STAGE-SPECIFIC OLIGONUCLEOTIDE UPTAKE IN MURINE BONE-MARROW B-CELL PRECURSORS

被引:48
|
作者
ZHAO, QY
WALDSCHMIDT, T
FISHER, E
HERRERA, CJ
KRIEG, AM
机构
[1] UNIV IOWA,COLL MED,DEPT INTERNAL MED,IOWA CITY,IA 52242
[2] UNIV IOWA,DEPT PATHOL,IOWA CITY,IA 52242
[3] AMGEN BOULDER INC,BOULDER,CO
关键词
D O I
10.1182/blood.V84.11.3660.bloodjournal84113660
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fluorescein isothiocyanate (FITC)-conjugated phosphodiester and phosphorothioate oligonucleotides were used in four-color flow cytometry with murine bone marrow cells stained with monoclonal antibody specific for the differentiation markers B220, S7 (CD43), and BP-1 to show possible stage-specific oligonucleotide uptake. Relatively low uptake was observed among pre-Pro- and early Pro-B cells. Late Pro-B- and pre-B cells had increased oligonucleotide uptake, whereas B cells had a lower level. cell membrane binding of oligonucleotides varied during B-cell differentiation in parallel with internalization, which was documented by confocal microscopy. An FITC-conjugated polyanionic dextran sulfate also showed differentiation-related B-cell association, suggesting the presence of cell membrane binding sites specific for polyanions as opposed to a unique feature of the DNA backbone. Interpretation of antisense experiments in murine bone marrow cells will need to account for the heterogeneous oligonucleotide uptake among differentiating B cells. (C) 1994 by The American Society of Hematology.
引用
收藏
页码:3660 / 3666
页数:7
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