Xu Katherine, Takabe Yared, Amaral Fábio E, Mohan Sumit, Wax Rebecca, Corbin Kaitlyn, Sanna-Cherchi Simone, Mori Kiyoshi, Johnson Lynne, Nickolas Thomas, D'Agati Vivette, Lin Chyuan-Sheng, Qiu Andong, Al-Awqati Qais, Ratner Adam J, Barasch Jonathan

出版信息

J Clin Invest. 2014 Jul;124(7):2963-76. doi: 10.1172/JCI71630. Epub 2014 Jun 17.

DOI:10.1172/JCI71630
PMID:24937428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4071397/
Abstract

α-Intercalated cells (A-ICs) within the collecting duct of the kidney are critical for acid-base homeostasis. Here, we have shown that A-ICs also serve as both sentinels and effectors in the defense against urinary infections. In a murine urinary tract infection model, A-ICs bound uropathogenic E. coli and responded by acidifying the urine and secreting the bacteriostatic protein lipocalin 2 (LCN2; also known as NGAL). A-IC-dependent LCN2 secretion required TLR4, as mice expressing an LPS-insensitive form of TLR4 expressed reduced levels of LCN2. The presence of LCN2 in urine was both necessary and sufficient to control the urinary tract infection through iron sequestration, even in the harsh condition of urine acidification. In mice lacking A-ICs, both urinary LCN2 and urinary acidification were reduced, and consequently bacterial clearance was limited. Together these results indicate that A-ICs, which are known to regulate acid-base metabolism, are also critical for urinary defense against pathogenic bacteria. They respond to both cystitis and pyelonephritis by delivering bacteriostatic chemical agents to the lower urinary system.

摘要

肾集合管中的α-闰细胞(A-ICs)对于酸碱平衡至关重要。在此,我们已表明A-ICs在抵御泌尿系统感染中既是哨兵又是效应器。在小鼠泌尿系统感染模型中,A-ICs结合致病性大肠杆菌,并通过酸化尿液和分泌抑菌蛋白lipocalin 2(LCN2;也称为NGAL)做出反应。A-ICs依赖性LCN2分泌需要TLR4,因为表达对LPS不敏感形式的TLR4的小鼠LCN2水平降低。尿液中LCN2的存在对于通过螯合铁来控制泌尿系统感染既是必要的也是充分的,即使在尿液酸化的苛刻条件下也是如此。在缺乏A-ICs的小鼠中,尿液LCN2和尿液酸化均降低,因此细菌清除受到限制。这些结果共同表明已知调节酸碱代谢的A-ICs对于泌尿系统抵御病原菌也至关重要。它们通过向下泌尿系统输送抑菌化学物质来应对膀胱炎和肾盂肾炎。