Ly6d marks the earliest stage of B-cell specification and identifies the branchpoint between B-cell and T-cell development

被引:227
作者
Inlay, Matthew A. [1 ]
Bhattacharya, Deepta [2 ]
Sahoo, Debashis [3 ]
Serwold, Thomas [1 ]
Seita, Jun [1 ]
Karsunky, Holger [4 ]
Plevritis, Sylvia K. [5 ]
Dill, David L. [6 ]
Weissman, Irving L. [1 ]
机构
[1] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[3] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[4] Cellerant Therapeut, San Carlos, CA 94070 USA
[5] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
B-cell development; T-cell development; fate decisions; hematopoiesis; lymphopoiesis; COMMON LYMPHOID PROGENITORS; E2A PROTEINS; BONE-MARROW; LINEAGE; E47; DIFFERENTIATION; COMMITMENT; PRECURSOR; PROMOTE;
D O I
10.1101/gad.1836009
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Common lymphoid progenitors (CLPs) clonally produce both B-and T-cell lineages, but have little myeloid potential in vivo. However, some studies claim that the upstream lymphoid-primed multipotent progenitor (LMPP) is the thymic seeding population, and suggest that CLPs are primarily B-cell-restricted. To identify surface proteins that distinguish functional CLPs from B-cell progenitors, we used a new computational method of Mining Developmentally Regulated Genes (MiDReG). We identified Ly6d, which divides CLPs into two distinct populations: one that retains full in vivo lymphoid potential and produces more thymocytes at early time-points than LMPP, and another that behaves essentially as a B-cell progenitor.
引用
收藏
页码:2376 / 2381
页数:6
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