CCR7 plays no appreciable role in trafficking of central memory CD4 T cells to lymph nodes.
CCR7 plays no appreciable role in trafficking of central memory CD4 T cells to lymph nodes.
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DOI:
10.4049/jimmunol.1200938
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发表时间:
2013-09-15
期刊:
影响因子:
--
通讯作者:
Campbell JJ
中科院分区:
文献类型:
--
作者:
Vander Lugt B;Tubo NJ;Nizza ST;Boes M;Malissen B;Fuhlbrigge RC;Kupper TS;Campbell JJ
CCR7−/− mice exhibit profound anomalies in LN and spleen architecture, which complicates the study of CCR7-mediated T cell trafficking in vivo. To circumvent this problem, we established in vivo models in which WT and CCR7−/− populations coexist within mice possessing normal lymphoid organs, and must compete for developmental niches within the tissues of these mice. Under the conditions we have created in vivo, we find the entry of memory CD4 T cells into LN from the blood to be independent of CCR7. Thus, the central memory CD4 T cells that traffic though LN, which are often defined by their expression of CCR7, do not appear to gain any competitive homing advantage by expressing this receptor. Furthermore, in contrast to cutaneous DC populations, we found that CCR7 deficiency had no appreciable effect on the exit of CD4 T cells from inflamed skin. Finally, we found that WT and CCR7−/− precursors were equally represented within the major thymic subpopulations, despite previous findings that CCR7 plays a role in seeding the thymus from bone marrow-derived T cell precursors.
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影响因子:
56.9
作者:
Campbell, JJ;Hedrick, J;Butcher, EC
通讯作者:
Butcher, EC
DOI:
10.1084/jem.20031645
发表时间:
2004-04-19
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Scimone ML;Felbinger TW;Mazo IB;Stein JV;Von Andrian UH;Weninger W
通讯作者:
Weninger W
DOI:
10.1084/jem.171.3.801
发表时间:
1990-03-01
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Mackay CR;Marston WL;Dudler L
通讯作者:
Dudler L
影响因子:
6.4
作者:
Bjorkdahl, O;Barber, KA;Thomsen, LL
通讯作者:
Thomsen, LL
影响因子:
4.4
作者:
Campbell, JJ;Murphy, KE;Wu, LJ
通讯作者:
Wu, LJ