Negative selection of self-reactive chicken B cells requires B cell receptor signaling and is independent of the bursal microenvironment.

Negative selection of self-reactive chicken B cells requires B cell receptor signaling and is independent of the bursal microenvironment.
复制标题

DOI:
10.4049/jimmunol.1302394
复制
发表时间:
2014-04-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Ratcliffe MJ
Ratcliffe MJ
中科院分区:
其他
文献类型:
--
作者:
Davani D;Pancer Z;Cheroutre H;Ratcliffe MJ

文献摘要

参考文献

被引文献

相似文献

Although the negative selection of self-reactive B cells in the bone marrow of mammals has been clearly demonstrated, it remains unclear in models of gut-associated B cell lymphopoiesis, such as that of the chicken (Gallus gallus). We have generated chicken surface IgM–related receptors in which the diversity region of the lamprey variable lymphocyte receptor (VLR) has been fused to the C region of chicken surface IgM (Tμ). Expression of a VLR:Tμ receptor with specificity for PE supported normal development of B cells, whereas a VLR:Tμ receptor specific to hen egg lysozyme (a self-antigen with respect to chicken B cells) induced, in vivo, complete deletion of VLRHELTμ-expressing B cells. In ovo i.v. injection of PE resulted in deletion of VLRPETμ-expressing Β cells in the embryo spleen, demonstrating that negative selection was independent of the bursal microenvironment. Although chickens transduced with a murine CD8α:chicken Igα fusion protein contained B cells expressing mCD8α:chIgα, cotransfection of the mCD8α:chIgα construct, together with thymus leukemia Ag (a natural ligand for mCD8α), resulted in reduced levels of mCD8α:chIgα-expressing B cells in inverse proportion to the levels of thymus leukemia Ag–expressing cells. Deletion of mCD8a: chIga-expressing cells was specific for B cells and required active signaling downstream of the mCD8α:chIgα receptor. Ag-mediated negative selection of developing chicken B cells can therefore occur independently of the bursal microenvironment and is dependent on signaling downstream of the BCR.
DOI: 10.1084/jem.181.1.105
发表时间: 1995-01-01
期刊: The Journal of experimental medicine
影响因子: --
作者:
Paramithiotis E;Jacobsen KA;Ratcliffe MJ
通讯作者: Ratcliffe MJ
DOI: 10.1038/ni1076
发表时间: 2004-06-01
期刊: NATURE IMMUNOLOGY
影响因子: 30.5
作者:
Halverson, R;Torres, RM;Pelanda, R
通讯作者: Pelanda, R
DOI: 10.1016/s1074-7613(00)80285-x
发表时间: 1997-04-01
期刊: IMMUNITY
影响因子: 32.4
作者:
Healy, JI;Dolmetsch, RE;Goodnow, CC
通讯作者: Goodnow, CC
DOI: 10.1038/334676a0
发表时间: 1988-08-25
期刊: NATURE
影响因子: 64.8
作者:
GOODNOW, CC;CROSBIE, J;BASTEN, A
通讯作者: BASTEN, A
DOI: 10.1038/353765a0
发表时间: 1991-10-24
期刊: NATURE
影响因子: 64.8
作者:
HARTLEY, SB;CROSBIE, J;GOODNOW, CC
通讯作者: GOODNOW, CC