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lineage conversion

Pharmacological Perturbation of Mechanical Contractility Enables Robust Transdifferentiation of Human Fibroblasts into Neurons

[Advanced Science] The authors reported a robust method to convert fibroblasts to neurons through targeting the cytoskeleton followed by exposure to lineage-specification surroundings.

Ultraefficient Extracellular Vesicle–Guided Direct Reprogramming of Fibroblasts into Functional Cardiomyocytes

[Science Advances] Researchers demonstrated of the use of extracellular vesicles derived from ESCs undergoing cardiac differentiation as biomimetic tools to induce cardiac reprogramming with extremely high efficiency, establishing a general, more readily accessible platform for generating a variety of specialized somatic cells through direct lineage conversion.

Somatic Lineage Reprogramming

[Cold Spring Harbor Perspectives in Biology] Investigators found a set of four defined factors that could reprogram fibroblasts into iPSCs, which were shown to be molecularly and functionally equivalent to blastocyst-derived ESCs, thus essentially showing that defined factors could induce authentic reprogramming without the need of oocytes.

Lymph Node Stromal Cell–Intrinsic MHC Class II Expression Promotes MHC Class I–Restricted CD8 T Cell Lineage Conversion to Regulatory CD4 T Cells

[Journal of Immunology] Scientists examined the cellular and molecular elements that promote CD8-to-CD4 lineage conversion and the development of CI-Treg cells in mice.

An Erythroid to Myeloid Cell Fate Conversion Is Elicited by LSD1 Inactivation

[Blood] The authors examined the consequences of conditional inactivation of Lsd1 in adult red blood cells using a new Gata1creERT2 BAC transgene. The analogous phenotype was observed in human hematopoietic stem and progenitor cells, coincident with induction of myeloid transcription factors.

An Epigenetic GPI Anchor Defect Impairs TLR4 Signaling in the B Cell Transdifferentiation Model for Primary Human Monocytes BLaER1

[Scientific Reports] The authors identified an important caveat when investigating TLR4-driven signaling in BLaER1 cells. They showed that this model contained glycosylphosphatidylinositol anchor-deficient cells, which lacked CD14 surface expression when differentiated to monocytes, resulting in diminished LPS/TLR4 but not TLR7/TLR8 responsiveness.

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