Deimantė Narauskaitė on Muck Rack

Deimantė Narauskaitė

As seen in: PLOS ONE, MDPI
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Articles

How different cardioplegic solutions influence genes expression and cytokine response in an immature rat heart model of ischemia/reperfusion?

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By Rimantas Treinys, Deimantė Narauskaitė, Arslan Mamedov, Povilas Jakuška
| PLOS ONE
Citation: Mamedov A, Gečys D, Jakuška P, Treinys R, Narauskaitė D, Aitaliyev S, et al. (2025) How different cardioplegic solutions influence genes expression and cytokine response in an immature rat heart model of ischemia/reperfusion? PLoS One 20(7): e0329010. https://doi.org/10.1371/journal.pone.0329010 Editor: Doa'a G. F.
Open in Who Shared Issue with article?

IJMS | Free Full-Text | Differential Mitochondrial, Oxidative Stress and Inflammatory Responses to SARS-CoV-2 Spike Protein Receptor Binding Domain in Human Lung Microvascular, Coronary Artery Endothelial and Bronchial Epithelial Cells

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By Gabrielė Kulkovienė, Deimantė Narauskaitė, Agile Tunaityte, Zbigniev Balion
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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Comparison of mitochondrial response to SARS-CoV-2 spike protein receptor binding domain in human lung microvascular, coronary artery endothelial and bronchial epithelial cells

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By Gabrielė Kulkovienė, Deimantė Narauskaitė, Agile Tunaityte, Augusta Volkeviciute
| biorxiv.org
Abstract Recent evidence indicate that SARS-CoV-2 spike protein affects mitochondria with a cell type-dependent outcome. We elucidate the effect of SARS-CoV-2 receptor binding domain (RBD) on the mitochondrial network and cristae morphology, oxygen consumption, mitoROS produc-tion, and inflammatory cytokine expression in cultured human lung microvascular (HLMVEC) and coronary artery endothelial (HCAEC) and bronchial epithelial cells (HBEC).
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