Phenotypic, molecular, and functional characterization of human peripheral blood CD34(+)/Thy1(+) cells

被引:49
作者
Humeau, L
Bardin, F
Maroc, C
Alario, T
Galindo, R
Mannoni, P
Chabannon, C
机构
[1] INST J PAOLI I CALMETTES, CTR REG LUTTE CONTRE CANC, DEPT TRANSFERT GENE & THERAPIE GENIQUE, F-13273 MARSEILLE 9, FRANCE
[2] INSERM, U119, MARSEILLE, FRANCE
关键词
D O I
10.1182/blood.V87.3.949.bloodjournal873949
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A subset of mobilized CD34(+) cells present in patient aphereses expresses Thy1 (CDw90). This population contains most long-term culture initiating cells, as assayed with a murine stromal cell line. It also contains a significant proportion of colony-forming unit granulocyte macrophage, but very few burst-forming unit erythroid. The limited differentiation towards the erythroid lineage is further confirmed by the absence of GATA-1 mRNA in the CD34(+)/Thy1(+) subset, and by the low level of c-kit expression. The CD34(+)/Thy1(+) subset appears phenotypically and functionally heterogeneous, a finding consistent with its high representation, compared to phenotypes such as CD34(+)/CD38(-). Therefore, while at least some of CD34(+)/Thy1(+) cells may be infectable by retroviral vectors, as shown by the presence of a transcript for the receptor for murine amphotropic retroviruses, the use of this selection strategy to specifically target human stem cells appears questionable. (C) 1996 by The American Society of Hematology.
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收藏
页码:949 / 955
页数:7
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