Mehler Mark F
Departments of Neurology, Neuroscience and Psychiatry, Rose F. Kennedy Center for Research in Mental Retardation and Developmental Disabilities, Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Results Probl Cell Differ. 2002;39:27-52. doi: 10.1007/978-3-540-46006-0_2.
During mammalian cerebral cortical development, neural stem cells (NSCs) present within periventricular generative zones give rise to successive waves of neurons and radial glia, followed by oligodendrocytes and astrocytes. The molecular and cellular mechanisms that orchestrate these precisely timed and progressive maturational events are still largely undefined. These developmental processes are likely to involve the dynamic interplay of environmental signals, cell-cell interactions and transcriptional regulatory events. The bone morphogenetic proteins (BMPs), an expanding subclass of the transforming growth factor beta cytokine superfamily, may represent an important set of environmental cues for these progressive maturational events because of the broad profiles of developmental expression of the requisite BMP ligands, receptor subunits and intracellular transduction elements, and because of their versatile roles in promoting a spectrum of cellular processes intimately involved in progressive neural fate decisions. The BMPs also interact with complementary regional environmental signals such as the basic fibroblast growth factor (bFGF) and sonic hedgehog (Shh) that promote earlier stages of NSC expansion, self-renewal, lineage restriction and incipient lineage commitment. The ability of these cytokines and trophic signals to act within specific neurodevelopmental contexts may, in turn, depend on the composite actions of cell-cell contact-associated signals, such as Notch-Hes-mediated lateral inhibitory pathways, and additional transcriptional modulatory events, such as those mediated by members of the inhibitor of differentiation (ID) gene family that encode a novel set of negative basic helix-loop-helix (bHLH) transcription factors. In this chapter, we will examine the distinct roles of these different classes of developmental cues in defining the biological properties of an integrated cerebral cortical developmental signaling network. Ongoing studies in this exciting area of mammalian central nervous system (CNS) development will help to identify important molecular and cellular targets for evolving pharmacological, gene and stem cell therapeutic interventions to combat the pathological sequelae of a spectrum of acquired and genetic disorders of the central nervous system.
在哺乳动物大脑皮质发育过程中,脑室周围生成区的神经干细胞(NSCs)产生连续的神经元和放射状胶质细胞波,随后是少突胶质细胞和星形胶质细胞。协调这些精确计时且逐步成熟事件的分子和细胞机制在很大程度上仍未明确。这些发育过程可能涉及环境信号、细胞间相互作用和转录调控事件的动态相互作用。骨形态发生蛋白(BMPs)是转化生长因子β细胞因子超家族中不断扩大的一个亚类,可能代表了这些逐步成熟事件的一组重要环境线索,这是因为所需BMP配体、受体亚基和细胞内转导元件具有广泛的发育表达谱,还因为它们在促进一系列与神经命运逐步决定密切相关的细胞过程中具有多种作用。BMPs还与互补的区域环境信号相互作用,如碱性成纤维细胞生长因子(bFGF)和音猬因子(Shh),它们促进神经干细胞扩增、自我更新、谱系限制和初始谱系定向的早期阶段。这些细胞因子和营养信号在特定神经发育背景下发挥作用的能力,反过来可能取决于细胞间接触相关信号的复合作用,如Notch-Hes介导的侧向抑制途径,以及其他转录调节事件,如由分化抑制因子(ID)基因家族成员介导的事件,该家族编码一组新的负性碱性螺旋-环-螺旋(bHLH)转录因子。在本章中,我们将研究这些不同类型发育线索在定义整合的大脑皮质发育信号网络生物学特性中的独特作用。在这个令人兴奋的哺乳动物中枢神经系统(CNS)发育领域的持续研究将有助于确定重要的分子和细胞靶点,以发展药理学、基因和干细胞治疗干预措施,来对抗一系列中枢神经系统获得性和遗传性疾病的病理后遗症。