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血管紧张素转换酶2(ACE2)在人肝脏、食管、胃和结肠中的表达及可能意义

Expression and Possible Significance of ACE2 in the Human Liver, Esophagus, Stomach, and Colon.

作者信息

Liu Yiwen, Wu Qing, Wan Dongmei, He Huiqin, Lin Hailian, Wang Kelang, Que Genxiang, Wang Yuanyuan, Chen Yongjun, Tang Xiaoqing, Wu Lingbo, Yang Xuefeng

机构信息

The Affifiliated Nanhua Hospital, Department of Gastroenterology, Hengyang Medical School, University of South China, Hengyang 421001, Hunan, China.

The Affifiliated Nanhua Hospital, Department of General Practice, Hengyang Medical School, University of South China, Hengyang 421001, Hunan, China.

出版信息

Evid Based Complement Alternat Med. 2021 Aug 25;2021:6949902. doi: 10.1155/2021/6949902. eCollection 2021.

DOI:10.1155/2021/6949902
PMID:34484401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8410421/
Abstract

Angiotensin-converting enzyme 2 (ACE2) has been identified as the key receptor of SARS coronavirus that plays a key role in the pathogenesis of SARS. It is known that ACE2 mRNA can be expressed in most organs. However, the protein expression of ACE2 is not clear yet. To explore the role of ACE2 as a precipitating factor in digestive organ damage in COVID-19, this study investigated the expression of ACE2 protein in the human liver, esophagus, stomach, and colon. The result showed that ACE2 can be expressed in the liver, esophagus, stomach, and colon, which suggests SARS-CoV-2 may enter the digestive system through ACE2 and cause liver damage and gastrointestinal damage. It is hoped that the result of the study will provide a new strategy for the prevention and treatment of digestive organ damage under COVID-19.

摘要

血管紧张素转换酶2(ACE2)已被确定为严重急性呼吸综合征冠状病毒(SARS-CoV)的关键受体,在SARS发病机制中起关键作用。已知ACE2信使核糖核酸(mRNA)可在大多数器官中表达。然而,ACE2的蛋白表达情况尚不清楚。为探究ACE2作为2019冠状病毒病(COVID-19)消化器官损伤诱发因素的作用,本研究调查了ACE2蛋白在人肝脏、食管、胃和结肠中的表达。结果显示,ACE2可在肝脏、食管、胃和结肠中表达,这表明严重急性呼吸综合征冠状病毒2(SARS-CoV-2)可能通过ACE2进入消化系统并导致肝损伤和胃肠道损伤。希望该研究结果能为COVID-19下消化器官损伤的防治提供新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65ec/8410421/9199c0b7979e/ECAM2021-6949902.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65ec/8410421/9199c0b7979e/ECAM2021-6949902.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65ec/8410421/9199c0b7979e/ECAM2021-6949902.001.jpg

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本文引用的文献

1
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Front Med (Lausanne). 2021 Jan 13;7:563893. doi: 10.3389/fmed.2020.563893. eCollection 2020.
2
Digestive symptoms of COVID-19 and expression of ACE2 in digestive tract organs.新型冠状病毒肺炎的消化系统症状及消化道器官中血管紧张素转换酶2的表达
Cell Death Discov. 2020 Aug 11;6:76. doi: 10.1038/s41420-020-00307-w. eCollection 2020.
3
Epidemiological and clinical characteristics of COVID-19 patients in Hengyang, Hunan Province, China.
H拮抗剂、质子泵抑制剂与2019冠状病毒病
J Anesth. 2022 Jun;36(3):329-331. doi: 10.1007/s00540-021-03032-5. Epub 2022 Jan 24.
中国湖南省衡阳市新冠肺炎患者的流行病学和临床特征
World J Clin Cases. 2020 Jun 26;8(12):2554-2565. doi: 10.12998/wjcc.v8.i12.2554.
4
A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2.一种中和性人源抗体结合到了 SARS-CoV-2 的刺突蛋白的 N 端结构域。
Science. 2020 Aug 7;369(6504):650-655. doi: 10.1126/science.abc6952. Epub 2020 Jun 22.
5
SARS-CoV-2 infection of the liver directly contributes to hepatic impairment in patients with COVID-19.SARS-CoV-2 感染肝脏直接导致 COVID-19 患者肝损伤。
J Hepatol. 2020 Oct;73(4):807-816. doi: 10.1016/j.jhep.2020.05.002. Epub 2020 May 11.
6
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Cell. 2020 May 14;181(4):905-913.e7. doi: 10.1016/j.cell.2020.04.004. Epub 2020 Apr 24.
7
Clinical characteristics of non-ICU hospitalized patients with coronavirus disease 2019 and liver injury: A retrospective study.COVID-19 住院非 ICU 患者的临床特征与肝损伤:一项回顾性研究。
Liver Int. 2020 Jun;40(6):1321-1326. doi: 10.1111/liv.14449. Epub 2020 Apr 12.
8
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ACS Chem Neurosci. 2020 Apr 1;11(7):995-998. doi: 10.1021/acschemneuro.0c00122. Epub 2020 Mar 13.
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Cell. 2020 Apr 16;181(2):271-280.e8. doi: 10.1016/j.cell.2020.02.052. Epub 2020 Mar 5.