[HTML][HTML] Human stem cell models of neurodegeneration: From basic science of amyotrophic lateral sclerosis to clinical translation

E Giacomelli, BF Vahsen, EL Calder, Y Xu, J Scaber… - Cell Stem Cell, 2022 - cell.com
Neurodegenerative diseases are characterized by progressive cell loss leading to disruption
of the structure and function of the central nervous system. Amyotrophic lateral sclerosis …

Recent insights on astrocyte mechanisms in CNS homeostasis, pathology, and repair

CG Hart, S Karimi‐Abdolrezaee - Journal of neuroscience …, 2021 - Wiley Online Library
Astrocytes play essential roles in development, homeostasis, injury, and repair of the central
nervous system (CNS). Their development is tightly regulated by distinct spatial and …

Generation of Human iPSC-Derived Astrocytes with a mature star-shaped phenotype for CNS modeling

D Voulgaris, P Nikolakopoulou, A Herland - Stem Cell Reviews and …, 2022 - Springer
The generation of astrocytes from human induced pluripotent stem cells has been hampered
by either prolonged differentiation—spanning over two months—or by shorter protocols that …

Human astrocytes model derived from induced pluripotent stem cells

N Leventoux, S Morimoto, K Imaizumi, Y Sato… - Cells, 2020 - mdpi.com
Induced pluripotent stem cell (iPSC)-based disease modeling has a great potential for
uncovering the mechanisms of pathogenesis, especially in the case of neurodegenerative …

Metabolism in pluripotency: Both driver and passenger?

P Dahan, V Lu, RMT Nguyen, SAL Kennedy… - Journal of Biological …, 2019 - ASBMB
Pluripotent stem cells (PSCs) are highly proliferative cells characterized by robust metabolic
demands to power rapid division. For many years considered a passive component or" …

[HTML][HTML] MeCP2 controls neural stem cell fate specification through miR-199a-mediated inhibition of BMP-Smad signaling

H Nakashima, K Tsujimura, K Irie, T Imamura… - Cell Reports, 2021 - cell.com
Rett syndrome (RTT) is a severe neurological disorder, with impaired brain development
caused by mutations in MECP2; however, the underlying mechanism remains elusive. We …

Glial dysfunction in MeCP2 deficiency models: implications for Rett syndrome

U Kahanovitch, KC Patterson, R Hernandez… - International Journal of …, 2019 - mdpi.com
Rett syndrome (RTT) is a rare, X-linked neurodevelopmental disorder typically affecting
females, resulting in a range of symptoms including autistic features, intellectual impairment …

Emerging mechanisms underlying astrogenesis in the developing mammalian brain

J Takouda, S Katada, K Nakashima - Proceedings of the Japan …, 2017 - jstage.jst.go.jp
In the developing brain, the three major cell types, ie, neurons, astrocytes and
oligodendrocytes, are generated from common multipotent neural stem cells (NSCs). In …

A tale of two: when neural stem cells encounter hypoxia

Y Fan, J Li, B Fang - Cellular and molecular neurobiology, 2023 - Springer
Normoxia is defined as an oxygen concentration of 20.9%, as in room air, whereas hypoxia
refers to any oxygen concentration less than this. Any physiological oxygen deficiency or …

Astrocytic modulation of excitatory synaptic signaling in a mouse model of Rett syndrome

B Rakela, P Brehm, G Mandel - Elife, 2018 - elifesciences.org
Studies linking mutations in Methyl CpG Binding Protein 2 (MeCP2) to physiological defects
in the neurological disease, Rett syndrome, have focused largely upon neuronal dysfunction …