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Induction of multiple ovulation via modulation of angiotensin II receptors in in vitro ovarian follicle culture models

Authors
Kim, Yong JinKim, Yoon YoungKang, Byeong-CheolKim, Moon SukKo, In KapLiu, Hung ChingRosenwaks, ZevKu, Seung-Yup
Issue Date
11월-2017
Publisher
WILEY
Keywords
multifollicular cluster culture; angiotensin II receptor; ovary
Citation
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.11, no.11, pp.3100 - 3110
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE
Volume
11
Number
11
Start Page
3100
End Page
3110
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81819
DOI
10.1002/term.2214
ISSN
1932-6254
Abstract
In vitro culture of ovarian follicles is a promising bioengineering technique for retrieving fertilizable oocytes from preserved ovarian tissues of cancer survivors. However, current in vitro follicle culture techniques are labour-intensive and of low efficiency, as only single follicle culture (SFC) has been possible to date. The present study investigated the feasibility of multifollicular cluster culture (MFCC) system using angiotensin II receptor (ATII-Rc) analogues. Ovarian pre-antral follicles isolated from 2-week-old C57BL6 mice were cultured with ATII-Rc agonist or antagonist and their maturation outcomes were compared with control group. When single follicles were cultured, the ovulation and maturation rates were similar in all three groups. When three-follicle clusters were cultured, up to three follicles were ovulated in the ATII-Rc agonist group while none or one follicle ovulated in control or antagonist groups (p < 0.0001). Significantly higher numbers of mature oocytes were obtained in the agonist group (three-follicle 28.2 +/- 4.9 vs. SFC 11.0 +/- 1.3, per 25 cultured droplets) (p < 0.0001), and the development of each fertilized oocytes was comparable to those from SFC. It is therefore concluded that this novel MFCC system can significantly improve the efficiency of in vitro mature oocyte retrieval via ATII-Rc modulation. Copyright (c) 2016 John Wiley & Sons, Ltd.
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