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Autophagic damage in senescent bone marrow mesenchymal stromal cells: Impact on Piezo1 expression during osteoporosis progression
Cell Recycling Damage in Aging Bone Marrow Cells and Its Link to Piezo1 Levels During Osteoporosis Progression
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Abstract
Piezo1 expression was downregulated in bone tissues of patients with osteoporosis and ovariectomized mice.
- Aging and estrogen deficiency in osteoporosis lead to oxidative stress that impairs bone marrow mesenchymal stromal cell (BMSC) function.
- Increased senescence markers were observed in BMSCs from osteoporotic conditions.
- Oxidative stress was associated with reduced Piezo1 expression and a shift in BMSC differentiation towards fat cells instead of bone-forming cells.
- Impaired autophagic flux in senescent BMSCs was noted, which could be restored by activating autophagy with rapamycin.
- Rapamycin treatment enhanced Piezo1 expression, alleviated senescence, and improved bone mass and structure in ovariectomized mice.
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