scholarly journals Parthenogenesis and Human Assisted Reproduction

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Adriana Bos-Mikich ◽  
Fabiana F. Bressan ◽  
Rafael R. Ruggeri ◽  
Yeda Watanabe ◽  
Flávio V. Meirelles

Parthenogenetic activation of human oocytes obtained from infertility treatments has gained new interest in recent years as an alternative approach to create embryos with no reproductive purpose for research in areas such as assisted reproduction technologies itself, somatic cell, and nuclear transfer experiments and for derivation of clinical grade pluripotent embryonic stem cells for regenerative medicine. Different activating methods have been tested on human and nonhuman oocytes, with varying degrees of success in terms of parthenote generation rates, embryo development stem cell derivation rates. Success in achieving a standardized artificial activation methodology for human oocytes and the subsequent potential therapeutic gain obtained from these embryos depends mainly on the availability of gametes donated from infertility treatments. This review will focus on the creation of parthenotes from clinically unusable oocytes for derivation and establishment of human parthenogenetic stem cell lines and their potential applications in regenerative medicine.

2020 ◽  
Vol 47 ◽  
pp. 101885
Author(s):  
Yongli Shan ◽  
Lishi Ma ◽  
Cong Zhang ◽  
Yanqi Zhang ◽  
Jingyuan Zhang ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Dominika Dziedzicka ◽  
Mukul Tewary ◽  
Alexander Keller ◽  
Laurentijn Tilleman ◽  
Laura Prochazka ◽  
...  

AbstractLow differentiation propensity towards a targeted lineage can significantly hamper the utility of individual human pluripotent stem cell (hPSC) lines in biomedical applications. Here, we use monolayer and micropatterned cell cultures, as well as transcriptomic profiling, to investigate how variability in signalling pathway activity between human embryonic stem cell lines affects their differentiation efficiency towards definitive endoderm (DE). We show that endogenous suppression of WNT signalling in hPSCs at the onset of differentiation prevents the switch from self-renewal to DE specification. Gene expression profiling reveals that this inefficient switch is reflected in NANOG expression dynamics. Importantly, we demonstrate that higher WNT stimulation or inhibition of the PI3K/AKT signalling can overcome the DE commitment blockage. Our findings highlight that redirection of the activity of Activin/NODAL pathway by WNT signalling towards mediating DE fate specification is a vulnerable spot, as disruption of this process can result in poor hPSC specification towards DE.


2010 ◽  
Vol 46 (3-4) ◽  
pp. 367-375 ◽  
Author(s):  
Helen Priddle ◽  
Cinzia Allegrucci ◽  
Paul Burridge ◽  
Maria Munoz ◽  
Nigel M. Smith ◽  
...  

2005 ◽  
Vol 10 ◽  
pp. 29
Author(s):  
Y Verlinsky ◽  
V Kukharenko ◽  
N Strelchenko ◽  
S Rechitsky ◽  
N Ilkevitch ◽  
...  

2010 ◽  
Vol 4 (1) ◽  
pp. 1-13
Author(s):  
T. A. Krylova ◽  
A. M. Kol’tsova ◽  
V. V. Zenin ◽  
O. F. Gordeeva ◽  
A. S. Musorina ◽  
...  

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