Furne Céline, Rama Nicolas, Corset Véronique, Chédotal Alain, Mehlen Patrick
Apoptosis, Cancer, and Development Laboratory, Equipe labellisée La Ligue, Centre Léon Berard and Unité Mixte de Recherche 5238, Centre National de la Recherche Scientifique, Université de Lyon, 69008 Lyon, France.
Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14465-70. doi: 10.1073/pnas.0803645105. Epub 2008 Sep 16.
DCC (Deleted in Colorectal Cancer) is a putative tumor suppressor whose expression is lost in numerous cancers and whose tumor suppressor activity appears to be dependent on its ability to trigger apoptosis when disengaged by its ligand netrin-1. In this sense, netrin-1 is a survival factor that controls tumorigenesis. However, netrin-1 is also the prototypical axon guidance cue and has been shown to orient many neurons or axons, especially commissural axons, during spinal cord development. Here we show that netrin-1 is not only an attractive cue for developing commissural axons but also promotes their survival. In primary neuronal culture, in mice or in chick embryos, netrin-1 inhibits the proapoptotic activity of DCC in developing commissural neurons. Thus, adequate commissural neurons navigation requires both the attractive activity of netrin-1 and the anti-apoptotic function of this cue.
结直肠癌缺失基因(DCC)是一种假定的肿瘤抑制因子,其表达在多种癌症中缺失,并且其肿瘤抑制活性似乎取决于其在与配体网蛋白-1分离时触发细胞凋亡的能力。从这个意义上说,网蛋白-1是一种控制肿瘤发生的生存因子。然而,网蛋白-1也是典型的轴突导向信号,并且已被证明在脊髓发育过程中可引导许多神经元或轴突,特别是连合轴突。在这里我们表明,网蛋白-1不仅是发育中连合轴突的吸引信号,还能促进它们的存活。在原代神经元培养、小鼠或鸡胚中,网蛋白-1可抑制发育中连合神经元中DCC的促凋亡活性。因此,连合神经元的充分导航既需要网蛋白-1的吸引活性,也需要该信号的抗凋亡功能。