Abstract:
:TNF-alpha plays an important role in the development of secondary lymphoid tissues. Earlier studies showed that fibroblastic reticular cells express TNF-alpha receptor, suggesting that TNF-alpha may affect the development of FRCs. To test this, we analyzed the development and function of FRCs in wild-type or TNF-alpha knockout mice. We found that GP38 expression was down-regulated in the spleen of TNF-alpha knockout mice. Chemokines, mainly secreted by GP38(+) FRCs, were also down-regulated. Additionally, we found that absence of TNF-alpha decreased the homing ability to direct T cells to the spleen. However, absence of TNF-alpha did not affect the development of lymph nodes FRCs. These data reveal that TNF-alpha plays an important role in the development of spleen FRCs. Absence of TNF-alpha could cause abnormality of spleen FRCs, thereby weakening the homing ability of T cells to localize to the spleen T cell zone.
journal_name
Cell Immunoljournal_title
Cellular immunologyauthors
Zhao L,Chen J,Liu L,Gao J,Guo B,Zhu Bdoi
10.1016/j.cellimm.2015.01.006subject
Has Abstractpub_date
2015-02-01 00:00:00pages
130-6issue
2eissn
0008-8749issn
1090-2163pii
S0008-8749(15)00007-6journal_volume
293pub_type
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journal_title:Cellular immunology
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journal_title:Cellular immunology
pub_type: 杂志文章
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