Institute of Anatomy I, University of Jena School of Medicine, Jena University Hospital, Teichgraben 7, 07743, Jena, Germany.
Cerebellum. 2011 Sep;10(3):393-408. doi: 10.1007/s12311-010-0207-4.
Cadherins are cell adhesion molecules with multiple morphogenic functions in brain development, for example, in neuroblast migration and aggregation, axon navigation, neural circuit formation, and synaptogenesis. More than 100 members of the cadherin superfamily are expressed in the developing and mature brain. Most of the cadherins investigated, in particular classic cadherins and δ-protocadherins, are expressed in the cerebellum. For several cadherin subtypes, expression begins at early embryonic stages and persists until mature stages of cerebellar development. At intermediate stages, distinct Purkinje cell clusters exhibit unique rostrocaudal and mediolateral expression profiles for each cadherin. In the chicken, mouse, and other species, the Purkinje cell clusters are separated by intervening raphes of migrating granule cells. This pattern of Purkinje cell clusters/raphes is, at least in part, continuous with the parasagittal striping pattern that is apparent in the mature cerebellar cortex, for example, for zebrin II/aldolase C. Moreover, subregions of the deep cerebellar nuclei, vestibular nuclei and the olivary complex also express cadherins differentially. Neuroanatomical evidence suggests that the nuclear subregions and cortical domains that express the same cadherin subtype are connected to each other, to form neural subcircuits of the cerebellar system. Cadherins thus provide a molecular code that specifies not only embryonic structures but also functional cerebellar compartmentalization. By following the implementation of this code, it can be revealed how mature functional architecture emerges from embryonic patterning during cerebellar development. Dysfunction of some cadherins is associated with psychiatric diseases and developmental impairments and may also affect cerebellar function.
钙黏蛋白是细胞黏附分子,在脑发育中有多种形态发生功能,例如神经母细胞迁移和聚集、轴突导航、神经回路形成和突触发生。在发育和成熟的大脑中表达了钙黏蛋白超家族的 100 多个成员。研究最多的钙黏蛋白,特别是经典钙黏蛋白和δ-原钙黏蛋白,在小脑中有表达。对于几种钙黏蛋白亚型,其表达始于胚胎早期,并持续到小脑发育的成熟阶段。在中间阶段,不同的浦肯野细胞簇表现出每个钙黏蛋白独特的头尾和内外表达模式。在鸡、鼠和其他物种中,浦肯野细胞簇由迁移的颗粒细胞的中间隔带隔开。这种浦肯野细胞簇/隔带的模式至少部分与成熟小脑皮质中明显的矢状条纹模式连续,例如,对于脑苷脂 II/醛缩酶 C。此外,小脑深部核、前庭核和橄榄复合体的亚区也表现出不同的钙黏蛋白表达。神经解剖学证据表明,表达相同钙黏蛋白亚型的核亚区和皮质域相互连接,形成小脑系统的神经亚回路。钙黏蛋白因此提供了一种分子编码,不仅指定了胚胎结构,还指定了功能性小脑分区。通过遵循这个编码的实现,可以揭示成熟的功能结构如何从小脑发育过程中的胚胎模式中出现。一些钙黏蛋白的功能障碍与精神疾病和发育障碍有关,也可能影响小脑功能。