| 論文種別 | 原著(症例報告除く) |
| 言語種別 | 英語 |
| 査読の有無 | 査読あり |
| 表題 | Ccl21a, Rather Than Ccl21b, is Essential for Thymocyte Migration in Mouse. |
| 掲載誌名 | 正式名:European journal of immunology 略 称:Eur J Immunol ISSNコード:15214141/00142980 |
| 掲載区分 | 国外 |
| 巻・号・頁 | 55(12),pp.e70114 |
| 著者・共著者 | Ohigashi I, Kyuma H, Otsu E, Hayashi S, Takemoto T, Takahama Y |
| 発行年月 | 2025/12 |
| 概要 | Self-tolerance in T cells is a vital self-defense strategy for mammals to specifically respond to invading pathogens. During T cell development in the thymus, thymocytes migrate from the cortex to the medulla to sequentially acquire non-self-reactivity and self-tolerance. This cortex-to-medulla migration is regulated by CCR7-mediated chemokine signaling. Previous studies have identified CCL21 but not CCL19 as a functional ligand for this CCR7-dependent migration. CCL21 in the mouse is encoded by multiple genes, including CCL21Ser-encoding Ccl21a and several CCL21Leu-encoding genes, including Ccl21b. The importance of Ccl21a in thymocyte migration has been demonstrated, whereas the role of CCL21Leu-encoding genes remains unclear. By producing mice specifically deficient in Ccl21b, we show that Ccl21b plays little to no role in the cortex-to-medulla migration of developing thymocytes. CCL21Leu-encoding gene transcripts remain detectable even in the absence of Ccl21b, suggesting that Ccl21b is not a major source of CCL21Leu. We further show that the copy number of CCL21Leu-encoding genes is smaller than the currently estimated copy number in a public database. These findings underscore the predominant role of Ccl21a over Ccl21b in the mouse thymus. |
| DOI | 10.1002/eji.70114 |
| PMID | 41420491 |