Levels of expression of pluripotency genes declined in parallel with the levels of
stem cell surface antigens.
The pathways that connect expression of
stem cell surface glycoconjugates such as the TRA -1-60 / GCTM - 2 antigen, receptors, and growth factors in human and even mouse ES cells with the transcriptional networks that regulate pluripotency remain unclear.
Oct - 4 is most consistently expressed of the pluripotency genes that we have studied, and it is switched off only in populations that have lost other measurable features of pluripotency, such as
stem cell surface marker expression and the capacity for self - renewal.
Cells along the continuum show a progressively decreasing likelihood of self renewal as their expression of
stem cell surface markers and pluripotency genes wanes.
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.
The surprising discovery made by the Dresden - based researchers: two components in the stem cell environment — the extracellular matrix and thyroid hormones — work together with a protein molecule found on
the stem cell surface, a so - called integrin.
Not exact matches
When blank slate
stem cells are exposed to a soft as opposed to a hard
surface on which to grow, they begin to transform themselves into neurons, the large, complex
cells of the central nervous system.
Stiffer
surfaces favored the
stem cell state.
When they looked closely, however, they noted that the transformed
cells had
surface proteins that were common to
stem cells.
Now, in a new study published today, Sept. 8, in the Proceedings of the National Academy of Sciences, a team of researchers from the University of Wisconsin - Madison has added a new wrinkle to the
cell differentiation equation, showing that the stiffness of the
surfaces on which
stem cells are grown can exert a profound influence on
cell fate.
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.
Finally, the team grew the tissue in a three - dimensional system, which coaxed it into forming all the structures found in gut tissue, including the finger - like villi that protrude inwards to increase
surface area, and recesses called crypts containing the intestinal
stem cells that renew the gut lining weekly (Nature, DOI: 10.1038 / nature09691).
«Growing
stem cells on synthetic
surfaces with different levels of compliance showed that
stem cells would become a different
cell type depending solely on the mechanical environment they perceive.
«The antibody binds to a specific protein, called CD44s, which is expressed on the
surface of pancreatic cancer
stem cells.
There, the
stem cells gradually moved to a spot just under the ovary's
surface, where they settled down and turned into eggs.
Still, a few
stem cell therapies have now been approved, such as a treatment available in India that takes
stem cells from the patient's eye in order to regrow the
surface of their cornea, and a US product based on other people's bone
stem cells.
By mimicking the stiffness of bone (40 kilopascal) or cartilage (15 kilopascal), the gel causes
stem cells applied to its
surface to differentiate.
A caveat of the study is that the gel does not exactly replicate the microenvironment inside the body, so it's not clear whether
stem cells behave differently on the designed gel
surfaces.
In the paper, the scientists report that their method produced more than twice the yield of potential bone - makers (9 percent) compared to their best application of another method: sorting
cells based on
surface proteins presumed to indicate that a
cell is a
stem cell (4 percent).
Because HIV uses CD4 to infect
cells, the researchers used a CAR molecule that hijacks the essential interaction between HIV and the
cell surface molecule CD4 to make
stem cell - derived T -
cells target infected
cells.
Dr. Basu had previously developed a technique to obtain ocular
stem cells from tiny biopsies at the
surface of the eye and a region between the cornea and sclera known as the limbus.
We found that delivery of
stem cells initiates regeneration of healthy corneal tissue rather than scar leaving a clear, smooth
surface.»
When the scientists remove these
surface proteins from the niche glial
cells, the
stem cells begin to grow and prematurely form new daughter
cells.
In addition, Berger's team has identified two
surface proteins located on the neural
stem cells and the surrounding niche glial
cells that are responsible for the interactions between these
cells.
The EMT is a biological process wherein epithelial
cells (
cells that line the cavities and
surfaces of blood vessels and organs) become mesenchymal (skeletal)
stem cells that can move throughout the body and differentiate into a variety of
cell types.
A
stem cell is generally characterized by the presence of various proteins — or
cell markers — on its outer
surface.
Researchers at Karolinska Institutet have identified
cell surface markers specific for the very earliest
stem cells in the human embryo.
They have screened combinations of antibodies that bind to specific proteins on the
surface of the immature and mature
stem cells and that can be used for flow cytometry, a common laboratory technique for sorting
cells.
RIKEN launched an investigation after claims of image manipulation and plagiarism
surfaced regarding a research article and a letter published online in Nature on 29 January that described a new, simple way of creating
stem cells called STAP, for stimulus - triggered acquisition of pluripotency.
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.
Each microsphere is coated with collagen — a natural structural material — to provide a
surface on which the
stem and blood
cells can anchor themselves and proliferate.
For example, the researchers were able to identify previously unknown gene expression differences between the neural
stem cells that give rise to the brain's deep structures versus its neocortical
surface, and to show that molecular signatures of different neural
cell types arise much earlier in brain development than previously realized.
The undifferentiated
stem cells were then placed onto a circular - patterned
surface that served to physically regulate
cell differentiation and growth.
The nanoparticles with the negative biomolecules on their
surface promoted
stem cell proliferation but suppressed «matrix mineralization»: the process that leads to the deposition of minerals into the bone's scaffolding, which makes bones strong.
The
stem cells behaved as if they were on a soft
surface when in contact with the smallest patches because they can't firmly grip them.
In contrast,
stem cells grown on softer
surfaces do go on to differentiate.
The research builds on the team's previous work with a technique called three - dimensional culture, which involves incubating
stem cells in a floating ball - shaped aggregate, unlike traditional
cell culture in which
cells grow in a flat layer on the
surface of a culture dish.
«By changing the
surface properties like the shape of the substrate at the nanoscale level, we tricked the
stem cells to behave differently,» explains co-author Dr Julien Gautrot, from QMUL's School of Engineering and Materials Science and the Institute of Bioengineering.
Significantly,
cells with reduced mtDNA became self - renewing and expressed specific
cell surface markers characteristic of breast cancer
stem cells.
As these
stem cells divide, the cortex increases its
surface area, expanding like an inflating balloon, says neuroscientist Victor Borrell of the Institute of Neurosciences of Alicante in Spain.
Researchers at the Babraham Institute and the Karolinska Institute report today in
Cell Stem Cell that they have identified a set of proteins (molecular «flags») that are present on the surface of either naïve or primed human embryonic stem ce
Stem Cell that they have identified a set of proteins (molecular «flags») that are present on the
surface of either naïve or primed human embryonic
stem ce
stem cells.
In studies of neural development in mice, Stahl found that TRNP1 produces a protein that determines whether neural
stem cells self - replicate, leading to a balloonlike expansion of cortical
surface area, or whether they differentiate into a plethora of intermediate
stem cell types and neurons, thickening the cortex and forming more complex brain structures.
Researchers have identified a set of molecular «flags» that are present on the
surface of human
stem cells.
To devise a potential new therapy, the investigators engineered a population of neural
stem cells to express a potent version of a gene called TRAIL, which codes for a molecule that activates
cell - death - inducing receptors found only on the
surface of cancer
cells.
Another lab ran into a similar problem when it tried to replicate work by Stanford
stem cell biologist Irving Weissman and his colleagues, who reported in 2012 in the Proceedings of the National Academy of Sciences that an antibody to a tumor
cell surface receptor called CD47 can slow tumor growth in mice.
Doctoral student Laura Hamilton was astonished to find fat droplets near the
stem cells, on the inner
surface of the brain in mice predisposed to develop the disease.
In this case, the gold nanoparticles are conjugated with antibodies against SSEA - 5 or TRA -1-60, proteins that are found on the
surfaces of
stem cells.
«For the first time, we may have potentially found a way to direct a person's own
stem cells to the bone
surface where they can regenerate bone,» says co-investigator Dr. Nancy Lane of UC Davis.