Porphyra-334, a mycosporine-like amino acid, attenuates UV-induced apoptosis in HaCaT cells

Author:

Suh Sung-Suk1,Oh Se Kyung1,Lee Sung Gu23,Kim Il-Chan24,Kim Sanghee25

Affiliation:

1. Division of Polar Life Sciences Korea Polar Research Institute, Incheon , 21990, Korea (Republic of)

2. Division of Polar Life Sciences Korea Polar Research Institute Incheon, 21990 Incheon , Korea (Republic of)

3. Department of Polar Science University of Science and Technology, Incheon , 21990, Korea (Republic of)

4. Department of Polar Science University of Science and Technology, Incheon 21990, Korea (Republic of)

5. Department of Polar Science University of Science and Technology Incheon, 21990 Incheon , Korea (Republic of)

Abstract

Abstract The main aim of the current research was to study the effect of porphyra-334, one of mycosporine-like amino acids (MAAs), well known as UV-absorbing compounds, on UVinduced apoptosis in human immortalized keratinocyte (HaCaT) cells. Due to their UV-screening capacity and ability to prevent UV-induced DNA damage, MAAs have recently attracted considerable attention in both industry and research in pharmacology. Herein, human HaCaT cells were used to determine the biological activities of porphyra- 334 by various in vitro assays, including proliferation, apoptosis and Western blot assays. The proliferation rate of UV-irradiated HaCaT cells was significantly decreased compared to the control group. Pretreatment with porphyra- 334 markedly attenuated the inhibitory effect of UV and induced a dramatic decrease in the apoptotic rate. Expression of active caspase-3 protein was increased in response to UV irradiation, while caspase-3 levels were similar between cells treated with porphyra-334 and the non-irradiated control group. Taken together, our data suggest that porphyra-334 inhibits UV-induced apoptosis in HaCaT cells through attenuation of the caspase pathway.

Publisher

Walter de Gruyter GmbH

Subject

Pharmaceutical Science,Pharmacology,General Medicine

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