Exploring the multifaceted nature of the common lymphoid progenitor compartment

被引:4
作者
Jensen, Christina T. [1 ]
Strid, Tobias [2 ]
Sigvardsson, Mikael [1 ,2 ]
机构
[1] Lund Univ, Div Mol Hematol, S-22100 Lund, Sweden
[2] Linkoping Univ, Dept Clin & Expt Med, S-58183 Linkoping, Sweden
基金
瑞典研究理事会;
关键词
B-CELL FATE; BONE-MARROW; LINEAGE SPECIFICATION; MYELOID DIFFERENTIATION; TRANSCRIPTION FACTORS; T-CELLS; COMMITMENT; EXPRESSION; PAX5; INNATE;
D O I
10.1016/j.coi.2016.01.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
While the common lymphoid progenitor compartment was originally thought to be a rather homogenous cell population, it has become increasingly clear that this compartment is highly heterogeneous both with regard to phenotypic and functional features. The exploration of this cellular complexity has generated novel molecular insights into regulatory events in lymphoid lineage restriction and provided support for the idea that multiple lineage restriction events occur at this developmental stage. Furthermore, the identification of multiple lineage-restricted progenitors with mixed lineage potential challenges a strictly hierarchical model for lymphoid development. Instead we propose a model based on competence windows during which cell fates are established through the action of lineage determining factors.
引用
收藏
页码:121 / 126
页数:6
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