共 24 条
Isolation, propagation and characterization of cord blood derived CD4+ CD25+ regulatory T cells
被引:22
作者:

Bresatz, Suzanne
论文数: 0 引用数: 0
h-index: 0
机构: Discipline Paediat, Adelaide, SA, Australia

Sadlon, Tim
论文数: 0 引用数: 0
h-index: 0
机构: Discipline Paediat, Adelaide, SA, Australia

Millard, Debrah
论文数: 0 引用数: 0
h-index: 0
机构: Discipline Paediat, Adelaide, SA, Australia

Zola, Heddy
论文数: 0 引用数: 0
h-index: 0
机构: Discipline Paediat, Adelaide, SA, Australia

Barry, Simon C.
论文数: 0 引用数: 0
h-index: 0
机构: Discipline Paediat, Adelaide, SA, Australia
机构:
[1] Discipline Paediat, Adelaide, SA, Australia
[2] Univ Adelaide, Adelaide, SA, Australia
[3] Child Hlth Res Inst, Adelaide, SA, Australia
基金:
英国医学研究理事会;
关键词:
treg;
cord blood;
MACS;
FoxP3;
CD25+;
suppressor function;
D O I:
10.1016/j.jim.2007.06.006
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Regulatory T cells (Treg) have recently come to the fore in studies of immune regulation, particularly in autommmme disease and cancer. While there appear to be several distinct subsets of T cells with regulatory function, a population described as natural Treg and characterized by expression of the transcription factor FOXP3 has attracted particular interest. These cells can be enriched using the surface markers CD4 and CD25, and cord blood is a convenient source of CD25+ Treg. We present detailed protocols for the enrichment of Treg from cord blood using CD25 and a magnetic bead procedure, yielding populations > 80% positive for CD25 and 50-65% FOXP3 positive. This enrichment can be followed by a second magnetic bead or a flow sorting step, yielding > 95% CD25 and > 65% FOXP3 positive populations. Protocols are presented for propagation of these cells in culture (yielding > 80% FOXP3 positive cells) and for their phenotypic and functional characterization. (c) 2007 Elsevier B.V. All rights reserved.
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页码:53 / 62
页数:10
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