Ruebsaamen, Katharina and Liebisch, Gerhard and Boettcher, Alfred and Schmitz, Gerd (2010) Lipidomic analysis of platelet senescence. TRANSFUSION, 50 (8). pp. 1665-1676. ISSN 0041-1132,
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BACKGROUND: A hallmark of platelet (PLT) storage lesion is the loss of PLT lipids. Due to technical limitations a detailed lipidomic analysis of plateletpheresis products during storage was so far not available. STUDY DESIGN AND METHODS: Fifty plateletpheresis products were stored for 5 days at 22 C under agitation. Each day plasma and PLTs were isolated by gel filtration and lipid species analyzed by electrospray ionization tandem mass spectrometry. RESULTS: During 5 days of storage the total lipid content decreased by 10% in PLTs and increased by 5% in plasma. We observed the following changes in lipid class fractions during storage relative to the day of preparation: increases of 69% ceramide (Cer), 32% lysophosphatidylcholine (LPC), and 49% cholesteryl esters (CE) and a decrease of 10% free cholesterol (FC) in PLTs and elevation of 43% LPC and 14% CE and a decline of 20% phosphatidylcholine (PC) and 24% FC in plasma. Significant lipid species shifts were observed for phosphatidylserine, Cer, and LPC. Correlation analysis of lipid changes in plasma indicated that lecithin-cholesterol-acyltransferase (LCAT) activity may be responsible for the shift in plasma lipid composition. These lipid changes correlated between plasma and PLTs for LPC, FC, and CE fractions. CONCLUSIONS: This study presents for the first time detailed lipid species profiles of PLTs and plasma during storage of PLT concentrates. These data provide clear evidence for LCAT-mediated esterification of FC and LPC generation in the plasma of PLT concentrates. Moreover, we showed evidence that these changes also impact PLT lipid composition.
Item Type: | Article |
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Uncontrolled Keywords: | TANDEM MASS-SPECTROMETRY; HIGH-THROUGHPUT QUANTIFICATION; LOW-DENSITY-LIPOPROTEIN; AGING IN-VIVO; PHOSPHOLIPID ASYMMETRY; QUANTITATIVE-ANALYSIS; BLOOD-PLATELET; STORAGE LESION; FATTY-ACIDS; ESI-MS/MS; |
Subjects: | 600 Technology > 610 Medical sciences Medicine |
Divisions: | Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin |
Depositing User: | Dr. Gernot Deinzer |
Date Deposited: | 22 Jul 2020 05:55 |
Last Modified: | 22 Jul 2020 05:55 |
URI: | https://pred.uni-regensburg.de/id/eprint/24436 |
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