Gritti Angela, Bonfanti Luca
San Raffaele Telethon Institute for Gene Therapy, San Raffaele Scientific Institute, Via Olgettina 58, 20132-Milan, Italy.
Neuron Glia Biol. 2007 Nov;3(4):309-23. doi: 10.1017/S1740925X0800001X.
Essentially, three neuroectodermal-derived cell types make up the complex architecture of the adult CNS: neurons, astrocytes and oligodendrocytes. These elements are endowed with remarkable morphological, molecular and functional heterogeneity that reaches its maximal expression during development when stem/progenitor cells undergo progressive changes that drive them to a fully differentiated state. During this period the transient expression of molecular markers hampers precise identification of cell categories, even in neuronal and glial domains. These issues of developmental biology are recapitulated partially during the neurogenic processes that persist in discrete regions of the adult brain. The recent hypothesis that adult neural stem cells (NSCs) show a glial identity and derive directly from radial glia raises questions concerning the neuronal-glial relationships during pre- and post-natal brain development. The fact that NSCs isolated in vitro differentiate mainly into astrocytes, whereas in vivo they produce mainly neurons highlights the importance of epigenetic signals in the neurogenic niches, where glial cells and neurons exert mutual influences. Unravelling the mechanisms that underlie NSC plasticity in vivo and in vitro is crucial to understanding adult neurogenesis and exploiting this physiological process for brain repair. In this review we address the issues of neuronal/glial cell identity and neuronal-glial interactions in the context of NSC biology and NSC-driven neurogenesis during development and adulthood in vivo, focusing mainly on the CNS. We also discuss the peculiarities of neuronal-glial relationships for NSCs and their progeny in the context of in vitro systems.
从本质上讲,三种神经外胚层来源的细胞类型构成了成体中枢神经系统的复杂结构:神经元、星形胶质细胞和少突胶质细胞。这些细胞成分具有显著的形态、分子和功能异质性,在发育过程中,当干细胞/祖细胞经历渐进性变化并被驱动至完全分化状态时,这种异质性达到最大程度的表达。在此期间,分子标记物的短暂表达阻碍了细胞类别的精确识别,即使在神经元和神经胶质区域也是如此。成体大脑离散区域持续存在的神经发生过程部分重现了这些发育生物学问题。最近的假说认为,成体神经干细胞(NSC)具有神经胶质细胞的特征,并且直接来源于放射状胶质细胞,这引发了关于产前和产后大脑发育过程中神经元与神经胶质细胞关系的问题。体外分离的神经干细胞主要分化为星形胶质细胞,而在体内它们主要产生神经元,这一事实凸显了神经发生微环境中表观遗传信号的重要性,在该微环境中神经胶质细胞和神经元相互影响。阐明神经干细胞在体内和体外可塑性的潜在机制,对于理解成体神经发生以及利用这一生理过程进行脑修复至关重要。在这篇综述中,我们在神经干细胞生物学以及体内发育和成年期神经干细胞驱动的神经发生的背景下,探讨神经元/神经胶质细胞身份以及神经元 - 神经胶质细胞相互作用的问题,主要聚焦于中枢神经系统。我们还将讨论在体外系统背景下神经干细胞及其后代的神经元 - 神经胶质细胞关系的特殊性。