Circadian rhythm disruption promotes M1 macrophages polarization exacerbating the inflammatory response in rosacea.
Tu. Ying Y; Yang. Zhenghui Z; He. Yunting Y; Wang. Tingyu T; Hua. Piyan P; Yao. Qiuyan Q; Gu. Hua H
Key Findings
- Circadian rhythm disruption lowers clock proteins (Bmal1, Clock, Per1/2, Rev‑Erbα, RORα) and pushes macrophages toward the pro‑inflammatory M1 phenotype in a rosacea mouse model.
- M1‑polarized macrophages increase inflammatory cytokines (TNF‑α, IL‑6, IL‑1β), worsening skin lesions.
- Over‑expressing Bmal1 restores clock protein levels, reduces M1 polarization, and lowers inflammatory cytokine production.
Practical Outcomes
- Aim for consistent sleep timing and adequate rest to support your circadian clock, which may lessen rosacea flare‑ups. Consider lifestyle habits that reinforce circadian health, such as regular light exposure and avoiding late‑night screen time. No specific LL‑37 dosing guidance is provided, but maintaining clock protein balance appears beneficial.
Summary
The study shows that messing up your body’s internal clock (like staying up late or having irregular sleep) can make rosacea worse by turning immune cells into a more inflammatory type, leading to more skin redness and irritation. Boosting a clock protein called Bmal1 in cells reduced this inflammation, suggesting that keeping a regular sleep‑wake schedule might help manage rosacea symptoms.
Abstract
To explore the role of macrophage polarization induced by circadian rhythm disorder (CRD) in the aggravated inflammatory response of rosacea. The rosacesis-like animal model was established by intradermal injection of Cathelicidin antimicrobial peptide LL-37 (LL37) into the back of mice. HE staining, Western blot and immunofluorescence detection were used to investigate the effect of circadian rhythm disorder on the expression of inflammatory factors and macrophage polarization in rosacea. Overexpression of Brain and Muscle ARNT-Like 1 (Oe-Bmal1) was transfected into HaCaT cells and M0 macrophages treated with LL37 in vitro to investigate the role of Muscle ARNT-Like 1 (Bmal1) on rosacea. In LL37-induced rosacea mice, circadian rhythm disruption (CRD) suppressed the expression of circadian clock proteins, including Bmal1, Circadian Locomotor Output Cycles Kaput (Clock), Period Circadian Protein 1 (Per1), Period Circadian Protein 2 (Per2), Nuclear Receptor Subfamily 1 Group D Member 1 (Rev-erbα), and Retinoic Acid Receptor-Related Orphan Receptor Alpha (RORα), and induced the polarization of macrophages in rosacea-like mice towards the M1 phenotype. Subsequently, the expression of inflammatory factors, including Tumor Necrosis Factor-alpha (TNF-α), Interleukin-6 (IL-6), and Interleukin-1 beta (IL-1β), was promoted, which aggravated the inflammatory response of skin lesions. Over-expression of Bmal1 significantly increased the expression level of clock proteins and inhibited the polarization of macrophages to M1 type, consequently inhibiting the expression of inflammatory factors in the cell model of rosacea. Circadian rhythm disorder may aggravate the inflammatory response of rosacea by affecting macrophage polarization, which indicates that paying attention to regular sleep and rest may be necessary for the treatment and management of rosacea.
Study Information
pubmed
2025
2025-04-01T00:00:00.000Z
10.1007/s00403-025-04060-x
3
38