Crosstalk between Vitamin D Metabolism, VDR Signalling, and Innate Immunity

Author

Lin, Rui

Source

BioMed Research International

Issue

Vol. 2016, Issue 2016 (31 Dec. 2016), pp.1-5, 5 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2016-06-15

Country of Publication

Egypt

No. of Pages

5

Main Subjects

Medicine

Abstract EN

The primary function of vitamin D is to regulate calcium homeostasis, which is essential for bone formation and resorption.

Although diet is a source of vitamin D, most foods are naturally lacking vitamin D.

Vitamin D is also manufactured in the skin through a photolysis process, leading to a process called the “sunshine vitamin.” The active form of vitamin D, 1,25-dihydroxyvitamin D (calcitriol), is biosynthesised in the kidney through the hydroxylation of 25-hydroxycholecalciferol by the CYP27B1 enzyme.

It has been found that several immune cells express the vitamin D receptor (VDR) and CYP27B1; of the latter, synthesis is determined by several immune-specific signals.

The realisation that vitamin D employs several molecular mechanisms to regulate innate immune responses is more recent.

Furthermore, evidence collected from intervention studies indicates that vitamin D supplements may boost clinical responses to infections.

This review considers the current knowledge of how immune signals regulate vitamin D metabolism and how innate immune system function is modulated by ligand-bound VDR.

American Psychological Association (APA)

Lin, Rui. 2016. Crosstalk between Vitamin D Metabolism, VDR Signalling, and Innate Immunity. BioMed Research International،Vol. 2016, no. 2016, pp.1-5.
https://search.emarefa.net/detail/BIM-1096863

Modern Language Association (MLA)

Lin, Rui. Crosstalk between Vitamin D Metabolism, VDR Signalling, and Innate Immunity. BioMed Research International No. 2016 (2016), pp.1-5.
https://search.emarefa.net/detail/BIM-1096863

American Medical Association (AMA)

Lin, Rui. Crosstalk between Vitamin D Metabolism, VDR Signalling, and Innate Immunity. BioMed Research International. 2016. Vol. 2016, no. 2016, pp.1-5.
https://search.emarefa.net/detail/BIM-1096863

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1096863