The Reduction of Skin Photodamage by the Ectoine– Thermus thermophilus Cofermentation Products

TL;DR

This study shows that cofermentation products of Ectoine and Thermus thermophilus protect skin from UVB damage by reducing inflammation and oxidative stress.

Contribution

The novel contribution is demonstrating the enhanced anti-UVB and antioxidant properties of Ectoine–T. thermophilus cofermentation products compared to Ectoine alone.

Findings

D-Ectoine increased GSH-PX activity and scavenging capacity in skin cells.

D-Ectoine reduced UVB-induced inflammation and promoted collagen expression.

In 3D skin models, D-Ectoine improved cell survival and reduced DNA damage markers.

Abstract

Prolonged exposure to UVB (280–320 nm) can lead to skin oxidative damage, inflammatory response, and skin cancer. Many active ingredients in the fermentation products of
Thermus thermophilus
have been shown to play important roles in antioxidant and anti‐UVB photodamage, such as superoxide dismutase (SOD) and photolyase. Ectoine, as one of the most prevalent compatible solutes in halophilic bacteria, can protect cells, proteins, cell membranes, and nucleic acids from external extreme environments such as high temperature, freezing, irradiation, and drying. It has been applied in the industries of fine chemicals, biomedicine, and biomanufacturing worldwide.

In this study, we evaluated the antioxidant activities and anti‐UVB photodamage activities of Ectoine–
T. thermophilus
cofermentation products (D‐Ectoine).

The comparison between D‐Ectoine and Ectoine was analyzed with hydroxyl radical (OH·−) scavenging assay, superoxide anion (O2·−) assay, total antioxidant capacity (T‐AOC) assay, and 1,1‐diphenyl‐2‐picrylhydrazyl radical (DPPH) scavenging assay. We evaluated the antioxidant ability of D‐Ectoine by detecting malondialdehyde (MDA) levels: the activity of SOD, catalase (CAT), and glutathione peroxidase (GSH‐PX) in human skin fibroblast (HSF) cells. Inflammatory response was measured with lipopolysaccharides (LPS) induced expression of interleukin 6 (IL‐6) and interleukin 8 (IL‐8). We evaluated the protective ability of D‐Ectoine against UVB‐induced damage by detecting the content of collagen type I (Col I) and extracellular matrix metalloproteinase (MMP‐1) in the cells, and the number of cell survival, erythroid 2‐related factor 2 (Nrf2) and 8‐hydroxy‐2′‐deoxyguanosine (8‐OHdG) expression in 3D skin model.

The results showed that D‐Ectione could promote the GSH‐PX activity in HSF cells with stronger T‐AOC and DPPH scavenging capacity, reduce the expression of LPS‐induced inflammatory factors IL‐6 and IL‐8, increase Col I expression both with and without UVB and inhibit expression of MMP‐1 after UVB irradiation. In the 3D skin model, D‐Ectione could increase the number of cell survival and Nrf2 expression, and decrease 8‐OHdG expression after UVB irradiation.

These results demonstrated that D‐Ectione has protective effects against UVB‐induced skin photodamage and may contribute to the development of cosmetic products with anti‐UVB.

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