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Sphingosine but not Sphingosine-1-phosphate Stimulates Suicidal Erythrocyte Death
Author(s) -
Syed M. Qadri,
Julia Bauer,
Christine Zelenak,
Hasan Mahmud,
Yuliya Kucherenko,
Seung Hun Lee,
Klaus Ferlinz,
Florian Läng
Publication year - 2011
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000331750
Subject(s) - sphingosine , ceramide , sphingosine kinase , lipid signaling , sphingosine 1 phosphate , phosphatidylserine , annexin , programmed cell death , sphingosine kinase 1 , microbiology and biotechnology , biochemistry , kinase , chemistry , biology , apoptosis , enzyme , phospholipid , receptor , membrane
Sphingosine kinase 1 phosphorylates sphingosine, which is converted to ceramide by ceramide synthetase. Ceramide triggers eryptosis, the suicidal erythrocyte death characterized by cell shrinkage and phosphatidylserine (PS) exposure at the erythrocyte surface. Erythrocytes lack sphingosine phosphate-degrading enzymes and thus store large quantities of sphingosine phosphate. The present study explored the influence of sphingosine and sphingosine phosphate on eryptosis. [Ca(2+)](i), was estimated from Fluo3 fluorescence, cell volume from forward scatter and PS exposure from annexin V-binding in FACS analysis. Sphingosine (0.1 - 10 μM) but not sphingosine-1- phosphate (0.1 - 10 μM) increased [Ca(2+)](i), decreased cell volume and increased PS-exposure. The observations disclose sphingosine, but not sphingosine-1-phosphate, as a strong inducer of eryptosis.

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