β2-Microglobulin Is a Systemic Pro-Aging Factor that Impairs Cognitive Function and Neurogenesis Scientists identified β2-microglobulin, a component of major histocompatibility complex class 1 molecules, as a circulating factor that negatively regulates cognitive and regenerative function in the adult hippocampus in an age-dependent manner. [Nat Med] Abstract | Press Release Transcriptional Mechanisms of Proneural Factors and REST in Regulating Neuronal Reprogramming of Astrocytes Recently, the authors demonstrated that expression of Neurog2 or Ascl1 in postnatal mouse astrocytes generates glutamatergic or GABAergic neurons. In this study, they took advantage of this model to study dynamics of neuronal cell fate acquisition at the transcriptional level. [Cell Stem Cell] Abstract | Graphical Abstract Nuclear Pore Complex Remodeling by p75NTR Cleavage Controls TGF-β Signaling and Astrocyte Functions Scientists showed that cleaved p75 neurotrophin receptor (p75NTR) is a component of the nuclear pore complex required for glial scar formation and reduced gamma oscillations in mice via regulation of transforming growth factor (TGF)-β signaling. [Nat Neurosci] Abstract A Post-Transcriptional Mechanism Pacing Expression of Neural Genes with Precursor Cell Differentiation Status Scientists showed that 3′-untranslated regions of multiple neural transcripts contain AU-rich cis-elements (AREs) recognized by tristetraprolin (TTP/Zfp36), an RNA-binding protein previously implicated in regulation of mRNA stability. They also demonstrated that the efficiency of ARE-dependent mRNA degradation declines in the neural lineage because of a decrease in the TTP protein expression mediated by the nervous system-enriched microRNA miR-9. [Nat Commun] Full Article | Press Release Cytomegalovirus Infection Induces a Stem Cell Phenotype in Human Primary Glioblastoma Cells: Prognostic Significance and Biological Impact Researchers investigated the relation between human cytomegalovirus (HCMV) infection of glioblastoma (GBM) cells and the presence of glioma cancer stem cells (GCSCs). The extent to which HCMV infection of primary GBM cells induced a GCSC phenotype was evaluated in vitro. [Cell Death Differ] Abstract Generation and Isolation of Oligodendrocyte Progenitor Cells from Human Pluripotent Stem Cells This protocol describes a robust, fast and reproducible differentiation protocol to generate human oligodendrocytes from pluripotent stem cells using a chemically defined, growth factor-rich medium. [Nat Protoc] Abstract Ets Factors Regulate Neural Stem Cell Depletion and Gliogenesis in Ras Pathway Glioma Investigators provide evidence that disruption of the Nf1-Ras pathway in the ventricular zone at multiple signaling nodes uniformly results in rapid neural stem cell depletion, progenitor hyperproliferation, and gliogenic lineage restriction. [Cell Rep] Full Article | Graphical Abstract The Regulatory Machinery of Neurodegeneration in In Vitro Models of Amyotrophic Lateral Sclerosis Researchers assembled a genome-wide regulatory model, whose unbiased interrogation revealed 23 candidate causal master regulators of neurodegeneration in an in vitro model of amyotrophic lateral sclerosis, characterized by a loss of spinal motor neurons. [Cell Rep] Full Article | Graphical Abstract Physiologically Normal 5% O2 Supports Neuronal Differentiation and Resistance to Inflammatory Injury in Neural Stem Cell Cultures Scientists demonstrated that culturing under 5% O2 conditions results in higher levels of mitochondrial oxidative metabolism, decreased glycolysis, and reduced levels of reactive oxygen species in neural stem cell cultures. [J Neurosci Res] Abstract Generation of Late-Born Neurons in the Ventral Spinal Cord Requires the Coordination of Retinoic Acid and Notch Signaling Researchers investigated the role of Mindbomb (Mib)-mediated Notch signaling in the differentiation of neural progenitors during late neurogenesis by overexpressing Mib and administering retinoic acid to Tg[hsp70-Mib:EGFP]. [Neurosci Lett] Abstract Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein The authors derived induced pluripotent stem cells (iPSCs) from individuals with frontotemporal dementia-associated MAPT mutations and differentiated them into mature neurons. Patient iPSC-derived neurons demonstrated pronounced TAU pathology with increased fragmentation and phospho-TAU immunoreactivity, decreased neurite extension, and increased but reversible oxidative stress response to inhibition of mitochondrial respiration. [Stem Cell Rep] Full Article | Graphical Abstract | Press Release |