Klug David B, Carter Carla, Gimenez-Conti Irma B, Richie Ellen R
Department of Carcinogenesis, University of Texas, M. D. Anderson Cancer Center, Smithville, TX 78957, USA.
J Immunol. 2002 Sep 15;169(6):2842-5. doi: 10.4049/jimmunol.169.6.2842.
Thymic epithelial cells (TECs) in adult mice have been classified into distinct subsets based on keratin expression profiles. To explore the emergence of TEC subsets during ontogeny, we analyzed keratin 8 and keratin 5 expression at several stages of fetal development in normal C57BL/6J mice. In addition, thymic epithelial development and compartmentalization were explored in recombination-activating gene 2/common cytokine receptor gamma-chain-deficient and Ikaros-null mice that sustain early and profound blocks in thymocyte differentiation. The results demonstrate that initial patterning of the thymic epithelial compartment as defined by differential keratin expression does not depend on inductive signals from hematopoietic cells. However, thymocyte-derived signals are required during late fetal stages for continued development and maintenance of TEC subsets in the neonate and adult.
成年小鼠的胸腺上皮细胞(TECs)已根据角蛋白表达谱被分类为不同的亚群。为了探究TEC亚群在个体发育过程中的出现情况,我们分析了正常C57BL/6J小鼠胎儿发育几个阶段的角蛋白8和角蛋白5表达。此外,我们还在重组激活基因2/共同细胞因子受体γ链缺陷型和Ikaros基因敲除型小鼠中探究了胸腺上皮发育和分区情况,这些小鼠在胸腺细胞分化过程中存在早期且严重的阻滞。结果表明,由不同角蛋白表达所定义的胸腺上皮区室的初始模式并不依赖于造血细胞的诱导信号。然而,在胎儿后期,胸腺细胞衍生的信号对于新生儿和成年期TEC亚群的持续发育和维持是必需的。