Research progress on the regulation of epithelial cell senescence by Sirt1

In the process of enamel development, premature senescence and apoptosis of ameloblasts are important causes of hereditary enamel hypoplasia. Silence information regulator 2-related enzyme 1 (Sirt1) is a nicotinamide adenosine dinucleotide (NAD⁺)-dependent deacetylase that has been widely reported to be involved in the regulation of cell senescence. This paper reviews the research progress of Sirt1 regulating epithelial cell senescence, starting with the structural characteristics of Sirt1, and further expounds on the relationship between Sirt1 and senescence. When epithelial cells are stimulated, Sirt1 affects the senescence of epithelial cells in many ways, such as mitochondrial dysfunction. Sirt1 participates in regulating mitochondrial function and metabolic homeostasis, and telomere length is negatively related to senescence. Sirt1 regulates the expression of telomere reverse transcriptase needed for telomere extension, thus positively regulating telomere homeostasis. DNA damage will undergo damage repair, unrepaired DNA damage will cause cell senescence, and the Sirt1/p53 pathway can inhibit epithelial cell senescence by reducing DNA damage. Senescent cells are the source of chronic inflammation, and chronic inflammation can also promote aging in many ways. Sirt1 inhibits epithelial cell senescence by relieving inflammatory symptoms. In future research, we can focus on the effect of Sirt1 on ameloblast senescence and explore its specific mechanism of action on ameloblasts to find a breakthrough in the etiology and treatment of enamel hypoplasia.