scholarly journals Engineering the ovarian cycle using in vitro follicle culture

2015 ◽  
Vol 30 (6) ◽  
pp. 1386-1395 ◽  
Author(s):  
Robin M. Skory ◽  
Yuanming Xu ◽  
Lonnie D. Shea ◽  
Teresa K. Woodruff

2011 ◽  
Vol 85 (Suppl_1) ◽  
pp. 706-706
Author(s):  
Min Xu ◽  
Erin Jackson ◽  
Lonnie D. Shea ◽  
Teresa K Woodruff


2019 ◽  
Vol 20 (24) ◽  
pp. 6190
Author(s):  
Amandine Anastácio ◽  
Max Waterstone ◽  
Xia Hao ◽  
Catherine Poirot ◽  
Kenny A. Rodriguez-Wallberg

There is currently a lack of knowledge about the feasibility of performing procedures for fertility preservation after chemotherapy treatment has been initiated. In this experimental controlled study using adolescent mice, we aimed to investigate if the chance of rescuing and growing in vitro secondary follicles (SeF) would be affected three days after a single injection of cyclophosphamide (CPA). The main outcomes included were: (1) The number of SeF with good morphologic quality obtained per ovary 3 days after CPA injection, (2) SeF development in culture, (3) small follicle density (SFD) on histology, and (4) apoptosis markers, including terminal deoxynucleotidyl transferase dUTP nick end-labelling (TUNEL), mRNA expression, and distribution of p 53 upregulated modulator of apoptosis (Puma) and phosphatase and tensin homolog (Pten). We found a 60% reduction of SeF obtained per ovary in all CPA-treated groups vs. controls. However, in vitro survival rates at culture day 12 and antrum formation were similar among all groups. On histology, SFD was only significantly reduced in the high CPA dose group. Apoptotic cells were mainly found in large growing follicles of CPA groups. Our study indicates the feasibility of SeF isolation and in vitro follicle culture 3 days following CPA treatment and a still preserved SFD, particularly following a low-dose CPA treatment.



2021 ◽  
Vol 140 ◽  
pp. 111422
Author(s):  
Du Xiang ◽  
Yang Liu ◽  
Encheng Zhou ◽  
Yanfeng Wang


2009 ◽  
Vol 92 (3) ◽  
pp. S8
Author(s):  
J.E. Hirshfeld-Cytron ◽  
J.K. Jozefik ◽  
M. Xu ◽  
A. Shikanov ◽  
L.D. Shea ◽  
...  


2011 ◽  
Vol 85 (Suppl_1) ◽  
pp. 663-663
Author(s):  
Francesca E. Duncan ◽  
Jessica E. Hornick ◽  
Erin Jackson ◽  
Teresa Woodruff


2017 ◽  
Vol 69 (7) ◽  
pp. 477-484 ◽  
Author(s):  
Ting Zhang ◽  
Ying Chen ◽  
Yang Yang ◽  
Zhonghui Wang ◽  
Qi Pan ◽  
...  


Reproduction ◽  
2009 ◽  
Vol 138 (2) ◽  
pp. 247-255 ◽  
Author(s):  
A Nation ◽  
L Selwood

A model marsupial culture system has been developed whereby individual primary follicles, obtained from adult ovaries, can be grown in vitro to the antral stage and oocytes retrieved from these follicles can achieve nuclear maturation (metaphase II) in the presence of LH. Primary follicles isolated from adult Sminthopsis macroura ovaries were cultured individually in one of four systems: microdrops under oil, upright, inverted, or roller culture. After 6 days of culture, cumulus–oocyte complexes (COCs) were excised from early antral follicles and incubated for an additional 24 h to assess meiotic competence and the effects of LH and lithium on oocyte maturation. Histology and transmission electron microscopy established normal in vivo standards and verified oocyte and follicular integrity following culture. On day 6 of culture, follicle viability was significantly greater in the inverted system (73%) than in the other three systems (10–46%). The inverted system was the most effective in supporting development with follicles demonstrating progressive growth during culture and showing antral signs by day 4. Meiotic resumption during COC culture was facilitated by LH, but hindered by lithium. The ability to resume meiosis and progress to metaphase II was equivalent in oocytes retrieved following follicle culture and those matured in vivo. This study highlights the importance of oxygen and nutrient availability during marsupial follicle culture, and demonstrates for the first time that primary follicles isolated from adult mammalian ovaries can undergo normal growth and development in vitro, to produce mature, meiotically competent oocytes.



Author(s):  
Eugene Galdones ◽  
Lonnie D. Shea ◽  
Teresa K. Woodruff


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