Thrombopoietin induces histidine decarboxylase gene expression in c-mpl transfected UT7 cells

被引:10
作者
Pacilio, M
Debili, N
Arnould, A
Machavoine, F
Rolli-Derkinderen, M
Bodger, M
Arock, M
Duménil, D
Dy, M
Schneider, E
机构
[1] Univ Paris 05, Hop Necker Enfants Malad, CNRS, UMR 8063, F-75743 Paris 15, France
[2] Inst Gustave Roussy, INSERM, U 362, F-94805 Villejuif, France
[3] Environm & Sci Res Ltd, Christchurch, New Zealand
[4] Fac Pharm, Lab Hematol Cellulaire & Mol, Paris, France
关键词
histamine; histidine decarboxylase; basophil; differentiation; cytokines; thrombopoietin; megakaryopoiesis; kinase; signal transduction;
D O I
10.1006/bbrc.2001.5296
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The leukemic cell line UT7 is endowed with both megakaryocyte and basophil differentiation potential, as judged by its capacity to respond to PALA. by displaying megakaryocytic and basophilic markers and to produce histamine by neosynthesis. Herein, we addressed the question whether the biological activities characteristic of basophil differentiation were still induced when c-mpl-transfected UT7 cells received a specific megakaryocytic differentiation signal delivered by thrombopoietin (TPO). Surprisingly, we found that histamine synthesis did effectively occur in response to the growth factor. This activity was not associated with megakaryopoiesis since it was not detected in megakaryocytes generated from CD34(+) cells cultured in the presence of TPO. Comparing different e-mpl-transfected cell lines, we found that the amount of histamine generated in response to TPO correlated with their responsiveness to PMA, but not with their level of c-mpl expression, thus revealing an intrinsic basophil differentiation potential. Both PMA- and TPO-induced histamine synthesis was reduced by PKC and MEKs inhibitors, indicating that the induction occurred through a common signalling pathway. (C) 2001 Academic Press.
引用
收藏
页码:1095 / 1101
页数:7
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