期刊
JOURNAL OF NEUROCHEMISTRY
卷 -, 期 -, 页码 -出版社
WILEY
DOI: 10.1111/jnc.15925
关键词
amyloid precursor protein; cortex development; neuronal migration; Rab21 GTPase
The development of mammalian neocortex requires migration of neurons from the ventricular zone to the cortical plate. This migration is regulated by small GTPase Rab21, which influences cell migration by controlling the trafficking of endocytic vesicles containing adhesion molecules. In this study, it is demonstrated that Rab21 plays a critical role in cortical neuronal differentiation and migration by regulating amyloid precursor protein levels on the neuronal cell surface. These findings improve our understanding of cerebral cortex development and cortical development disorders associated with Rab21 signaling effectors malfunction.
Development of the mammalian neocortex requires proper inside-out migration of developing cortical neurons from the germinal ventricular zone toward the cortical plate. The mechanics of this migration requires precise coordination of different cellular phenomena including cytoskeleton dynamics, membrane trafficking, and cell adhesion. The small GTPases play a central role in all these events. The small GTPase Rab21 regulates migration and neurite growth in developing neurons. Moreover, regulators and effectors of Rab21 have been implicated in brain pathologies with cortical malformations, suggesting a key function for the Rab21 signaling pathway in cortical development. Mechanistically, it has been posited that Rab21 influences cell migration by controlling the trafficking of endocytic vesicles containing adhesion molecules. However, direct evidence of the participation of Rab21 or its mechanism of action in the regulation of cortical migration is still incomplete. In this study, we demonstrate that Rab21 plays a critical role in the differentiation and migration of pyramidal neurons by regulating the levels of the amyloid precursor protein on the neuronal cell surface. Rab21 loss of function increased the levels of membrane-exposed APP, resulting in impaired cortical neuronal differentiation and migration. These findings further our understanding of the processes governing the development of the cerebral cortex and shed light onto the molecular mechanisms behind cortical development disorders derived from the malfunctioning of Rab21 signaling effectors.
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