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解析 ACE2 作为 SARS-CoV-2 的结合受体在炎症性肠病中的作用。

Unraveling the Role of ACE2, the Binding Receptor for SARS-CoV-2, in Inflammatory Bowel Disease.

机构信息

Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy of University of Porto, Porto, Portugal.

LAQV@REQUIMTE, University of Porto, Porto, Portugal.

出版信息

Inflamm Bowel Dis. 2020 Nov 19;26(12):1787-1795. doi: 10.1093/ibd/izaa249.

Abstract

Angiotensin-converting enzyme 2 (ACE2) has been highlighted for its role as a receptor for SARS-CoV-2, responsible for the current COVID-19 pandemic. This review summarizes current knowledge about ACE2 as a multifunctional protein, focusing on its relevance in inflammatory bowel disease (IBD). As an enzyme, ACE2 may be protective in IBD because it favors the counter-regulatory arm of the renin-angiotensin system or deleterious because it metabolizes other anti-inflammatory/repairing elements. Meanwhile, as a receptor for SARS-CoV-2, the impact of ACE2 expression/activity on infection is still under debate because no direct evidence has been reported and, again, both protective and deleterious pathways are possible. Research has shown that ACE2 regulates the expression of the neutral amino acid transporter B0AT1, controlling tryptophan-associated intestinal inflammation and nutritional status. Finally, intact membrane-bound or shed soluble ACE2 can also trigger integrin signaling, modulating the response to anti-integrin biologic drugs used to treat IBD (such as vedolizumab) and fibrosis, a long-term complication of IBD. As such, future studies on ACE2 expression/activity in IBD can improve monitoring of the disease and explore an alternative pharmacological target.

摘要

血管紧张素转换酶 2(ACE2)作为 SARS-CoV-2 的受体,在当前的 COVID-19 大流行中发挥了重要作用。这篇综述总结了 ACE2 作为一种多功能蛋白的现有知识,重点介绍了其在炎症性肠病(IBD)中的相关性。作为一种酶,ACE2 在 IBD 中可能具有保护作用,因为它有利于肾素-血管紧张素系统的代偿性分支,也可能具有有害作用,因为它代谢其他抗炎/修复元素。同时,作为 SARS-CoV-2 的受体,ACE2 表达/活性对感染的影响仍存在争议,因为没有报道直接证据,而且可能存在保护性和有害性途径。研究表明,ACE2 调节中性氨基酸转运体 B0AT1 的表达,控制色氨酸相关的肠道炎症和营养状况。最后,完整的膜结合或脱落的可溶性 ACE2 也可以触发整合素信号,调节用于治疗 IBD(如 vedolizumab)和纤维化的抗整合素生物药物的反应,纤维化是 IBD 的一种长期并发症。因此,未来对 IBD 中 ACE2 表达/活性的研究可以改善对疾病的监测,并探索替代的药理靶点。

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