Ultraviolet (UV) causes skin disorders by inducing reactive oxygen species (ROS) and inflammation. Therefore, oral intake of ergothioneine (
ERGO
), which has antioxidant and anti-inflammatory activities, may protect from UV-induced skin damage since
ERGO
is efficiently absorbed from diet via its specific transporter OCTN1/SLC
22
A4 expressed in various tissues including epidermis . In the present study, we investigated the effect of novel strain of Pleurotus sp. (NPS), which highly contains
ERGO
, on UVB-induced skin damage in mice and human keratinocyte HaCaT cells. First, HR-1 hairless mice fed with 2.5% NPS containing diet or control diet were irradiated with UVB for 10 weeks. In the NPS ingested group,
ERGO
concentrations were ~130 µg/g tissue in the epidermis and ~40 µM in the plasma. In the skin, an oxidative marker 8-OHdG measured by ELISA and expression of TNF evaluated by western blotting were significantly lower than those in control group. In undifferentiated HaCaT cells, OCTN1 was detected in both plasma membranes and intracellular compartment. [3H]
ERGO
was taken up in HaCaT cells in a time-dependent manner, and transfection of siRNA targeted to OCTN1 remarkably suppressed the uptake.
ERGO
-containing NPS significantly suppressed intracellular ROS induced by UVB treatment. Taken together, NPS ingestion may lead to a high
ERGO
distribution to the skin, suppressing UVB-induced oxidative stress and inflammation possibly via protective effect exerted by
ERGO
taken up by its specific uptake transporter OCTN1 in keratinocytes.
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