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Polyamines, PI(4,5)P 2 , and actin polymerization
Author(s) -
Coburn Ronald F.,
LaBelle Edward F.,
Baron Carl B.
Publication year - 2006
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.20729
Subject(s) - putrescine , inositol , phosphatidylinositol , spermine , spermidine , pi , polyamine , inositol phosphate , biochemistry , phospholipid , kinase , biology , microbiology and biotechnology , chemistry , enzyme , receptor , membrane
Spermine (SPM) and spermidine (SPD) activate isolated phosphatidylinositol‐4‐phosphate 5‐kinases (PI(4)P5K), enzymes that convert phosphatidylinositol‐4‐phosphate to phosphatidylinositol 4,5‐bisphosphate (PI(4,5)P 2 ). PI(4,5)P 2 formation is known to be involved in cellular actin reorganization and motility, functions that are also influenced by polyamines. It has not been proven that endogenous polyamines can control inositol phospholipid metabolism. We evoked large decreases in SPD and putrescine (PUT) contents in HL60 cells, using the ornithine decarboxylase inhibitor, alpha‐difluoromethylornithine (DFMO), which resulted in decreases in PI(4,5)P 2 content per cell and inositol phosphate formation to 76.9 ± 3.5% and 81.5 ± 4.0% of control, respectively. Accurately reversing DFMO‐evoked decreases in SPD content by incubating cells with exogenous SPD for 20 min rescued these decreases. DFMO treatment and SPD rescues also changed the ratio of total cellular PI(4,5)P 2 to PIP suggesting involvement of a SPD‐sensitive PI(4)P5K. PUT and SPM were not involved in DFMO‐evoked changes in cellular PI(4,5)P 2 contents. In DFMO‐treated HL60 cells, the percent of total actin content that was filamentous was decreased to 59.1 ± 5.8% of that measured in paired control HL60 cells, a finding that was rescued following reversal of DFMO‐evoked decreases in SPD and PI(4,5)P 2 contents. In slowly proliferating DMSO‐differentiated HL60 cells, inositol phospholipid metabolism was uncoupled from SPD control. We conclude: in rapidly proliferating HL60 cells, but not in slowly proliferating differentiated HL60 cells, there are endogenous SPD‐sensitive PI(4,5)P 2 pools, probably formed via SPD‐sensitive PI(4)P5K, that likely control actin polymerization. J. Cell. Physiol. 209: 405–412, 2006. © 2006 Wiley‐Liss, Inc.