Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Jan:175:82-87.
doi: 10.1016/j.jsbmb.2016.11.001. Epub 2016 Nov 3.

Role of vitamin D on gut microbiota in cystic fibrosis

Affiliations
Review

Role of vitamin D on gut microbiota in cystic fibrosis

Mansi Kanhere et al. J Steroid Biochem Mol Biol. 2018 Jan.

Abstract

This review explores the potential for vitamin D to favorably alter the gut microbiota, given emerging evidence of the role of vitamin D in controlling mucosal inflammation in the gut. It will focus on cystic fibrosis (CF) patients, a population with both vitamin D deficiency due to gut malabsorption and an altered gut microbiota composition. Recent evidence shows that vitamin D acts to maintain the integrity of the gut mucosal barrier by enhancement of intercellular junctions that control mucosal permeability and reduction of pro-inflammatory cytokines such as IL-8. In addition, vitamin D receptor-mediated signaling has been shown to inhibit inflammation-induced apoptosis of intestinal epithelial cells. As a result of these effects on the intestinal mucosa, maintenance of sufficient vitamin D status may be essential for the development of a healthy gut microbiota, particularly in conditions defined by chronic mucosal inflammation such as CF. We hypothesize here that high dose vitamin D may be used to favorably manipulate the aberrant mucosa seen in patients with CF. This may result in improved clinical outcomes in association with a low inflammatory environment that allows beneficial bacteria to outcompete opportunistic pathogens. Current evidence is sparse but encouraging, and additional evidence is needed to establish vitamin D as a therapeutic approach for gut microbiota modification.

Keywords: Cystic fibrosis; Inflammation; Intestinal microbiota; Vitamin D; Vitamin D receptor.

PubMed Disclaimer

Conflict of interest statement

Conflicts of interest: None

Figures

Figure 1
Figure 1. A schematic representation of mechanisms by which vitamin D may decrease intestinal mucosal inflammation and thus alter dysbiosis in CF
Description: Microbial dysbiosis is a hallmark of the CF gut underlying to chronic mucosal inflammation. Vitamin D has been proposed to decrease intestinal inflammation through the inhibition of inflammation-induced epithelial cell apoptosis and enhancement of intercellular junctions that are important in maintaining mucosal permeability. In addition it reduces cytokine-induced NF-κB nuclear translocation thus resulting in a suppression of inflammatory mediators. Together, these effects may restore gastrointestinal homeostasis and prevent intestinal dysbiosis in CF.

Similar articles

Cited by

References

    1. Strong TV, Boehm K, Collins FS. Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization. The Journal of clinical investigation. 1994;93:347–354. - PMC - PubMed
    1. Chesdachai S, Tangpricha V. Treatment of vitamin D deficiency in cystic fibrosis. The Journal of steroid biochemistry and molecular biology. 2015 - PMC - PubMed
    1. Wang TT, Nestel FP, Bourdeau V, Nagai Y, Wang Q, Liao J, Tavera-Mendoza L, Lin R, Hanrahan JW, Mader S, White JH. Cutting edge: 1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. Journal of immunology (Baltimore, Md : 1950) 2004;173:2909–2912. - PubMed
    1. Liu PT, Stenger S, Tang DH, Modlin RL. Cutting edge: vitamin D-mediated human antimicrobial activity against Mycobacterium tuberculosis is dependent on the induction of cathelicidin. Journal of immunology (Baltimore, Md : 1950) 2007;179:2060–2063. - PubMed
    1. Zhu Y, Mahon BD, Froicu M, Cantorna MT. Calcium and 1 alpha,25-dihydroxyvitamin D3 target the TNF-alpha pathway to suppress experimental inflammatory bowel disease. European journal of immunology. 2005;35:217–224. - PubMed

Publication types

MeSH terms