Adipocyte-Derived Exosomal NOX4-Mediated Oxidative Damage Induces Premature Placental Senescence in Obese Pregnancy
- Int J Nanomedicine. 2023 Aug 17;18:4705-4726. doi: 10.2147/IJN.S419081.
- 1. Department of Obstetrics, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, People's Republic of China.
- 2. Chongqing Key Laboratory of Maternal and Fetal Medicine, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
- 3. Department of Emergency & Intensive Care Units, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
- 4. Department of Obstetrics, Chongqing University Three Gorges Hospital, Chongqing, 404100, People's Republic of China.
- 5. Maternal and Child Health Hospital of Hubei Province, Wuhan City, Hubei Province, 430070, People's Republic of China.
- 6. Women and Children's Hospital of Chongqing Medical University, Chongqing, 401147, People's Republic of China.
- # Contributed equally.
Background: A recent study has reported that maternal Obesity is linked to placental oxidative damage and premature senescence. NADPH Oxidase 4 (NOX4) is massively expressed in adipose tissue, and its induced reactive oxygen species have been found to contribute to Cellular Senescence. While, whether, in obese pregnancy, adipose tissue-derived NOX4 is the considerable cause of placental senescence remained elusive.
Methods: This study collected term placentas from obese and normal pregnancies and obese pregnant mouse model was constructed by a high fat diet to explore placental senescence. Furthermore, adipocyte-derived Exosomes were isolated from primary adipocyte medium of obese and normal pregnancies to examine their effect on placenta functions in vivo and vitro.
Results: The placenta from the obese group showed a significant increase in placental oxidative damage and senescence. Exosomes from obese adipocytes contained copies of NOX4, and when cocultured with HTR8/SVneo cells, they induced severe oxidative damage, Cellular Senescence, and suppressed proliferation and invasion functions when compared with the control group. In vivo, adipocyte-derived NOX4-containing Exosomes could induce placental oxidative damage and senescence, ultimately leading to adverse pregnancy outcomes.
Conclusion: In Obesity, adipose tissue can secrete Exosomes containing NOX4 which can be delivered to trophoblast resulting in severe DNA oxidative damage and premature placental senescence, ultimately leading to adverse pregnancy outcomes.
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