Multilineage gene expression precedes commitment in the hemopoietic system

被引:596
作者
Hu, M
Krause, D
Greaves, M
Sharkis, S
Dexter, M
Heyworth, C
Enver, T
机构
[1] INST CANC RES, CHESTER BEATTY LABS, LEUKAEMIA RES FUND CTR, LONDON SW3 6JB, ENGLAND
[2] YALE UNIV, DEPT LAB MED, NEW HAVEN, CT 06520 USA
[3] JOHNS HOPKINS UNIV, CTR ONCOL, BALTIMORE, MD 21287 USA
[4] CHRISTIE HOSP & HOLT RADIUM INST, PATERSON INST CANC RES, MANCHESTER M20 9BX, LANCS, ENGLAND
关键词
hemopoietic stem cells; lineage specification; cytokine receptors;
D O I
10.1101/gad.11.6.774
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have tested the hypothesis that multipotential hemopoietic stem and progenitor cells prime several different lineage-affiliated programs of gene activity prior to unilineage commitment and differentiation. Using single cell RT-PCR we show that erythroid (beta-globin) and myeloid (myeloperoxidase) gene expression programs can be initiated by the same cell prior to exclusive commitment to the erythroid or granulocytic lineages. furthermore, the multipotential state is characterized by the coexpression of several lineage-affiliated cytokine receptors. These data support a model of hemopoietic lineage specification in which unilineage commitment is prefaced by a ''promiscuous'' phase of multilineage locus activation.
引用
收藏
页码:774 / 785
页数:12
相关论文
共 41 条
[1]   FUNCTIONAL ISOLATION AND CHARACTERIZATION OF HUMAN HEMATOPOIETIC STEM-CELLS [J].
BERARDI, AC ;
WANG, AL ;
LEVINE, JD ;
LOPEZ, P ;
SCADDEN, DT .
SCIENCE, 1995, 267 (5194) :104-108
[2]   GRANZYME-B AND PERFORIN LYTIC PROTEINS ARE EXPRESSED IN CD34(+) PERIPHERAL-BLOOD PROGENITOR CELLS MOBILIZED BY CHEMOTHERAPY AND GRANULOCYTE-COLONY-STIMULATING FACTOR [J].
BERTHOU, C ;
MAROLLEAU, JP ;
LAFAURIE, C ;
SOULIE, A ;
DALCORTIVO, L ;
BOURGE, JF ;
BENBUNAN, M ;
SASPORTES, M .
BLOOD, 1995, 86 (09) :3500-3506
[3]   ANALYSIS OF GENE-EXPRESSION IN A COMPLEX DIFFERENTIATION HIERARCHY BY GLOBAL AMPLIFICATION OF CDNA FROM SINGLE CELLS [J].
BRADY, G ;
BILLIA, F ;
KNOX, J ;
HOANG, T ;
KIRSCH, IR ;
VOURA, EB ;
HAWLEY, RG ;
CUMMING, R ;
BUCHWALD, M ;
SIMINOVITCH, K ;
MIYAMOTO, N ;
BOEHMELT, G ;
ISCOVE, NN .
CURRENT BIOLOGY, 1995, 5 (08) :909-922
[4]   THE GENE ENCODING THE STEM-CELL ANTIGEN, CD34, IS CONSERVED IN MOUSE AND EXPRESSED IN HEMATOPOIETIC PROGENITOR-CELL LINES, BRAIN, AND EMBRYONIC FIBROBLASTS [J].
BROWN, J ;
GREAVES, MF ;
MOLGAARD, HV .
INTERNATIONAL IMMUNOLOGY, 1991, 3 (02) :175-184
[5]   IRREVERSIBLE GENE REPRESSION MODEL FOR CONTROL OF DEVELOPMENT [J].
CAPLAN, AI ;
ORDAHL, CP .
SCIENCE, 1978, 201 (4351) :120-130
[6]   ILLEGITIMATE TRANSCRIPTION - TRANSCRIPTION OF ANY GENE IN ANY CELL TYPE [J].
CHELLY, J ;
CONCORDET, JP ;
KAPLAN, JC ;
KAHN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (08) :2617-2621
[7]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[8]   GROWTH-FACTORS IN DEVELOPMENT, TRANSFORMATION, AND TUMORIGENESIS [J].
CROSS, M ;
DEXTER, TM .
CELL, 1991, 64 (02) :271-280
[9]  
CROSS MA, 1994, ONCOGENE, V9, P3013
[10]   PROGRESSIVE INACTIVATION OF THE EXPRESSION OF AN ERYTHROID TRANSCRIPTIONAL FACTOR IN GM-CSF-DEPENDENT AND G-CSF-DEPENDENT MYELOID CELL-LINES [J].
CROTTA, S ;
NICOLIS, S ;
RONCHI, A ;
OTTOLENGHI, S ;
RUZZI, L ;
SHIMADA, Y ;
MIGLIACCIO, AR ;
MIGLIACCIO, G .
NUCLEIC ACIDS RESEARCH, 1990, 18 (23) :6863-6869