Instruction of hematopoietic lineage choice by cytokine signaling

被引:32
作者
Endele, Max [1 ]
Etzrodt, Martin [1 ]
Schroeder, Timm [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, CH-4058 Basel, Switzerland
关键词
Cytokines; Signaling; Lineage choice; Biosensors; Hematopoiesis; INHIBITS NEUTROPHIL DEVELOPMENT; FACTOR-I RECEPTOR; PROGENITOR CELLS; STEM-CELLS; C/EBP-ALPHA; C-FMS; COMMITMENT; EXPRESSION; PHOSPHORYLATION; SPECIFICITY;
D O I
10.1016/j.yexcr.2014.07.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hematopoiesis is the cumulative consequence of finely tuned signaling pathways activated through extrinsic factors, such as local niche signals and systemic hematopoietic cytokines. Whether extrinsic factors actively instruct the lineage choice of hematopoietic stem and progenitor cells or are only selectively allowing survival and proliferation of already intrinsically lineage-committed cells has been debated over decades. Recent results demonstrated that cytokines can instruct lineage choice. However, the precise function of individual cytokine-triggered signaling molecules in inducing cellular events like proliferation, lineage choice, and differentiation remains largely elusive. Signal transduction pathways activated by different cytokine receptors are highly overlapping, but support the production of distinct hematopoietic lineages. Cellular context signaling dynamics, and the crosstalk of different signaling pathways determine the cellular response of a given extrinsic signal. New tools to manipulate and continuously quantify signaling events at the single cell level are therefore required to thoroughly interrogate how dynamic signaling networks yield a specific cellular response. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:207 / 213
页数:7
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