Wilsch-Bräuninger Michaela, Huttner Wieland B
Max-Planck-Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Front Neurosci. 2021 Oct 21;15:755867. doi: 10.3389/fnins.2021.755867. eCollection 2021.
During mammalian brain development, neural stem and progenitor cells generate the neurons for the six-layered neocortex. The proliferative capacity of the different types of progenitor cells within the germinal zones of the developing neocortex is a major determinant for the number of neurons generated. Furthermore, the various modes of progenitor cell divisions, for which the orientation of the mitotic spindle of progenitor cells has a pivotal role, are a key parameter to ensure the appropriate size and proper cytoarchitecture of the neocortex. Here, we review the roles of primary cilia and centrosomes of progenitor cells in these processes during neocortical development. We specifically focus on the apical progenitor cells in the ventricular zone. In particular, we address the alternating, dual role of the mother centriole (i) as a component of one of the spindle poles during mitosis, and (ii) as the basal body of the primary cilium in interphase, which is pivotal for the fate of apical progenitor cells and their proliferative capacity. We also discuss the interactions of these organelles with the microtubule and actin cytoskeleton, and with junctional complexes. Centriolar appendages have a specific role in this interaction with the cell cortex and the plasma membrane. Another topic of this review is the specific molecular composition of the ciliary membrane and the membrane vesicle traffic to the primary cilium of apical progenitors, which underlie the ciliary signaling during neocortical development; this signaling itself, however, is not covered in depth here. We also discuss the recently emerging evidence regarding the composition and roles of primary cilia and centrosomes in basal progenitors, a class of progenitors thought to be of particular importance for neocortex expansion in development and evolution. While the tight interplay between primary cilia and centrosomes makes it difficult to allocate independent roles to either organelle, mutations in genes encoding ciliary and/or centrosome proteins indicate that both are necessary for the formation of a properly sized and functioning neocortex during development. Human neocortical malformations, like microcephaly, underpin the importance of primary cilia/centrosome-related processes in neocortical development and provide fundamental insight into the underlying mechanisms involved.
在哺乳动物大脑发育过程中,神经干细胞和祖细胞生成了具有六层结构的新皮层中的神经元。发育中的新皮层生发区内不同类型祖细胞的增殖能力是所生成神经元数量的主要决定因素。此外,祖细胞的各种分裂模式对于确保新皮层的适当大小和正常细胞结构至关重要,其中祖细胞有丝分裂纺锤体的方向起着关键作用。在此,我们综述了祖细胞的初级纤毛和中心体在新皮层发育这些过程中的作用。我们特别关注脑室区的顶端祖细胞。具体而言,我们探讨母中心粒的双重交替作用:(i)在有丝分裂期间作为纺锤体极之一的组成部分;(ii)在间期作为初级纤毛的基体,这对顶端祖细胞的命运及其增殖能力至关重要。我们还讨论了这些细胞器与微管和肌动蛋白细胞骨架以及连接复合体的相互作用。中心粒附属物在与细胞皮层和质膜的这种相互作用中具有特定作用。本综述的另一个主题是纤毛膜的特定分子组成以及向顶端祖细胞初级纤毛的膜囊泡运输,这是新皮层发育期间纤毛信号传导的基础;然而,这里不深入讨论这种信号传导本身。我们还讨论了关于初级纤毛和中心体在基底祖细胞中的组成和作用的最新证据,基底祖细胞被认为在发育和进化中对新皮层扩展特别重要。虽然初级纤毛和中心体之间紧密的相互作用使得难以给任何一个细胞器分配独立的作用,但编码纤毛和/或中心体蛋白的基因突变表明,两者对于发育过程中形成大小合适且功能正常的新皮层都是必需的。人类新皮层畸形,如小头畸形,突显了初级纤毛/中心体相关过程在新皮层发育中的重要性,并为所涉及的潜在机制提供了基本见解。