Cytokine mRNA in Gaucher disease

被引:45
作者
Lichtenstein, M
Zimran, A
Horowitz, M
机构
[1] SHAARE ZEDEK MED CTR,GAUCHER CLIN,IL-91031 JERUSALEM,ISRAEL
[2] TEL AVIV UNIV,DEPT CELL RES & IMMUNOL,RAMAT AVIV,ISRAEL
关键词
Gaucher disease; glucocerebroside; glucocerebrosidase; cytokine; TNF alpha; IL-1; beta; monocytes/macrophages; polymerase chain reaction; mRNA expression;
D O I
10.1006/bcmd.1997.0156
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gaucher disease, the most common glycolipid storage disease, is caused by glucocerebrosidase deficiency, resulting in accumulation of glucocerebrosides within the macrophages of the reticuloendothelial system. The disease is characterized by great phenotypic heterogeneity, which can be explained only in part by the various mutations in the glucocerebrosidase gene, and by the amount of storage material in affected organs and tissues, Therefore, it has been postulated that some of the biochemical and clinical features may be related to the fact that ''Gaucher'' cells, as activated macrophages, express and release cytokines such as IL-1 beta, IL-8, IL-6 and TNF-alpha which play a role in different physiological processes, In the present study, cytokine mRNA expression was measured in monocytes isolated from Gaucher patients and from healthy controls, using RT-PCR methodology with semiquantitative analysis. We found significantly increased expression of IL-1 beta mRNA, as well as a trend to elevated TNF-alpha mRNA in Gaucher patients relative to healthy individuals. There were no statistically significant differences between Gaucher disease patients and controls with respect to two other tested cytokines (IL-6 and IL-8).
引用
收藏
页码:395 / 401
页数:7
相关论文
共 29 条
[1]   ABNORMAL NEUTROPHIL CHEMOTAXIS IN GAUCHER DISEASE [J].
AKER, M ;
ZIMRAN, A ;
ABRAHAMOV, A ;
HOROWITZ, M ;
MATZNER, Y .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 83 (02) :187-191
[2]  
Allen MJ, 1997, QJM-MON J ASSOC PHYS, V90, P19
[3]  
[Anonymous], 2001, The Immune System in Health and Disease
[4]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[5]  
BENJAMIN D, 1979, SCAND J HAEMATOL, V22, P179
[6]   CACHECTIN AND TUMOR-NECROSIS-FACTOR AS 2 SIDES OF THE SAME BIOLOGICAL COIN [J].
BEUTLER, B ;
CERAMI, A .
NATURE, 1986, 320 (6063) :584-588
[7]  
BEUTLER E, 1995, METABOLIC BASIS INHE
[8]   EFFECTS OF INTERLEUKIN-1 ON BONE TURNOVER IN NORMAL MICE [J].
BOYCE, BF ;
AUFDEMORTE, TB ;
GARRETT, IR ;
YATES, AJP ;
MUNDY, GR .
ENDOCRINOLOGY, 1989, 125 (03) :1142-1150
[9]   NUCLEOTIDE-SEQUENCE OF THE ACEB GENE ENCODING MALATE SYNTHASE-A IN ESCHERICHIA-COLI [J].
BYRNE, C ;
STOKES, HW ;
WARD, KA .
NUCLEIC ACIDS RESEARCH, 1988, 16 (19) :9342-9342
[10]  
Dinarello C A, 1986, Year Immunol, V2, P68