EFFECT OF BUTYRIC-ACID ON INDUCTION OF DIFFERENTIATION INTO EOSINOPHIL-LIKE CELLS IN HUMAN EOSINOPHILIC LEUKEMIA-CELLS, EOL-1 CELL-LINE - POSSIBLE ROLE OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AS AN AUTOCRINE DIFFERENTIATING FACTOR

被引:25
作者
SAITO, H
HAYAKAWA, T
MITA, H
AKIYAMA, K
SHIDA, T
机构
[1] Clinical Research Center for Rheumato-Allergology, Sagamihara National Hospital, Sagamihara
关键词
EOSINOPHILIC LEUKEMIA CELLS; EOL-1 CELL LINE; BUTYRIC ACID; AUTOCRINE DIFFERENTIATING FACTOR; GM-CSF;
D O I
10.1159/000236418
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
EoL-1 cells differentiated into mature eosinophil-like cells when incubate with butyric acid (BA). The differentiated cells possessed many granules that stained with Luxol fast blue and acquired the ability to produce leukotriene C4 and eosinophil cationic protein (ECP), and migrated toward some eosinophilotactic attractants, including PAF, IL-5, IL-3 and GM-CSF. Monoclonal antibody to GM-CSF and IL-5, especially GM-CSF, strongly decreased the ability of BA to induce differentiation, whereas antibody to IL-3 did not. Recombinant human (rh) IL-3, rhGM-CSF and recombinant mouse (rm) IL-5, by themselves, did not have the ability to induce differentiation. On the other hand, the presence of these cytokines significantly (p < 0.01) augmented BA-induced cell differentiation. Other cytokines including rhIL-1alpha/beta, rhIL-2, rhIL-4, rhIL-6, rhIL-8, rhTNF-alpha and rhIFN-gamma had no effect on differentiation. Expression of GM-CSF and GM-CSF receptor mRNA was detected in cellular RNA obtained from BA-stimulated EoL-1 cells. Moreover, about 5-10 pg/ml of GM-CSF was detected in the culture supernatant of BA-stimulated EoL-1 cells. These findings suggested that BA-induced EoL-1 cell differentiation was elicited under the influence of GM-CSF endogenously produced in these cells. GM-CSF also seemed to be an autocrine differentiating factor in EoL-1 cells.
引用
收藏
页码:240 / 247
页数:8
相关论文
共 23 条
[1]   INDUCTION OF BASOPHILIC DIFFERENTIATION IN THE HUMAN BASOPHILIC CELL-LINE KU812 [J].
ALMLOF, I ;
NILSSON, K ;
JOHANSSON, V ;
AKERBLOM, E ;
SLOTTE, H ;
AHLSTEDT, S ;
MATSSON, P .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1988, 28 (03) :293-300
[2]  
BUTTERWORTH AE, 1984, ADV PARASIT, V23, P143, DOI 10.1016/S0065-308X(08)60287-0
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
CLUTTERBUCK EJ, 1990, BLOOD, V75, P1774
[5]   A 48-WELL MICRO CHEMOTAXIS ASSEMBLY FOR RAPID AND ACCURATE MEASUREMENT OF LEUKOCYTE MIGRATION [J].
FALK, W ;
GOODWIN, RH ;
LEONARD, EJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1980, 33 (03) :239-247
[6]  
FRANK L, 1985, P NATL ACAD SCI USA, V82, P4360
[7]   EOSINOPHILS AND LYMPHOCYTES-T IN LATE-PHASE ALLERGIC REACTIONS [J].
FREW, AJ ;
KAY, AB .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 85 (03) :533-539
[8]   THE EOSINOPHIL AND THE PATHOPHYSIOLOGY OF ASTHMA [J].
FRIGAS, E ;
GLEICH, GJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1986, 77 (04) :527-537
[9]   THE EOSINOPHIL AND BRONCHIAL-ASTHMA - CURRENT UNDERSTANDING [J].
GLEICH, GJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 85 (02) :422-436
[10]  
GOLDE DW, 1978, BLOOD, V52, P1068