Wurbel M A, Philippe J M, Nguyen C, Victorero G, Freeman T, Wooding P, Miazek A, Mattei M G, Malissen M, Jordan B R, Malissen B, Carrier A, Naquet P
Centre d'Immunologie INSERM-CNRS de Marseille-Luminy, Marseille, France.
Eur J Immunol. 2000 Jan;30(1):262-71. doi: 10.1002/1521-4141(200001)30:1<262::AID-IMMU262>3.0.CO;2-0.
Chemokines are key regulators of migration in lymphoid tissues. In the thymus, maturing thymocytes move from the outer capsule to the inner medulla and thereby interact with different types of stromal cells that control their maturation and selection. In the process of searching for molecules specifically expressed at different stages of mouse thymic differentiation, we have characterized the cDNA coding for the thymus-expressed chemokine (TECK) and its receptor CCR9. The TECK receptor gene was isolated and shown to be localized on the mouse chromosome 9F1-F4. Thymic dendritic cells have been initially thought to be a prevalent source of TECK. In contrast, our results indicate that thymic epithelial cells constitute the predominant source of TECK. Consistent with the latter distribution, the TECK receptor is highly expressed by double-positive thymocytes, and TECK can chemoattract both double-positive and single-positive thymocytes. The TECK transcript is also abundantly expressed in the epithelial cells lining the small intestine. In conclusion, the interplay of TECK and its receptor CCR9 is likely to have a significant role in the recruitment of developing thymocytes to discrete compartments of the thymus.
趋化因子是淋巴组织中迁移的关键调节因子。在胸腺中,成熟的胸腺细胞从外膜迁移至内髓质,从而与控制其成熟和选择的不同类型的基质细胞相互作用。在寻找小鼠胸腺分化不同阶段特异性表达分子的过程中,我们对编码胸腺表达趋化因子(TECK)及其受体CCR9的cDNA进行了表征。TECK受体基因被分离出来,并显示定位于小鼠9号染色体F1 - F4区域。胸腺树突状细胞最初被认为是TECK的主要来源。相反,我们的结果表明胸腺上皮细胞是TECK的主要来源。与后一种分布一致,TECK受体在双阳性胸腺细胞中高度表达,并且TECK可以趋化双阳性和单阳性胸腺细胞。TECK转录本在小肠内衬上皮细胞中也大量表达。总之,TECK及其受体CCR9之间的相互作用可能在将发育中的胸腺细胞募集到胸腺的离散区域中发挥重要作用。