1. Academic Validation
  2. MFG-E8 stabilized by deubiquitinase USP14 suppresses cigarette smoke-induced ferroptosis in bronchial epithelial cells

MFG-E8 stabilized by deubiquitinase USP14 suppresses cigarette smoke-induced ferroptosis in bronchial epithelial cells

  • Cell Death Dis. 2023 Jan 3;14(1):2. doi: 10.1038/s41419-022-05455-8.
Yanan Cui 1 2 3 Lijuan Luo 1 2 3 Zihang Zeng 1 2 3 Xiangming Liu 1 2 3 Tiao Li 1 2 3 Xue He 1 2 3 Yiming Ma 1 2 3 Weiwei Meng 1 2 3 Huihui Zeng 1 2 3 Yingjiao Long 1 2 3 Dandan Zong 1 2 3 Yan Chen 4 5 6
Affiliations

Affiliations

  • 1 Department of Pulmonary and Critical Care Medicine, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
  • 2 Research Unit of Respiratory Disease, Central South University, Changsha, Hunan, China.
  • 3 Diagnosis and Treatment Center of Respiratory Disease, Changsha, Hunan, China.
  • 4 Department of Pulmonary and Critical Care Medicine, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China. chenyan99727@csu.edu.cn.
  • 5 Research Unit of Respiratory Disease, Central South University, Changsha, Hunan, China. chenyan99727@csu.edu.cn.
  • 6 Diagnosis and Treatment Center of Respiratory Disease, Changsha, Hunan, China. chenyan99727@csu.edu.cn.
Abstract

Milk fat globule epidermal growth factor 8 (MFG-E8) participates in a range of cellular processes, including reducing Apoptosis and oxidative stress. However, its protective activity against cigarette smoke-induced Ferroptosis in the pathogenesis of the chronic obstructive pulmonary disease (COPD) and the modulation of MFG-E8 remain unclear. Here, we showed that cigarette smoke diminished MFG-E8 protein levels but had no significant effect on its mRNA levels in lung tissues of humans and mice and in two human bronchial epithelial cell lines. MFG-E8 could attenuate Ferroptosis induced by cigarette smoke extract (CSE) in vivo and in vitro. We identified Ubiquitin-Specific Protease 14 (USP14) as a Deubiquitinase of MFG-E8 in human bronchial epithelial cells. USP14 interacted with, deubiquitinated and stabilized MFG-E8. Furthermore, USP14 inhibited CSE-induced MFG-E8 proteasomal degradation. USP14 expression downregulated by CSE decreased MFG-E8 abundance and further reduced the antiferroptotic effect of MFG-E8. These findings suggest that USP14 is an essential regulator of MFG-E8 through the proteasomal pathway and that the USP14/MFG-E8 axis plays a critical role in regulating CSE-induced Ferroptosis of bronchial epithelial cells.

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