# Functional Characterization of Naematelia aurantialba Basidiospore Polysaccharides in L929 Cells: Photoprotective, Antioxidant, and Anti-Inflammatory Effects Against UVB-Induced Damage

**Authors:** Lihan Sun, Sijie Liu, Tao Sun, Rui Wang, Yian Gu, Liang Sun, Hong Xu, Peng Lei

PMC · DOI: 10.3390/foods15030598 · Foods · 2026-02-06

## TL;DR

This study shows that a polysaccharide from a medicinal fungus protects skin cells from UVB damage by reducing oxidative stress and inflammation.

## Contribution

The novel contribution is the functional characterization of NAPS-A as a photoprotective, antioxidant, and anti-inflammatory agent derived from Naematelia aurantialba.

## Key findings

- NAPS-A reduced UVB-induced cytotoxicity and oxidative stress in L929 cells.
- NAPS-A inhibited pro-inflammatory cytokines and maintained extracellular matrix homeostasis.
- NAPS-A showed potential as a sustainable bioactive ingredient for functional foods and nutricosmetics.

## Abstract

Ultraviolet (UV) radiation is a primary driver of skin photoaging, characterized by oxidative stress, persistent inflammatory responses, and excessive degradation of the extracellular matrix (ECM). Naematelia aurantialba is a traditional medicinal and edible fungus recognized for its diverse pharmacological activities. In this study, N. aurantialba polysaccharides (NAPS-A)—high-value bioactive compounds obtained through liquid fermentation—were subjected to detailed functional characterization to evaluate their restorative potential against UVB-induced damage. The results demonstrated that NAPS-A treatment effectively mitigated UVB-induced cytotoxicity. Furthermore, NAPS-A significantly suppressed the accumulation of reactive oxygen species (ROS) and malondialdehyde (MDA), while robustly revitalizing the endogenous antioxidant defense system by restoring superoxide dismutase (SOD) and catalase (CAT) activities. Moreover, NAPS-A exerted potent anti-inflammatory effects by inhibiting the secretion of nitric oxide (NO) and pro-inflammatory cytokines, including IL-1β, IL-6, and TNF-α. NAPS-A maintained ECM homeostasis by counteracting collagen depletion, exhibiting inhibitory activity against collagenase and elastase, and modulating the mRNA expression of Col1a1 and Col3a1. These findings suggested that NAPS-A protects fibroblasts from UVB-induced damage through a synergistic mechanism involving radical scavenging, the enhancement of cellular redox homeostasis, and the modulation of ECM metabolism. Overall, NAPS-A represents a promising, sustainably produced, food-derived bioactive ingredient with significant potential for the development of functional foods and nutricosmetics aimed at mitigating UVB-induced skin damage.

## Linked entities

- **Genes:** COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277], COL3A1 (collagen type III alpha 1 chain) [NCBI Gene 1281]
- **Proteins:** Cat (Catalase), cela1.2.L (chymotrypsin like elastase 1, gene 2 L homeolog)
- **Chemicals:** malondialdehyde (PubChem CID 10964), nitric oxide (PubChem CID 145068), IL-6 (PubChem CID 165368475)
- **Species:** Naematelia aurantialba (taxon 371454)

## Full-text entities

- **Genes:** Col1a1 (collagen, type I, alpha 1) [NCBI Gene 12842] {aka Col1a-1, Cola-1, Cola1, Mov-13, Mov13}, Col3a1 (collagen, type III, alpha 1) [NCBI Gene 12825] {aka Col3a-1, Tsk-2, Tsk2}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Diseases:** cytotoxicity (MESH:D064420), skin damage (MESH:D012871), Inflammatory (MESH:D007249)
- **Chemicals:** N. aurantialba polysaccharides (-), NO (MESH:D009569), ROS (MESH:D017382), MDA (MESH:D008315)
- **Species:** Naematelia aurantialba (species) [taxon 371454]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896858/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12896858/full.md

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Source: https://tomesphere.com/paper/PMC12896858