Vitamin C Modulates TET1 Function During Somatic Cell Reprogramming Researchers report that TET1 either positively or negatively regulates somatic cell reprogramming depending on the absence or presence of vitamin C. TET1 deficiency enhances reprogramming, and its overexpression impairs reprogramming in the context of vitamin C, by modulating the obligatory mesenchymal-to-epithelial transition. [Nat Genet] Abstract Hierarchical Mechanisms for Direct Reprogramming of Fibroblasts to Neurons Researchers revealed a hierarchical mechanism in the direct conversion of fibroblasts into induced neuronal cells mediated by the transcription factors Ascl1, Brn2, and Myt1l. Ascl1 acts as an “on-target” pioneer factor by immediately occupying most cognate genomic sites in fibroblasts. [Cell] Abstract | Graphical Abstract Identification and Rescue of α-Synuclein Toxicity in Parkinson Patient-Derived Neurons Investigators exploited mutation correction of induced pluripotent stem cells and conserved proteotoxic mechanisms from yeast to humans to discover and reverse phenotypic responses to α-Synuclein, a key protein involved in Parkinson’s disease. [Science] Abstract | Press Release Vascular Progenitors from Cord Blood-Derived iPSC Possess Augmented Capacity for Regenerating Ischemic Retinal Vasculature To evaluate the potential of human induced pluripotent stem cells (hiPSC) for treating ischemic retinopathies, scientists generated vascular progenitors from a repertoire of viral-integrated and non-integrated fibroblast and cord blood-derived hiPSC lines, and tested their capacity for homing and engrafting into murine retina in an ischemia-reperfusion model. [Circulation] Abstract Targeting RNA Foci in iPSC-Derived Motor Neurons from ALS Patients with a C9ORF72 Repeat Expansion Researchers report a cellular model of C9ORF72 gene-amyotrophic lateral sclerosis (ALS) with motor neurons differentiated from induced pluripotent stem cells derived from ALS patients carrying the C9ORF72 repeat expansion. No significant loss of C9ORF72 expression was observed, and knockdown of the transcript was not toxic to cultured human motor neurons. [Sci Transl Med] Abstract | Press Release Reprogramming of MLL-AF9 Leukemia Cells into Pluripotent Stem Cells Investigators established an acute myeloid leukemia model by over-expressing the human mixed lineage leukemia AF9 (MLL-AF9) fusion gene in mouse hematopoietic cells that carry Yamanaka factors under the control of doxycycline. [Leukemia] Full Article Human Induced Pluripotent Stem Cell-Derived Cortical Neurons Integrate in Stroke-Injured Cortex and Improve Functional Recovery At two months after transplantation into a stroke-damaged rat cortex, cortically fated cells showed less proliferation and more efficient conversion to mature neurons with morphological and immunohistochemical characteristics of a cortical phenotype and higher axonal projection density as compared with non-fated cells. [Brain] Abstract | Press Release Pcid2 Inactivates Developmental Genes in Human and Mouse Embryonic Stem Cells to Sustain their Pluripotency by Modulation of Eid1 Stability Researchers demonstrated that Pcid2 is required for the maintenance of self-renewal both in mouse and human embryonic stem cells. [Stem Cells] Abstract Partial Restoration of Cardiovascular Function by Embryonic Neural Stem Cell Grafts after Complete Spinal Cord Transection To restore supraspinal control of sympathetic preganglionic neurons, scientists grafted embryonic brainstem-derived neural stem cells or spinal cord-derived neural stem cells expressing green fluorescent protein into the T4 complete transection site of adult rats. [J Neurosci] Abstract Human Endogenous Retrovirus K (HML-2) RNA and Protein Expression Is a Marker for Human Embryonic and Induced Pluripotent Stem Cells Using RTPCR and Western Blot, scientists demonstrate HML-2 RNA and protein expression in undifferentiated human embryonic stem cell and induced pluripotent stem cells. [Retrovirology] Abstract | Full Article |