Beffert Uwe, Morfini Gerardo, Bock Hans H, Reyna Huichuan, Brady Scott T, Herz Joachim
Department of Molecular Genetics, Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9046, USA.
J Biol Chem. 2002 Dec 20;277(51):49958-64. doi: 10.1074/jbc.M209205200. Epub 2002 Oct 9.
Reelin is a large secreted protein that controls cortical layering by signaling through the very low density lipoprotein receptor and apolipoprotein E receptor 2, thereby inducing tyrosine phosphorylation of the adaptor protein Disabled-1 (Dab1) and suppressing tau phosphorylation in vivo. Here we show that binding of Reelin to these receptors stimulates phosphatidylinositol 3-kinase, resulting in activation of protein kinase B and inhibition of glycogen synthase kinase 3beta. We present genetic evidence that this cascade is dependent on apolipoprotein E receptor 2, very low density lipoprotein receptor, and Dab1. Reelin-signaling components are enriched in axonal growth cones, where tyrosine phosphorylation of Dab1 is increased in response to Reelin. These findings suggest that Reelin-mediated phosphatidylinositol 3-kinase signaling in neuronal growth cones contributes to final neuron positioning in the mammalian brain by local modulation of protein kinase B and glycogen synthase kinase 3beta kinase activities.
Reelin是一种大型分泌蛋白,它通过极低密度脂蛋白受体和载脂蛋白E受体2发出信号来控制皮质分层,从而在体内诱导衔接蛋白Disabled-1(Dab1)的酪氨酸磷酸化并抑制tau蛋白磷酸化。我们在此表明,Reelin与这些受体的结合会刺激磷脂酰肌醇3激酶,导致蛋白激酶B激活并抑制糖原合酶激酶3β。我们提供了遗传学证据,证明该级联反应依赖于载脂蛋白E受体2、极低密度脂蛋白受体和Dab1。Reelin信号成分在轴突生长锥中富集,其中Dab1的酪氨酸磷酸化会因Reelin而增加。这些发现表明,神经元生长锥中Reelin介导的磷脂酰肌醇3激酶信号传导通过局部调节蛋白激酶B和糖原合酶激酶3β激酶活性,有助于哺乳动物大脑中最终神经元的定位。