Thrombospondin‐1 Regulates Trophoblast Necroptosis via NEDD4‐Mediated Ubiquitination of TAK1 in Preeclampsia

• Published in: Advanced science Vol. 11; no. 21; pp. e2309002 - n/a
• Main Authors: Hu, Haoyue, Ma, Jing, Peng, You, Feng, Rixuan, Luo, Chenling, Zhang, Minyi, Tao, Zixin, Chen, Lu, Zhang, Tao, Chen, Wenqian, Yin, Qian, Zhai, Jinguo, Chen, Jun, Yin, Ailan, Wang, Chi Chiu, Zhong, Mei
• Format: Journal Article
• Language: English
• Published: Germany John Wiley & Sons, Inc 01.06.2024; John Wiley and Sons Inc; Wiley
• Subjects: Adult; Blood pressure; Enzymes; Female; Humans; Inflammation; Kinases; MAP Kinase Kinase Kinases - genetics; MAP Kinase Kinase Kinases - metabolism; necroptosis; Necroptosis - genetics; Nedd4 Ubiquitin Protein Ligases - genetics; Nedd4 Ubiquitin Protein Ligases - metabolism; Pathogenesis; Placenta; Placenta - metabolism; Pre-Eclampsia - genetics; Pre-Eclampsia - metabolism; Preeclampsia; Pregnancy; Proteins; Proteomics; Thrombospondin 1 - genetics; Thrombospondin 1 - metabolism; thrombospondin‐1; trophoblast; Trophoblasts - metabolism; Ubiquitination; thrombospondin‐1; preeclampsia; trophoblast; ubiquitination; necroptosis
• ISSN: 2198-3844; 2198-3844
• DOI: 10.1002/advs.202309002

Preeclampsia (PE) is considered as a disease of placental origin. However, the specific mechanism of placental abnormalities remains elusive. This study identified thrombospondin‐1 (THBS1) is downregulated in preeclamptic placentae and negatively correlated with blood pressure. Functional studies show that THBS1 knockdown inhibits proliferation, migration, and invasion and increases the cycle arrest and apoptosis rate of HTR8/SVneo cells. Importantly, THBS1 silencing induces necroptosis in HTR8/SVneo cells, accompanied by the release of damage‐associated molecular patterns (DAMPs). Necroptosis inhibitors necrostatin‐1 and GSK′872 restore the trophoblast survival while pan‐caspase inhibitor Z‐VAD‐FMK has no effect. Mechanistically, the results show that THBS1 interacts with transforming growth factor B‐activated kinase 1 (TAK1), which is a central modulator of necroptosis quiescence and affects its stability. Moreover, THBS1 silencing up‐regulates the expression of neuronal precursor cell‐expressed developmentally down‐regulated 4 (NEDD4), which acts as an E3 ligase of TAK1 and catalyzes K48‐linked ubiquitination of TAK1 in HTR8/SVneo cells. Besides, THBS1 attenuates PE phenotypes and improves the placental necroptosis in vivo. Taken together, the down‐regulation of THBS1 destabilizes TAK1 by activating NEDD4‐mediated, K48‐linked TAK1 ubiquitination and promotes necroptosis and DAMPs release in trophoblast cells, thus participating in the pathogenesis of PE. The down‐regulation of THBS1 can destabilize TAK1 via NEDD4‐mediated, K48‐linked TAK1 ubiquitination, resulting in the activation of the necroptosis and DAMPs release in trophoblast cells, thus participating in the pathogenesis of PE.