Both animal and human studies have demonstrated the important roles of neurotrophins (BDNF, NTF3 and NTF4)
in oocyte maturation mediated by their receptors (NTRK1 — 3 and NGFRAP1)[20], [25].
To find out more about the pathway's role
in oocyte maturation, Nick Duesbery, a postdoc in Vande Woude's lab, was seeking compounds that block MAPK's activity.
Not exact matches
They were interested
in one of the cell's key signaling pathways, the MAPK pathway, which helps control cell growth, embryonic development, and the
maturation of
oocytes into eggs.
In biology, folliculogenesis refers to the
maturation of the ovarian follicle, a densely - packed shell of somatic cells that contains an immature
oocyte.
Following incubation
in medium supplemented with ovarian factors (BDNF, IGF - I, estradiol, GDNF, FGF2 and leptin), a greater percentage of
oocytes demonstrated nuclear
maturation and subsequently, underwent parthenogenesis relative to control.
As outlined below, we used a microfluidic quantitative PCR (qPCR) system to elucidate the gene expression profiles of individual human
oocytes and small numbers of cumulus cells using a combination of a large number of samples and targets [12], and then extended our studies via the use of parthenogenesis,
in conjunction with gene expression profiling, as a functional assay of cytoplasmic
maturation of
oocytes.
Oocyte maturation and embryo development data were entered into a two - by - two contingency table, and Fisher's exact test was used to generate P - values
in Prism version 5.02 for windows (GraphPad Software, Inc.).
However, detailed protein expression of individual ovarian factors and their receptors
in oocytes need to be further studied
in order to elucidate the factors that may affect
oocytes in specific
maturation stages.
In contrast, nuclear maturation of MI oocytes was much more efficient with values ranging from 75 to 94 % in the three different medi
In contrast, nuclear
maturation of MI
oocytes was much more efficient with values ranging from 75 to 94 %
in the three different medi
in the three different media.
We derived a protocol for paracrine / autocrine supplementation for
in vitro
maturation of cumulus - free
oocytes that includes supplementation with BDNF, IGF - I, GDNF, leptin, FGF2 and estradiol as shown
in Figure 2C.
In order to improve culture conditions for maturation of cumulus - free oocytes in vitro, we began by assaying the expression of 15 growth factors (BDNF, IGF - I, estradiol, GDNF, leptin, FGF1, FGF2, GM - CSF, EGF, TGF - α, TGF - β1; 2; 3, and ET - 1; 2) and 27 of their cognate receptors that have been shown to regulate oocyte maturatio
In order to improve culture conditions for
maturation of cumulus - free
oocytes in vitro, we began by assaying the expression of 15 growth factors (BDNF, IGF - I, estradiol, GDNF, leptin, FGF1, FGF2, GM - CSF, EGF, TGF - α, TGF - β1; 2; 3, and ET - 1; 2) and 27 of their cognate receptors that have been shown to regulate oocyte maturatio
in vitro, we began by assaying the expression of 15 growth factors (BDNF, IGF - I, estradiol, GDNF, leptin, FGF1, FGF2, GM - CSF, EGF, TGF - α, TGF - β1; 2; 3, and ET - 1; 2) and 27 of their cognate receptors that have been shown to regulate
oocyte maturation.
Following
in vitro
maturation,
oocytes at metaphase II with the presence of a first polar body were activated using 10 µM calcium ionophore A23187 (Sigma - Aldrich) for 5 min followed by 2 mM DMAP (Sigma - Aldrich) for 4 h at 37 °C
in 6 % CO2, 5 % O2 and 89 % N2.
Since the first report of
in vitro human
oocyte maturation in 1969 [3], several reports have documented blastocyst (BL) development or live birth achieved from
oocytes matured
in vitro [1], [4], [5].
Based on our gene expression data, FGF2 could affect
oocyte maturation in a paracrine manner via the cumulus cells.
Oxygen concentration during mouse
oocyte in vitro
maturation affects embryo and fetal development.
Simulated physiological
oocyte maturation (SPOM): a novel
in vitro
maturation system that substantially improves embryo yield and pregnancy outcomes.