Towards a New Understanding of Decision-Making by Hematopoietic Stem Cells

被引:5
作者
Brown, Geoffrey [1 ]
机构
[1] Univ Birmingham, Inst Clin Sci, Sch Biomed Sci, Birmingham B15 2TT, W Midlands, England
关键词
hematopoiesis; stem cells; decision-making; cytokines; environmental niches; COLONY-STIMULATING FACTOR; GRANULOCYTE-MACROPHAGE-COLONY; FATE DETERMINATION; PROGENITOR CELLS; CLONAL ANALYSIS; SELF-RENEWAL; C-KIT; ERYTHROPOIETIN; CSF-1; THROMBOPOIETIN;
D O I
10.3390/ijms21072362
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
Cells within the hematopoietic stem cell compartment selectively express receptors for cytokines that have a lineage(s) specific role; they include erythropoietin, macrophage colony-stimulating factor, granulocyte colony-stimulating factor, granulocyte/macrophage colony-stimulating factor and the ligand for the fms-like tyrosine kinase 3. These hematopoietic cytokines can instruct the lineage fate of hematopoietic stem and progenitor cells in addition to ensuring the survival and proliferation of cells that belong to a particular cell lineage(s). Expression of the receptors for macrophage colony-stimulating factor and granulocyte colony-stimulating factor is positively autoregulated and the presence of the cytokine is therefore likely to enforce a lineage bias within hematopoietic stem cells that express these receptors. In addition to the above roles, macrophage colony-stimulating factor and granulocyte/macrophage colony-stimulating factor are powerful chemoattractants. The multiple roles of some hematopoietic cytokines leads us towards modelling hematopoietic stem cell decision-making whereby these cells can 'choose' just one lineage fate and migrate to a niche that both reinforces the fate and guarantees the survival and expansion of cells as they develop.
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页数:11
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共 62 条
[1]   Single-cell RNA sequencing reveals developmental heterogeneity among early lymphoid progenitors [J].
Alberti-Servera, Llucia ;
von Muenchow, Lilly ;
Tsapogas, Panagiotis ;
Capoferri, Giuseppina ;
Eschbach, Katja ;
Beisel, Christian ;
Ceredig, Rhodri ;
Ivanek, Robert ;
Rolink, Antonius .
EMBO JOURNAL, 2017, 36 (24) :3619-3633
[2]   ERYTHROPOIETIN HAS A MITOGENIC AND POSITIVE CHEMOTACTIC EFFECT ON ENDOTHELIAL-CELLS [J].
ANAGNOSTOU, A ;
LEE, ES ;
KESSIMIAN, N ;
LEVINSON, R ;
STEINER, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5978-5982
[3]   The biology of stem cell factor and its receptor C-kit [J].
Ashman, LK .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1999, 31 (10) :1037-1051
[4]   The Evolution of Gene-Specific Transcriptional Noise Is Driven by Selection at the Pathway Level [J].
Barroso, Gustavo Valadares ;
Puzovic, Natasa ;
Dutheil, Julien Y. .
GENETICS, 2018, 208 (01) :173-189
[5]   Influence of the microenvironment on cell fate determination and migration [J].
Bloom, Alexander B. ;
Zaman, Muhammad H. .
PHYSIOLOGICAL GENOMICS, 2014, 46 (09) :309-314
[6]   Modeling the Hematopoietic Landscape [J].
Brown, Geoffrey ;
Ceredig, Rhodri .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2019, 7
[7]   GRANULOCYTE-COLONY AND GRANULOCYTE-MACROPHAGE-COLONY STIMULATING FACTORS INDUCE HUMAN-ENDOTHELIAL CELLS TO MIGRATE AND PROLIFERATE [J].
BUSSOLINO, F ;
WANG, JM ;
DEFILIPPI, P ;
TURRINI, F ;
SANAVIO, F ;
EDGELL, CJS ;
AGLIETTA, M ;
ARESE, P ;
MANTOVANI, A .
NATURE, 1989, 337 (6206) :471-473
[8]   Models of haematopoiesis: seeing the wood for the trees [J].
Ceredig, Rhodri ;
Rolink, Antonius G. ;
Brown, Geoffrey .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (04) :293-300
[9]   Transcriptome-wide noise controls lineage choice in mammalian progenitor cells [J].
Chang, Hannah H. ;
Hemberg, Martin ;
Barahona, Mauricio ;
Ingber, Donald E. ;
Huang, Sui .
NATURE, 2008, 453 (7194) :544-U10
[10]   Erythroblastic islands: niches for erythropoiesis [J].
Chasis, Joel Anne ;
Mohandas, Narla .
BLOOD, 2008, 112 (03) :470-478