TRANSCRIPTIONAL RATES OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR, GRANULOCYTE-COLONY-STIMULATING FACTOR, INTERLEUKIN-3, AND MACROPHAGE-COLONY-STIMULATING FACTOR GENES IN ACTIVATED CORD VERSUS ADULT MONONUCLEAR-CELLS - ALTERATION IN CYTOKINE EXPRESSION MAY BE SECONDARY TO POSTTRANSCRIPTIONAL INSTABILITY

被引:26
作者
LEE, SM [1 ]
KNOPPEL, E [1 ]
VANDEVEN, C [1 ]
CAIRO, MS [1 ]
机构
[1] CHILDRENS HOSP ORANGE CTY, DIV HEMATOL ONCOL, ORANGE, CA 92668 USA
关键词
D O I
10.1203/00006450-199311000-00002
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We have previously demonstrated that protein production and mRNA expression of granulocyte-macrophage colony-stimulating factor (GM-CSF), granulocyte colony-stimulating factor (G-CSF), and IL-3 are decreased in activated mononuclear cells (MNC) from human umbilical cord compared with adult peripheral blood. Reduced production of these colony-stimulating factors (CSF) during states of increased demand, as occurs during overwhelming bacterial infection, may play a role in the pathogenesis of neutropenia and thrombocytopenia in the newborn. To determine whether the reduced mRNA expression and CSF production from activated cord MNC is secondary to the decreased transcriptional activity of the corresponding genes, we determined the transcriptional rate of GM-CSF, G-CSF, IL-3, and M-CSF by nuclear run-on assays. Cord and adult MNC were isolated by Ficoll-Hypaque density centrifugation. A total of 10(8) MNC from cord and adult blood were stimulated as follows: GMCSF and G-CSF [32 nmol/L phorbol-l2-myristate-6-acetate (20 mu g/L) +/- 2 mg/L phytohemagglutinin for 6 h]; IL-3 [32 nmol/L phorbol-12-myristate-6-acetate (20 mu g/L)+/- 0.5 mu mol/L A 23187 for 6 h]; and macrophage CSF (2 mu g/L recombinant human GM-CSF for 24 h). The nuclei from unstimulated and stimulated cells were isolated and labeled with P-32-uridine triphosphate. Newly elongated P-32-labeled RNA transcripts were hybridized to slot blots of CSF DNA. To minimize cross hybridization artifacts, short fragments (0.5-1.0 kb) of cDNA were used. The transcriptional rate increase of GM-CSF, G-CSF, IL-3, and macrophage CSF upon stimulation appears to be similar in both cord and adult MNC [GM-CSF: 260 +/- 62% (cord) versus 270 +/- 33% (adult); G-CSF: 220 +/- 71% (cord) versus 220 +/- 44% (adult); IL-3: 150 +/- 25% (cord) versus 160 +/- 38% (adult); macrophage CSF: 130 +/- 10% (cord) versus 150 +/- 15% (adult), mean +/- SD]. These findings indicate that cord MNC transcribe these CSF genes at the same level as adult MNC during states of increased demand (stimulation). Therefore, the decrease in CSF mRNA expression in activated cord versus adult MNC is probably not secondary to defects in transcriptional regulation. Alteration in posttranscriptional events, such as dysregulation of mRNA stability, could account for the difference between newborn and adult CSF expression.
引用
收藏
页码:560 / 564
页数:5
相关论文
共 53 条
[1]  
BICKEL M, 1990, J IMMUNOL, V145, P840
[2]   MESSENGER-RNA DECAY - FINDING THE RIGHT TARGETS [J].
BRAWERMAN, G .
CELL, 1989, 57 (01) :9-10
[3]   DETERMINANTS OF MESSENGER-RNA STABILITY [J].
BRAWERMAN, G .
CELL, 1987, 48 (01) :5-6
[4]   POLY(A) SHORTENING AND DEGRADATION OF THE 3' A+U-RICH SEQUENCES OF HUMAN C-MYC MESSENGER-RNA IN A CELL-FREE SYSTEM [J].
BREWER, G ;
ROSS, J .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (04) :1697-1708
[6]  
BRORSON KA, 1991, J IMMUNOL, V147, P3601
[7]   GRANULOCYTE-COLONY AND GRANULOCYTE-MACROPHAGE-COLONY STIMULATING FACTORS INDUCE HUMAN-ENDOTHELIAL CELLS TO MIGRATE AND PROLIFERATE [J].
BUSSOLINO, F ;
WANG, JM ;
DEFILIPPI, P ;
TURRINI, F ;
SANAVIO, F ;
EDGELL, CJS ;
AGLIETTA, M ;
ARESE, P ;
MANTOVANI, A .
NATURE, 1989, 337 (6206) :471-473
[8]   NEONATAL NEUTROPHIL HOST DEFENSE - PROSPECTS FOR IMMUNOLOGICAL ENHANCEMENT DURING NEONATAL SEPSIS [J].
CAIRO, MS .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1989, 143 (01) :40-46
[9]   DECREASED STIMULATED GM-CSF PRODUCTION AND GM-CSF GENE-EXPRESSION BUT NORMAL NUMBERS OF GM-CSF RECEPTORS IN HUMAN TERM NEWBORNS COMPARED WITH ADULTS [J].
CAIRO, MS ;
SUEN, Y ;
KNOPPEL, E ;
VANDEVEN, C ;
NGUYEN, A ;
SENDER, L .
PEDIATRIC RESEARCH, 1991, 30 (04) :362-367
[10]   DECREASED G-CSF AND IL-3 PRODUCTION AND GENE-EXPRESSION FROM MONONUCLEAR-CELLS OF NEWBORN-INFANTS [J].
CAIRO, MS ;
YU, S ;
KNOPPEL, E ;
DANA, R ;
PARK, L ;
CLARK, S ;
VANDEVEN, C ;
SENDER, L .
PEDIATRIC RESEARCH, 1992, 31 (06) :574-578