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肠道中细菌甾体 17α-羟化酶/17,20-裂合酶的作用

Gut feelings about bacterial steroid-17,20-desmolase.

机构信息

Microbiome Metabolic Engineering Theme, Carl R. Woese Institute for Genomic Biology, Urbana, IL, 61801, USA; Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA; Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

Microbiome Metabolic Engineering Theme, Carl R. Woese Institute for Genomic Biology, Urbana, IL, 61801, USA; Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

出版信息

Mol Cell Endocrinol. 2021 Apr 5;525:111174. doi: 10.1016/j.mce.2021.111174. Epub 2021 Jan 24.

Abstract

Advances in technology are only beginning to reveal the complex interactions between hosts and their resident microbiota that have co-evolved over centuries. In this review, we present compelling evidence that implicates the host-associated microbiome in the generation of 11β-hydroxyandrostenedione, leading to the formation of potent 11-oxy-androgens. Microbial steroid-17,20-desmolase cleaves the side-chain of glucocorticoids (GC), including cortisol (and its derivatives of cortisone, 5α-dihydrocortisol, and also (allo)- 3α, 5α-tetrahydrocortisol, but not 3α-5β-tetrahydrocortisol) and drugs (prednisone and dexamethasone). In addition to side-chain cleavage, we discuss the gut microbiome's robust potential to transform a myriad of steroids, mirroring much of the host's metabolism. We also explore the overlooked role of intestinal steroidogenesis and efflux pumps as a potential route for GC transport into the gut. Lastly, we propose several health implications from microbial steroid-17,20-desmolase function, including aberrant mineralocorticoid, GC, and androgen receptor signaling in colonocytes, immune cells, and prostate cells, which may exacerbate disease states.

摘要

技术的进步才刚刚开始揭示宿主与其常驻微生物群之间的复杂相互作用,这些相互作用是经过数百年共同进化而来的。在这篇综述中,我们提出了令人信服的证据,表明宿主相关的微生物组参与了 11β-羟基雄烯二酮的产生,导致了强效的 11-氧基雄激素的形成。微生物甾体 17,20-脱氨酶切割糖皮质激素(GC)的侧链,包括皮质醇(及其衍生物可的松、5α-二氢皮质醇,以及(allo)-3α,5α-四氢皮质醇,但不包括 3α-5β-四氢皮质醇)和药物(泼尼松和地塞米松)。除了侧链切割外,我们还讨论了肠道微生物组强大的转化多种类固醇的潜力,这反映了宿主代谢的大部分情况。我们还探讨了肠道类固醇生成和外排泵被忽视的作用,因为它可能是 GC 进入肠道的一种途径。最后,我们从微生物甾体 17,20-脱氨酶的功能提出了一些健康影响,包括结肠细胞、免疫细胞和前列腺细胞中异常的盐皮质激素、GC 和雄激素受体信号转导,这可能会加重疾病状态。

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