scholarly journals CHANGES IN THE CAPACITY FOR CLONAL GROWTH AND DIFFERENTIATION IN VITRO OF THE VERTEBRAL CARTILAGE CELLS WITH EMBRYONIC DEVELOPMENT II. VITALIZING EFFECT OF CONDITIONED MEDIUM ON THE CELLS OF YOUNGER EMBRYOS

1971 ◽  
Vol 13 (2) ◽  
pp. 107-118 ◽  
Author(s):  
KAZUO WATANABE
2015 ◽  
Vol 27 (1) ◽  
pp. 155
Author(s):  
M. Barcelo-Fimbres ◽  
J. N. Gouze ◽  
N. R. Mtango ◽  
R. Koppang ◽  
J. P. Verstegen

Beneficial effects on embryonic development of co-culture with Vero cells during in vitro culture have been previously reported and related to Vero cells growth factors/cytokines secretion into the medium (1998 Human Reprod. 1600–1605). However, co-culture increases the probability of microorganism contamination during culture. In this study, we aimed to overcome this problem by culturing bovine embryos in conditioned medium derived from Vero cells culture (CM). Vero cells (GenBiotech, Antibes, France) were cultured for 24 h, and then the medium was removed, filtered, and frozen until its use. A total of 701 slaughterhouse bovine cumulus oocytes complexes were matured and fertilized in vitro under standard conditions. After fertilization, zygotes were allocated to 4 different treatments [0 (control), 5, 10, and 20% of CM v/v] for in vitro culture in BBH7 medium (BoviPro®, MOFA Global, Verona, WI, USA) at 38.5°C in 5% O2, 5% CO2, 90% N2 atmosphere for 7 days. A total of 8 replicates were done. Cleavage rates were assessed at 2.5 days, blastocyst rates and embryonic stage at 7 days, and blastocyst total cell number at 7.5 days after fertilization. Data were analysed by ANOVA using GLM; the percentages were transformed using arcsin square root. If the ANOVA was significant (P < 0.05), means were separated by Tukey's procedure using Statistix 10 software (Tallahassee, FL, USA). No differences in cleavage rates were found between treatments (P > 0.1; Table 1). However, the addition of conditioned medium at all levels increased the blastocyst production at Day 7 of culture (between 11 to 19 percentage points) compared with the control group (P < 0.01; Table 1); likewise, CM addition was superior in total embryo production (Day 7 morulae plus all blastocysts; P < 0.01; Table 1), between 12.5 to 15 percentage points higher than the control group. No differences were found between treatments for blastocyst total cell number at 7.5 days of culture (P > 0.1; Table 1) and overall embryonic developmental stage (P > 0.1; Table 1). In conclusion, we found a superior embryonic development when Vero cells conditioned medium was added at Day 0 of in vitro culture; the positive effect on total embryo production was observed even at 5% of conditioned medium. Table 1.Means (± s.e.m.) of embryonic development of bovine embryos


2016 ◽  
pp. 137-139
Author(s):  
K.P. Golovatyuk ◽  

The objective: was to investigate the levels of cytokines IL-4 and IL-17 in serum and conditioned medium cultures of blood mononuclear cells (MNC) and evaluation association between their products and miscarriage, which occurred in IVF cycles. Patients and methods. We observed 240 patients with recurrent miscarriage, came in IVF cycles, and 100 apparently healthy fertile women in the control group. The concentrations of IL-4 and IL-17 in serum and conditioned medium of MNC cultures were determined. Results. The levels of IL-4 in the serum and conditioned medium in spontaneous and stimulated mitogen secretion was not significantly different from those in the control group, whereas IL-17 levels were higher than those in the control group serum, in conditioned media of stimulated and non-stimulated MNCs. Conclusion. Disregulation of activity of circulating blood mononuclear cells in women with recurrent miscarriage that followed IVF, is accompanied by increased secretion of IL-17 and almost constant production of IL-4 on the back of high stimulation index of production of these cytokines. Key words: in vitro fertilization, miscarriage, interleukin-4, interleukin-17, serum stimulated and non-stimulated mononuclear blood.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ning Zhou ◽  
Lei Wang ◽  
Ping Fu ◽  
Zihao Cui ◽  
Yuhang Ge ◽  
...  

Abstract Background Oligovascular niche mediates interactions between cerebral endothelial cells and oligodendrocyte precursor cells (OPCs). Disruption of OPC-endothelium trophic coupling may aggravate the progress of cerebral white matter injury (WMI) because endothelial cells could not provide sufficient support under diseased conditions. Endothelial progenitor cells (EPCs) have been reported to ameliorate WMI in the adult brain by boosting oligovascular remodeling. It is necessary to clarify the role of the conditioned medium from hypoxic endothelial cells preconditioned EPCs (EC-pEPCs) in WMI since EPCs usually were recruited and play important roles under blood-brain barrier disruption. Here, we investigated the effects of EC-pEPCs on oligovascular remodeling in a neonatal rat model of WMI. Methods In vitro, OPC apoptosis induced by the conditioned medium from oxygen-glucose deprivation-injured brain microvascular endothelial cells (OGD-EC-CM) was analyzed by TUNEL and FACS. The effects of EPCs on EC damage and the expression of cytomokine C-X-C motif ligand 12 (CXCL12) were examined by western blot and FACS. The effect of the CM from EC-pEPCs against OPC apoptosis was also verified by western blot and silencing RNA. In vivo, P3 rat pups were subjected to right common carotid artery ligation and hypoxia and treated with EPCs or EC-pEPCs at P7, and then angiogenesis and myelination together with cognitive outcome were evaluated at the 6th week. Results In vitro, EPCs enhanced endothelial function and decreased OPC apoptosis. Meanwhile, it was confirmed that OGD-EC-CM induced an increase of CXCL12 in EPCs, and CXCL12-CXCR4 axis is a key signaling since CXCR4 knockdown alleviated the anti-apoptosis effect of EPCs on OPCs. In vivo, the number of EPCs and CXCL12 protein level markedly increased in the WMI rats. Compared to the EPCs, EC-pEPCs significantly decreased OPC apoptosis, increased vascular density and myelination in the corpus callosum, and improved learning and memory deficits in the neonatal rat WMI model. Conclusions EC-pEPCs more effectively promote oligovascular remodeling and myelination via CXCL12-CXCR4 axis in the neonatal rat WMI model.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Karina Cañón-Beltrán ◽  
Yulia N. Cajas ◽  
Serafín Peréz-Cerezales ◽  
Claudia L. V. Leal ◽  
Ekaitz Agirregoitia ◽  
...  

AbstractIn vitro culture can alter the development and quality of bovine embryos. Therefore, we aimed to evaluate whether nobiletin supplementation during EGA improves embryonic development and blastocyst quality and if it affects PI3K/AKT signaling pathway. In vitro zygotes were cultured in SOF + 5% FCS (Control) or supplemented with 5, 10 or 25 µM nobiletin (Nob5, Nob10, Nob25) or with 0.03% dimethyl-sulfoxide (CDMSO) during minor (2 to 8-cell stage; MNEGA) or major (8 to 16-cell stage; MJEGA) EGA phase. Blastocyst yield on Day 8 was higher in Nob5 (42.7 ± 1.0%) and Nob10 (44.4 ± 1.3%) for MNEGA phase and in Nob10 (61.0 ± 0.8%) for MJEGA phase compared to other groups. Mitochondrial activity was higher and lipid content was reduced in blastocysts produced with nobiletin, irrespective of EGA phase. The mRNA abundance of CDK2, H3-3B, H3-3A, GPX1, NFE2L2 and PPARα transcripts was increased in 8-cells, 16-cells and blastocysts from nobiletin groups. Immunofluorescence analysis revealed immunoreactive proteins for p-AKT forms (Thr308 and Ser473) in bovine blastocysts produced with nobiletin. In conclusion, nobiletin supplementation during EGA has a positive effect on preimplantation bovine embryonic development in vitro and corroborates on the quality improvement of the produced blastocysts which could be modulated by the activation of AKT signaling pathway.


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