«In the future, this will move us towards a way to understand how to generate a cardiac muscle or other specific cell type without having to try an unwieldy number
of cell culture conditions.»
Not exact matches
Under experimental
conditions, the researchers then demonstrated that elevated levels
of elastase dramatically reduce the survival and operation
of muscle stem
cells in
culture.
Despite a lack
of rigorous clinical trials to test safety or efficacy, a ban
of the treatment by health authorities, and a lack
of peer review by the scientific community, the privately funded Stamina Foundation has been using
cultured mesenchymal stem
cells that have been exposed to putative
conditions that favour neuronal differentiation to treat different diseases in severely or terminally ill patients.
Human chondrosarcoma HCS - 2 / 8
cells, which are a type
of benign bone cancer
cells, can be used to investigate how optimization
of culture conditions could improve the synthesis
of cartilage - specific molecules.»
«We also think this method could be applied towards the development
of culture conditions during differentiation
of human stem
cells.
Studies
of IBD are typically performed using
cell culture experiments or animal models, which don't mimic the precise
conditions that occur in the gut
of human patients.
«The
culture conditions needed to grow various kinds
of stem
cells can be very tricky,» down to the source
of the water, says neural stem
cell biologist David Anderson
of the California Institute
of Technology in Pasadena.
The scientists then tried the proline / polyproline combination in a test system
of adherent
cell cultures that were subjected to freeze - thaw
conditions.
«We isolated kidney progenitor
cells from mice and searched for the most favorable
culture conditions,» said Assistant Professor Shunsuke Tanigawa
of Kumamoto University.
They then combined these in a dish with testicular
cells from newborn mice in various
culture conditions — a process that took hundreds
of trials, says author Xiao - Yang Zhao, a stem
cell biologist now at Southern Medical University in Guangzhou, China.
Haruko Obokata
of the RIKEN Center for Developmental Biology (CDB) in Kobe, Japan, and colleagues at other Japanese institutions and at Harvard Medical School in Boston reported that simply subjecting blood
cells from newborn mice to a moderately acidic environment for 25 minutes and then tweaking
culture conditions could generate pluripotent stem
cells capable
of developing into nearly all
of a body's
cell types.
They then placed the
cells into
culture conditions containing certain cytokines, and instead
of differentiating into B -
cells, the
cells continued to divide as stem
cells.
«Indeed, this model
of cell culture may reproduce what happens under physiological
conditions.»
Also, in both
cell culture and a mouse model
of the
condition, blocking the excessive splintering reduced production
of reactive oxygen species, a potentially harmful byproduct
of metabolism, as well as
cell death.
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.
Phase - contrast images
of organ - derived endothelial
cells (37 °C
culture conditions) that had undergone two successive selection processes by flow cytometry.
The first step
of our program is to apply the previously established lab -
culture conditions that first commit human ES (hES) and iPS
cells into retinal precursors.
The second step will be to optimize
culture conditions for the commitment
of the iPS / hES
cell - derived retinal precursors towards the photoreceptor lineage.
Most
of these were invalidated when challenged with experimental data generated in Smith's laboratory, which measured gene expression
of ESCs across 23 different
cell culture conditions, all
of which maintained pluripotency.
Difficult - To - Express Proteins: Resolving Bioprocessing Challenges with a Scalable Perfusion Bioreactor Scott Waginer, Emily Wozniak, and Kyle Biesecker (The
Cell Culture Company) Among some other recombinant glycoproteins, bi - and tri-specific antibodies are labeled as «difficult - to - express» proteins because
of low titers and sensitivity to environmental
conditions.
Bartosz Balana (Ravens, TUD)-- «Influence
of culture conditions on differentiation and bioelectrical properties
of human mesenchymal stem
cells» (2005)
Low - serum
conditions for expansion
culture of multiple
cell types.
Scientists developing new
cell therapy methods for the treatment
of disorders such as sickle
cell disease or leukemia need to consider how their
culture conditions may affect the success
of their translational research.
Whether a protocol uses
cell culture methods to expand edited
cells for downstream assays, to increase the efficiency
of lentiviral transduction or to let
cells «rest» after electroporation, optimized
culture conditions are key to maintaining
cell viability and biological function.
The most well - known
of these are so - called «senescent»
cells, originally characterized by Leonard Hayflick as mitotic
cells that reached growth arrest after a limited replicative lifespan (later associated with telomere attrition) under unphysiological
conditions in
culture.
Previous studies
of cell cultures from diabetic subjects
cultured under basal physiological
conditions showed that the basal as well as the insulin - stimulated FV0.1 values are reduced (4,5).
Consistent with their previous studies in
cell culture, mice exposed to paraquat under realistic
conditions developed an increased burden
of senescent
cells in their brains (Figure 1, (a-c)-RRB--- and this plague was almost entirely restricted to astrocytes (Figure 1 (d)-RRB-.
Previous studies
of cell cultures established from diabetic subjects and
cultured under basal physiological
conditions showed that the basal as well as the insulin - stimulated FV values are reduced (4,5).
To highlight the potentially important role
of 3D
culture conditions, the authors compared 2D monolayers
of hepatocyte progenitors, fetal liver stromal
cells, or adult bone marrow - derived stromal progenitor
cells to their 3D counterparts
cultured on liver extracellular matrix (3D - ECM) constructs.
This ensures that sister
cultures from the same subjects are similar in
cell composition and differentiation state, and it avoids the influence
of experimental
conditions on the differentiation process (1).
To determine the effect
of the
conditioned medium on NGF - induced neurite outgrowth, PC12
cells were dissociated and plated on polyornithine - coated tissue
culture dishes in the following
conditions: 1) HT22
conditioned medium, 2) J147 treated HT22
conditioned medium, 3) DMEM alone plus J147, 4) DMEM plus NGF at 50 nanograms per ml, 5) J147 treated HT22
conditioned medium pre-incubated for one hour with 10 μg / ml anti-NGF and N2 supplement (Invitrogen).
Bone marrow
cells cultured with
conditioned medium derived from ABL1 / ABL2 knockdown 1833 and SKBR3 breast cancer
cells had decreased numbers
of TRAP +
cells compared to the control groups (Fig. 5, B and C, and fig.
In light
of the observation that iPS
cell derivation takes place under the same
culture conditions used for ES
cells [20], we hypothesized that these human feeder
cells could offer a stable tool for defining molecular hallmarks during conversion
of differentiated somatic
cells to the pluripotent state.
(A) Purified CD4 + naive T
cells were
cultured with different concentrations
of VPA under Th1 - polarizing
conditions.
Our improved IVM
culture conditions may be used for obtaining mature oocytes for clinical purposes and / or for derivation
of embryonic stem
cells following parthenogenesis or nuclear transfer.
(A, B)
Culturing wild - type brains with
conditioned media from GBP1 and GBP2 expressing
cells induces low level
of ILP2 (A) and ILP5 (B) accumulation in the insulin - producing
cells.
(C, D)
Culturing wild - type brains with
conditioned media from GBP1 and GBP2 expressing
cells decreases the densities
of ILP2 (C) and ILP5 (D) signals in the insulin - producing
cells.
No expression
of SCP3 was detected in the EBs examined, whereas there was an increase
of SCP1 expression in the day 28 EBs
cultured in ovarian
cell -
conditioned medium.
The low levels
of Hex transcript observed in undifferentiated ES
cells (Figure S2C) were sufficient to generate a significant Venus positive (V +) sub-population in undifferentiated ES
cell cultures grown under standard feeder free
conditions.
Inverted microscopes represent the perfect solution for
cell culture in which a variety
of cells are grown under controlled
conditions.
HV
cells cultured under self - renewing
conditions were subjected to flow cytometry to separate Venus positive and negative ES
cell subpopulations and injected into Rosa26 LacZ expressing blastocysts within 1 h
of purification.
(A) Flow cytometry
of two independent HV clones (HV 5.1 and HV 16.1)
cultured either under self - renewing
conditions or in the absence
of LIF show the presence
of a subpopulation
of cells positive for Venus and / or the ES
cell surface marker SSEA - 1.
The current findings could provide important clues to determine the
culture conditions for promoting the differentiation
of primate ES
cells into mature gametes, and to understand molecular mechanisms
of primate gametogenesis including the timing
of germ
cell induction, the regulation
of germ
cell gene expression, and the response to growth factors for germ
cell differentiation.
Our results demonstrated that our 3D
cell culture device enables a real - time imaging
of giant vacuole formation and tracers crossing the
cultured endothelial
cell monolayer in a controlled experimental
condition.
Culture media for tumor cells were supplemented with 10 % FBS, whereas culture medium for HUVEC was supplemented with 20 % FBS, with the exception of the experiment under low proliferation rate conditions (2
Culture media for tumor
cells were supplemented with 10 % FBS, whereas
culture medium for HUVEC was supplemented with 20 % FBS, with the exception of the experiment under low proliferation rate conditions (2
culture medium for HUVEC was supplemented with 20 % FBS, with the exception
of the experiment under low proliferation rate
conditions (2 % FBS).
In the case
of EB formation using mouse testicular or ovarian
cell -
conditioned medium (see below), the EBs were
cultured in ES medium for 24 hr, and then in a
conditioned medium.
Increased permissivity
of monkey
cells to human adenovirus multiplication is affected by
culturing conditions and correlates with both synthesis
of virion fiber protein and altered splicing
of its mRNA
The existence
of a paracrine inter-dependent equilibrium would suggest that the
culture conditions have selected for the stable coexistence
of mutually dependent and metastable
cell types that only transiently exist in vivo.
VASA was detected earlier in
cells cultured in testicular
cell -
conditioned medium than in those
cultured in non-
conditioned medium or in ovarian
cell -
conditioned medium, suggesting that the initiation
of germ
cell differentiation in testicular
cell -
conditioned medium was faster than that in ovarian
cell -
conditioned medium.
As expected the
culture of HV
cells under these
conditions resulted in a significant reduction in the V+S + population (Figure 6B).