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embryonic stem cells

Site-Specific O-GlcNAcylation of Psme3 Maintains Mouse Stem Cell Pluripotency by Impairing P-Body Homeostasis

[Cell Reports] The authors identified O-GlcNAcylation of proteasome activator subunit 3 (Psme3) protein as a node of the ESC pluripotency network. Mechanistically, O-GlcNAc modification of serine 111 (S111) of Psme3 promoted degradation of Ddx6, which was essential for processing body assembly, resulting in the maintenance of ESC pluripotent state.

TAGLN, a Canonical Marker of Smooth Muscle Cells, Is Present in Endothelial Cells and Involved in Angiogenesis

[Journal of Cell Science] Human umbilical vein endothelial cells (HUVECs) elongated, activated TAGLN promoter and increased TAGLN transcripts in angiogenesis model. Genetic disruption of TAGLN augmented angiogenic behaviors of HUVECs, as did the disruption of TAGLN2 and TAGLN3 genes.

Zfp57 Inactivation Illustrates the Role of ICR Methylation in Imprinted Gene Expression during Neural Differentiation of Mouse ESCs

[Scientific Reports] To study of the relationship between DMR methylation and imprinted gene expression, scientists differentiated wild-type and Zfp57-/- hybrid mouse ESCs into neural precursor cells and evaluated allelic expression of imprinted genes.

JMJD3: A Critical Epigenetic Regulator in Stem Cell Fate

[Cell Communication and Signaling] JMJD3 has been found to enhance self-renewal ability and reduce the differentiation capacity of ESCs and multipotent stem cells. The authors discuss the recent advances of JMJD3 function in stem cell fate.

Differentiation of Embryonic Stem Cells into a Putative Hair Cell-Progenitor Cells via Co-Culture with HEI-OC1 Cells

[Scientific Reports] Scientists investigated whether co-culture of ESCs with HEI-OC1 cells promoted differentiation. Dissociated or embryonic bodies of ESCs were introduced to a conditioned and inactivated confluent layer of HEI-OC1 cells for 14 days.

Cell-Intrinsic Glial Pathology Is Conserved across Human and Murine Models of Huntington’s Disease

[Cell Reports] The authors investigated mutant HTT-associated changes in gene expression by mouse and human striatal astrocytes, as well as in mouse microglia, to identify commonalities in glial pathobiology across species and models.

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