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Expression of the SARS-CoV-2 cell receptor gene ACE2 in a wide variety of human tissues

机译:SARS-COV-2细胞受体基因ACE2在各种人体组织中的表达

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Since its discovery in December 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected more than 2?180 000 people worldwide and has caused more than 150 000 deaths as of April 16, 2020. SARS-CoV-2, which is the virus causing coronavirus disease 2019 (COVID-19), uses the angiotensin-converting enzyme 2 (ACE2) as a cell receptor to invade human cells. Thus, ACE2 is the key to understanding the mechanism of SARS-CoV-2 infection. This study is to investigate the ACE2 expression in various human tissues in order to provide insights into the mechanism of SARS-CoV-2 infection. We compared ACE2 expression levels across 31 normal human tissues between males and females and between younger (ages ≤?49?years) and older (ages ?49?years) persons using two-sided Student’s t test. We also investigated the correlations between ACE2 expression and immune signatures in various tissues using Pearson’s correlation test. ACE2 expression levels were the highest in the small intestine, testis, kidneys, heart, thyroid, and adipose tissue, and were the lowest in the blood, spleen, bone marrow, brain, blood vessels, and muscle. ACE2 showed medium expression levels in the lungs, colon, liver, bladder, and adrenal gland. ACE2 was not differentially expressed between males and females or between younger and older persons in any tissue. In the skin, digestive system, brain, and blood vessels, ACE2 expression levels were positively associated with immune signatures in both males and females. In the thyroid and lungs, ACE2 expression levels were positively and negatively associated with immune signatures in males and females, respectively, and in the lungs they had a positive and a negative correlation in the older and younger groups, respectively. Our data indicate that SARS-CoV-2 may infect other tissues aside from the lungs and infect persons with different sexes, ages, and races equally. The different host immune responses to SARS-CoV-2 infection may partially explain why males and females, young and old persons infected with this virus have markedly distinct disease severity. This study provides new insights into the role of ACE2 in the SARS-CoV-2 pandemic.
机译:自2019年12月发现以来,严重的急性呼吸综合征冠状病毒2(SARS-COV-2)感染了超过2?18万人,截至4月16日,截至2020年4月16日,造成了超过150 000人死亡。SARS-COV-2 ,这是导致冠状病毒疾病2019(Covid-19)的病毒,使用血管紧张素转换酶2(ACE2)作为侵入人细胞的细胞受体。因此,ACE2是理解SARS-COV-2感染机制的关键。该研究是探讨各种人体组织中的ACE2表达,以便为SARS-COV-2感染的机制提供见解。我们将ACE2表达水平与男性和女性之间的31种正常人体组织进行比较,年轻(年龄≤?49岁)和较大的(年龄>?49?岁)使用双面学生的T测试。我们还研究了使用Pearson相关试验的各种组织中ACE2表达和免疫签名之间的相关性。 Ace2表达水平是小肠,睾丸,肾脏,心脏,甲状腺和脂肪组织中最高的,并且血液,脾脏,骨髓,脑,血管和肌肉中最低。 ACE2显示肺部,结肠,肝脏,膀胱和肾上腺中的培养基表达水平。 ACE2在雄性和女性之间或任何组织中的年轻人和年龄较大的人之间没有差异表达。在皮肤,消化系统,脑和血管中,ACE2表达水平与男性和女性的免疫签名呈正相关。在甲状腺和肺部,ACE2表达水平分别与男性和女性的免疫签名和肺部分别与免疫签名产生阳性和负面相关,它们分别在较旧的群体和较年轻的群体中具有正相关和负相关。我们的数据表明,SARS-COV-2可能会感染除了肺部和感染不同性别,年龄和平等的感染者的其他组织。对SARS-COV-2感染的不同宿主免疫应答可能部分解释为什么男性和女性,感染这种病毒的年轻人和雌性都具有明显不同的疾病严重程度。本研究为ace-cov-2大流行中的ACE2作用提供了新的见解。

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