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Mitochondrial Respiration of Platelets: Comparison of Isolation Methods
Multiple non-aggregatory functions of human platelets (PLT) are widely acknowledged, yet their functional examination is limited mainly due to a lack of standardized isolation and analytic methods. Platelet apheresis (PA) is an established clinical method for PLT isolation aiming at the treatment of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698846/ https://www.ncbi.nlm.nih.gov/pubmed/34944675 http://dx.doi.org/10.3390/biomedicines9121859 |
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author | Vernerova, Andrea Garcia-Souza, Luiz Felipe Soucek, Ondrej Kostal, Milan Rehacek, Vit Kujovska Krcmova, Lenka Gnaiger, Erich Sobotka, Ondrej |
author_facet | Vernerova, Andrea Garcia-Souza, Luiz Felipe Soucek, Ondrej Kostal, Milan Rehacek, Vit Kujovska Krcmova, Lenka Gnaiger, Erich Sobotka, Ondrej |
author_sort | Vernerova, Andrea |
collection | PubMed |
description | Multiple non-aggregatory functions of human platelets (PLT) are widely acknowledged, yet their functional examination is limited mainly due to a lack of standardized isolation and analytic methods. Platelet apheresis (PA) is an established clinical method for PLT isolation aiming at the treatment of bleeding diathesis in severe thrombocytopenia. On the other hand, density gradient centrifugation (DC) is an isolation method applied in research for the analysis of the mitochondrial metabolic profile of oxidative phosphorylation (OXPHOS) in PLT obtained from small samples of human blood. We studied PLT obtained from 29 healthy donors by high-resolution respirometry for comparison of PA and DC isolates. ROUTINE respiration and electron transfer capacity of living PLT isolated by PA were significantly higher than in the DC group, whereas plasma membrane permeabilization resulted in a 57% decrease of succinate oxidation in PA compared to DC. These differences were eliminated after washing the PA platelets with phosphate buffer containing 10 mmol·L(−1) ethylene glycol-bis (2-aminoethyl ether)-N,N,N′,N′-tetra-acetic acid, suggesting that several components, particularly Ca(2+) and fuel substrates, were carried over into the respiratory assay from the serum in PA. A simple washing step was sufficient to enable functional mitochondrial analysis in subsamples obtained from PA. The combination of the standard clinical PA isolation procedure with PLT quality control and routine mitochondrial OXPHOS diagnostics meets an acute clinical demand in biomedical research of patients suffering from thrombocytopenia and metabolic diseases. |
format | Online Article Text |
id | pubmed-8698846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86988462021-12-24 Mitochondrial Respiration of Platelets: Comparison of Isolation Methods Vernerova, Andrea Garcia-Souza, Luiz Felipe Soucek, Ondrej Kostal, Milan Rehacek, Vit Kujovska Krcmova, Lenka Gnaiger, Erich Sobotka, Ondrej Biomedicines Article Multiple non-aggregatory functions of human platelets (PLT) are widely acknowledged, yet their functional examination is limited mainly due to a lack of standardized isolation and analytic methods. Platelet apheresis (PA) is an established clinical method for PLT isolation aiming at the treatment of bleeding diathesis in severe thrombocytopenia. On the other hand, density gradient centrifugation (DC) is an isolation method applied in research for the analysis of the mitochondrial metabolic profile of oxidative phosphorylation (OXPHOS) in PLT obtained from small samples of human blood. We studied PLT obtained from 29 healthy donors by high-resolution respirometry for comparison of PA and DC isolates. ROUTINE respiration and electron transfer capacity of living PLT isolated by PA were significantly higher than in the DC group, whereas plasma membrane permeabilization resulted in a 57% decrease of succinate oxidation in PA compared to DC. These differences were eliminated after washing the PA platelets with phosphate buffer containing 10 mmol·L(−1) ethylene glycol-bis (2-aminoethyl ether)-N,N,N′,N′-tetra-acetic acid, suggesting that several components, particularly Ca(2+) and fuel substrates, were carried over into the respiratory assay from the serum in PA. A simple washing step was sufficient to enable functional mitochondrial analysis in subsamples obtained from PA. The combination of the standard clinical PA isolation procedure with PLT quality control and routine mitochondrial OXPHOS diagnostics meets an acute clinical demand in biomedical research of patients suffering from thrombocytopenia and metabolic diseases. MDPI 2021-12-08 /pmc/articles/PMC8698846/ /pubmed/34944675 http://dx.doi.org/10.3390/biomedicines9121859 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vernerova, Andrea Garcia-Souza, Luiz Felipe Soucek, Ondrej Kostal, Milan Rehacek, Vit Kujovska Krcmova, Lenka Gnaiger, Erich Sobotka, Ondrej Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title | Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title_full | Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title_fullStr | Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title_full_unstemmed | Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title_short | Mitochondrial Respiration of Platelets: Comparison of Isolation Methods |
title_sort | mitochondrial respiration of platelets: comparison of isolation methods |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698846/ https://www.ncbi.nlm.nih.gov/pubmed/34944675 http://dx.doi.org/10.3390/biomedicines9121859 |
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