Panigada M, Porcellini S, Sutti F, Doneda L, Pozzoli O, Consalez G G, Guttinger M, Grassi F
Department of Biological and Technological Research (DIBIT), San Raffaele Scientific Institute (HSR), Milan, Italy.
Mech Dev. 1999 Mar;81(1-2):103-13. doi: 10.1016/s0925-4773(98)00237-8.
Gut-enriched Krüppel-like factor (GKLF) is a transcriptional regulator expressed in differentiated epithelia. We identified GKLF transcript as a regulated element in thymic epithelium of recombinase-deficient mice during thymus development induced by anti-CD3 antibody injection. This treatment recapitulates the organogenetic process depending on productive rearrangement of T cell receptor (TCR) beta gene with thymocytes expansion and acquisition of the CD4+8+ double positive phenotype. In wildtype mice, GKLF is expressed very early in embryogenesis and becomes intensely up-regulated in thymus epithelium at day 18 of gestation when TCR beta expressing cells have selectively expanded and express both CD4 and CD8. The results presented here suggest that thymocytes may regulate GKLF transcriptionally in the cortical epithelium at the developmental check-point controlled by TCR beta gene rearrangement. Furthermore, GKLF expression in hematopoietic stroma might suggest the thus far uncharacterised participation of this factor in hematopoiesis.
肠道富集型锌指蛋白(GKLF)是一种在分化上皮中表达的转录调节因子。我们将GKLF转录本鉴定为在抗CD3抗体注射诱导的胸腺发育过程中,重组酶缺陷小鼠胸腺上皮中的一个受调控元件。这种处理模拟了依赖于T细胞受体(TCR)β基因有效重排以及胸腺细胞扩增和获得CD4+8+双阳性表型的器官发生过程。在野生型小鼠中,GKLF在胚胎发育早期就有表达,并且在妊娠第18天,当表达TCRβ的细胞选择性扩增并同时表达CD4和CD8时,在胸腺上皮中强烈上调。此处呈现的结果表明,胸腺细胞可能在由TCRβ基因重排控制的发育检查点处,对皮质上皮中的GKLF进行转录调控。此外,GKLF在造血基质中的表达可能表明该因子在造血过程中迄今尚未被描述的参与情况。