Cultivation of Cells in a Physiological Plasmax Medium Increases Mitochondrial Respiratory Capacity and Reduces Replication Levels of RNA Viruses.
Cultivation of Cells in a Physiological Plasmax Medium Increases Mitochondrial Respiratory Capacity and Reduces Replication Levels of RNA Viruses.
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DOI:
10.3390/antiox11010097
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发表时间:
2021-12-30
期刊:
影响因子:
--
通讯作者:
Ivanov AV
中科院分区:
文献类型:
--
作者:
Golikov MV;Karpenko IL;Lipatova AV;Ivanova ON;Fedyakina IT;Larichev VF;Zakirova NF;Leonova OG;Popenko VI;Bartosch B;Kochetkov SN;Smirnova OA;Ivanov AV
Changes in metabolic pathways are often associated with the development of various pathologies including cancer, inflammatory diseases, obesity and metabolic syndrome. Identification of the particular metabolic events that are dysregulated may yield strategies for pharmacologic intervention. However, such studies are hampered by the use of classic cell media that do not reflect the metabolite composition that exists in blood plasma and which cause non-physiological adaptations in cultured cells. In recent years two groups presented media that aim to reflect the composition of human plasma, namely human plasma-like medium (HPLM) and Plasmax. Here we describe that, in four different mammalian cell lines, Plasmax enhances mitochondrial respiration. This is associated with the formation of vast mitochondrial networks and enhanced production of reactive oxygen species (ROS). Interestingly, cells cultivated in Plasmax displayed significantly less lysosomes than when any standard media were used. Finally, cells cultivated in Plasmax support replication of various RNA viruses, such as hepatitis C virus (HCV) influenza A virus (IAV), severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) and several others, albeit at lower levels and with delayed kinetics. In conclusion, studies of metabolism in the context of viral infections, especially those concerning mitochondria, lysosomes, or redox systems, should be performed in Plasmax medium.
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影响因子:
64.8
作者:
Birsoy, Kivanc;Possemato, Richard;Lorbeer, Franziska K.;Bayraktar, Erol C.;Thiru, Prathapan;Yucel, Burcu;Wang, Tim;Chen, Walter W.;Clish, Clary B.;Sabatini, David M.
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Sabatini, David M.
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Fafournoux P
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3.7
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Ivanov AV;Smirnova OA;Ivanova ON;Masalova OV;Kochetkov SN;Isaguliants MG
通讯作者:
Isaguliants MG
影响因子:
5.6
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Chalecka M;Kazberuk A;Palka J;Surazynski A
通讯作者:
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影响因子:
29
作者:
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Moraes-Vieira, Pedro M.