1. Cold exposure-induced plasma exosomes impair bone mass by inhibiting autophagy.
- Author
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Lei LM, Li FX, Lin X, Xu F, Shan SK, Guo B, Zheng MH, Tang KX, Wang Y, Xu QS, Ouyang WL, Duan JY, Wu YY, Cao YC, Zhou ZA, He SY, Wu YL, Chen X, Lin ZJ, Pan Y, Yuan LQ, and Li ZH
- Subjects
- Animals, Mice, Mesenchymal Stem Cells metabolism, Osteoporosis pathology, Cell Differentiation drug effects, Bone and Bones metabolism, Female, Bone Density, Sirolimus pharmacology, Autophagy drug effects, Exosomes metabolism, MicroRNAs metabolism, MicroRNAs genetics, Cold Temperature, Osteogenesis drug effects, Mice, Inbred C57BL
- Abstract
Recently, environmental temperature has been shown to regulate bone homeostasis. However, the mechanisms by which cold exposure affects bone mass remain unclear. In our present study, we observed that exposure to cold temperature (CT) decreased bone mass and quality in mice. Furthermore, a transplant of exosomes derived from the plasma of mice exposed to cold temperature (CT-EXO) can also impair the osteogenic differentiation of BMSCs and decrease bone mass by inhibiting autophagic activity. Rapamycin, a potent inducer of autophagy, can reverse cold exposure or CT-EXO-induced bone loss. Microarray sequencing revealed that cold exposure increases the miR-25-3p level in CT-EXO. Mechanistic studies showed that miR-25-3p can inhibit the osteogenic differentiation and autophagic activity of BMSCs. It is shown that inhibition of exosomes release or downregulation of miR-25-3p level can suppress CT-induced bone loss. This study identifies that CT-EXO mediates CT-induced osteoporotic effects through miR-25-3p by inhibiting autophagy via targeting SATB2, presenting a novel mechanism underlying the effect of cold temperature on bone mass., (© 2024. The Author(s).)
- Published
- 2024
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