Constitutively active mutant D816VKit induces megakayocyte and mast cell differentiation of early haemopoietic cells from murine foetal liver

被引:23
作者
Ferrao, PT
Gonda, TJ
Ashman, LK
机构
[1] Univ Newcastle, Fac Hlth, Sch Biomed Sci, Callaghan, NSW 2308, Australia
[2] Inst Med & Vet Sci, Hanson Ctr Canc Res, Adelaide, SA 5000, Australia
关键词
c-Kit; D816V mutation; transformation; differentiation; megakaryocyte; mast cell;
D O I
10.1016/S0145-2126(02)00272-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations of Kit at position D816 have been implicated in mastocytosis, acute myeloid leukaemia and germ cell tumours. Expression of this mutant Kit in cell lines results in factor-independent growth, differentiation and increased survival in vitro and tumourigenicity in vivo. Mutant D816VKit and wild-type Kit were expressed in murine primary haemopoietic cells and grown in stem cell factor (SCF) or the absence of factors. Expression of D816VKit did not lead to transformation as assessed by a colony assay, but resulted in enhanced differentiation of cells when compared to control cells. D816VKit induced an increase in the number of cells differentiating along the megakaryocyte lineage in the absence of factors. SCF had an added effect with an increase in differentiation of mast cells. Expression of wild-type Kit in the presence of SCF also failed to cause transformation and induced differentiation of mast cells and megakaryocytes. We conclude that constitutive expression of D816VKit in primary haemopoietic cells is not a sufficient transforming stimulus but leads to the survival and maturation of cells whose phenotype is influenced by the presence of SCF. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:547 / 555
页数:9
相关论文
共 64 条
[41]   SPECIFICITY OF A MOUSE MONOCLONAL-ANTIBODY RAISED AGAINST ACUTE MYELOID-LEUKEMIA CELLS FOR MAST-CELLS IN HUMAN MUCOSAL AND CONNECTIVE TISSUES [J].
MAYRHOFER, G ;
GADD, SJ ;
SPARGO, LDJ ;
ASHMAN, LK .
IMMUNOLOGY AND CELL BIOLOGY, 1987, 65 :241-250
[42]   Expression of activated mutants of the human interleukin-3/interleukin-5 granulocyte-macrophage colony-stimulating factor receptor common beta subunit in primary hematopoietic cells induces factor-independent proliferation and differentiation [J].
McCormack, MP ;
Gonda, TJ .
BLOOD, 1997, 90 (04) :1471-1481
[43]  
MCNEIL HP, 1992, J IMMUNOL, V149, P2466
[44]  
Moriyama Y, 1996, J BIOL CHEM, V271, P3347
[45]   IDENTIFICATION OF A POINT MUTATION IN THE CATALYTIC DOMAIN OF THE PROTOONCOGENE C-KIT IN PERIPHERAL-BLOOD MONONUCLEAR-CELLS OF PATIENTS WHO HAVE MASTOCYTOSIS WITH AN ASSOCIATED HEMATOLOGIC DISORDER [J].
NAGATA, H ;
WOROBEC, AS ;
OH, CK ;
CHOWDHURY, BA ;
TANNENBAUM, S ;
SUZUKI, Y ;
METCALFE, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10560-10564
[46]   Activating mutations of c-kit at codon 816 confer drug resistance in human leukemia cells [J].
Ning, ZQ ;
Li, J ;
Arceci, RJ .
LEUKEMIA & LYMPHOMA, 2001, 41 (5-6) :513-522
[47]   Signal transducer and activator of transcription 3 activation is required for Asp816 mutant c-Kit-mediated cytokine-independent survival and proliferation in human leukemia cells [J].
Ning, ZQ ;
Li, J ;
Arceci, RJ .
BLOOD, 2001, 97 (11) :3559-3567
[48]   Oncogenic mutation in the Kit receptor tyrosine kinase alters substrate specificity and induces degradation of the protein tyrosine phosphatase SHP-1 [J].
Piao, XH ;
Paulson, R ;
vanderGeer, P ;
Pawson, T ;
Bernstein, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14665-14669
[49]   A point mutation in the catalytic domain of c-kif induces growth factor independence, tumorigenicity, and differentiation of mast cells [J].
Piao, XH ;
Bernstein, A .
BLOOD, 1996, 87 (08) :3117-3123