Cold exposure-induced plasma exosomes impair bone mass by inhibiting autophagy

Author:

Lei Li-Min,Li Fu-Xing-Zi,Lin Xiao,Xu Feng,Shan Su-Kang,Guo Bei,Zheng Ming-Hui,Tang Ke-Xin,Wang Yi,Xu Qiu-Shuang,Ouyang Wen-Lu,Duan Jia-Yue,Wu Yun-Yun,Cao Ye-Chi,Zhou Zhi-Ang,He Si-Yang,Wu Yan-Lin,Chen Xi,Lin Zheng-Jun,Pan Yi,Yuan Ling-Qing,Li Zhi-Hong

Abstract

AbstractRecently, 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.

Funder

National Natural Science Foundation of China

Kunming medicine joint special project

National Key Research & Development Program

National Clinical Key Specialties Major Research Projects

The Health Research Project in Hunan Province

Health Research Project of Hunan Provincial Health Commission

the Natural Science Foundation of Hunan Province

National Undergraduate Innovation Training Program of Central South University

Publisher

Springer Science and Business Media LLC

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