Patten Brooke A, Peyrin Jean Michel, Weinmaster Gerry, Corfas Gabriel
Division of Neuroscience, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Neurosci. 2003 Jul 9;23(14):6132-40. doi: 10.1523/JNEUROSCI.23-14-06132.2003.
Radial glia cells both generate neurons and physically guide nascent neurons to their target destination in the cortex, and as such they are essential for CNS development. It has been proposed that in the developing cerebellum, neuronal contact induces radial glia formation, however, the mechanisms involved in this process are not well understood. Here we demonstrate that neuronal induction of radial glia formation is the result of sequential signaling through Notch1 and erbB receptors. First, Notch1 activation by neuronal contact induces the glial expression of the brain lipid binding protein (BLBP) and erbB2 genes. Interestingly, two different signaling pathways mediate these effects of Notch1 on transcription, BLBP expression being dependent on Su(H), whereas erbB2 is regulated by a yet unidentified Notch1 pathway. The subsequent increase in erbB2 receptor expression makes the glia more responsive to neuronal NRG, which then induces the morphological transformation into radial glia. Thus, these results unveil some of the mechanisms underlying radial glia formation.
放射状胶质细胞既能产生神经元,又能将新生神经元物理引导至皮质中的目标位置,因此它们对中枢神经系统的发育至关重要。有人提出,在发育中的小脑中,神经元接触会诱导放射状胶质细胞形成,然而,这一过程所涉及的机制尚不清楚。在此我们证明,神经元诱导放射状胶质细胞形成是通过Notch1和erbB受体进行顺序信号传导的结果。首先,神经元接触激活Notch1会诱导脑脂质结合蛋白(BLBP)和erbB2基因的胶质细胞表达。有趣的是,两条不同的信号通路介导了Notch1对转录的这些影响,BLBP的表达依赖于Su(H),而erbB2则由一条尚未明确的Notch1通路调控。随后erbB2受体表达的增加使胶质细胞对神经元神经调节蛋白(NRG)更敏感,进而诱导其形态转变为放射状胶质细胞。因此,这些结果揭示了放射状胶质细胞形成的一些潜在机制。