Autophagy attenuates particulate matter 2.5-induced damage in HaCaT cells

Background: Keratinocyte is a key component of the skin barrier and maintains skin homeostasis. As an environmental pathogenic factor, PM2.5 can cause epidermal cell damage, but the mechanism remains to be elucidated. The present study aimed to evaluate the effect caused by PM2.5 in HaCaT cells and investigate the underlying mechanisms.

Methods: HaCaT cells were treated with PM2.5 for 12 h or 24 h, either alone or combined with UVB irradiation. A Cell Counting Kit (CCK-8) assay was carried out to detect the effect of PM2.5 on HaCaT cell viability. Flow cytometry, Western Blot, and AO staining were employed to detect the changes of Apoptosis and Autophagy. The changes of cytotoxicity and Apoptosis in HaCaT cells were analyzed by CCK-8 and flow cytometry after pretreatment with Autophagy Inhibitor 3-MA.

Results: The results showed that PM2.5 induced cytotoxicity by increasing cell Apoptosis and activating Autophagy. Apoptosis was determined to be increased significantly after Autophagy inhibition. Moreover, solar radiation intensified PM2.5-induced damage in HaCaT cells, which further enhanced the Autophagy. However, there was no significant difference in Apoptosis after inhibition of Autophagy in combined treatment.

Conclusions: Our data reveals that PM2.5 induces damage in HaCaT cells, and Autophagy plays a protective role to promote cell survival.