4.6 Article

Expression of antimicrobial peptide genes oscillates along day/night rhythm protecting mice skin from bacteria

Journal

EXPERIMENTAL DERMATOLOGY
Volume 30, Issue 10, Pages 1418-1427

Publisher

WILEY
DOI: 10.1111/exd.14229

Keywords

antimicrobial peptides; circadian clock; gene expression; skin

Categories

Funding

  1. NIH [1R01AR073004-01A1, R01AR071189-01A1, R21 AI1520]
  2. National Science Centre in Poland (NCN) [UMO-2014/12/W/NZ6/00454]

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The gene expression of Rarres2, Camp, and Defb1 in mouse skin was highest during high activity periods, but this rhythm was masked under constant darkness, while the gene expression of Defb3 and Defb14 showed the highest levels during sleep and were maintained under constant darkness. This indicates a correlation between specific antimicrobial peptides and different physiological states, with some being influenced by light-dark cycles and others being regulated by a circadian clock.
Antimicrobial peptides (AMPs) are important components of the innate immune system and are involved in skin protection against environmental insults and in wound healing. Herein, we assessed the gene expression of chemerin (Rarres2), cathelicidin CRAMP (Camp), and three beta-defensins (Defb1, Defb3, and Defb14) in mouse skin during light/dark cycle (LD 12:12) and constant darkness (DD). Next, we examined the survival of bacteria applied on the skin at specific times during the day. We found that the expression of Rarres2, Camp, and Defb1 was the highest at 4 h after the beginning of darkness, during high activity of mice. These rhythms, however, were not maintained under DD in the skin but were present in the liver. This indicated that in the case of skin, a circadian input was masked by daily changes of light in the environment. In contrast, Defb3 and Defb14 showed the highest mRNA levels when the mice slept, and these rhythmic mRNA oscillations were maintained under DD. This shows that Rarres2, Camp, and Defb1 levels in the skin are correlated with high locomotor activity in mice and they are controlled by daily changes of light and dark. Alternatively, oscillations in the mRNA levels of Defb3 and Defb14 seem to protect skin and heal wounds during sleep. These rhythms are maintained under DD, indicating that they are regulated by a circadian clock. Our study suggests that daily AMP expression affects the survival of bacteria on the surface of skin, which depends on the phase of AMP cycling.

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