Differentiating embryonal stem cells are a rich source of haemopoietic gene products and suggest erythroid preconditioning of primitive haemopoietic stem cells

被引:17
作者
Baird, JW [1 ]
Ryan, KM [1 ]
Hayes, I [1 ]
Hampson, L [1 ]
Heyworth, CM [1 ]
Clark, A [1 ]
Wootton, M [1 ]
Ansell, JD [1 ]
Menzel, U [1 ]
Hole, N [1 ]
Graham, GJ [1 ]
机构
[1] Beatson Inst Canc Res, Canc Res Campaign, Beatson Labs, Glasgow G61 1BD, Lanark, Scotland
关键词
D O I
10.1074/jbc.M008354200
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 difficulties associated with studying molecular mechanisms important in hemopoietic stem cell (HSC) function such as the problems of purifying homogeneous stem cell populations, have prompted us to adapt the murine ES cell system as an in vitro model of HSC generation and function. We now report that careful analysis of the time course of HSC generation in differentiating ES cells allows them to be used as a source of known and novel hemopoietic gene products. We have generated a subtracted library using cDNA from ES cells collected just prior to and just following the emergence of HSCs. Analysis of this library shows it to be a rich source of known hemopoietic and hemopoietic related gene products with 44% of identifiable cDNAs falling into these camps. We have demonstrated the value of this system as a source of novel genes of relevance to HSC function by characterizing a novel membrane protein encoding cDNA that is preferentially expressed in primitive hemopoietic cells. Intriguingly, further analysis of the known components of the subtracted library is suggestive of erythroid preconditioning of the ES cell-derived HSC. We have used dot-blot and in situ analysis to indicate that this erythroid preconditioning is probably restricted to primitive but not definitive HSC.
引用
收藏
页码:9189 / 9198
页数:10
相关论文
共 63 条
[11]   EXPRESSION CLONING OF AN INTERFERON-INDUCIBLE 17-KDA MEMBRANE-PROTEIN IMPLICATED IN THE CONTROL OF CELL-GROWTH [J].
DEBLANDRE, GA ;
MARINX, OP ;
EVANS, SS ;
MAJJAJ, S ;
LEO, O ;
CAPUT, D ;
HUEZ, GA ;
WATHELET, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23860-23866
[12]  
DOETSCHMAN TC, 1985, J EMBRYOL EXP MORPH, V87, P27
[13]  
FRAICHARD A, 1995, J CELL SCI, V108, P3181
[14]   New insights into functions of erythroid proteins in nonerythroid cells [J].
Gascard, P ;
Mohandas, N .
CURRENT OPINION IN HEMATOLOGY, 2000, 7 (02) :123-129
[15]   The SCL gene specifies haemangioblast development from early mesoderm [J].
Gering, M ;
Rodaway, ARF ;
Göttgens, B ;
Patient, RK ;
Green, AR .
EMBO JOURNAL, 1998, 17 (14) :4029-4045
[16]   Haemopoietic stem cells: their heterogeneity and regulation [J].
Graham, GJ ;
Wright, EG .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 1997, 78 (04) :197-218
[17]  
GUIMARAES MJ, 1995, DEVELOPMENT, V121, P3335
[18]   INVITRO DIFFERENTIATION OF EMBRYONIC STEM-CELLS INTO LYMPHOCYTE PRECURSORS ABLE TO GENERATE LYMPHOCYTES-T AND LYMPHOCYTES-B INVIVO [J].
GUTIERREZRAMOS, JC ;
PALACIOS, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (19) :9171-9175
[19]   A limited temporal window for the derivation of multilineage repopulating hematopoietic progenitors during embryonal stem cell differentiation in vitro [J].
Hole, N ;
Graham, GJ ;
Menzel, U ;
Ansell, JD .
BLOOD, 1996, 88 (04) :1266-1276
[20]  
Hole Nicholas, 1994, P235