Sen J, Venkataraman L, Shinkai Y, Pierce J W, Alt F W, Burakoff S J, Sen R
Rosenstiel Basic Medical Sciences Research Center, Brandeis University, Waltham, MA 02254.
J Immunol. 1995 Apr 1;154(7):3213-21.
Thymocytes mature in response to the cues from the thymic micro-environment, which regulate stage-specific gene expression during development. We find that several proteins that bind the kappa B sequence in vitro are constitutively activated in freshly isolated thymocytes. These include the rel-related p50 homodimers, p50/p65 heterodimers, low levels of c-rel, and two other factors that may be thymus specific. Disruption of the thymic micro-environment resulted in loss of DNA-binding, suggesting that lymphocyte-stromal cell interactions induce and maintain these proteins in a DNA-binding form. Phorbol ester and ionomycin treatment induced p50, p65, and p68 c-rel kappa B DNA-binding activity. Expression of p68 c-rel protein, but not p50 or p65, was suppressed by the immunosuppressive drug FK506. Because FK506 specifically inhibits the appearance of mature single-positive thymocytes, gene expression regulated by p68 c-rel may play a role in selection and maturational signals involved in the double-positive to single-positive transition.
胸腺细胞在胸腺微环境的信号作用下成熟,胸腺微环境在发育过程中调节阶段特异性基因表达。我们发现,几种在体外与κB序列结合的蛋白质在新鲜分离的胸腺细胞中被组成性激活。这些蛋白质包括rel相关的p50同二聚体、p50/p65异二聚体、低水平的c-rel以及另外两种可能是胸腺特异性的因子。胸腺微环境的破坏导致DNA结合能力丧失,这表明淋巴细胞与基质细胞的相互作用诱导并维持这些蛋白质处于DNA结合形式。佛波酯和离子霉素处理可诱导p50、p65和p68 c-rel的κB DNA结合活性。免疫抑制药物FK506可抑制p68 c-rel蛋白的表达,但不影响p50或p65的表达。由于FK506特异性抑制成熟单阳性胸腺细胞的出现,因此由p68 c-rel调节的基因表达可能在双阳性到单阳性转变过程中的选择和成熟信号中发挥作用。