The sequential determination model of hematopoiesis

被引:28
作者
Brown, Geoffrey [1 ]
Hughes, Philip J.
Michell, Robert H.
Rolink, Antonius G.
Ceredig, Rod
机构
[1] Univ Birmingham, Sch Med, Div Immun & Infect, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[3] Univ Basel, Dept Clin & Biol Sci, Biomed Ctr, Basel, Switzerland
[4] Etab Francais Sang Bourgogne Franche Comte, INSERM U645, UPRES EA2284, Immunol Lab,IFR 133, Besancon, France
关键词
D O I
10.1016/j.it.2007.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Analysis of hematopoietic development has for decades been central to understanding lineage diversification. Some models consider hematopoietic commitment to be random, and branching lineage maps often include an early myeloid or lymphoid bifurcation. However, the existence of joint lymphoid or myeloid intermediate progenitors argues against both. One of us earlier proposed the sequential determination (SD) model, which features a limited and stepwise set of binary choices across the full hematopoietic spectrum. This model arose from observations that hematopoietic progenitors show preferences for particular associations of lineage potentials - indicating that these linked fates are neighbours developmentally. An updated SD model complemented by several recently recognized processes - spatiotemporal fluctuations in transcription factor concentrations, asymmetric cell division, and Notch signalling - still offers a sound summary of hematopoiesis.
引用
收藏
页码:442 / 448
页数:7
相关论文
共 55 条
[1]
Identification of Flt3+ lympho-myeloid stem cells lacking erythro-megakaryocytic potential:: A revised road map for adult blood lineage commitment [J].
Adolfsson, J ;
Månsson, R ;
Buza-Vidas, N ;
Hultquist, A ;
Liuba, K ;
Jensen, CT ;
Bryder, D ;
Yang, LP ;
Borge, OJ ;
Thoren, LAM ;
Anderson, K ;
Sitnicka, E ;
Sasaki, Y ;
Sigvardsson, M ;
Jacobsen, SEW .
CELL, 2005, 121 (02) :295-306
[2]
Frontline:: A B220+ CD117+ CD19- hematopoietic progenitor with potent lymphoid and myeloid developmental potential [J].
Balciunaite, G ;
Ceredig, R ;
Massa, S ;
Rolink, AG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (07) :2019-2030
[3]
Asymmetric cell division within the human hernatopoietic stem and progenitor cell compartment: identification of asymmetrically segregating proteins [J].
Beckmann, Julia ;
Scheitza, Sebastian ;
Wernet, Peter ;
Fischer, Johannes C. ;
Giebel, Bernd .
BLOOD, 2007, 109 (12) :5494-5501
[4]
MACROPHAGE LINEAGE SWITCHING OF MURINE EARLY PRE-B LYMPHOID-CELLS EXPRESSING TRANSDUCED FMS GENES [J].
BORZILLO, GV ;
ASHMUN, RA ;
SHERR, CJ .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (06) :2703-2714
[5]
DERIVATION OF MACROPHAGE-LIKE LINES FROM THE PRE-LYMPHOMA-B ABLS 8.1 USING 5-AZACYTIDINE [J].
BOYD, AW ;
SCHRADER, JW .
NATURE, 1982, 297 (5868) :691-693
[6]
GROWTH OF MOUSE BONE MARROW CELLS IN VITRO [J].
BRADLEY, TR ;
METCALF, D .
AUSTRALIAN JOURNAL OF EXPERIMENTAL BIOLOGY AND MEDICAL SCIENCE, 1966, 44 :287-&
[7]
THE DEVELOPMENT OF CELL LINEAGES - A SEQUENTIAL MODEL [J].
BROWN, G ;
BUNCE, CM ;
LORD, JM ;
MCCONNELL, FM .
DIFFERENTIATION, 1988, 39 (02) :83-89
[8]
SEQUENTIAL DETERMINATION OF LINEAGE POTENTIALS DURING HEMATOPOIESIS [J].
BROWN, G ;
BUNCE, CM ;
GUY, GR .
BRITISH JOURNAL OF CANCER, 1985, 52 (05) :681-686
[9]
Potential of CD34 in the regulation of symmetrical and asymmetrical divisions by hematopoietic progenitor cells [J].
Bullock, Tabitha E. ;
Wen, Baiping ;
Marley, Stephen B. ;
Gordon, Myrtle Y. .
STEM CELLS, 2007, 25 (04) :844-851
[10]
NEAR-NEIGHBOR ANALYSIS OF VARIANT CELL-LINES DERIVED FROM THE PROMYELOID CELL-LINE HL60 [J].
BUNCE, CM ;
LORD, JM ;
WONG, AKY ;
BROWN, G .
BRITISH JOURNAL OF CANCER, 1988, 57 (06) :559-563