Water‐soluble intracellular extract of Desmodesmus sp. YT enhanced the antioxidant capacity of human skin fibroblast to protect the skin from UV damage

Author:

Ying Ming123,Zeng Zuye1,Li Qin1,Chen Xianglan1,Xiong Ying4,Wu Bo4,Peng Liang5,Zhang Qian6,Wang Li7,Dai Zhongming8,Li Shuangfei1,Chen Huirong1,Yang Xuewei1

Affiliation:

1. Guangdong Key Laboratory of Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, College of Life Sciences and Oceanography Shenzhen University Shenzhen China

2. Innova Bay (Shenzhen) Technology Co. Ltd Shenzhen China

3. Pingshan Translational Medicine Center Shenzhen Bay Laboratory Shenzhen China

4. Department of Dermatology, Affiliated Shenzhen Maternity and Child Healthcare Hospital Southern Medical University Shenzhen China

5. Shenzhen Mental Health Center Shenzhen Kangning Hospital Shenzhen China

6. The Sixth Affiliated Hospital of Shenzhen University and Huazhong University of Science and Technology Union Shenzhen Hospital Shenzhen China

7. Department of Dermatology Shenzhen University General Hospital Shenzhen China

8. Shenzhen University General Hospital Shenzhen China

Abstract

AbstractBackgroundThe oxidative stress induced by ultraviolet (UV) radiation is a pivotal factor in skin aging and can even contribute to the development of skin cancer.AimThis study explored the antioxidant effect and mechanism of water‐soluble intracellular extract (WIE) of Desmodesmus sp.YT (YT), aiming to develop a natural antioxidant suitable for incorporation into cosmetics.MethodsThe study evaluated the scavenging capacity of YT‐WIE against free radicals and assessed its impact on human skin fibroblasts (HSF) cell viability and UV resistance using Cell Counting Kit‐8 (CCK‐8). Transcriptome sequencing was employed to elucidate the mechanism of action, while RT‐qPCR and western blot were used to validate the expression of key genes.ResultsYT‐WIE displayed robust antioxidant activity, demonstrating potent scavenging abilities against 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH; IC50 = 0.55 mg mL−1), 2,2′‐Azino‐bis (3 ethylbenzothiazoline‐6‐sulfonic acid; ABTS; IC50 = 3.11 mg mL−1), Hydroxyl (·OH; IC50 = 2.21 mg mL−1), and Superoxide anion (O2•−; IC50 = 0.98 mg mL−1). Furthermore, compared to the control group, the YT‐WIE group exhibited an 89.30% enhancement in HSF viability and a 44.63% increase in survival rate post‐UV irradiation. Significant upregulation of antioxidant genes (GCLC, GCLM, TXNRD1, HMOX1, NQO1) was observed with YT‐WIE treatment at 400 μg mL−1, with fold increases ranging from 1.13 to 5.85 times.ConclusionYT‐WIE demonstrated considerable potential as an antioxidant, shielding human cells from undue oxidative stress triggered by external stimuli such as UV radiation. This suggests its promising application in cosmetics antioxidants.

Funder

Natural Science Foundation of Guangdong Province

Publisher

Wiley

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