Phenotypic characterizations reveal high levels of CD44, α2β1 integrin, and β - catenin expression in holoclones, whereas meroclones and paraclones show markedly reduced expression
of these stem cell markers.
Not exact matches
Previous research shows human induced pluripotent
stem cells (hiPSCs)-- generated directly from adult
cells — can express
markers for a wide variety
of cells, including those that secrete NP.
Several studies have used
cell - surface
markers — proteins found on the outer membranes
of tumor
cells — to identify glioblastoma
stem cells; but the specific
markers used have been controversial and can not reflect molecular processes going on within tumor
cells.
They also showed that the
cells have most
of the surface «
markers» considered as identifiers
of embryonic
stem cells and form «embryoid bodies» — characteristic clumps
of cells formed by ESCs.
When Busch turned on the
marker in adult animals, it became visible that at least one third (approximately 5000
cells)
of a mouse's hematopoietic
stem cells produce differentiated progenitor
cells.
Three
of the four projects receiving CIRM money capitalize on Victoria's expertise at finding
markers for differentiated
stem cells versus
cells that still have tumor - forming potential.
Based on anatomy and molecular
markers, we propose that it arose by duplication
of a neighboring
stem cell, which may have enabled finer neuronal control over leg - related behaviors, such as walking and grooming.»
Using fluorescent
markers, Fuchs and her colleagues isolated two distinct populations
of stem cells from mouse skin.
They found that ONC201 alters the gene expression
of cancer
stem cell markers and signaling pathways prior to killing the tumor
cells, providing pharmacodynamic biomarkers
of response.
Dr Mohamed Elrayess, from ADLQ, said: «In this study we have shown that the impaired ability
of fat
stem cells to store excess fat was partially due to increased levels
of the inflammatory
marker interleukin - 6 in the blood.
A
stem cell is generally characterized by the presence
of various proteins — or
cell markers — on its outer surface.
In a statement put on the Web this morning, NIH reported that all 64 lines «show characteristics
of stem cell morphology» and have undergone several population doublings, and most
of them have demonstrated all the protein
markers «known to be associated with human embryonic
stem cells.»
Whitehead Institute researchers have determined that the transcription factor Nanog, which plays a critical role in the self - renewal
of embryonic
stem cells, is expressed in a manner similar to other pluripotency
markers.
Comparing the
markers on these
stem cells with those on the surfaces
of cancer
cells, Johnson adds, will also help scientists determine if
stem cells contribute to prostate malignancies.
«We've not had
cell surface
markers for the different
stem cell states before, which has made it hard to study them,» says Fredrik Lanner, assistant professor at Karolinska Institutet's Department
of Clinical Science, Intervention and Technology.
To trace the lineage
of liver
cells, scientists used a telltale
marker — the
cells» response to signals delivered by a known
stem -
cell regulator called Wnt.
But on the right, the deletion
of a MicroRNA called miR - 34a causes
stem cells (green
markers in the top right image and red
markers in the bottom right image) to divide out
of control.
A series
of genetic
markers sprinkled throughout the
cells» chromosomes show the same pattern found in parthenogenetic mice as opposed to cloned mice, according to a report published online today in the journal
Cell Stem Cell.
Mouse embryonic
stem cells injected into rat brains express the AHD2 protein
marker (yellow) characteristic
of cells lost in Parkinson's disease.
Significantly,
cells with reduced mtDNA became self - renewing and expressed specific
cell surface
markers characteristic
of breast cancer
stem cells.
Intrigued, the team inserted a human version
of L1 into rat neural
stem cells, along with a
marker that would make the
cells glow green whenever L1 made a jump.
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.
A section
of a head and neck tumor — red and green
markers show the proliferation
of cancer
stem cells — that formed when one
of several newly characterized genes, Myh9, was suppressed.
Nearly 30 years after the discovery
of the hematopoietic
stem cell, Stanford researchers have found a
marker that allows them to study the version
of these
stem cells that continues to replicate.
For example, labeling
of these
cells with
stem - like
cell associated
markers (p63, nestin, and telomerase) have heavily implicated these
cells as
stem cells [13].
Middle: Immunofluorescence analysis
of TRP1 (melanosomes
marker) in melanocytes derived from pluripotent
stem cells.
However, we have found a fluorescent
marker for nestin, a neural crest
stem cell marker, in the posterior limbal region
of the human anterior segment in the vicinity
of both the trabecular meshwork and Schwalbe's line (unpublished).
Expression
of the Wnt inhibitor Dickkopf - 1 is required for the induction
of neural
markers in mouse embryonic
stem cells differentiating in response to retinoic acid.
When transplanted to the subretinal space
of mice lacking functional photoreceptors, human embryonic
stem cells directed toward a retinal lineage integrate into the outer nuclear layer, express photoreceptor
markers, and restore a light response as determined by the electroretinogram (ERG)[5].
Methods: Human corneas with attached scleral rims were obtained from eye banks and were assayed for telomerase activity and BrdU (bromodeoxyridine) incorporation to determine, respectively, the presence
of a
stem - like
cell marker and replicative activity.
Ihor Zahanich (Ravens, TUD)-- «Differentiation potential
of human mesenchymal
stem cells: expression
of molecular
markers, ion channels and gap junction channels» (2006)
Further research uncovered a broad spectrum
of cell surface
stem cell markers (e.g., CD133, CD44, and CD24) that allow the identification
of CSCs in human solid tumors, including brain, breast, prostate, pancreas, liver, ovary, skin, colon cancers, and melanoma (3 - 6)(Figure 1 based on 7).
A lot
of effort in tumor
stem cell research has always been directed to finding a so - called
marker, a molecule whose presence on a
cell reliably identifies it as a cancer
stem cell.
This gave a mixed population
of cells with 20 % expressing CD34, a hematopoietic
stem cell marker, with some co-expression
of endothelial
cell markers (CD31, Flk1, and VE - cadherin).
Pluripotent
marker expression and differentiation
of human second trimester mesenchymal
stem cells.
Solid tumours are reported to possess a sub set
of cells called Side Population expressing various
stem like
cell markers, self - renewal capacity and ability to give rise to differentiated
cells [23, 24].
Review
of «In Vitro
Cell Motility as a Potential Mesenchymal
Stem Cell Marker for Multipotency» from
Stem Cells TM by Stuart P. Atkinson
Significance
of CD44 and CD24 as Cancer
Stem Cell Markers: An Enduring Ambiguity.
Biological
markers of Mesenchymal Stromal
Cells as Predictors
of response to Autologous
Stem Cell Transplantation in Patients with Amyotrophic Lateral Sclerosis; an Investigator - Initiated Trial and in Vivo Study.
Since very few studies have demonstrated the formation
of macro-metastasis from low numbers
of sorted CSCs and currently proposed CSC
markers might not be sufficient to identify all
stem cell populations [13], we believe that our study presents a promising approach to isolate
stem - like and metastatic breast CSCs as opposed to the
cell - sorting strategy based on putative
stem cell surface
markers.
Title: Single - molecule transcript counting
of stem -
cell markers in the mouse intestine Authors: Itzkovitz S, Lyubimova A, Blat IC, Maynard M, van Es J, Lees J, Jacks T, Clevers H, van Oudenaarden A Date: 2011 Publication Details: Nat Cell B
cell markers in the mouse intestine Authors: Itzkovitz S, Lyubimova A, Blat IC, Maynard M, van Es J, Lees J, Jacks T, Clevers H, van Oudenaarden A Date: 2011 Publication Details: Nat
Cell B
Cell Biol.
Now, in a study published in
Stem Cells, the laboratory
of Seung Hyun Kim (Hanyang University, Seoul, Korea) report on an open ‐ label, single ‐ arm, investigator ‐ initiated trial to identify biological
markers of MSCs to predict response to in patients with ALS [3].
However, as demonstrated by a recent report from Stuelten and colleagues [13], the complexity
of CSC
markers continues to pose challenges for identifying and isolating the putative tumor
stem cell populations by the
cell - sorting approach.
Review
of «Biological
markers of Mesenchymal Stromal
Cells as Predictors
of response to Autologous
Stem Cell Transplantation in Patients with Amyotrophic Lateral Sclerosis; an Investigator - Initiated Trial and in Vivo Study» from
Stem Cells by Stuart P. Atkinson
(C) Confocal image
of P150 dystrophic inner retina transplanted with hNPCctx — GDNF and double stained with antibodies against nestin, a neural
stem and progenitor
cell marker (green) and human nuclear antigen (red).
Neural crest - like
stem cells (NCLSC) share many properties with aggressive melanoma
cells, such as high migratory capabilities and expression
of neural crest
markers.
With this reporter we split ES
cell cultures into two fractions that both express certain
stem cell markers but only one
of which expresses low levels
of an endodermal
marker gene.
The expression
of the tumoral multidrug resistance gene (MDR1), which encodes P - glycoprotein, and NANOG, a
stem -
cell marker and a regulator
of the expression
of drug resistance genes, was determined using qRT - PCR.
Of note, mouse neural stem cells (NSCs) were reprogrammed using only one (Oct4) or two factors (Oct4 and Klf4), due to the endogenously high expression of pluripotent genes, such as Sox2 and c - Myc, as well as several intermediate reprogramming markers [14], [17], [18
Of note, mouse neural
stem cells (NSCs) were reprogrammed using only one (Oct4) or two factors (Oct4 and Klf4), due to the endogenously high expression
of pluripotent genes, such as Sox2 and c - Myc, as well as several intermediate reprogramming markers [14], [17], [18
of pluripotent genes, such as Sox2 and c - Myc, as well as several intermediate reprogramming
markers [14], [17], [18].
Support to date for the existence
of an hypoxic niche in marrow blood
stem cells came from indirect evidence such as expression
of the hypoxia protein Hif - 1 and related genes and staining with surrogate
markers of hypoxia.