7-Ketocholesterol Induces Oxiapoptophagy and Inhibits Osteogenic Differentiation in MC3T3-E1 Cells.
Jing OuyangYaosheng XiaoQun RenJishang HuangQingluo ZhouShanshan ZhangLinfu LiWeimei ShiZhixi ChenLonghuo WuPublished in: Cells (2022)
7-Ketocholesterol (7KC) is one of the oxysterols produced by the auto-oxidation of cholesterol during the dysregulation of cholesterol metabolism which has been implicated in the pathological development of osteoporosis (OP). Oxiapoptophagy involving oxidative stress, autophagy, and apoptosis can be induced by 7KC. However, whether 7KC produces negative effects on MC3T3-E1 cells by stimulating oxiapoptophagy is still unclear. In the current study, 7KC was found to significantly decrease the cell viability of MC3T3-E1 cells in a concentration-dependent manner. In addition, 7KC decreased ALP staining and mineralization and down-regulated the protein expression of OPN and RUNX2, inhibiting osteogenic differentiation. 7KC significantly stimulated oxidation and induced autophagy and apoptosis in the cultured MC3T3-E1 cells. Pretreatment with the anti-oxidant acetylcysteine (NAC) could effectively decrease NOX4 and MDA production, enhance SOD activity, ameliorate the expression of autophagy-related factors, decrease apoptotic protein expression, and increase ALP, OPN, and RUNX2 expression, compromising 7KC-induced oxiapoptophagy and osteogenic differentiation inhibition in MC3T3-E1 cells. In summary, 7KC may induce oxiapoptophagy and inhibit osteogenic differentiation in the pathological development of OP.
Keyphrases
- cell cycle arrest
- induced apoptosis
- cell death
- oxidative stress
- endoplasmic reticulum stress
- signaling pathway
- mesenchymal stem cells
- pi k akt
- bone marrow
- transcription factor
- diabetic rats
- poor prognosis
- dna damage
- ischemia reperfusion injury
- cell proliferation
- postmenopausal women
- drug induced
- bone mineral density
- flow cytometry