Stewart H J
Department of Anatomy and Developmental Biology, University College London, UK.
Eur J Neurosci. 1995 Jun 1;7(6):1366-75. doi: 10.1111/j.1460-9568.1995.tb01128.x.
In order to identify the transcription factors that may be involved in the development and differentiation of rat Schwann cells we examined the expression of c-Jun, Jun B, Jun D and the cAMP response element binding protein (CREB) in vivo and in vitro. We found that CREB was expressed at high levels throughout nerve development by both Schwann cells and their precursors. Jun family members, on the other hand, were expressed only at low levels in a few nuclei of the developing nerve. After sciatic nerve transection, however, c-Jun levels were rapidly up-regulated in many Schwann cells of the distal stump but CREB, Jun B and Jun D levels were not affected. When nerve contact was resumed after crush injury c-Jun levels returned to control values. Interestingly, unlike the situation in vivo, when Schwann cells were removed from the nerve and cultured, levels of all three Jun family members were rapidly up-regulated. This also occurred in Schwann cell precursors. In other experiments we found that Schwann cell c-Jun, but not Jun B or Jun D, expression was down-regulated by the adenylate cyclase activator, forskolin. In addition, we show that the forskolin induced down-regulation of c-Jun is not necessary for Schwann cell proliferation or myelination to occur.
为了鉴定可能参与大鼠雪旺细胞发育和分化的转录因子,我们在体内和体外检测了c-Jun、Jun B、Jun D以及环磷酸腺苷反应元件结合蛋白(CREB)的表达。我们发现,在整个神经发育过程中,雪旺细胞及其前体细胞均高水平表达CREB。另一方面,Jun家族成员仅在发育中神经的少数细胞核中低水平表达。然而,坐骨神经横断后,远侧断端的许多雪旺细胞中c-Jun水平迅速上调,但CREB、Jun B和Jun D水平未受影响。挤压伤后恢复神经接触时,c-Jun水平恢复到对照值。有趣的是,与体内情况不同,当雪旺细胞从神经中分离并培养时,所有三种Jun家族成员的水平均迅速上调。雪旺细胞前体细胞中也出现这种情况。在其他实验中,我们发现腺苷酸环化酶激活剂福斯可林可下调雪旺细胞c-Jun的表达,但对Jun B或Jun D无此作用。此外,我们还表明,福斯可林诱导的c-Jun下调对于雪旺细胞增殖或髓鞘形成并非必需。