McMahon S B, Monroe J G
Department of Pathology and Laboratory Medicine, School of Medicine, University of Pennsylvania, Philadelphia 19104.
J Exp Med. 1995 Jan 1;181(1):417-22. doi: 10.1084/jem.181.1.417.
The primary response gene egr-1 encodes a sequence-specific transcription factor whose expression is necessary for antigen receptor-stimulated activation of B lymphocytes. The molecular processes involved in linking egr-1 induction to antigen receptor signaling have not been defined. The present study demonstrates that expression of an activated form of p21ras results in egr-1 induction similar to that previously shown after antigen receptor cross-linking. In addition, both antigen receptor cross-linking and p21ras use the same element in the egr-1 promoter to exert their effects. Using dominant-negative mutants of p21ras and raf-1, we demonstrate that induction of egr-1 after antigen receptor cross-linking is mediated by activation of the p21ras/mitogen-activated protein kinase signaling pathway. While regulation of the p21ras pathway during B cell activation has been intensively studied, this report represents the first description of a biologically relevant event associated with its activation.
初级反应基因egr-1编码一种序列特异性转录因子,其表达对于抗原受体刺激的B淋巴细胞活化是必需的。将egr-1诱导与抗原受体信号传导联系起来的分子过程尚未明确。本研究表明,活化形式的p21ras的表达导致egr-1诱导,类似于先前在抗原受体交联后所显示的情况。此外,抗原受体交联和p21ras均使用egr-1启动子中的相同元件来发挥其作用。使用p21ras和raf-1的显性负性突变体,我们证明抗原受体交联后egr-1的诱导是由p21ras/丝裂原活化蛋白激酶信号通路的激活介导的。虽然在B细胞活化过程中对p21ras途径的调节已进行了深入研究,但本报告首次描述了与其激活相关的生物学相关事件。