Positive correlation between circulating cathelicidin antimicrobial peptide (hCAP18/LL-37) and 25-hydroxyvitamin D levels in healthy adults

被引:59
|
作者
Dixon B.M. [1 ]
Barker T. [2 ]
McKinnon T. [1 ]
Cuomo J. [1 ]
Frei B. [3 ]
Borregaard N. [4 ]
Gombart A.F. [3 ]
机构
[1] USANA Health Sciences Inc, 3838 West Parkway Boulevard, Salt Lake City
[2] Sport Science Department, Orthopedic Specialty Hospital, Murray
[3] Linus Pauling Institute, Department of Biochemistry and Biophysics, Oregon State University, Corvallis
[4] Granulocyte Research Laboratory, Department of Hematology, National University Hospital, Copenhagen
基金
美国国家卫生研究院;
关键词
25-hydroxyvitamin D; CAMP; Cathelicidin; hCAP18; Immunity; Infection; LL-37; Plasma; Serum; Vitamin D;
D O I
10.1186/1756-0500-5-575
中图分类号
学科分类号
摘要
Abstract. Background: Transcription of the cathelicidin antimicrobial peptide (CAMP) gene is induced by binding of the bioactive form of vitamin D, 1,25-dihydroxyvitamin D, to the vitamin D receptor. Significant levels of the protein hCAP18/LL-37 are found in the blood and may protect against infection and/or sepsis. We hypothesized that serum vitamin D levels may modulate the circulating levels of hCAP18. Only three studies have shown a positive correlation between circulating 25-hydroxyvitamin D and hCAP18 levels. Here we provide additional evidence for such a correlation in healthy, middle-aged adults. Findings. Serum levels of 25-hydroxyvitamin D [25(OH)D] and plasma levels of hCAP18 were determined in 19 healthy middle-aged (mean of 50.1 years) adult men and women. Plasma hCAP18 concentrations correlated with serum 25(OH)D concentrations in subjects with 25(OH)D levels ≤ 32 ng/ml (r = 0.81, p < 0.005) but not in subjects with concentrations > 32 ng/ml (r = 0.19, p = 0.63). Conclusions: We conclude that plasma hCAP18 levels correlate with serum 25(OH)D levels in subjects with concentrations of 25(OH)D ≤ 32 ng/ml as opposed to those with concentrations > 32 ng/ml and that vitamin D status may regulate systemic levels of hCAP18/LL-37. © 2012 Dixon et al.; licensee BioMed Central Ltd.
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