2. Academic Validation
  3. HTR1B regulates mitochondrial homeostasis and mitophagy by activating the ERK/ MAPK signalling pathway during human embryonic arrest

HTR1B regulates mitochondrial homeostasis and mitophagy by activating the ERK/ MAPK signalling pathway during human embryonic arrest

  • Heliyon. 2024 Jun 17;10(12):e33132. doi: 10.1016/j.heliyon.2024.e33132.
Si-Min Ding 1 2 3 4,  Ling-Ge Shi 1 2 3 4,  Zhen-Ping Cao 5,  Na-Na Zhu 6,  Yun-Yun Liu 1 2 3,  Meng-Yao Wang 1 2 3,  Shuang-Shuang Cui 1 2 3,  Hui-Ru Cheng 2,  Dan Liang 1 2 3,  Yun-Xia Cao 1 2 3 4 7 8,  Ya-Jing Liu 1 2 3 4 7 8
Affiliations

Affiliations

  • 1 Reproductive Medicine Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.
  • 2 NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract, Anhui Medical University, Hefei, 230022, China.
  • 3 Key Laboratory of Population Health Across Life Cycle (Anhui Medical University),Ministry of Education of the People's Republic of China, No 81 Meishan Road, Hefei, 230032, Anhui, China.
  • 4 Anhui Province Key Laboratory of Reproductive Disorders and Obstetrics and Gynaecology Diseases, No 81 Meishan Road, Hefei, 230032, Anhui, China.
  • 5 The Third People's Hospital of Hefei, The Third Clinical Teaching Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
  • 6 The Second People's Hospital of Hefei, The Second Clinical Teaching Hospital of Anhui Medical University, Hefei, 230011, Anhui, China.
  • 7 Biopreservation and Artificial Organs, Anhui Provincial Engineering Research Center, Anhui Medical University, No 81 Meishan Road, Hefei, 230032, Anhui, China.
  • 8 Anhui Provincial Institute of Translational Medicine,No 81 Meishan Road, Hefei, 230032, Anhui, China.
PMID: 39022094 DOI: 10.1016/j.heliyon.2024.e33132
Abstract

Background: Previous studies have shown that serotonin and its receptors are widely distributed in mammalian reproductive tisssues and play an important role in embryonic development. However, the specific effects of the serotonergic system on embryonic arrest (EA) and the underlying mechanism require further investigation.

Methods: Chorionic villi were collected from patients with EA and healthy pregnant women. Western blotting (WB) and immunohistochemistry (IHC) were used to detect serotonin receptor 1B (HTR1B) levels and evaluate mitochondrial function. Additionally, HTR-8/SVneo cells were transfected with an HTR1B overexpression plasmid. Quantitative real-time polymerase chain reaction(qRT-PCR), Cell Counting Kit-8 (CCK-8), and wound healing assays were utilized to evaluate Mitophagy level, cell proliferation and cell migration, respectively.

Results: We discovered elevated HTR1B levels in the chorionic villi of the patients with EA compared to controls. Concurrently, we observed enhanced levels of nucleus-encoded proteins including mitofilin, Succinate Dehydrogenase complex subunit A (SDHA), and cytochrome c oxidase subunit 4 (COXIV), along with the mitochondrial fusion protein optic atrophy 1(OPA1), fission proteins mitochondrial fission protein 1(FIS1) and mitochondrial fission factor (MFF) in the EA group. Additionally, there was an excessive Mitophagy levels in EA group. Furthermore, a notable activation of mitogen-activated protein kinase (MAPK) signaling pathway proteins including extracellular regulating kinase (ERK), c-Jun N-terminal kinase (JNK), and P38 was observed in the EA group. By overexpressing HTR1B in HTR-8/SVneo cells, we observed a significant reduction in cell proliferation and migration. HTR1B overexpression also caused an increase in levels of SDHA and FIS1, as well as an upregulation of Mitophagy. Notably, the ERK Inhibitor U0126 effectively mitigated these effects.

Conclusion: These findings show that HTR1B influences mitochondrial homeostasis, promoting excessive Mitophagy and impairing cell proliferation and migration by activating the MAPK signalling pathway during post-implantation EA. Therefore, HTR1B may serve as a potential therapeutic target for patients with EA.

Keywords

Embryonic arrest; Excessive mitophagy; HTR1B; MAPK; Mitochondrial fission protein; Mitochondrial fusion protein.

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