Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia

被引:300
作者
Hart, A
Melet, F
Grossfeld, P
Chien, K
Jones, C
Tunnacliffe, A
Favier, R
Bernstein, A
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Program Mol Biol & Canc, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[3] Canadian Inst Hlth Res, Ottawa, ON K1A 0W9, Canada
[4] Univ Calif San Diego, Sch Med, Salk Program Mol Med, La Jolla, CA 92093 USA
[5] St Bartholomews & Royal London Med & Dent Sch, Dept Expt Hematol, London E1 2AD, England
[6] Univ Cambridge, Inst Biotechnol, Cambridge CB2 1QT, England
[7] Hop Enfants Armand Trousseau, INSERM, U91, F-75571 Paris, France
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(00)00017-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ETS gene Fli-1 is involved in the induction of erythroleukemia in mice by Friend murine leukemia virus and Ewings sarcoma in children. Mice with a targeted null mutation in the Fli-1 locus die at day 11.5 of embryogenesis with loss of vascular integrity leading to bleeding within the vascular plexus of the cerebral meninges and specific downregulation of Tek/Tie-2, the receptor for angiopoietin-1. We also show that dysmegakaryopoiesis in Fli-1 null embryos resembles that frequently seen in patients with terminal deletions of 11q (Jacobsen or Paris-Trousseau Syndrome). We map the megakaryocytic defects in 14 Jacobsen patients to a minimal region on 11q that includes the Fli-1 gene and suggest that dysmegakaryopoiesis in these patients may be caused by hemizygous loss of Fli-1.
引用
收藏
页码:167 / 177
页数:11
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