Karahoda Rona, Du Toit Therina, Fuenzalida Barbara, Kallol Sampada, Groessl Michael, Anderle Pascale, Ontsouka Edgar, Staud Frantisek, Flueck Christa E, Albrecht Christiane
Department of Pharmacology and Toxicology, Charles University, Faculty of Pharmacy in Hradec Kralove, Hradec Kralove, Czech Republic.
Department of Biomedical Research, Inselspital, University of Bern, Bern, Switzerland.
Mol Cell Proteomics. 2025 Jun;24(6):100976. doi: 10.1016/j.mcpro.2025.100976. Epub 2025 Apr 23.
Recent advances in analytical methods have revolutionized our understanding of steroid biochemistry. The emergence of novel steroids such as 11-oxy androgens and 11-oxy progesterones has necessitated a reevaluation of steroid biosynthesis and metabolism within the maternal-placental-fetal unit. In this study, we employed a validated liquid chromatography high-resolution mass spectrometry method to quantify 51 steroids in paired maternal serum, neonatal serum, and placenta samples from 37 healthy pregnancies. Additionally, we characterized steroid release in various placental models, including human placenta perfusion, explants, and primary trophoblast cells isolated from human term placenta. Our findings emphasize the predominance of keto derivatives of androgens in the placenta compared to hydroxylated forms, which are dominant in maternal serum and neonatal serum. We also observed high levels of classic and novel progesterones in the placenta and across all models, with significant release on the maternal side. These results suggest that the placenta possesses an active enzymatic machinery capable of producing and metabolizing novel progesterones. Furthermore, we demonstrated that the catalytic activity of 11β-hydroxysteroid dehydrogenase type 2 extends beyond cortisol regulation to hydroxylated androgens, highlighting its significance in the broader context of steroid metabolism within the maternal-placental-fetal unit. These findings contribute to our understanding of placental physiology and impact on fetal development.
分析方法的最新进展彻底改变了我们对类固醇生物化学的理解。新型类固醇如11-氧代雄激素和11-氧代孕酮的出现,使得有必要重新评估母胎-胎盘-胎儿单位内的类固醇生物合成和代谢。在本研究中,我们采用了一种经过验证的液相色谱高分辨率质谱法,对来自37例健康妊娠的配对母血、新生儿血和胎盘样本中的51种类固醇进行定量。此外,我们还对各种胎盘模型中的类固醇释放进行了表征,包括人胎盘灌注、外植体以及从足月人胎盘中分离的原代滋养层细胞。我们的研究结果强调,与在母血和新生儿血中占主导地位的羟基化形式相比,雄激素的酮衍生物在胎盘中占优势。我们还观察到,在胎盘和所有模型中,经典和新型孕酮的水平都很高,且在母体一侧有大量释放。这些结果表明,胎盘拥有一种活跃的酶机制,能够产生和代谢新型孕酮。此外,我们证明2型11β-羟基类固醇脱氢酶的催化活性不仅限于皮质醇调节,还扩展到羟基化雄激素,突出了其在母胎-胎盘-胎儿单位内更广泛的类固醇代谢背景下的重要性。这些发现有助于我们理解胎盘生理学及其对胎儿发育的影响。