In this study, we found that nuclear receptors FXR and LXR (originally characterized as regulatory factors involved in cholesterol/bile acid homeostasis) regulate the expression of Oct3/4, a marker for cell differentiation, in both normal renal-derived cell line HK-2 and renal adenocarcinoma cell line ACHN. Down-regulation of Oct3/4 expression by activating FXR and LXR occurs only in normal renal cell-derived HK-2 cells. We also found that the RNA-binding protein, ELAVL2, oppositely regulates Oct3/4 expressions in HK-2 and ACHN cells. Moreover, we revealed that LXR-alpha and LXR-beta regulate each other’s expression. Although an LXR-beta-specific agonist is assumed to be the basis for an anti-arteriosclerotic drug that only stimulates reverse cholesterol transport, our findings show that the development of such an anti-arteriosclerotic drug would require further elucidation of the complex mechanism of LXR-alpha and LXR-beta regulation.
CITATION STYLE
Fujino, T., Sugizaki, K., Kato, R., Beppu, M., Murakami, S., Lee, H., … Hayakawa, M. (2020). Farnesoid x receptor and liver x receptors regulate oct3/4 expression by multiple feedback regulating system in normal renal-derived cells and renal adenocarcinoma cells. Journal of Toxicological Sciences, 45(1), 25–35. https://doi.org/10.2131/jts.45.25
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