Suppr超能文献

稳定细胞屏障:对抗 COVID-19 的盾牌。

Stabilizing Cellular Barriers: Raising the Shields Against COVID-19.

机构信息

Aphaia Pharma AG, Zug, Switzerland.

Department of Physiology, University of Toronto, Toronto, ON, Canada.

出版信息

Front Endocrinol (Lausanne). 2020 Sep 30;11:583006. doi: 10.3389/fendo.2020.583006. eCollection 2020.

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its clinical manifestation (COVID-19; coronavirus disease 2019) have caused a worldwide health crisis. Disruption of epithelial and endothelial barriers is a key clinical turning point that differentiates patients who are likely to develop severe COVID-19 outcomes: it marks a significant escalation in respiratory symptoms, loss of viral containment and a progression toward multi-organ dysfunction. These barrier mechanisms are independently compromised by known COVID-19 risk factors, including diabetes, obesity and aging: thus, a synergism between these underlying conditions and SARS-CoV-2 mechanisms may explain why these risk factors correlate with more severe outcomes. This review examines the key cellular mechanisms that SARS-CoV-2 and its underlying risk factors utilize to disrupt barrier function. As an outlook, we propose that glucagon-like peptide 1 (GLP-1) may be a therapeutic intervention that can slow COVID-19 progression and improve clinical outcome following SARS-CoV-2 infection. GLP-1 signaling activates barrier-promoting processes that directly oppose the pro-inflammatory mechanisms commandeered by SARS-CoV-2 and its underlying risk factors.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)及其临床表现(COVID-19;冠状病毒病 2019)已引发全球性健康危机。上皮和内皮屏障的破坏是区分可能发生严重 COVID-19 结局的患者的关键临床转折点:它标志着呼吸道症状显著加重、病毒失控以及向多器官功能障碍进展。这些屏障机制分别受到 COVID-19 已知风险因素的损害,包括糖尿病、肥胖症和衰老:因此,这些潜在条件和 SARS-CoV-2 机制之间的协同作用可能解释了为什么这些风险因素与更严重的结局相关。本综述检查了 SARS-CoV-2 及其潜在风险因素利用来破坏屏障功能的关键细胞机制。作为展望,我们提出胰高血糖素样肽 1(GLP-1)可能是一种治疗干预措施,可减缓 COVID-19 进展并改善 SARS-CoV-2 感染后的临床结局。GLP-1 信号激活促进屏障的过程,这些过程直接对抗 SARS-CoV-2 及其潜在风险因素所利用的促炎机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4128/7554589/562f13848794/fendo-11-583006-g0001.jpg

相似文献

1
Stabilizing Cellular Barriers: Raising the Shields Against COVID-19.
Front Endocrinol (Lausanne). 2020 Sep 30;11:583006. doi: 10.3389/fendo.2020.583006. eCollection 2020.
2
Obesity and COVID-19.
Front Endocrinol (Lausanne). 2020 Sep 30;11:581356. doi: 10.3389/fendo.2020.581356. eCollection 2020.
3
Obesity, Diabetes and COVID-19: An Infectious Disease Spreading From the East Collides With the Consequences of an Unhealthy Western Lifestyle.
Front Endocrinol (Lausanne). 2020 Sep 17;11:582870. doi: 10.3389/fendo.2020.582870. eCollection 2020.
4
From Influenza Virus to Novel Corona Virus (SARS-CoV-2)-The Contribution of Obesity.
Front Endocrinol (Lausanne). 2020 Oct 6;11:556962. doi: 10.3389/fendo.2020.556962. eCollection 2020.
5
COVID-19: a conundrum to decipher.
Eur Rev Med Pharmacol Sci. 2020 May;24(10):5830-5841. doi: 10.26355/eurrev_202005_21378.
6
Diabetes and COVID-19: Global and regional perspectives.
Diabetes Res Clin Pract. 2020 Aug;166:108303. doi: 10.1016/j.diabres.2020.108303. Epub 2020 Jul 3.
7
Hypercoagulopathy and Adipose Tissue Exacerbated Inflammation May Explain Higher Mortality in COVID-19 Patients With Obesity.
Front Endocrinol (Lausanne). 2020 Jul 28;11:530. doi: 10.3389/fendo.2020.00530. eCollection 2020.
8
Melatonin is a potential adjuvant to improve clinical outcomes in individuals with obesity and diabetes with coexistence of Covid-19.
Eur J Pharmacol. 2020 Sep 5;882:173329. doi: 10.1016/j.ejphar.2020.173329. Epub 2020 Jun 30.
10
COVID-19, Renin-Angiotensin System and Endothelial Dysfunction.
Cells. 2020 Jul 9;9(7):1652. doi: 10.3390/cells9071652.

引用本文的文献

2
Coagulation and Inflammation in COVID-19: Reciprocal Relationship between Inflammatory and Coagulation Markers.
Ann Hematol. 2024 Jun;103(6):1819-1831. doi: 10.1007/s00277-024-05630-1. Epub 2024 Feb 13.
3
Cardiovascular signatures of COVID-19 predict mortality and identify barrier stabilizing therapies.
EBioMedicine. 2022 Apr;78:103982. doi: 10.1016/j.ebiom.2022.103982. Epub 2022 Apr 8.
4
The age again in the eye of the COVID-19 storm: evidence-based decision making.
Immun Ageing. 2021 May 20;18(1):24. doi: 10.1186/s12979-021-00237-w.

本文引用的文献

1
Chest CT Findings in Cases from the Cruise Ship with Coronavirus Disease (COVID-19).
Radiol Cardiothorac Imaging. 2020 Mar 17;2(2):e200110. doi: 10.1148/ryct.2020200110. eCollection 2020 Apr.
2
A molecular cell atlas of the human lung from single-cell RNA sequencing.
Nature. 2020 Nov;587(7835):619-625. doi: 10.1038/s41586-020-2922-4. Epub 2020 Nov 18.
3
The protein expression profile of ACE2 in human tissues.
Mol Syst Biol. 2020 Jul;16(7):e9610. doi: 10.15252/msb.20209610.
4
Single-Cell RNA Expression Profiling of ACE2, the Receptor of SARS-CoV-2.
Am J Respir Crit Care Med. 2020 Sep 1;202(5):756-759. doi: 10.1164/rccm.202001-0179LE.
5
The molecular virology of coronaviruses.
J Biol Chem. 2020 Sep 11;295(37):12910-12934. doi: 10.1074/jbc.REV120.013930. Epub 2020 Jul 13.
6
COVID-19 hypothesis: Activated protein C for therapy of virus-induced pathologic thromboinflammation.
Res Pract Thromb Haemost. 2020 Jun 12;4(4):506-509. doi: 10.1002/rth2.12362. eCollection 2020 May.
7
Role of Aging and the Immune Response to Respiratory Viral Infections: Potential Implications for COVID-19.
J Immunol. 2020 Jul 15;205(2):313-320. doi: 10.4049/jimmunol.2000380. Epub 2020 Jun 3.
8
A Randomized Trial of Hydroxychloroquine as Postexposure Prophylaxis for Covid-19.
N Engl J Med. 2020 Aug 6;383(6):517-525. doi: 10.1056/NEJMoa2016638. Epub 2020 Jun 3.
9
Two hits to the renin-angiotensin system may play a key role in severe COVID-19.
Kaohsiung J Med Sci. 2020 Jun;36(6):389-392. doi: 10.1002/kjm2.12237. Epub 2020 Jun 3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验