The regulatory role of COX-2 in the interaction between Cr(VI)-induced endoplasmic reticulum stress and autophagy in DF-1 cells

Hexavalent chromium (Cr(VI)) is a common environmental pollutant. Exposure of Cr(VI) can lead to cell Autophagy, but the preventive measures for diminishing Cr(VI)-induced Autophagy need further study. COX-2 can be induced by several heavy metals and can lead to endoplasmic reticulum (ER) stress and autophagy; thus, COX-2, ER stress, and Autophagy may be related. This study mainly investigated the role of COX-2 in the eIF2α-ATF4 pathway, which is a major pathway in cell Autophagy. In this study, Cr(VI) was used as a xenobiotic to determine changes in the parameters of ER stress, Autophagy, and COX-2 levels. At the same time, a clear contrast was obtained by assigning positive and negative controls of ER stress and Autophagy. The results showed that during Cr(VI) invasion, the parameters of ER stress and Autophagy (such as BiP, PERK, p62, LC3-II, and mTOR) were enhanced, similarly to the positive control of ER stress and/or the Autophagy controls. Such enhancement is a protective mechanism for cell survival. Additionally, the COX-2 levels increased. Moreover, when COX-2 was inhibited, the PERK level remained high, whereas the LC3-II level decreased. This finding suggests that COX-2 specifically affects the interaction between ER stress and Autophagy. Notably, this study reveals that Cr(VI) can induce ER stress and Autophagy in DF-1 cells and that COX-2 plays an essential role in the interaction between ER stress and Autophagy.