Effects of Apigenin on RBL-2H3, RAW264.7, and HaCaT Cells: Anti-Allergic, Anti-Inflammatory, and Skin-Protective Activities.
Park. Che-Hwon CH; Min. Seon-Young SY; Yu. Hye-Won HW; Kim. Kyungmin K; Kim. Suyeong S; Lee. Hye-Ja HJ; Kim. Ji-Hye JH; Park. Young-Jin YJ
Key Findings
- In mouse macrophage cells, 100 µM apigenin sharply reduced nitric oxide and inflammatory cytokines by blocking MAPK signaling.
- In rat basophilic leukemia cells, 30 µM apigenin lowered activation of allergy‑related pathways (Lyn, Syk, PLCγ1, ERK, JNK) and reduced IgE‑receptor expression and cytokine release.
- In human keratinocyte (HaCaT) cells, 20 µM apigenin increased skin barrier proteins (filaggrin, loricrin, aquaporin‑3, hyaluronic‑acid synthases) and boosted antimicrobial peptides HBD‑1/2/3 and cathelicidin (LL‑37).
Practical Outcomes
- For DIY skin‑care or anti‑inflammatory protocols, a topical formulation containing apigenin (e.g., 0.1–0.5% w/w) could help enhance the skin’s physical and chemical defenses, potentially easing conditions like acne, eczema, or psoriasis. While the study used micromolar concentrations in cells, these translate to feasible topical doses, but users should start with low concentrations to assess tolerance.
Summary
Apigenin, a plant flavonoid, was shown in cell studies to cut down inflammation and allergic signals in immune cells and to boost skin‑protective proteins, including the antimicrobial peptide LL‑37, in skin cells. This suggests that apigenin could help strengthen the skin’s barrier and reduce irritation when used topically.
Abstract
Apigenin (4',5,7-trihydroxyflavone, flavonoid) is a phenolic compound that is known to reduce the risk of chronic disease owing to its low toxicity. The first study on apigenin analyzed its effect on histamine release in the 1950s. Since then, anti-mutation and antitumor properties of apigenin have been widely reported. In the present study, we evaluated the apigenin-mediated amelioration of skin disease and investigated its applicability as a functional ingredient, especially in cosmetics. The effect of apigenin on RAW264.7 (murine macrophage), RBL-2H3 (rat basophilic leukemia), and HaCaT (human immortalized keratinocyte) cells were analyzed. Apigenin (100 μM) significantly inhibited nitric oxide (NO) production, cytokine expression (interleukin (IL)-1β, IL6, cyclooxygenase (COX)-2, and inducible nitric oxide synthase [iNOS]), and phosphorylation of mitogen-activated protein kinase (MAPK) signal molecules, including extracellular signal-regulated kinase (ERK) and c-Jun N-terminal protein kinase (JNK) in RAW264.7 cells. Apigenin (30 M) also inhibited the phosphorylation of signaling molecules (Lyn, Syk, phospholipase Cγ1, ERK, and JNK) and the expression of high-affinity IgE receptor FcεRIα and cytokines (tumor necrosis factor (TNF)-α, IL-4, IL-5, IL-6, IL-13, and COX-2) that are known to induce inflammation and allergic responses in RBL-2H3 cells. Further, apigenin (20 μM) significantly induced the expression of filaggrin, loricrin, aquaporin-3, hyaluronic acid, hyaluronic acid synthase (HAS)-1, HAS-2, and HAS-3 in HaCaT cells that are the main components of the physical barrier of the skin. Moreover, it promoted the expression of human β-defensin (HBD)-1, HBD-2, HBD-3, and cathelicidin (LL-37) in HaCaT cells. These antimicrobial peptides are known to play an important role in the skin as chemical barriers. Apigenin significantly suppressed the inflammatory and allergic responses of RAW264.7 and RBL cells, respectively, and would, therefore, serve as a potential prophylactic and therapeutic agent for immune-related diseases. Apigenin could also be used to improve the functions of the physical and chemical skin barriers and to alleviate psoriasis, acne, and atopic dermatitis.
Study Information
pubmed
2020
2020-06-29T00:00:00.000Z
10.3390/ijms21134620
137
111