# Camellia sinensis Seed Flavonoids Attenuate UVB-Induced Inflammation and UVA-Induced Photodamage via MAPK/NF-κB and AP-1 Pathways

**Authors:** Xiao-Xiao Duo, Ru-Biao Hou, Yuan-Cheng Huang, Lei Li, Jian-Ming Deng, Min Yu, Guang-Li Wang, Jing Wang

PMC · DOI: 10.3390/molecules31050871 · 2026-03-05

## TL;DR

This study shows that Camellia sinensis seed flavonoids can reduce UV-induced skin damage and inflammation by targeting specific cellular pathways.

## Contribution

The study reveals the novel anti-inflammatory and anti-photoaging mechanisms of Camellia sinensis seed flavonoids via MAPK/NF-κB and AP-1 pathways.

## Key findings

- CSF reduced ROS and inflammatory factors in keratinocytes via p38/JNK and NF-κB inhibition.
- CSF upregulated skin barrier proteins and counteracted UVA damage in fibroblasts via AP-1 and TGF-β/Smad pathways.
- CSF demonstrated coordinated anti-inflammatory, barrier-repair, and anti-photoaging effects.

## Abstract

This study evaluated the anti-inflammation and anti-photoaging effects of Camellia sinensis seed flavonoids (CSF) against UVB and UVA irradiation and elucidated the underlying mechanisms. Using UVB-irradiated human keratinocytes and UVA-irradiated human dermal fibroblasts, we found that CSF significantly reduced intracellular ROS and suppressed the secretion of inflammatory factors (PGE-2, TNF-α, IL-6, IL-8) by inhibiting the p38/JNK and NF-κB pathways, along with iNOS and COX-2 expression. In keratinocytes, CSF also downregulated Caspase-3 and upregulated barrier proteins filaggrin and Claudin-1. In fibroblasts, CSF counteracted UVA damage by upregulating collagen IV and XVII at the dermo-epidermal junction and enhancing the production of collagen I, III, and hyaluronic acid in the dermis, mediated via AP-1 inhibition and TGF-β/Smad pathway modulation. These results demonstrate that CSF coordinated anti-inflammatory, barrier-repair, and anti-photoaging actions, highlighting its potential as a promising skincare ingredient.

## Linked entities

- **Genes:** CRK (CRK proto-oncogene, adaptor protein) [NCBI Gene 1398], MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], Smox (Smad on X) [NCBI Gene 31738], Casp3 (caspase 3) [NCBI Gene 12367], LOC102285057 (hornerin) [NCBI Gene 102285057], CLDN7 (claudin 7) [NCBI Gene 1366]
- **Proteins:** ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase), ptges2.L (prostaglandin E synthase 2 L homeolog), TNF (tumor necrosis factor), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), NOS2 (nitric oxide synthase 2), COX2 (cytochrome c oxidase subunit II), vkg (viking)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, ISYNA1 (inositol-3-phosphate synthase 1) [NCBI Gene 51477] {aka INO1, INOS, IPS, IPS 1, IPS-1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, FLG (filaggrin) [NCBI Gene 2312] {aka ATOD2, FLG-1, FLG1}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}
- **Diseases:** Inflammation (MESH:D007249)
- **Chemicals:** PGE-2 (MESH:D015232), CSF (-), hyaluronic acid (MESH:D006820)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12986526/full.md

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Source: https://tomesphere.com/paper/PMC12986526