Urich H
Clin Exp Neurol. 1984;20:203-15.
Dendritic plasticity in man is analysed on the example of the Purkinje cell. The conspicuous and easily demonstrable dendrites of this cell lend themselves particularly to such a study. Abnormalities of the dendritic tree have been observed in a variety of conditions, some of them originating in early infancy, others acquired in later life, all of them associated with a substantial loss of granule cells. While differences between the various diseases undoubtedly exist, the basic pattern remains remarkably constant. Three types of dendritic abnormality may be present: (i) persistence or neoformation of somal dendrites; (ii) expansion and malorientation of primary apical dendrites (the staghorn deformity); and (iii) bizarre ramification of secondary and tertiary dendrites, sometimes associated with expansions known as cactus, stellate or sunray figures. It is suggested that all these features should be interpreted as a response of the Purkinje cell to partial deafferentation and not as congenital malformations. In addition, dislocation of the Purkinje cell into the molecular layer is frequently seen in this group of cases. This may be ascribed to loss of tethering of the cell by its afferent fibres.
以浦肯野细胞为例对人类树突可塑性进行分析。该细胞明显且易于显示的树突特别适合此类研究。在多种情况下都观察到了树突树的异常,其中一些始于婴儿早期,另一些则在晚年获得,所有这些都与颗粒细胞的大量丧失有关。虽然各种疾病之间无疑存在差异,但基本模式仍非常恒定。可能存在三种类型的树突异常:(i)体细胞树突的持续存在或新形成;(ii)初级顶树突的扩张和方向异常(鹿角畸形);(iii)次级和三级树突的奇异分支,有时与称为仙人掌、星状或射线状图形的扩张有关。有人认为,所有这些特征都应解释为浦肯野细胞对部分传入神经阻滞的反应,而不是先天性畸形。此外,在这组病例中经常可以看到浦肯野细胞移位到分子层。这可能归因于细胞被其传入纤维的束缚丧失。