Vessel-on-a-Chip: A Powerful Tool for Investigating Endothelial COVID-19 Fingerprints

被引:2
作者
Shevchuk, Oksana [1 ]
Palii, Svitlana [1 ]
Pak, Anastasiia [2 ]
Chantada, Nuria [3 ]
Seoane, Nuria [4 ]
Korda, Mykhaylo [2 ]
Campos-Toimil, Manuel [3 ,4 ]
alvarez, Ezequiel [3 ,5 ,6 ]
机构
[1] I Horbachevsky Ternopil Natl Med Univ, Dept Pharmacol & Clin Pharmacol, UA-46001 Ternopol, Ukraine
[2] I Horbachevsky Ternopil Natl Med Univ, Dept Med Biochem, UA-46001 Ternopol, Ukraine
[3] Univ Santiago Compostela, Dept Farmacol Farm & Tecnol Farmaceut, Santiago De Compostela 15782, Spain
[4] Univ Santiago Compostela, Physiol & Pharmacol Chron Dis FIFAEC Ctr Res Mol M, Santiago De Compostela 15782, Spain
[5] Univ Santiago Compostela CHUS, Complexo Hosp, Inst Invest Sanitaria Santiago Compostela IDIS, SERGAS, Travesia Choupana S-N, Santiago De Compostela 15706, Spain
[6] Inst Hlth Carlos III, CIBERCV, Madrid 28220, Spain
关键词
COVID-19; endothelial dysfunction; long COVID; microfluidic system; personalized COVID-19 follow-up; vessel-on-a-chip model; 3D MICROVASCULAR NETWORKS; PHENOTYPIC HETEROGENEITY; SARS CORONAVIRUS; CELLS; DYSFUNCTION; RISK; ACE2; PATHOPHYSIOLOGY; INFECTION; RECEPTOR;
D O I
10.3390/cells12091297
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Coronavirus disease (COVID-19) causes various vascular and blood-related reactions, including exacerbated responses. The role of endothelial cells in this acute response is remarkable and may remain important beyond the acute phase. As we move into a post-COVID-19 era (where most people have been or will be infected by the SARS-CoV-2 virus), it is crucial to define the vascular consequences of COVID-19, including the long-term effects on the cardiovascular system. Research is needed to determine whether chronic endothelial dysfunction following COVID-19 could lead to an increased risk of cardiovascular and thrombotic events. Endothelial dysfunction could also serve as a diagnostic and therapeutic target for post-COVID-19. This review covers these topics and examines the potential of emerging vessel-on-a-chip technology to address these needs. Vessel-on-a-chip would allow for the study of COVID-19 pathophysiology in endothelial cells, including the analysis of SARS-CoV-2 interactions with endothelial function, leukocyte recruitment, and platelet activation. "Personalization" could be implemented in the models through induced pluripotent stem cells, patient-specific characteristics, or genetic modified cells. Adaptation for massive testing under standardized protocols is now possible, so the chips could be incorporated for the personalized follow-up of the disease or its sequalae (long COVID) and for the research of new drugs against COVID-19.
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页数:23
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