|
|
Previous Article | Table of Contents | Next Article 
Expression of c-jun protooncogene in human myelomonocytic cells
A Bertani, N Polentarutti, A Sica, A Rambaldi, A Mantovani and F Colotta
Instituto di Ricerche Farmacologiche Mario Negri, Milano Italy.
A prototypic "immediate early" gene, c-fos, has been extensively
investigated in relation to the differentiation and activation of
myelomonocytic cells. The c-fos gene product is associated in
transcriptional complexes with the c-jun product. These protooncogenes are
part of the regulatory network of gene expression. The present study was
designed to investigate expression of the c-jun protooncogene in human
circulating myelomonocytic cells. We found that c-jun is constitutively
expressed in normal monocytes and granulocytes, whereas low levels of
transcripts are found in lymphocytes. Acute myelogenous leukemia (AML)
samples of French-American-British Cooperative Group (FAB) subtypes 1
through 4 express appreciable levels of this protooncogene. Normal
phytohemagglutinin (PHA)-activated lymphocytes express high levels of
c-jun. Expression in normal myelomonocytic cells is detectable even after
18 hours of culture. The c-jun transcripts in myelomonocytic cells have a
half-life of approximately 20 minutes and are superinduced by
cycloheximide, which affects both the degradation rate of mRNA and the
transcriptional activity of the c-jun gene. Functional activation of
monocytes and granulocytes with phorbol esters, lipopolysaccharide, and
tumor necrosis factor (TNF) increase c- jun expression. This induction is
rapid, transient, and does not require intervening protein synthesis.
Runoff experiments showed that in freshly isolated untreated monocytes, the
c-jun gene is constitutively transcribed, and that induction by
lipopolysaccharide is at least in part at the transcriptional level.
Moreover, lipopolysaccharide (LPS) treatment reduced the degradation rate
of c- jun transcripts, prolonging the half-life to approximately two hours.
Expression of c-jun in resting and activated monocytes and granulocytes
suggests that this protooncogene may play a role in the differentiation and
activation of cells belonging to the myelomonocytic lineage.
Volume 74,
Issue 5,
pp. 1811-1816,
10/01/1989
Copyright © 1989 by The American Society of Hematology

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
A. Cloutier, T. Ear, O. Borissevitch, P. Larivee, and P. P. McDonald
Inflammatory Cytokine Expression Is Independent of the c-Jun N-Terminal Kinase/AP-1 Signaling Cascade in Human Neutrophils
J. Immunol.,
October 1, 2003;
171(7):
3751 - 3761.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Bourke, A. Cassetti, A. Villa, E. Fadlon, F. Colotta, and A. Mantovani
IL-1{beta} Scavenging by the Type II IL-1 Decoy Receptor in Human Neutrophils
J. Immunol.,
June 15, 2003;
170(12):
5999 - 6005.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Rangatia, R. K. Vangala, N. Treiber, P. Zhang, H. Radomska, D. G. Tenen, W. Hiddemann, and G. Behre
Downregulation of c-Jun Expression by Transcription Factor C/EBP{alpha} Is Critical for Granulocytic Lineage Commitment
Mol. Cell. Biol.,
December 15, 2002;
22(24):
8681 - 8694.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. R. Himes, H. Tagoh, N. Goonetilleke, T. Sasmono, D. Oceandy, R. Clark, C. Bonifer, and D. A. Hume
A highly conserved c-fms gene intronic element controls macrophage-specific and regulated expression
J. Leukoc. Biol.,
November 1, 2001;
70(5):
812 - 820.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Penton-Rol, S. Orlando, N. Polentarutti, S. Bernasconi, M. Muzio, M. Introna, and A. Mantovani
Bacterial Lipopolysaccharide Causes Rapid Shedding, Followed by Inhibition of mRNA Expression, of the IL-1 Type II Receptor, with Concomitant Up-Regulation of the Type I Receptor and Induction of Incompletely Spliced Transcripts
J. Immunol.,
March 1, 1999;
162(5):
2931 - 2938.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Yan, S. Wang, S. P. Rafferty, R. A. Wesley, and R. L. Danner
Endogenously Produced Nitric Oxide Increases Tumor Necrosis Factor-alpha Production in Transfected Human U937 Cells
Blood,
August 1, 1997;
90(3):
1160 - 1167.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. H. Steer, K. M. Kroeger, L. J. Abraham, and D. A. Joyce
Glucocorticoids Suppress Tumor Necrosis Factor-alpha Expression by Human Monocytic THP-1 Cells by Suppressing Transactivation through Adjacent NF-kappa B and c-Jun-Activating Transcription Factor-2 Binding Sites in the Promoter
J. Biol. Chem.,
June 9, 2000;
275(24):
18432 - 18440.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|