The temporal relationship between oocyte maturation and early fertilisation events in relation to the pre-ovulatory LH peak and preimplantation embryo development in red deer (Cervus elaphus)

2008 ◽  
Vol 105 (3-4) ◽  
pp. 332-343 ◽  
Author(s):  
D.K. Berg ◽  
J.G. Thompson ◽  
A.J. Peterson ◽  
G.W. Asher
iScience ◽  
2020 ◽  
Vol 23 (9) ◽  
pp. 101523
Author(s):  
Alaa A. Eisa ◽  
Scott Bang ◽  
Katherine J. Crawford ◽  
Emily M. Murphy ◽  
William W. Feng ◽  
...  

2009 ◽  
Vol 19 (2) ◽  
pp. 181-190 ◽  
Author(s):  
Yinghui Ye ◽  
Kazuhiro Kawamura ◽  
Mitsue Sasaki ◽  
Nanami Kawamura ◽  
Peter Groenen ◽  
...  

Reproduction ◽  
2011 ◽  
Vol 141 (4) ◽  
pp. 417-424 ◽  
Author(s):  
Pan-Pan Cheng ◽  
Jun-Jie Xia ◽  
Hai-Long Wang ◽  
Ji-Bing Chen ◽  
Fei-Yu Wang ◽  
...  

Maternal diabetes adversely affects preimplantation embryo development and oocyte maturation. Thus, it is important to identify ways to eliminate the effects of maternal diabetes on preimplantation embryos and oocytes. The objectives of this study were to investigate whether islet transplantation could reverse the effects of diabetes on oocytes. Our results revealed that maternal diabetes induced decreased ovulation; increased the frequency of meiotic spindle defects, chromosome misalignment, and aneuploidy; increased the relative expression levels of Mad2 and Bub1; and enhanced the sensitivity of oocytes to parthenogenetic activation. Islet transplantation prevented these detrimental effects. Therefore, we concluded that islet transplantation could reverse the effects of diabetes on oocytes, and that this technique may be useful to treat the fundamental reproductive problems of women with diabetes mellitus.


2016 ◽  
Vol 65 ◽  
pp. 159-169 ◽  
Author(s):  
Eric J. Schoevers ◽  
Regiane R. Santos ◽  
Johanna Fink-Gremmels ◽  
Bernard A.J. Roelen

2019 ◽  
Vol 20 (2) ◽  
pp. 409 ◽  
Author(s):  
Tao Lin ◽  
Jae Lee ◽  
Jung Kang ◽  
Hyeon Shin ◽  
Ju Lee ◽  
...  

Mammalian oocytes and early embryos derived from in vitro production are highly susceptible to a variety of cellular stresses. During oocyte maturation and preimplantation embryo development, functional proteins must be folded properly in the endoplasmic reticulum (ER) to maintain oocyte and embryo development. However, some adverse factors negatively impact ER functions and protein synthesis, resulting in the activation of ER stress and unfolded protein response (UPR) signaling pathways. ER stress and UPR signaling have been identified in mammalian oocytes and embryos produced in vitro, suggesting that modulation of ER stress and UPR signaling play very important roles in oocyte maturation and the development of preimplantation embryos. In this review, we briefly describe the current state of knowledge regarding ER stress, UPR signaling pathways, and their roles and mechanisms in mammalian (excluding human) oocyte maturation and preimplantation embryo development.


2019 ◽  
Vol 101 (2) ◽  
pp. 262-270 ◽  
Author(s):  
Megan Lim ◽  
Hannah M Brown ◽  
Karen L Kind ◽  
Jeremy G Thompson ◽  
Kylie R Dunning

Abstract Hemoglobin (Hb) is commonly known for its capacity to bind and transport oxygen and carbon dioxide in erythroid cells. However, it plays additional roles in cellular function and health due to its capacity to bind other gases including nitric oxide. Further, Hb acts as a potent antioxidant, quenching reactive oxygen species. Despite its potential roles in cellular function, the preponderance of Hb research remains focused on its role in oxygen regulation. There is increasing evidence that Hb expression is more ubiquitous than previously thought, with Hb and its variants found in a myriad of cell types ranging from macrophages to spermatozoa. The majority of nonerythroid cell types that express Hb are situated within hypoxic environments, suggesting Hb may play a role in hypoxia-inducible factor-regulated gene expression by controlling the level of oxygen available or as an adaptation to low oxygen providing a mechanism to store oxygen. Oocyte maturation and preimplantation embryo development occur within the low oxygen environments of the antral follicle and oviduct/uterus, respectively. Interestingly, Hb was recently found in human cumulus and granulosa cells and murine cumulus–oocyte complexes and preimplantation embryos. Here, we consolidate and analyze the research generated todate on Hb expression in nonerythroid cells with a particular focus on reproductive cell types. We outline future directions of this research to elucidate the role of Hb during oocyte maturation and preimplantation embryo development and finally, we explore the potential clinical applications and benefits of Hb supplementation during the in vitro culture of gametes and embryos.


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