Swansea University Medical School, ILS1 Building, Singleton Park, Swansea SA2 8PP, UK.
Centre for Translational Myeloma Research, NIHR Biomedical Research Centre, Botnar Research Centre, University of Oxford, Oxford OX3 7LD, UK.
Open Biol. 2023 May;13(5):220313. doi: 10.1098/rsob.220313. Epub 2023 May 3.
Most biologically active oxysterols have a 3β-hydroxy-5-ene function in the ring system with an additional site of oxidation at C-7 or on the side-chain. In blood plasma oxysterols with a 7α-hydroxy group are also observed with the alternative 3-oxo-4-ene function in the ring system formed by ubiquitously expressed 3β-hydroxy-Δ-C-steroid oxidoreductase Δ-isomerase, HSD3B7. However, oxysterols without a 7α-hydroxy group are not substrates for HSD3B7 and are not usually observed with the 3-oxo-4-ene function. Here we report the unexpected identification of oxysterols in plasma derived from umbilical cord blood and blood from pregnant women taken before delivery at 37+ weeks of gestation, of side-chain oxysterols with a 3-oxo-4-ene function but no 7α-hydroxy group. These 3-oxo-4-ene oxysterols were also identified in placenta, leading to the hypothesis that they may be formed by a previously unrecognized 3β-hydroxy-Δ-C-steroid oxidoreductase Δ-isomerase activity of HSD3B1, an enzyme which is highly expressed in placenta. Proof-of-principle experiments confirmed that HSD3B1 has this activity. We speculate that HSD3B1 in placenta is the source of the unexpected 3-oxo-4-ene oxysterols in cord and pregnant women's plasma and may have a role in controlling the abundance of biologically active oxysterols delivered to the fetus.
大多数具有生物活性的氧化固醇在环系统中具有 3β-羟基-5-烯功能,并且在 C-7 或侧链上还有另外一个氧化部位。在血浆中,也观察到具有 7α-羟基基团的氧化固醇,其环系统中存在替代的 3-酮-4-烯功能,这是由广泛表达的 3β-羟基-Δ-C-甾体氧化还原酶 Δ-异构酶 HSD3B7 形成的。然而,没有 7α-羟基基团的氧化固醇不是 HSD3B7 的底物,通常不会观察到 3-酮-4-烯功能。在这里,我们报告了一个意外的发现,即在脐血和妊娠 37+周分娩前孕妇的血浆中,存在具有 3-酮-4-烯功能但没有 7α-羟基基团的侧链氧化固醇。这些 3-酮-4-烯氧化固醇也在胎盘,导致假说它们可能是由以前未被识别的 HSD3B1 的 3β-羟基-Δ-C-甾体氧化还原酶 Δ-异构酶活性形成的,这种酶在胎盘组织中高度表达。验证性实验证实 HSD3B1 具有这种活性。我们推测胎盘组织中的 HSD3B1 是脐血和孕妇血浆中意外的 3-酮-4-烯氧化固醇的来源,可能在控制向胎儿输送的具有生物活性的氧化固醇的丰度方面发挥作用。