Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10770047 | Biochemical and Biophysical Research Communications | 2005 | 6 Pages |
Abstract
In this study, we observed that lysophosphatidylserine (LPS) stimulated intracellular calcium ([Ca2+]i) increase in leukemic cells but not in normal human peripheral blood mononuclear cells. LPS also stimulated [Ca2+]i increase in human leukemic THP-1 cells. LPS-stimulated [Ca2+]i increase was inhibited by U-73122 but not by U-73343. LPS also stimulated inositol phosphates formation in THP-1 cells, suggesting that LPS stimulates calcium signaling via phospholipase C activation. Moreover, pertussis toxin (PTX) completely inhibited [Ca2+]i increase by LPS, indicating the activation of PTX-sensitive G-proteins. We also found that LPS-induced [Ca2+]i increase was completely inhibited by suramin, suggesting G-protein coupled receptor activation. Since LPS specifically stimulates PTX-sensitive G-proteins, phospholipase C-dependent [Ca2+]i increase in leukemic cells but not normal peripheral blood leukocytes, LPS receptor may be associated with leukemia.
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Authors
Kyoung Sun Park, Ha Young Lee, Mi-Kyoung Kim, Eun Ha Shin, Yoe-Sik Bae,