Slug, a highly conserved zinc finger transcriptional repressor, protects hematopoietic progenitor cells from radiation-induced apoptosis in vivo

被引:152
作者
Inoue, A
Seidel, MG
Wu, WS
Kamizono, S
Ferrando, AA
Bronson, RT
Iwasaki, H
Akashi, K
Morimoto, A
Hitzler, JK
Pestina, TI
Jackson, CW
Tanaka, R
Chong, MJ
McKinnon, PJ
Inukai, T
Grosveld, GC
Look, AT
机构
[1] St Jude Childrens Res Hosp, Dept Expt Oncol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Div Expt Hematol, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Genet, Memphis, TN 38105 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/S1535-6108(02)00155-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We show here that a zinc finger transcriptional repressor, Slug, which is aberrantly upregulated by the E2A-HLF oncoprotein in pro-B cell acute leukemia, functions as an antiapoptotic factor in normal hematopoietic progenitor cells. Slug(-/-) mice were much more radiosensitive than wild-type mice, dying earlier and showing accentuated decreases in peripheral blood cell counts, as well as abundant microhemorrhages and widely disseminated bacterial microabscesses throughout the body. Slug expression was detected in diverse subsets of hematopoietic progenitors, but not in more differentiated B and T lymphoid cells, and there was a significant increase in apoptotic (TUNEL-positive) bone marrow progenitor cells in irradiated Slug(-/-) mice compared to wild-type controls. These results implicate Slug in a novel survival pathway that protects hematopoietic progenitors from apoptosis after DNA damage.
引用
收藏
页码:279 / 288
页数:10
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