Dr. Sonntag studies this concept on the molecular and cellular level using a translational research approach that integrates the analysis of human material, such as postmortem brains, primary cell systems, and neural
cell populations generated from patients» - or healthy individuals» - derived induced pluripotent stem cells (iPSC), or induced neurons (iNs), in combination with molecular, biochemistry, and lentivirus - mediated gene - engineering technologies.
Different clonal memory cell populations had different B cell or macrophage helper compositions that matched effector
cell populations generated much earlier in the response.
Attempts to eliminate the tumor - initiating
cell population generated by EMT are hampered by their increased resistance against most conventional cancer therapeutics.
Not exact matches
In the clearest possible case, the ANT - OAR
cell would differ from a zygote on all of the parameters noted above: The ANT - OAR
cell would have a pattern of gene expression that is clearly distinct from a zygote; it would
generate a homogeneous
population of
cells rather than multiple
cell types; it would undergo simple cleavage divisions and not produce any multicellular structures.
They observed that after allergic sensitization, some mouse strains
generated large
populations of MMC9
cells while other strains did not.
Frey and his colleagues made use of mathematical models to analyze the complex interplay between ecological factors and
population dynamics, and were able to demonstrate that
populations can indeed respond in a coordinated fashion to chemical information even when the signal molecules are
generated by only a subset of the
cells.
According to the authors, future studies should aim to improve the efficiency of the approach to
generate a pure
population of
cells that closely mimic adult Leydig
cells.
She said that a failure to maintain NFkB signals at this point, or even after memory T
cells have been produced, leads to a loss of the
population of memory T
cells that have been
generated after the infection.
Mycobacteria can
generate daughter
cells through asymmetric growth, resulting in genetically identical, but physiologically diverse,
populations.
These results collectively suggest that neural stem
cells need MSI1 to
generate enough neurons for normal brain size, but the presence of MSI1 also increases the vulnerability of these
cells to Zika infection, leading to the death of the
population which ultimately results in microcephaly.
«In combination with recent advances in sorting
cells on a biophysical basis, the biomechanical stemness markers we identified hold the potential to rapidly
generate corneal transplants with highly enriched stem
cell populations, which could one day translate into better outcomes for these patients.»
Interestingly, CD44 + / CD24 −
population can be
generated by induction of epithelial — mesenchymal transition (EMT) by treating breast epithelial
cells with EMT - inducing agents such as TGF - β1 (6).
For isolated
cell populations, SuperScript III was used to
generate cDNA.
The selection strategy targeted
cell populations expressing the inducible endothelial
cell adhesion molecules, E-selectin and VCAM - 1, and proved successful in
generating microvascular endothelial
cell lines from a number of different organs.
Thus, our selection strategies, which were based on targeting endothelial
populations that expressed both of these inducible glycoproteins, suggest that the endothelial
cell lines
generated in this study are most likely from this microcirculatory region.
The results of our limiting dilution analysis confirmed that the isolated CSCs (CD24 − / CD44 + / ESA +)
population has significantly stronger ability of
generating tumors compared with non-stem
cell population (Table 1).
However, unlike HUVECs or other commercially available endothelial
cell lines, the endothelial
cells generated from the H - 2Kb - tsA58 mice retained their ability to mobilize these adhesion molecules despite undergoing numerous
population doublings (currently 30 passages).
Within five to nine days we can
generate virtually all the pure
cell populations that we need.»
In this study, we used an in vivo strategy to determine if functional retinas could be
generated from a defined
population of pluripotent Xenopus laevis
cells.
The ability to make pure
populations of these
cells within days rather than the weeks or months previously required is a key step toward clinically useful regenerative medicine — potentially allowing researchers to
generate new beating heart
cells to repair damage after a heart attack or to create cartilage or bone to reinvigorate creaky joints or heal from trauma.
The researchers also found that another
population known as progenitor
cells — differentiated daughter
cells of stem
cells — started to behave like stem
cells: They began to live much longer than their usual lifespan of a few days, and they could also
generate mini-intestines when grown outside of the body.
The ability to quickly
generate purified
populations of specialized precursor
cells has opened new doors to further study.
Homogenous and functional
population of keratinocytes and melanocytes derived from pluripotent stem
cells were
generated by designing a multi-step sequential protocol respecting the chronobiology of epidermis formation during human ontogenesis.
«The ability to
generate pure
populations of these
cell types is very important for any kind of clinically important regenerative medicine,» said Loh, «as well as to develop a basic road map of human embryonic development.
The study of mice suggests that a high - fat diet drives a
population boom of intestinal stem
cells and also
generates a pool of other
cells that behave like stem
cells — that is, they can reproduce themselves indefinitely and differentiate into other
cell types.
«Often, we want to
generate a particular
cell population from stem
cells for introduction into patients,» says co-senior author Young - sup Yoon, MD, PhD, professor of medicine (cardiology) and director of stem
cell biology at Emory University School of Medicine.
His team also discovered how to
generate functional hemangioblasts — a
population of «ambulance»
cells — from hESCs.
Today, analyzing and editing genomes, proteomes and metabolomes has become a standard for many model systems; imaging beyond the diffraction limit of light and new technologies for studying protein structures provide insights deeper than ever before; the characterization of large
populations of
cells or organisms brings unprecedented statistical power; and studying nearly all organisms of an ecosystems as a whole allows
generating comprehensive models.
Starting with transplants of human oligodendrocytes in the late 1980s [40], and more recently with
populations of human oligodendrocyte progenitor
cells isolated from the developing or adult CNS, or from human embryonic stem
cells, it has been possible to
generate extensive myelination upon transplantation into spinal cord injury or into congenital mouse models of hypomyelination [41]--[48].
The Hematopoietic stem
cell population resident in bone marrow is responsible for
generating blood
cells and immune
cells.
We show that subpopulations of human astrocytes,
generated by activation of different signaling pathways in the same
population of human glial precursor
cells, have markedly different effects when transplanted into the injured spinal cord.
We now show that astrocytes
generated from the same
population of human fetal glial precursor
cells, by exposure to either bone morphogenetic protein (BMP) or ciliary neurotrophic factor (CNTF), promote widely divergent outcomes with respect to repairing the injured adult spinal cord.
Further challenges include the identification of signaling molecules that promote the generation of beneficial
populations of astrocytes, identification of appropriate stem and / or progenitor
cell populations that can be the source of such
cells, and determination of whether there are situations in which it is more useful to transplant astrocytes themselves rather than to transplant stem or progenitor
cells that might
generate astrocytes in vivo in response to signals present in the host environment.
As a first step towards determining whether human glial progenitor
cells (hGPCs) can
generate functionally distinct astrocyte
populations, we exposed embryonic hGPCs isolated from spinal cords of 9.5 week old abortuses to BMP or CNTF.
Thus while the majority of the V +
population existing in ES
cell cultures are indistinguishable from undifferentiated ES
cells, we also observe differentiated
cells expressing high levels of the Venus transgene (arrows in Figure 2B) that resemble the high - level Venus expressors
generated in response to differentiation and that probably represent spontaneous PrEn differentiation.
Clinical trials are now underway that aim to see if the large
populations of T regulatory
cells generated in the thymus can be exploited to better protect against type 1 diabetes.
This approach involves first
generating many monoclonal antibodies raised against «crude» tumor
cell antigen
populations — whole
cells and
cell membranes — and then screening for those that block the metastatic ability of the
cell.
Despite remarkable improvement in the generation of hPSC - CMs, without purification, these protocols can only
generate mixed
cell populations including undifferentiated hPSCs or non-CMs, which may elicit adverse outcomes.
The researchers now hypothesize that microbes in the gut, where most of this pTreg
cell population is switched on, may be responsible for
generating these protective
cells and thus protecting against the autoimmune attack on pancreatic beta
cells that cause type 1 diabetes.
More than half of mammalian genes
generate multiple messenger RNA isoforms that differ in their 3 ′ untranslated regions (3 ′ UTRs) and therefore in regulatory sequences, often associated with
cell proliferation and cancer; however, the mechanisms coordinating alternative 3 ′ - UTR processing for specific mRNA
populations remain poorly defined.
There are
populations of
cells that divide in the mature brain, and the knowledge we gain from the in vitro studies could help influence how one might be able to manipulate and use that newly
generated population of
cells in the brain in more therapeutic ways.
Against common wisdom even the adult and aging brain can
generate new neurons from a
population of resident stem
cells but it does so only in two privileged regions and on a minute scale.
The low density culture protocol helps in
generating larger number of CD133 + endothelial
population from initially fewer CD133 + endothelial progenitor
cells; EPCs (Figure S1).
Among other projects, according to Pop!Tech, she's designing a cheap wind turbine capable of
generating enough electricity to charge a
cell phone or power LED lighting in Guatemala, where 75 percent of the
population lives below the poverty line.