Vitamin D-deficient mice have more invasive urinary tract infection

被引:16
作者
Hertting, Olof [1 ,2 ,3 ]
Luthje, Petra [1 ,2 ]
Sullivan, Devin [4 ]
Aspenstrom, Pontus [5 ]
Brauner, Annelie [1 ,2 ]
机构
[1] Karolinska Univ Hosp, Div Clin Mircrobiol, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
[2] Karolinska Inst, Stockholm, Sweden
[3] Karolinska Univ Hosp, Astrid Lindgren Childrens Hosp, Pediat Infect Dis Unit, Stockholm, Sweden
[4] KTH Royal Inst Technol, Sci Life Lab, Sch Biotechnol, Stockholm, Sweden
[5] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Stockholm, Sweden
来源
PLOS ONE | 2017年 / 12卷 / 07期
基金
瑞典研究理事会;
关键词
UROPATHOGENIC ESCHERICHIA-COLI; HUMAN UROTHELIAL CELLS; CATHELICIDIN; EXPRESSION; IMMUNITY;
D O I
10.1371/journal.pone.0180810
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vitamin D deficiency is a common health problem with consequences not limited to bone and calcium hemostasis. Low levels have also been linked to tuberculosis and other respiratory infections as well as autoimmune diseases. We have previously shown that supplementation with vitamin D can induce the antimicrobial peptide cathelicidin during ex vivo infection of human urinary bladder. In rodents, however, cathelicidin expression is not linked to vitamin D and therefore this vitamin D-related effect fighting bacterial invasion is not relevant. To determine if vitamin D had further protective mechanisms during urinary tract infections, we therefore used a mouse model. In vitamin D-deficient mice, we detected more intracellular bacterial communities in the urinary bladder, higher degree of bacterial spread to the upper urinary tract and a skewed cytokine response. Furthermore, we show that the vitamin D receptor was upregulated in the urinary bladder and translocated into the cell nucleus after E. coli infection. This study supports a more general role for vitamin D as a local immune response mediator in the urinary tract.
引用
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页数:13
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