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首页> 外文期刊>Cell stem cell >Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
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Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men

机译:雄激素信号调节SARS-COV-2受体水平,与男性的严重Covid-19症状相关

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摘要

SARS-CoV-2 infection has led to a global health crisis, and yet our understanding of the disease and potential treatment options remains limited. The infection occurs through binding of the virus with angiotensin converting enzyme 2 (ACE2) on the cell membrane. Here, we established a screening strategy to identify drugs that reduce ACE2 levels in human embryonic stem cell (hESC)-derived cardiac cells and lung organoids. Target analysis of hit compounds revealed androgen signaling as a key modulator of ACE2 levels. Treatment with antiandrogenic drugs reduced ACE2 expression and protected hESC-derived lung organoids against SARS-CoV-2 infection. Finally, clinical data on COVID-19 patients demonstrated that prostate diseases, which are linked to elevated androgen, are significant risk factors and that genetic variants that increase androgen levels are associated with higher disease severity. These findings offer insights on the mechanism of disproportionate disease susceptibility in men and identify antiandrogenic drugs as candidate therapeutics for COVID-19.
机译:SARS-CoV-2感染已导致全球健康危机,但我们对该疾病和潜在治疗方案的了解仍然有限。感染是通过病毒与细胞膜上的血管紧张素转换酶2(ACE2)结合而发生的。在这里,我们建立了一个筛选策略,以确定降低人类胚胎干细胞(hESC)衍生的心脏细胞和肺类器官中ACE2水平的药物。hit化合物的靶向分析显示雄激素信号是ACE2水平的关键调节因子。抗雄激素药物治疗可降低ACE2表达,保护人胚胎干细胞衍生的肺类器官免受SARS-CoV-2感染。2019冠状病毒疾病的临床资料表明,前列腺疾病与雄激素升高有关,是显著的危险因素,增加雄激素水平的遗传变异与较高的疾病严重程度有关。这些发现提供2019冠状病毒疾病易感性的机制和鉴定抗雄激素药物作为候选治疗COVID-19的见解。

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  • 来源
    《Cell stem cell》 |2020年第6期|共26页
  • 作者单位

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Yale Sch Med Dept Internal Med New Haven CT 06510 USA;

    Harvard &

    MIT Broad Inst Program Med &

    Populat Genet Cambridge MA 02142 USA;

    Univ Calif San Francisco Dept Biochem &

    Biophys San Francisco CA 94158 USA;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Univ Calif San Francisco Dept Biochem &

    Biophys San Francisco CA 94158 USA;

    Gladstone Inst San Francisco CA 94158 USA;

    Univ Calif San Francisco Dept Med San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Med San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Microbiol &

    Immunol San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Microbiol &

    Immunol San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Biochem &

    Biophys San Francisco CA 94158 USA;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

    Yale Univ Program Computat Biol &

    Bioinformat New Haven CT 06510 USA;

    Univ Calif San Francisco Dept Microbiol &

    Immunol San Francisco CA 94143 USA;

    Yale Univ Program Computat Biol &

    Bioinformat New Haven CT 06510 USA;

    Harvard &

    MIT Broad Inst Program Med &

    Populat Genet Cambridge MA 02142 USA;

    Univ Calif San Francisco Dept Med San Francisco CA 94143 USA;

    Gladstone Inst San Francisco CA 94158 USA;

    Univ Calif San Francisco Dept Biochem &

    Biophys San Francisco CA 94158 USA;

    Univ Calif San Francisco Eli &

    Edythe Broad Ctr Regenerat Med &

    Stem Cell San Francisco CA 94143;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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