Publication Date:
2013-04-12
Description:
Under stress conditions such as infection or inflammation the body rapidly needs to generate new blood cells that are adapted to the challenge. Haematopoietic cytokines are known to increase output of specific mature cells by affecting survival, expansion and differentiation of lineage-committed progenitors, but it has been debated whether long-term haematopoietic stem cells (HSCs) are susceptible to direct lineage-specifying effects of cytokines. Although genetic changes in transcription factor balance can sensitize HSCs to cytokine instruction, the initiation of HSC commitment is generally thought to be triggered by stochastic fluctuation in cell-intrinsic regulators such as lineage-specific transcription factors, leaving cytokines to ensure survival and proliferation of the progeny cells. Here we show that macrophage colony-stimulating factor (M-CSF, also called CSF1), a myeloid cytokine released during infection and inflammation, can directly induce the myeloid master regulator PU.1 and instruct myeloid cell-fate change in mouse HSCs, independently of selective survival or proliferation. Video imaging and single-cell gene expression analysis revealed that stimulation of highly purified HSCs with M-CSF in culture resulted in activation of the PU.1 promoter and an increased number of PU.1(+) cells with myeloid gene signature and differentiation potential. In vivo, high systemic levels of M-CSF directly stimulated M-CSF-receptor-dependent activation of endogenous PU.1 protein in single HSCs and induced a PU.1-dependent myeloid differentiation preference. Our data demonstrate that lineage-specific cytokines can act directly on HSCs in vitro and in vivo to instruct a change of cell identity. This fundamentally changes the current view of how HSCs respond to environmental challenge and implicates stress-induced cytokines as direct instructors of HSC fate.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679883/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679883/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mossadegh-Keller, Noushine -- Sarrazin, Sandrine -- Kandalla, Prashanth K -- Espinosa, Leon -- Stanley, E Richard -- Nutt, Stephen L -- Moore, Jordan -- Sieweke, Michael H -- CA 32551/CA/NCI NIH HHS/ -- R01 CA032551/CA/NCI NIH HHS/ -- England -- Nature. 2013 May 9;497(7448):239-43. doi: 10.1038/nature12026. Epub 2013 Apr 10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre d'Immunologie de Marseille-Luminy, Aix-Marseille Universite, UM2, Campus de Luminy, Case 906, 13288 Marseille Cedex 09, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23575636" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Cell Differentiation/*drug effects
;
Cell Lineage/*drug effects
;
Cell Proliferation/drug effects
;
Cell Survival/drug effects
;
Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology
;
Hematopoietic Stem Cells/*cytology/*drug effects
;
Macrophage Colony-Stimulating Factor/*pharmacology
;
Mice
;
Mice, Inbred C57BL
;
Myeloid Cells/*cytology/*drug effects
;
Promoter Regions, Genetic/genetics
;
Proto-Oncogene Proteins/biosynthesis/genetics/metabolism
;
Single-Cell Analysis
;
Trans-Activators/biosynthesis/genetics/metabolism
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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