alpha-Intercalated cells defend the urinary system from bacterial infection

作者: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 Fabio 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
来源:Journal of Clinical Investigation, 2014, 124(7): 2963-2976.
DOI:10.1172/JCI71630

摘要

alpha-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.

  • 出版日期2014-7