The let-7/LIN-41 Pathway Regulates Reprogramming to Human Induced Pluripotent Stem Cells by Controlling Expression of Prodifferentiation Genes Scientists showed that the let-7 family of microRNAs acts as an inhibitory influence on the reprogramming process through a regulatory pathway involving prodifferentiation factors, including EGR1. Inhibiting let-7 in human cells promotes reprogramming to a comparable extent to c-MYC when combined with OCT4, SOX2, and KLF4, and persistence of let-7 inhibits reprogramming. [Cell Stem Cell] Abstract | Graphical Abstract A Fully Defined and Scalable 3D Culture System for Human Pluripotent Stem Cell Expansion and Differentiation Researchers report a simple, defined, efficient, scalable, and good manufacturing practice-compatible 3D culture system for human pluripotent stem cells expansion and differentiation. [Proc Natl Acad Sci USA] Abstract Analysis of DNA Methylation Reveals a Partial Reprogramming of the Müller Glia Genome during Retina Regeneration Because somatic cell reprogramming during induced pluripotent stem cell generation is accompanied by changes in DNA methylation, especially in pluripotency factor gene promoters, scientists aimed to determine whether DNA methylation changes also underlie Müller glia reprogramming following retinal injury. [Proc Natl Acad Sci USA] Abstract Oct4 Is Required ~E7.5 for Proliferation in the Primitive Streak Using a tamoxifen-inducible Cre recombinase and floxed alleles of Oct4, scientists investigated the effect of depleting Oct4 in mouse embryos between the pre-streak and headfold stages, ~E6.0-E8.0, when Oct4 is found in dynamic patterns throughout the embryonic compartment of the mouse egg cylinder. [PLoS Genet] Full Article RNAi-Dependent and Independent Control of LINE1 Accumulation and Mobility in Mouse Embryonic Stem Cells Scientists showed that Dicer- and Ago2-dependent RNAi restricts long-interspersed elements-1 accumulation and retrotransposition in undifferentiated mouse embryonic stem cells, derived from blastocysts. [PLoS Genet] Full Article Comparative Receptor Tyrosine Kinase Profiling Identifies a Novel Role for AXL in Human Stem Cell Pluripotency Researchers present the first detailed and distinct repertoire of receptor tyrosine kinases (RTKs) characteristic for human pluripotent stem cell pluripotency by determining both the expression and phosphorylation profiles of RTKs in human embryonic stem cells and human induced pluripotent stem cells using RT-PCR with degenerate primers that target conserved tyrosine kinase domains and phospho-RTK array, respectively. [Hum Mol Genet] Abstract Dual Functions of Hypoxia Inducible Factor-1 Alpha for the Commitment of Mouse Embryonic Stem Cells Toward a Neural Lineage Investigators demonstrated that the oxygen-sensitive hypoxia-inducible transcription factor, Hif-1α, is an essential regulator for neural commitment of embryonic stem cells. [Stem Cell Dev] Abstract EDA-Containing Fibronectin Increases Proliferation of Embryonic Stem Cells The authors investigated if the fibronectin isoform that contains the extra domain A (FN EDA+) increased proliferation of mouse and human embryonic stem cells. They analyzed cell proliferation using conditioned media produced by different mouse embryonic fibroblast lines genetically engineered to express FN constitutively including or excluding the EDA domain, and in media supplemented with recombinant peptides containing or not the EDA. [PLoS One] Full Article MiR-223 Regulates Human Embryonic Stem Cell Differentiation by Targeting the Insulin-Like Growth Factor Receptor/Akt Signaling Pathway Levels of MicroRNA-223 (miR-223) were detected in differentiated versus undifferentiated human embryonic stem cells (hESCs). In addition, proliferation, apoptosis, and differentiation were assayed in these two hESC populations and were compared in the presence of exogenous miR-223 and miR-223 inhibitor. [PLoS One] Full Article The Presenilin-1 ΔE9 Mutation Results in Reduced γ-Secretase Activity, but Not Total Loss of PS1 Function, in Isogenic Human Stem Cells Scientists used isogenic euploid human induced pluripotent stem cell lines to generate and study an allelic series of Presenilin 1 (PS1) mutations, including heterozygous null mutations and homozygous and heterozygous familial Alzheimer’s disease PS1 mutations. [Cell Rep] Full Article | Graphical Abstract | Press Release |