Veselý J, Macáková J, Dostálová K, Riegrová D, Cervenková K
Ustav patologické fyziologie, LF UP Olomouc.
Cesk Fysiol. 2003 Feb;52(1):10-4.
Expression of cyclin-dependent kinase 5 (Cdk5) gradually increases during embryonal development until it reaches maximal levels that persist in the adult brain. Cdk5 represents a key component in the reelin signalling cascade. Activity of p35/Cdk5 is critical for the development of normal, six-layered structure of the mammalian brain cortex. Although it is not required for splitting of the cortical pre-plate into the marginal zone and sub-plate, a process that is affected in absence of the reelin and/or Dab1, it is substantial for the later-born neurons to bypass sub-plate neurons and to enter into the embryonal cortical plate. The defect of p35/Cdk5 disrupts the classical inside-out histogenetic pattern of neocortex. Neurons that fail to migrate past older layers of cells accumulate beneath the sub-plate thus forming an abnormal, inverted outside-in configuration in p35/Cdk5 defective animals. Exploration of neuronal migration disturbancies can shed new light on some diseases of human brain development including different heterotopias and lissencephaly. From an evolutionary point of view, the involvement of Cdk5 in the reelin signalling cascade could define a new step in the brain gray matter development.
细胞周期蛋白依赖性激酶5(Cdk5)的表达在胚胎发育过程中逐渐增加,直至达到在成人大脑中持续存在的最高水平。Cdk5是Reelin信号级联反应中的关键成分。p35/Cdk5的活性对于哺乳动物大脑皮层正常六层结构的发育至关重要。虽然它对于将皮质前板分裂为边缘区和亚板不是必需的(在缺乏Reelin和/或Dab1时该过程会受到影响),但对于较晚生成的神经元绕过亚板神经元并进入胚胎皮质板来说却是至关重要的。p35/Cdk5的缺陷会破坏新皮质经典的由内向外的组织发生模式。未能迁移越过较老细胞层的神经元会在亚板下方积聚,从而在p35/Cdk5缺陷动物中形成异常的、由外向内倒置的结构。对神经元迁移障碍的研究可以为一些人类大脑发育疾病,包括不同类型的异位症和无脑回畸形,提供新的线索。从进化的角度来看,Cdk5参与Reelin信号级联反应可能标志着大脑灰质发育的一个新步骤。