Cerebral cortex (New York, N.Y. : 1991) · 2019
PDK1 Deficit Impairs the Development of the Dentate Gyrus in Mice.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Xu Min, Han Xiaoning, Liu Rui, Li Yanjun, Qi Cui, Yang Zhongzhou, Zhao Chunjie, Gao Jun
Аннотация
3-Phosphoinositide-dependent protein kinase-1 (PDK1) is crucial for the development of the dentate gyrus (DG), the first gateway receiving afferent inputs from the entorhinal cortex. However, the role of PDK1 in DG development is unclear. In the present study, by crossing Pdk1fl/fl mice with the Emx1-cre line, we identified that the ablation of PDK1 disrupted the development of DG via decreasing the proliferation, and increasing the differentiation of dentate neural progenitor cells, downregulating AKT activity and upregulating GSK3β signaling. Moreover, PDK1 deletion disrupted the distribution of Reelin+ cells and decreased the level of Reelin mRNA which may contribute to the defective migration of progenitor cells and the disrupted radial glial scaffolds. Furthermore, the inhibition of GSK3β activity partially restored the decreased proliferation of primary neural stem cells in vitro. Taken together, our data indicated that the ablation of PDK1 affected the proliferation and differentiation of dentate neural progenitor cells in mice.
Предметные рубрики MeSH
3-Phosphoinositide-Dependent Protein KinasesAnimalsCell Adhesion Molecules, NeuronalCell DifferentiationCell ProliferationCells, CulturedDentate GyrusExtracellular Matrix ProteinsFemaleGlycogen Synthase Kinase 3 betaMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsNeural Stem CellsNeurogliaProto-Oncogene Proteins c-aktReelin ProteinSerine EndopeptidasesSignal Transduction