Transcriptomes of the B and T lineages compared by multiplatform microarray profiling.

Transcriptomes of the B and T lineages compared by multiplatform microarray profiling.
复制标题

DOI:
10.4049/jimmunol.1002695
复制
发表时间:
2011-03-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Immunological Genome Project Consortium
Immunological Genome Project Consortium
中科院分区:
其他
文献类型:
--
作者:
Painter MW;Davis S;Hardy RR;Mathis D;Benoist C;Immunological Genome Project Consortium

文献摘要

参考文献

被引文献

相似文献

T and B lymphocytes are developmentally and functionally related cells of the immune system, representing the two major branches of adaptive immunity. Although originating from a common precursor, they play very different roles: T cells contribute to and drive cell-mediated immunity, while B cells secrete antibodies. Because of their functional importance and well-characterized differentiation pathways, T and B lymphocytes are ideal cell-types with which to understand how functional differences are encoded at the transcriptional level. Although there has been a great deal of interest in defining regulatory factors that distinguish T and B cells, a truly genome-wide view of the transcriptional differences between these two cells types has not yet been taken. To obtain a more global perspective of the transcriptional differences underlying T and B cells, we exploited the statistical power of combinatorial profiling on different microarray platforms, and the breadth of the Immunological Genome Project (ImmGen) gene-expression database, to generate robust differential signatures. We find that differential expression in T and B cells is pervasive, the majority of transcripts showing statistically significant differences. These distinguishing characteristics are acquired gradually, though all stages of B and T differentiation. On the other hand, very few T vs. B signature genes are uniquely expressed in these lineages, but are shared throughout immune cells.
DOI: 10.4049/jimmunol.173.9.5434
发表时间: 2004-11-01
影响因子: 4.4
作者:
Mick, VE;Starr, TK;Hogquist, KA
通讯作者: Hogquist, KA
DOI: 10.4049/jimmunol.170.3.1339
发表时间: 2003-02-01
影响因子: 4.4
作者:
Hoffmann, R;Bruno, L;Melchers, F
通讯作者: Melchers, F
DOI: 10.1016/s1074-7613(03)00328-5
发表时间: 2003-12-01
期刊: IMMUNITY
影响因子: 32.4
作者:
Pai, SY;Truitt, ML;Ho, IC
通讯作者: Ho, IC
DOI: 10.1073/pnas.0808070105
发表时间: 2008-10-14
影响因子: 11.1
作者:
Venanzi, Emily S.;Melamed, Rachel;Benoist, Christophe
通讯作者: Benoist, Christophe
DOI: 10.1007/s12026-008-8043-z
发表时间: 2008-10-01
影响因子: 4.4
作者:
Northrup, Daniel L.;Allman, David
通讯作者: Allman, David