| Literature DB >> 11869682 |
Tomoo Ueno1, Kyoko Hara, Melissa Swope Willis, Mark A Malin, Uta E Höpken, Daniel H D Gray, Kouji Matsushima, Martin Lipp, Timothy A Springer, Richard L Boyd, Osamu Yoshie, Yousuke Takahama.
Abstract
Most T lymphocytes are generated within the thymus. It is unclear, however, how newly generated T cells relocate out of the thymus to the circulation. The present study shows that a CC chemokine CCL19 attracts mature T cells out of the fetal thymus organ culture. Another CC chemokine CCL21, which shares CCR7 with CCL19 but has a unique C-terminal extension containing positively charged amino acids, failed to show involvement in thymic emigration. Neonatal appearance of circulating T cells was defective in CCL19-neutralized mice as well as in CCR7-deficient mice but not in CCL21-neutralized mice. In the thymus, CCL19 is predominantly localized in the medulla including endothelial venules. These results indicate a CCL19- and CCR7-dependent pathway of thymic emigration, which represents a major pathway of neonatal T cell export.Entities:
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Year: 2002 PMID: 11869682 DOI: 10.1016/s1074-7613(02)00267-4
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745