Abstract

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.

Highlights

  • Phospholipids are essential structural components of cell membranes and plasma lipoproteins, and are involved in numerous biological responses, including membrane protein regulation, membrane trafficking, apoptosis, cellular signalling and lipoprotein metabolism[1,2,3,4,5,6,7,8,9]

  • PI(3)P and PI(4,5)P2 exhibited only negligible fluorescence increases (

  • To understand the control of cellular phospholipid metabolism in detail, we investigated whether the overexpression of phosphatidylinositol synthase (PIS), CDP-diacylglycerol synthase 1 (CDS1) or CDS2 affected the phospholipid composition of the intracellular organelles

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Summary

Results and Discussion

By performing comprehensive analyses of major phospholipid classes, we demonstrated that the cellular contents of phospholipid classes were largely dependent on cell density and that overexpression of PIS, CDS1 or CDS2 affected the phospholipid composition of microsomal and mitochondrial membranes. These simple methods may be applicable to animal tissues, fluids, lipoproteins and extracellular vesicles. Our enzymatic fluorometric methods for quantifying phospholipid classes will be helpful in understanding the biological functions of phospholipids in various organisms

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