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一种改良的静水压微流控无泵装置,用于体外小鼠卵巢组织培养,作为生育力保存的研究模型。

A modified hydrostatic microfluidic pumpless device for in vitro murine ovarian tissue culture as research model for fertility preservation.

作者信息

Thuwanut Paweena, Pimpin Alongkorn, Thatsanabunjong Fueangrat, Srisuwatanasagul Sayamon, Sereepapong Wisan, Sirayapiwat Porntip

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Research Unit of Reproductive Medicine and Fertility Preservation, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Obstet Gynecol Sci. 2022 Jul;65(4):376-381. doi: 10.5468/ogs.22012. Epub 2022 Jun 16.

DOI:10.5468/ogs.22012
PMID:35707972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9304444/
Abstract

This study aimed to compare the efficacies of conventional and non-conventional (modified hydrostatic microfluidic pumpless device, MHPD) systems on ovarian tissue culture and in vitro follicle growth using a mouse model. A total of 56 ovarian cortical tissues retrieved from seven wild-type mice were divided into three groups: 1) fresh control, 2) conventional culture system (control), and 3) non-conventional system with MHPD. Ovarian tissues were cultured for 96 hours and evaluated for follicle morphology, developmental stage, intact follicle density, and relative gene expression levels (proliferating cell nuclear antigen, insulin like growth factor 1, BAX, and Bcl-2). Our major data demonstrated that the mean percentage of primary follicle development was increased by the MHPD (P<0.05). In addition, this device could maintain and support follicle development better than the conventional culture systems. However, the overall outcomes were not significantly improved by our first-design prototype. Consequently, nextgeneration platforms should be developed as alternative medical tools for fertility preservation research.

摘要

本研究旨在使用小鼠模型比较传统和非传统(改良型静水微流无泵装置,MHPD)系统对卵巢组织培养和体外卵泡生长的效果。从7只野生型小鼠获取的总共56个卵巢皮质组织被分为三组:1)新鲜对照组,2)传统培养系统(对照组),3)带有MHPD的非传统系统。卵巢组织培养96小时,并对卵泡形态、发育阶段、完整卵泡密度和相对基因表达水平(增殖细胞核抗原、胰岛素样生长因子1、BAX和Bcl-2)进行评估。我们的主要数据表明,MHPD使初级卵泡发育的平均百分比增加(P<0.05)。此外,该装置比传统培养系统能更好地维持和支持卵泡发育。然而,我们的第一代设计原型并未显著改善总体结果。因此,应开发下一代平台作为生育力保存研究的替代医学工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1415/9304444/088d923b0cf1/ogs-22012f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1415/9304444/088d923b0cf1/ogs-22012f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1415/9304444/088d923b0cf1/ogs-22012f1.jpg

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本文引用的文献

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Fertility-sparing treatment in early endometrial cancer: current state and future strategies.早期子宫内膜癌的保留生育功能治疗:现状与未来策略
Obstet Gynecol Sci. 2020 Jul;63(4):417-431. doi: 10.5468/ogs.19169. Epub 2020 Jul 8.
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In vitro spermatogenesis in two-dimensionally spread mouse testis tissues.二维铺展的小鼠睾丸组织中的体外精子发生
Reprod Med Biol. 2019 Aug 13;18(4):362-369. doi: 10.1002/rmb2.12291. eCollection 2019 Oct.
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Ovarian tissue cryopreservation for fertility preservation: clinical and research perspectives.
用于生育力保存的卵巢组织冷冻保存:临床与研究视角
Hum Reprod Open. 2017 Mar 29;2017(1):hox001. doi: 10.1093/hropen/hox001. eCollection 2017.
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Future developments: In vitro growth (IVG) of human ovarian follicles.未来的发展:人类卵巢滤泡的体外生长(IVG)。
Acta Obstet Gynecol Scand. 2019 May;98(5):653-658. doi: 10.1111/aogs.13592. Epub 2019 Apr 5.
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Acta Obstet Gynecol Scand. 2019 May;98(5):659-664. doi: 10.1111/aogs.13552. Epub 2019 Feb 24.
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A Microfluidic Device for Culturing an Encapsulated Ovarian Follicle.一种用于培养封装卵巢卵泡的微流控装置。
Micromachines (Basel). 2017 Nov 20;8(11):335. doi: 10.3390/mi8110335.
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Flow perfusion rate modulates cell deposition onto scaffold substrate during cell seeding.在细胞接种过程中,流动灌注速率调节细胞在支架上的沉积。
Biomech Model Mechanobiol. 2018 Jun;17(3):675-687. doi: 10.1007/s10237-017-0985-4. Epub 2017 Nov 29.
9
Pumpless microfluidic system driven by hydrostatic pressure induces and maintains mouse spermatogenesis in vitro.由静水压力驱动的无泵微流控系统在体外诱导并维持小鼠精子发生。
Sci Rep. 2017 Nov 13;7(1):15459. doi: 10.1038/s41598-017-15799-3.
10
A microfluidic culture model of the human reproductive tract and 28-day menstrual cycle.一种人类生殖道的微流控培养模型和 28 天的月经周期。
Nat Commun. 2017 Mar 28;8:14584. doi: 10.1038/ncomms14584.