Perfluorinated fatty acids alter merocyanine 540 dye binding to plasma membranes.

We have evaluated the effect of the perfluorinated fatty acids pentadecafluoro-n-octanoic acid (PFOA) and nonadecafluoro-n-decanoic acid (NDFDA) on the ability of a human B-lymphoblastoid cell line to bind the lipid-binding, membrane-impermeant, fluorescent dye merocyanine 540 (MC540). Subtoxic concentrations of perfluorinated fatty acids (0.9 mM PFOA; 0.5 mM NDFDA) greatly diminish binding of MC540 by normal plasma membranes, as determined by fluorescence flow cytometry. When perfluorinated fatty acids are added to cells at toxic or lethal concentrations (1.2 mM PFOA; 0.75 mM NDFDA), MC540 binding increases dramatically, with entrance of dye to internal membrane domains. Neither perfluorinated fatty acid molecule reduces the ability of surface immunoglobulin to migrate laterally and cap on cells. Our data suggest that perfluorinated fatty acids either interact directly with lipid binding sites for MC540, and thereby inhibit dye intercalation, or alter membrane lipid architecture and lipid packing to diminish MC540 binding. Both possibilities support a direct, physical, membrane-altering mechanism for perfluorinated fatty acid toxicity on mammalian cells.

[1]  A. Liss,et al.  Toxicity of perfluorinated fatty acids for human and murine B cell lines. , 1986, Toxicology and applied pharmacology.

[2]  D. Levitt,et al.  Binding, ingestion, and growth of Chlamydia trachomatis (L2 serovar) analyzed by flow cytometry. , 1986, Cytometry.

[3]  R. Schlegel,et al.  Alterations in plasma membrane lipid organization during lymphocyte differentiation , 1986, Journal of cellular physiology.

[4]  D. Levitt,et al.  Binding, ingestion, and multiplication of Chlamydia trachomatis (L2 serovar) in human leukocyte cell lines , 1985, Infection and immunity.

[5]  L. Hendershot,et al.  Effects of mycoplasma contamination on immunoglobulin biosynthesis by human B lymphoblastoid cell lines , 1985, Infection and immunity.

[6]  P. Williamson,et al.  Merocyanine 540 recognizes membrane abnormalities of erythrocytes in chronic myelogenous leukemia. , 1985, Cell biology international reports.

[7]  J. Spivak,et al.  Selective killing of leukemic cells by merocyanine 540-mediated photosensitization. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[8]  P. Williamson,et al.  Plasma membrane lipid order of leukemic and normal immature avian erythroid cells. , 1984, Experimental cell research.

[9]  P. Raval,et al.  Phospholipid asymmetry in the membranes of intact human erythrocytes and in spectrin-free microvesicles derived from them. , 1984, Biochimica et biophysica acta.

[10]  P. Williamson,et al.  Alteration of lipid organization following fertilization of sea urchin eggs. , 1984, Biochimica et biophysica acta.

[11]  M E Andersen,et al.  The acute toxicity of perfluorooctanoic and perfluorodecanoic acids in male rats and effects on tissue fatty acids. , 1983, Toxicology and applied pharmacology.

[12]  P. Williamson,et al.  Merocyanine 540, a fluorescent probe sensitive to lipid packing. , 1983, Biochimica et biophysica acta.

[13]  J. Spivak,et al.  Susceptibility to merocyanine 540‐mediated photosensitization: A differentiation marker on murine hematopoietic progenitor cells , 1983, Journal of cellular physiology.

[14]  G. M. Humphries,et al.  Cholesterol-free phospholipid domains may be the membrane feature selected by Nε-dansyl-L-lysine and merocyanine 540 , 1983 .

[15]  M E Andersen,et al.  Mutagenicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin and perfluoro-n-decanoic acid in L5178Y mouse-lymphoma cells. , 1982, Mutation research.

[16]  R D Klausner,et al.  The concept of lipid domains in membranes , 1982, The Journal of cell biology.

[17]  P. Williamson,et al.  Enucleation eliminates a differentiation-specific surface marker from normal and leukemic murine erythroid cells. , 1982, Experimental cell research.

[18]  M. Loken,et al.  Flow cytometry as an analytical and preparative tool in immunology. , 1982, Journal of immunological methods.

[19]  P. Williamson,et al.  Lectin‐induced rearrangement of an immature hematopoietic cell surface marker , 1982, Journal of cellular physiology.

[20]  P. Williamson,et al.  Binding of merocyanine 540 to normal and leukemic erythroid cells , 1980, Cell.

[21]  R. Klausner,et al.  Model for capping derived from inhibition of surface receptor capping by free fatty acids. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Valinsky,et al.  Merocyanine 540 as a fluorescent probe of membranes: Selective staining of leukemic and immature hemopoietic cells , 1978, Cell.