Not exact matches
The results showed that, when applied, a long - term inhibition
of Rho - kinase signaling increased the expressions
of chondrocyte - specific genes and
differentiation markers in human chondrosarcoma 2/8 cells.
Expanding from their previous studies with mice, the researchers first established that under specific conditions, culturing human embryonic stem cells with fibroblast growth factor 2 (FGF2) leads to neural
differentiation particular to the midbrain / hindbrain region — the location
of the cerebellum — within three weeks, and the expression
of markers for the cerebellar plate neuroepithelium — the part
of the developing nervous system specific for the cerebellum — within five.
By contrast, the R206H ACVR1 mutant only slightly enhances the expression
of initial and early chondrogenesis
markers (collagen type II and aggrecan), consistent with a milder stimulatory effect
of the FOP ACVR1 mutation on chondrocyte
differentiation.
A short - term inhibition
of Rho - kinase failed to induce extracellular matrix production in fibroblasts or in HCS - 2 / 8 cells, while its long - term exposure increased the expressions
of chondrocyte - specific genes and
differentiation markers, and also promoted the synthesis
of sulfated glycosaminoglycans by chondrocytic cells.
While expression levels
of all
marker genes remained almost unchanged in wild - type ACVR1 cultures compared with the empty viral vector, the expression profile induced by caACVR1 Q207D displayed evidence
of advanced chondrogenic
differentiation as shown by decreased levels
of the early
differentiation stage
marker collagen type II together with enhanced expression
of the later - stage
markers Ihh and collagen type X. Indian hedgehog has been shown previously to be induced by BMP signaling transmitted via the ACVR1 receptor (9).
We will develop mathematical models to predict the pathways
of differentiation from naive to memory and effector T - cell subsets based on the characterisation
of surface
marker expression, transcription factors and cytokines production at early and late time points after immunisation.
After 15 days, a subset
of cells expressed regulators
of RGC
differentiation (Atoh7, Brn3b, and Islet1), while a smaller subset co-expressed Brn3b and the mature RGC
marker Thy1, thus confirming a RGC identity.
Ihor Zahanich (Ravens, TUD)-- «
Differentiation potential
of human mesenchymal stem cells: expression
of molecular
markers, ion channels and gap junction channels» (2006)
Pluripotent
marker expression and
differentiation of human second trimester mesenchymal stem cells.
MyoD is normally only expressed in skeletal muscle, and it was later found to be a transcription factor involved in the
differentiation of muscle cells and also a very early
marker of muscle cell fate commitment.
Both BMP and CNTF - induced astrocyte populations express GFAP (Fig. 1 A — C), AQP4 and S100β (Fig. 1 D), three widely used
markers of astrocyte
differentiation [17]--[22].
For definitive endoderm
differentiation, spontaneously formed EBs on day 6 were plated onto matrigel - coated dishes and maintained in a low concentration
of fetal bovine serum (FBS) in combination with a high concentration
of recombinant Activin A. Scale - like cells appeared (Figure 5A), which were positive for definitive endoderm
markers such as Foxa2, Sox17 and Gata4.
«The observed increase in the ratio
of cytotoxic CD4 T cells to CD4 helper T cells indicates that they are an important component
of the protective immune response to viral infections and that their induction should be an important
marker for successful vaccinations against certain viral diseases,» says postdoctoral researcher and first author Veena Patil, Ph.D. «But we really didn't know enough about their molecular profile and the mechanisms that drive their
differentiation and maintenance.»
In addition, the expression
of other germ cell
markers, such as NANOS and PIWIL1 genes, was also up - regulated as the EB
differentiation progressed.
Among the early germ cell
markers examined, VASA is a candidate gene for detecting pre-meiotic germ cell
differentiation from monkey ES cells, because its expression is detected earlier in the primordial stage
of germ cell development in comparison to that
of PIWI family genes in vivo in mice and humans [11], [36]--[38], [49].
Genetic studies using samples along the distribution range
of both subspecies and based on a few dozen nuclear
markers have revealed loci
of relatively high divergence (0.3 — 1.2 %) between subspecies embedded in a genome otherwise characterized by low levels
of differentiation and high levels
of bidirectional gene flow [21], [24]--[26], likely facilitated by high effective population sizes, high dispersal, and a relatively short generation time [21], [24]--[26].
A combination
of several germ cell
markers will thus be necessary to detect germ cell
differentiation from ES cells.
To explore the
differentiation markers for detecting germ cells differentiated from ES cells, the expression
of various germ cell
marker genes was examined in tissues and ES cells
of the cynomolgus monkey (Macaca fascicularis).
Here, ES cells transduced with HOXB4 were analyzed for the expression
of hematopoietic
markers after 26 days
of differentiation.
We have previously reported that our 26 - d protocol closely recapitulates key stages
of biliary development, starting with the
differentiation of hPSCs into endoderm and subsequently into foregut progenitor (FP) cells, followed by the generation
of hepatoblasts (HBs), cholangiocyte progenitors (CPs) expressing early biliary
markers and mature CLCs displaying cholangiocyte functionality.
After 4 weeks
of differentiation, the majority
of the cells (> 60 %) expressed the postmitotic neuronal
marker β - III tubulin with a subset (about 50 %
of total neurons) additionally expressing TH, a
marker for midbrain dopaminergic neurons (Fig. 3A — D).
Fluorescence - based assays Fluorescent
markers such as EGFP, YFP, mCherry and mTomato or fluorescent biosensors can be used to measure a variety
of real - time cell - based activities, including, intracellular transport, protein signaling, receptor desensitization, migration, division, apoptosis, metabolism,
differentiation, chemotaxis, transcription and translation.