Increased Activity of Small GTP-binding Protein-dependent Phospholipase D during Differentiation in Human Promyelocytic Leukemic HL60 Cells*

In response to dibutyryl cyclic AMP (dbcAMP) and all-trans retinoic acid, human promyelocytic leukemic HL60 cells differentiate into granulocyte-like cells. In cell lysate and in vitro reconstitution system, phospholipase D (PLD) activity in response to guanosine 5′-O-(3-thiotriphosphate) (GTPγS) was up-regulated by dbcAMP or all-trans retinoic acid treatment. In the present study, the mechanism(s) for increased PLD activity during differentiation was examined. Western blot analysis revealed that the contents of ADP-ribosylation factor, Rac2, and Cdc42Hs but not RhoA and Rac1 in the cytosolic fraction were elevated during differentiation. However, the cytosolic fraction from undifferentiated cells was almost equally potent as the cytosolic fraction from differentiated cells in the ability to stimulate membrane PLD activity. It was shown that the GTPγS-dependent PLD activity in membranes from differentiated cells was much higher than that in membranes from undifferentiated cells, suggesting that the increased PLD activity during differentiation was due to alterations in some membrane component(s). Clostridium botulinum ADP-ribosyltransferase C3 and C. difficile toxin B, which are known as inhibitors of RhoA and Rho family proteins, respectively, effectively suppressed PLD activity in membranes from differentiated cells. In fact, the amount of membrane-associated RhoA was increased during differentiation. Furthermore, the extent of GTPγS-dependent PLD activity partially purified from membranes from differentiated cells was greater than that from membranes from undifferentiated cells in the presence of recombinant ADP-ribosylation factor 1. The PLD (hPLD1) mRNA level was observed to be up-regulated during differentiation, as inferred by reverse transcription-polymerase chain reaction. Our results suggest the possibility that the increased Rho proteins in membranes and the changed level of PLD itself may be, at least in part, responsible for the increase in GTPγS-dependent PLD activity during granulocytic differentiation of HL60 cells.

[1]  A. Ridley,et al.  Stimulation of actin stress fibre formation mediated by activation of phospholipase D , 1996, Current Biology.

[2]  S. Nakashima,et al.  Regulation of Membrane-bound Phospholipase D by Protein Kinase C in HL60 Cells , 1996, The Journal of Biological Chemistry.

[3]  S. Hammond,et al.  Human ADP-ribosylation Factor-activated Phosphatidylcholine-specific Phospholipase D Defines a New and Highly Conserved Gene Family (*) , 1995, The Journal of Biological Chemistry.

[4]  K. Aktories,et al.  Monoglucosylation of low-molecular-mass GTP-binding Rho proteins by clostridial cytotoxins. , 1995, Trends in cell biology.

[5]  T. Katada,et al.  Synergistic Activation of Rat Brain Phospholipase D by ADP-ribosylation Factor and rhoA p21, and Its Inhibition by Clostridium botulinum C3 Exoenzyme (*) , 1995, The Journal of Biological Chemistry.

[6]  K. Waite,et al.  Cell-free activation of neutrophil NADPH oxidase by a phosphatidic acid-regulated protein kinase. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[7]  G. Bokoch,et al.  Resolved Phospholipase D Activity Is Modulated by Cytosolic Factors Other than Arf (*) , 1995, The Journal of Biological Chemistry.

[8]  R. Kahn,et al.  Partial Purification and Characterization of Arf-sensitive Phospholipase D from Porcine Brain (*) , 1995, The Journal of Biological Chemistry.

[9]  S. Nakashima,et al.  Activation of membrane-bound phospholipase D by protein kinase C in HL60 cells: synergistic action of a small GTP-binding protein RhoA. , 1995, Biochemical and biophysical research communications.

[10]  L. Cantley,et al.  Signal transduction and membrane traffic: The PITP/phosphoinositide connection , 1995, Cell.

[11]  T. Sasaki,et al.  Rho as a regulator of the cytoskeleton. , 1995, Trends in biochemical sciences.

[12]  M. Roth,et al.  Phospholipase D is present on Golgi-enriched membranes and its activation by ADP ribosylation factor is sensitive to brefeldin A. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[13]  M. Symons,et al.  Regulation of Phospholipase D in HL60 Cells , 1995, The Journal of Biological Chemistry.

[14]  R. Kahn,et al.  Arf proteins: the membrane traffic police? , 1995, Trends in biochemical sciences.

[15]  S. Nakashima,et al.  Endogenous Cleavage of Phospholipase C-β3 by Agonist-induced Activation of Calpain in Human Platelets (*) , 1995, The Journal of Biological Chemistry.

[16]  S. Nakashima,et al.  Defective phospholipase D activation in Ki-ras-transformed NIH3T3 cells: evidence for downstream effector of PLC-gamma 1 in PDGF-mediated signal transduction. , 1995, Biochemical and biophysical research communications.

[17]  P. Hawkins,et al.  Activation of the small GTP-binding proteins rho and rac by growth factor receptors. , 1995, Journal of cell science.

[18]  S. Okamura,et al.  Purification and characterization of phosphatidylcholine phospholipase D from pig lung. , 1994, The Journal of biological chemistry.

[19]  J. Moss,et al.  Activation of rat brain phospholipase D by ADP-ribosylation factors 1,5, and 6: separation of ADP-ribosylation factor-dependent and oleate-dependent enzymes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[20]  M. Symons,et al.  Activation of rat liver phospholipase D by the small GTP-binding protein RhoA. , 1994, The Journal of biological chemistry.

[21]  L. Cantley,et al.  Novel function of phosphatidylinositol 4,5-bisphosphate as a cofactor for brain membrane phospholipase D. , 1994, The Journal of biological chemistry.

[22]  M. Aepfelbacher,et al.  Spreading of differentiating human monocytes is associated with a major increase in membrane-bound CDC42. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Exton Phosphatidylcholine breakdown and signal transduction. , 1994, Biochimica et biophysica acta.

[24]  J. Moss,et al.  Effect of ADP-ribosylation factor amino-terminal deletions on its GTP-dependent stimulation of cholera toxin activity. , 1994, The Journal of biological chemistry.

[25]  J. Shayman,et al.  Phospholipase D-mediated diradylglycerol formation coincides with H2O2 and lactoferrin release in adherent human neutrophils. , 1994, The Journal of biological chemistry.

[26]  I. Gout,et al.  Phospholipase D: a downstream effector of ARF in granulocytes. , 1994, Science.

[27]  B. McConnell,et al.  Regulation of phospholipase A2 activity in undifferentiated and neutrophil-like HL60 cells. Linkage between impaired responses to agonists and absence of protein kinase C-dependent phosphorylation of cytosolic phospholipase A2. , 1994, The Journal of biological chemistry.

[28]  H. Brown,et al.  ADP-ribosylation factor, a small GTP-dependent regulatory protein, stimulates phospholipase D activity , 1993, Cell.

[29]  J. Lambeth,et al.  Neutrophil phospholipase D is activated by a membrane-associated Rho family small molecular weight GTP-binding protein. , 1993, The Journal of biological chemistry.

[30]  S. Cockcroft,et al.  Correlation between secretion and phospholipase D activation in differentiated HL60 cells. , 1993, The Biochemical journal.

[31]  D. Bass,et al.  Activation of NADPH oxidase and phospholipase D in permeabilized human neutrophils. Correlation between oxidase activation and phosphatidic acid production. , 1992, The Journal of biological chemistry.

[32]  R. Klausner,et al.  Brefeldin A inhibits Golgi membrane-catalysed exchange of guanine nucleotide onto ARF protein , 1992, Nature.

[33]  J. Lambeth,et al.  Role of phospholipase D-derived diradylglycerol in the activation of the human neutrophil respiratory burst oxidase. Inhibition by phosphatidic acid phosphohydrolase inhibitors. , 1992, Journal of immunology.

[34]  M. Record,et al.  Human neutrophil phospholipase D activation by N-formylmethionyl-leucylphenylalanine reveals a two-step process for the control of phosphatidylcholine breakdown and oxidative burst. , 1992, The Biochemical journal.

[35]  S. Cockcroft,et al.  Synergistic activation of phospholipase D by protein kinase C- and G-protein-mediated pathways in streptolysin O-permeabilized HL60 cells. , 1992, The Biochemical journal.

[36]  F. Thévenod,et al.  Dual regulation of arachidonic acid release by P2U purinergic receptors in dibutyryl cyclic AMP-differentiated HL60 cells. , 1992, The Journal of biological chemistry.

[37]  J. Lambeth,et al.  Phospholipase D activation in a cell-free system from human neutrophils by phorbol 12-myristate 13-acetate and guanosine 5'-O-(3-thiotriphosphate). Activation is calcium dependent and requires protein factors in both the plasma membrane and cytosol. , 1991, The Journal of biological chemistry.

[38]  G. Dubyak,et al.  Regulation of phospholipase D and primary granule secretion by P2-purinergic- and chemotactic peptide-receptor agonists is induced during granulocytic differentiation of HL-60 cells. , 1991, The Journal of clinical investigation.

[39]  Y. Nozawa,et al.  Phospholipase D activation by platelet-activating factor, leukotriene B4, and formyl-methionyl-leucyl-phenylalanine in rabbit neutrophils. Phospholipase D activation is involved in enzyme release. , 1991, Journal of immunology.

[40]  J. Lambeth,et al.  Fluoride activates diradylglycerol and Superoxide generation in human neutrophils via PLD/PA phosphohydrolase‐dependent and ‐independent pathways , 1990, FEBS letters.

[41]  M. Billah,et al.  The regulation and cellular functions of phosphatidylcholine hydrolysis. , 1990, The Biochemical journal.

[42]  N. Thompson,et al.  Phospholipase D activation is functionally linked to superoxide generation in the human neutrophil. , 1989, The Biochemical journal.

[43]  L. Ercolani,et al.  Isolation and complete sequence of a functional human glyceraldehyde-3-phosphate dehydrogenase gene. , 1988, The Journal of biological chemistry.

[44]  S. Collins,et al.  The HL-60 promyelocytic leukemia cell line: proliferation, differentiation, and cellular oncogene expression. , 1987, Blood.

[45]  J. Tobert New developments in lipid-lowering therapy: the role of inhibitors of hydroxymethylglutaryl-coenzyme A reductase. , 1987, Circulation.

[46]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[47]  J. Niedel,et al.  Cyclic nucleotide-induced maturation of human promyelocytic leukemia cells. , 1982, The Journal of clinical investigation.

[48]  S. Collins,et al.  Induction of differentiation of the human promyelocytic leukemia cell line (HL-60) by retinoic acid. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[49]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[50]  S. Collins,et al.  Terminal differentiation of human promyelocytic leukemia cells induced by dimethyl sulfoxide and other polar compounds. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[51]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.