Phenotypic distinction and functional characterization of pro-B cells in adult mouse bone marrow

被引:17
|
作者
Mojica, MP
Perry, SS
Searles, AE
Etenitoba-Johnson, KSJ
Pierce, LJ
Wiesmann, A
Slayton, WB
Spangrude, GJ
机构
[1] Univ Utah, Dept Oncol Sci, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Human Genet, Salt Lake City, UT 84132 USA
[3] Univ Utah, Dept Pathol, Salt Lake City, UT 84132 USA
[4] Univ Utah, Dept Med, Div Hematol, Salt Lake City, UT 84132 USA
[5] Univ Utah, Dept Pediat, Salt Lake City, UT 84132 USA
来源
JOURNAL OF IMMUNOLOGY | 2001年 / 166卷 / 05期
关键词
D O I
10.4049/jimmunol.166.5.3042
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A lymphoid-committed progenitor population was isolated from mouse bone marrow based on the cell sur-face phenotype Thy-1.1(neg)Sca-1(pos)c-Kit(low)Lin(neg). These cells were CD43(pos)CD24(pos) on isolation and proliferated in response to the cytokine combination of steel factor, IL-7, and Flt3 ligand, Lymphoid-committed progenitors could be segregated into more primitive and more differentiated subsets based on expression of AA4.1. The more differentiated subset generated only B lymphoid cells in 92% of total colonies assayed, lacked T lineage potential, and expressed Pax5. These studies have therefore defined and isolated a B lymphoid-committed progenitor population at a developmental stage corresponding to the initial expression of CD45R.
引用
收藏
页码:3042 / 3051
页数:10
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