SEPHS1 attenuates intervertebral disc degeneration by delaying nucleus pulposus cell senescence through the Hippo-Yap/Taz pathway

Author:

Hu Tao12ORCID,Shi Zhongming2,Sun Yongjin2,Hu Feng3,Rong Yuluo2,Wang Jia2,Wang Liang2,Xu Wenbin2,Zhang Feng2,Zhang Wen-Zhi1ORCID

Affiliation:

1. Department of Orthopedics, Provincial Hospital Affiliated to Anhui Medical University, Hefei, People’s Republic of China

2. Division of Life Sciences and Medicine, Department of Orthopedics, Centre for Leading Medicine and Advanced Technologies of IHM, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, People’s Republic of China

3. Department of Orthopedics, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University, Shanghai, People’s Republic of China

Abstract

Selenophosphate synthetase 1 (SEPHS1) deficiency leads to an increase in reactive oxygen species levels and in the subsequent activation of the Hippo-Yap/Taz signaling pathway. In the rat model of intervertebral disc degeneration (IVDD), overexpression of SEPHS1 and inhibition of Hippo-YAP/Taz mitigated the progression of disc degeneration indicating the involvement of SEPHS1 in IVDD. SEPHS1 is a promising therapeutic target for IVDD.

Funder

安徽省科学技术厅 | Natural Science Foundation of Anhui Province

Research Funds of Centre for Leading Medicine and Advanced Technologies of IHM

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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