Role of c-jun in the inhibition of erythropoietin receptor-mediated apoptosis

被引:17
作者
Shimizu, R
Komatsu, N
Nakamura, Y
Nakauchi, H
Nakabeppu, Y
Miura, Y
机构
[1] JICHI MED SCH,DEPT MED,DIV HEMATOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[2] UNIV TSUKUBA,INST BASIC MED SCI,DEPT IMMUNOL,TSUKUBA,IBARAKI 305,JAPAN
[3] INST PHYS & CHEM RES,LAB CELL GROWTH & DIFFERENTIAT,TSUKUBA,IBARAKI 305,JAPAN
[4] KYUSHU UNIV,MED INST BIOREGULAT,DEPT BIOCHEM,FUKUOKA 812,JAPAN
关键词
PROGRAMMED CELL-DEATH; FOS JUN; EXPRESSION; GENE; CLONING; BCL-2; MYC; ACTIVATION; INDUCTION; SURVIVAL;
D O I
10.1006/bbrc.1996.0688
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
Human bone marrow cells express both a truncated and full-length form of the erythropoietin receptor (EpoR-T and EpoR-F, respectively). Transfection experiments using the murine interleukin (IL)-3-dependent cell Line, Ba/F3, revealed that the cells coexpressing EpoR-F and EpoR-T (Ba/F3-FT) were more likely to undergo programmed cell death (apoptosis) than cells expressing EpoR-F (Ba/F3-FF), even in the presence of erythropoietin (Epo). When Ba/F3-FF cells were stimulated with Epo or IL-3, rapid induction of c-myc, c-fos, c-jun and junB genes was observed. A similar effect was also seen in IL-3-stimulated Ba/F3-Ft cells. However, in Ba/F3-FT cells expression of the c-jun gene was not induced by Epo stimulation. Administration of Epo could prevent apoptosis induced by IL-3 deprivation in Ba/F3-FT cells expressing ectopic c-Jun protein. These results indicate that induction of c-Jun through the Epo signaling pathway has an important role in the inhibition of apoptosis. (C) 1996 Academic Press. Inc.
引用
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页码:1 / 6
页数:6
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