Conti L, De Fraja C, Gulisano M, Migliaccio E, Govoni S, Cattaneo E
Institute of Pharmacological Sciences, University of Milano, Via Balzaretti 9, Milan 20133, Italy.
Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):8185-90. doi: 10.1073/pnas.94.15.8185.
The adult mammalian brain comprises many functionally distinct neuronal types, which are generated during development as a result of a coordinated signaling cascade that drives neuroblasts from proliferation into differentiation. We investigated whether and how ShcA adaptor proteins, which are known to function as initiators of the Ras signaling cascade in various nonneuronal systems where they have been considered to be expressed ubiquitously, are involved in the proliferative and differentiative phases of the developing brain. We found that in the forebrain expression and activation of ShcA proteins were strictly regulated during embryonic development, both temporally and spatially. The mRNAs encoded by the ShcA gene were expressed exclusively within an area to which active proliferation of immature neuroblasts was confined, the ventricular zone. In postnatal and adult brain, ShcA mRNAs and proteins were present only faintly. In the adult olfactory epithelium, in which neuronal cell renewal occurs throughout life, ShcA remained strongly expressed. These phenomena were peculiar to ShcA, since Grb2 adaptor protein remained expressed at constant level throughout development. The embryonically expressed ShcA proteins were functionally active, since p52(ShcA) became phosphorylated on tyrosine and associated with Grb2 following intraventricular injection of epidermal growth factor in the embryonic brain. Our data indicate that, through an orderly pattern of expression, ShcA gene products may play a role in the control of the switch between proliferation and differentiation of brain neuroblasts.
成年哺乳动物的大脑包含许多功能不同的神经元类型,这些神经元类型在发育过程中由协调的信号级联反应产生,该信号级联反应促使神经母细胞从增殖阶段进入分化阶段。我们研究了ShcA衔接蛋白是否以及如何参与发育中大脑的增殖和分化阶段,已知ShcA衔接蛋白在各种非神经元系统中作为Ras信号级联反应的启动子发挥作用,并且在这些系统中被认为是普遍表达的。我们发现,在前脑,ShcA蛋白的表达和激活在胚胎发育过程中在时间和空间上都受到严格调控。ShcA基因编码的mRNA仅在未成熟神经母细胞活跃增殖的区域即脑室区表达。在出生后和成年大脑中,ShcA的mRNA和蛋白仅微弱存在。在成年嗅上皮中,神经元细胞终生更新,ShcA仍强烈表达。这些现象是ShcA特有的,因为Grb2衔接蛋白在整个发育过程中保持恒定水平的表达。胚胎期表达的ShcA蛋白具有功能活性,因为在胚胎脑室内注射表皮生长因子后,p52(ShcA)在酪氨酸上磷酸化并与Grb2结合。我们的数据表明,通过有序的表达模式,ShcA基因产物可能在控制脑成神经细胞增殖和分化之间的转换中发挥作用。