Tang Y, Marwaha S, Rutkowski J L, Tennekoon G I, Phillips P C, Field J
Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5139-44. doi: 10.1073/pnas.95.9.5139.
Neurofibromatosis type 1 (NF1), a common autosomal dominant disorder caused by loss of the NF1 gene, is characterized clinically by neurofibromas and more rarely by neurofibrosarcomas. Neurofibromin, the protein encoded by NF1, possesses an intrinsic GTPase accelerating activity for the Ras proto-oncogene. Through this activity, it is a negative regulator of Ras. The Pak protein kinase is a candidate for a downstream signaling protein that may mediate Ras signals because it is activated by Rac and Cdc42, two small G proteins required for Ras signaling. Here, we use Pak mutants to explore the role of Pak in Ras signaling in Schwann cells, the cells affected in NF1. Whereas an activated Pak mutant does not transform cells, dominant negative Pak mutants are potent inhibitors of Ras transformation of rat Schwann cells and of a neurofibrosarcoma cell line from an NF1 patient. Although activated Pak stimulated jun-N-terminal kinase, inhibition of Ras transformation by dominant negative Pak did not require inhibition of jun-N-terminal kinase. Instead, the Pak mutants appeared to inhibit transformation by preventing Ras activation of the ERK/mitogen-activated protein kinase cascade. These results have implications for our understanding of NF1 because a neurofibrosarcoma cell line derived from a patient with NF1 was reverted by stable expression of the Pak dominant negative mutants.
1型神经纤维瘤病(NF1)是一种由NF1基因缺失引起的常见常染色体显性疾病,其临床特征为神经纤维瘤,较少见的为神经纤维肉瘤。神经纤维瘤蛋白是由NF1编码的蛋白质,对Ras原癌基因具有内在的GTP酶加速活性。通过这种活性,它是Ras的负调节因子。Pak蛋白激酶是下游信号蛋白的候选者,可能介导Ras信号,因为它被Rac和Cdc42激活,这是Ras信号传导所需的两种小G蛋白。在这里,我们使用Pak突变体来探索Pak在雪旺细胞(NF1中受影响的细胞)的Ras信号传导中的作用。虽然激活的Pak突变体不会转化细胞,但显性负性Pak突变体是大鼠雪旺细胞和来自NF1患者的神经纤维肉瘤细胞系的Ras转化的有效抑制剂。虽然激活的Pak刺激了Jun氨基末端激酶,但显性负性Pak对Ras转化的抑制并不需要抑制Jun氨基末端激酶。相反,Pak突变体似乎通过阻止Ras激活ERK/丝裂原活化蛋白激酶级联反应来抑制转化。这些结果对我们理解NF1有启示意义,因为来自NF1患者的神经纤维肉瘤细胞系通过Pak显性负性突变体的稳定表达而恢复正常。