@article{Lu2024, 
author = {Weicheng Lu and Jianfei Yan and Chenyu Wang and Wenpin Qin and Xiaoxiao Han and Zixuan Qin and Yu Wei and Haoqing Xu and Jialu Gao and Changhe Gao and Tao Ye and Franklin R. Tay and Lina Niu and Kai Jiao},
title = {Interorgan communication in neurogenic heterotopic ossification: the role of brain-derived extracellular vesicles},
year = {2024},
journal = {Bone Research},
volume = {12},
pages = {11},
url = {https://www.sciopen.com/article/10.1038/s41413-023-00310-8},
doi = {10.1038/s41413-023-00310-8},
abstract = {Brain-derived extracellular vesicles participate in interorgan communication after traumatic brain injury by transporting pathogens to initiate secondary injury. Inflammasome-related proteins encapsulated in brain-derived extracellular vesicles can cross the blood‒brain barrier to reach distal tissues. These proteins initiate inflammatory dysfunction, such as neurogenic heterotopic ossification. This recurrent condition is highly debilitating to patients because of its relatively unknown pathogenesis and the lack of effective prophylactic intervention strategies. Accordingly, a rat model of neurogenic heterotopic ossification induced by combined traumatic brain injury and achillotenotomy was developed to address these two issues. Histological examination of the injured tendon revealed the coexistence of ectopic calcification and fibroblast pyroptosis. The relationships among brain-derived extracellular vesicles, fibroblast pyroptosis and ectopic calcification were further investigated in vitro and in vivo. Intravenous injection of the pyroptosis inhibitor Ac-YVAD-cmk reversed the development of neurogenic heterotopic ossification in vivo. The present work highlights the role of brain-derived extracellular vesicles in the pathogenesis of neurogenic heterotopic ossification and offers a potential strategy for preventing neurogenic heterotopic ossification after traumatic brain injury.}
}