A
blastocyst is a tiny, early stage of a developing human or animal embryo. It's a cluster of cells that forms about 5-7 days after fertilization.
Full definition
Currently, the NIH defines acceptable hESCs as «cells that are derived from the inner cell mass of
blastocyst stage human embryos.»
The existence of ES cell precursors to this lineage is supported by the observed heterogeneous expression of other PrEn genes, Lefty1, Cerl, and Gata6 in the ICM
of blastocyst stage embryos, the stage from which ES cells are derived [17], [44]--[46].
The first reports of the generation of human induced pluripotent stem cells (hiPSCs) from fibroblasts [1, 2] were greeted with great enthusiasm over their ability to mimic the properties and function of embryonic stem cells without entailing the ethical controversies and resourcing issues associated with the use of human
blastocysts in derivation.
After the babies were delivered, researchers took blood from their umbilical cords and swabbed their cheeks for DNA samples to compare with those taken
from blastocysts at implantation.
Cells with normal karyotype were injected
into blastocysts isolated from C57BL / 6 mice.
In preimplantation diagnosis, eggs are fertilized in vitro and allowed to develop for five or six days to the so -
called blastocyst stage.
That this occurs once cells enter differentiation, is consistent with a requirement for sustained FGF signalling for commitment and segregation of the PrEn lineage in cultured blastocysts [57].
Paper on creation of stem cell line from human
blastocyst contains fabricated data, university committee concludes
To access ESCs, researchers puncture the outer walls of early stage embryos, known
as blastocysts, and reach into the inner cell mass to extract them — a process that destroys the rest of the embryo.
He was one of the first physicians to perform and report on
blastocyst transfer in the United States.
Most embryo transfers at Pacific Fertility Center are done
with blastocyst stage embryos.
«The authors went on to study the resulting
blastocysts for aneuploidy (frequency of abnormal chromosomes), and pattern of gene expression (which genes are active and at what level).
The goal was to demonstrate that the Eeva System may be used to identify embryos at cleavage stage (Day 3) that are most likely to
form blastocysts (Day 5).
In IVF, eggs from a woman are fertilized by male sperm in a Petri dish and allowed to grow for five days until they
become blastocysts consisting of about 50 to 65 cells.
Increased
human blastocyst viability by changing the start temperature and cooling rate in a slow freezing protocol.
Reviewing embryology records from March 2014 to July 2015, PFC researchers looked only at
blastocysts on Day 5, 6, or 7.
Gardner DK, Stilley KS, Lane M. High protein diet inhibits inner cell mass formation and increases apoptosis in
mouse blastocysts developed in vivo by increasing ammonium in the female tract.
Changes in the manipulation medium, as well as a move from late to early stages after first appearance of pronuclei, produced
blastocysts which were statistically indistinguishable from those produced in normal IVF by measures of morphology, ploidy and gene expression.
ES cells are an in vitro cell line derived from the inner cell mass (ICM) of the early
mammalian blastocyst [1], [2].
Thomson's group
used blastocysts from in vitro fertilization (IVF) clinics with full donor consent.
Human embryonic stem cells are isolated from early - stage embryos in the
late blastocyst stage, about four or five days after fertilization.
Herrmann D, Dahl JA, Lucas - Hahn A, Collas P, Niemann H Histone modifications and mRNA expression in the inner cell mass and trophectoderm of
bovine blastocysts Epigenetics, 8 (3)(in press) PubMed 23406883
Multiple pregnancy (twins, triplets, etc.) is associated with greatly increased risks of prematurity and very low birthweight, so the transfer of a
single blastocyst in all patients was a vital improvement.
Chazaud et al. observed that heterogeneous expression of Nanog and Gata6 in
early blastocysts was dependent on Grb2 - MAPK signalling and suggested that the reason that ES cells are unable to colonize the PrEn meant they had lost the capacity to respond to this signal [56].
The key goals were to produce good
quality blastocysts, similar to those shown to produce successful live births after IVF, and to reduce the carryover of mutant mitochondria to levels which strongly reduce the likelihood of developing (< 18 %) or transmitting (< 5 %) the disease.
Ideally we will achieve higher and higher rates of live births with transfers of single
healthy blastocysts.
The conclusion was that good quality
ePNT blastocysts could not be distinguished from controls.»
ES cell generation will include the isolation of the inner cell mass and subsequent growth of ES cells from
blastocysts obtained from five to ten superovulated females.
Live mice are supplied from a production colony, from a colony recovered from cryopreservation, or via micro-injection of a cell line into
host blastocysts.
These results validate our observations obtained with
blastocyst injection and indicate that the V − S + fraction is particularly effective at contributing to the epiblast (Table 2).
The abstract is entitled «Supernumerary
Frozen Blastocyst Transfers Result in Unacceptable Rates of Multiple Gestation and Preterm Delivery.»
Under these conditions,
blastocyst formation was the same in unmanipulated and control samples (zygotes that received their own pronuclei back).
In collaboration with Pacific Fertility Center (PFC), we are able to provide patients with a donor egg program that guarantees two
cryopreserved blastocyst embryos.
We take a human embryonic stem cell, and we inject it into a
monkey blastocyst [the first 130 or so cells in a newly formed embryo].
Based on these patterns, computer - automated programs have the potential to predict by day two of embryo development which embryo (s) are more likely to become
viable blastocysts and, as suggested by the current Penn study, result in a viable pregnancy.
The loss in ability to contribute to
blastocysts generated in this transient PrEn - like state was interesting, but we wanted to establish if these cells had gained new properties.
Part of the normal variation, which is equally present
between blastocysts of both groups, can be observed in the gene expression of levels mtDNA encoded OXPHOS proteins.
Consequently, most research facilities that use hESCs do not
isolate blastocysts and create hESC lines themselves, but purchase the cell lines from a large cell - banking facility or a collaborator.
Both lines were tested for chimera generation before any genetic manipulations by a collaborator who found that using injections with BALB /
c blastocysts produced germline chimeras.
Changing the start temperature and cooling rate in a slow - freezing protocol increases human
blastocyst viability.
No one has yet shown success with SCNT using human tissue: The closest effort so far has been the cloned
blastocyst reported last year by workers at the Newcastle Fertility Centre in the U.K., but that did not yield ES cells.
Phrases with «blastocyst»