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Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles
Cell membrane phospholipids regulate various biological functions. We previously reported enzymatic fluorometric methods for quantifying phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, sphingomyelin, phosphatidylglycerol and cardiolipin. In the present report, a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565719/ https://www.ncbi.nlm.nih.gov/pubmed/31197208 http://dx.doi.org/10.1038/s41598-019-45185-0 |
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author | Tsuji, Tokuji Morita, Shin-ya Ikeda, Yoshito Terada, Tomohiro |
author_facet | Tsuji, Tokuji Morita, Shin-ya Ikeda, Yoshito Terada, Tomohiro |
author_sort | Tsuji, Tokuji |
collection | PubMed |
description | Cell membrane phospholipids regulate various biological functions. We previously reported enzymatic fluorometric methods for quantifying phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, sphingomyelin, phosphatidylglycerol and cardiolipin. In the present report, a new enzymatic fluorometric assay was developed for quantifying phosphatidylinositol. These simple, sensitive and high-throughput methods enabled us to quantify all major phospholipid classes in cultured cells and intracellular organelles. By conducting comprehensive quantitative analyses of major phospholipid classes, we demonstrated that the contents of phospholipid classes in HEK293 cells changed with cell density and that overexpression of phosphatidylinositol synthase or CDP-diacylglycerol synthase significantly affected the phospholipid compositions of microsomal and mitochondrial membranes. These enzymatic fluorometric assays for measuring all major phospholipid classes may be applicable to tissues, fluids, lipoproteins, extracellular vesicles and intracellular organelles of many organisms and will further our understanding of cellular, physiological and pathological processes. |
format | Online Article Text |
id | pubmed-6565719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65657192019-06-20 Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles Tsuji, Tokuji Morita, Shin-ya Ikeda, Yoshito Terada, Tomohiro Sci Rep Article Cell membrane phospholipids regulate various biological functions. We previously reported enzymatic fluorometric methods for quantifying phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, sphingomyelin, phosphatidylglycerol and cardiolipin. In the present report, a new enzymatic fluorometric assay was developed for quantifying phosphatidylinositol. These simple, sensitive and high-throughput methods enabled us to quantify all major phospholipid classes in cultured cells and intracellular organelles. By conducting comprehensive quantitative analyses of major phospholipid classes, we demonstrated that the contents of phospholipid classes in HEK293 cells changed with cell density and that overexpression of phosphatidylinositol synthase or CDP-diacylglycerol synthase significantly affected the phospholipid compositions of microsomal and mitochondrial membranes. These enzymatic fluorometric assays for measuring all major phospholipid classes may be applicable to tissues, fluids, lipoproteins, extracellular vesicles and intracellular organelles of many organisms and will further our understanding of cellular, physiological and pathological processes. Nature Publishing Group UK 2019-06-13 /pmc/articles/PMC6565719/ /pubmed/31197208 http://dx.doi.org/10.1038/s41598-019-45185-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tsuji, Tokuji Morita, Shin-ya Ikeda, Yoshito Terada, Tomohiro Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title | Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title_full | Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title_fullStr | Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title_full_unstemmed | Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title_short | Enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
title_sort | enzymatic fluorometric assays for quantifying all major phospholipid classes in cells and intracellular organelles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565719/ https://www.ncbi.nlm.nih.gov/pubmed/31197208 http://dx.doi.org/10.1038/s41598-019-45185-0 |
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