Human fallopian tube organoids provide a favourable environment for sperm motility

IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY
Nicolas Gatimel, Guillaume Perez, Eloïse Bruno, David Sagnat, Corinne Rolland, Yan Tanguy-Le-Gac, Emeline Di Donato, Claire Racaud, Roger Léandri, Célia Bettiol, Céline Deraison, Jean-Paul Motta, Eric Huyghe, Nathalie Vergnolle
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In order to better understand the tubal physiology and tubal factors involved in these reproductive functions, and to improve still suboptimal in vitro conditions for gamete preparation and embryo culture during IVF, we sought to develop an HFT organoid model from isolated adult stem cells to allow spermatozoa co-culture in the apical compartment. STUDY DESIGN, SIZE, DURATION Over a 2-year period, fallopian tube tissues were collected for organoid culture purposes from 10 ‘donor’ patients undergoing bilateral salpingectomy by laparoscopy for definitive sterilization. After tissue digestion, isolated cells from the isthmus and ampulla regions were separately seeded in 3D Matrigel and cultured with conventional growth factors for organoid culture and specific factors for differentiation of the female genital tract. PARTICIPANTS/MATERIALS, SETTING, METHODS HFT organoids were characterized by light microscopy, scanning and transmission electron microscopy, immunofluorescence, and transcriptome analysis. Following simultaneous organoid culture on specific inserts, spermatozoa from five donors were placed either in control media or in the apical compartment of colon or HFT organoids (isthmus and ampulla separately) for 96 h. Vitality and motility and kinematic parameters were assessed at 0, 48, and 96 h on 200 spermatozoa in each condition and in duplicate and compared using the Wilcoxon test. MAIN RESULTS AND THE ROLE OF CHANCE Specific fallopian tube differentiation of our model was confirmed by immunofluorescence, transcriptome analysis, and electron microscopy observations that exhibited ciliated and secretory cells. We succeeded in releasing spermatozoa in the apical compartment of HFT organoids and in recovering them for sperm analysis. Sperm vitality values were similar in HFT organoids and in commercial sperm media. We demonstrated a superiority of the HFT organoid apical compartment for sperm motility compared with other controls (colon organoids, organoid culture media, and conventional commercial sperm fertilization media). At 48 h of incubation, progressive sperm motility was higher in the apical compartment of HFT organoids (ampulla 31% ± 17, isthmus 29% ± 15) than in commercial fertilization media (15% ± 15) (P < 0.05) and compared with all other conditions. At 96 h, progressive sperm motility was almost nil (<1%) in all conditions except for spermatozoa in HFT organoids (P < 0.05): 12% ± 15 and 13% ± 17 in ampulla and isthmus organoids, respectively. Computer-assisted sperm analysis (CASA) analysis also showed that the organoids were able to maintain significantly higher levels of kinematic parameters (curvilinear velocity, average path velocity, straight linear velocity, and amplitude of lateral movement of the head) and therefore more efficient mobility compared with commercial IVF media. LARGE SCALE DATA N/A. LIMITATIONS, REASONS FOR CAUTION This was an in vitro study in which conditions of organoid culture could not exactly mimic the in vivo environment of the extracellular matrix and vascularization of fallopian tubes. WIDER IMPLICATIONS OF THE FINDINGS This work opens up perspectives for better understanding of HFT physiology. For the first time, it highlights the possibility of developing HFT organoids for reproductive purposes. In the future, it could help us to improve gamete fertilizing abilities and embryo culture conditions during human ARTs. STUDY FUNDING/COMPETING INTEREST(S) This study was funded by a grant from the Occitanie region, and by financial allocations from the DEFE and IRSD research teams. The authors have no conflicts of interest to report.","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":"129 1","pages":""},"PeriodicalIF":6.0000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human reproduction","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/humrep/deae258","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

STUDY QUESTION Does a human fallopian tube (HFT) organoid model offer a favourable apical environment for human sperm survival and motility? SUMMARY ANSWER After differentiation, the apical compartment of a new HFT organoid model provides a favourable environment for sperm motility, which is better than commercial media. WHAT IS KNOWN ALREADY HFTs are the site of major events that are crucial for achieving an ongoing pregnancy, such as gamete survival and competence, fertilization steps, and preimplantation embryo development. In order to better understand the tubal physiology and tubal factors involved in these reproductive functions, and to improve still suboptimal in vitro conditions for gamete preparation and embryo culture during IVF, we sought to develop an HFT organoid model from isolated adult stem cells to allow spermatozoa co-culture in the apical compartment. STUDY DESIGN, SIZE, DURATION Over a 2-year period, fallopian tube tissues were collected for organoid culture purposes from 10 ‘donor’ patients undergoing bilateral salpingectomy by laparoscopy for definitive sterilization. After tissue digestion, isolated cells from the isthmus and ampulla regions were separately seeded in 3D Matrigel and cultured with conventional growth factors for organoid culture and specific factors for differentiation of the female genital tract. PARTICIPANTS/MATERIALS, SETTING, METHODS HFT organoids were characterized by light microscopy, scanning and transmission electron microscopy, immunofluorescence, and transcriptome analysis. Following simultaneous organoid culture on specific inserts, spermatozoa from five donors were placed either in control media or in the apical compartment of colon or HFT organoids (isthmus and ampulla separately) for 96 h. Vitality and motility and kinematic parameters were assessed at 0, 48, and 96 h on 200 spermatozoa in each condition and in duplicate and compared using the Wilcoxon test. MAIN RESULTS AND THE ROLE OF CHANCE Specific fallopian tube differentiation of our model was confirmed by immunofluorescence, transcriptome analysis, and electron microscopy observations that exhibited ciliated and secretory cells. We succeeded in releasing spermatozoa in the apical compartment of HFT organoids and in recovering them for sperm analysis. Sperm vitality values were similar in HFT organoids and in commercial sperm media. We demonstrated a superiority of the HFT organoid apical compartment for sperm motility compared with other controls (colon organoids, organoid culture media, and conventional commercial sperm fertilization media). At 48 h of incubation, progressive sperm motility was higher in the apical compartment of HFT organoids (ampulla 31% ± 17, isthmus 29% ± 15) than in commercial fertilization media (15% ± 15) (P < 0.05) and compared with all other conditions. At 96 h, progressive sperm motility was almost nil (<1%) in all conditions except for spermatozoa in HFT organoids (P < 0.05): 12% ± 15 and 13% ± 17 in ampulla and isthmus organoids, respectively. Computer-assisted sperm analysis (CASA) analysis also showed that the organoids were able to maintain significantly higher levels of kinematic parameters (curvilinear velocity, average path velocity, straight linear velocity, and amplitude of lateral movement of the head) and therefore more efficient mobility compared with commercial IVF media. LARGE SCALE DATA N/A. LIMITATIONS, REASONS FOR CAUTION This was an in vitro study in which conditions of organoid culture could not exactly mimic the in vivo environment of the extracellular matrix and vascularization of fallopian tubes. WIDER IMPLICATIONS OF THE FINDINGS This work opens up perspectives for better understanding of HFT physiology. For the first time, it highlights the possibility of developing HFT organoids for reproductive purposes. In the future, it could help us to improve gamete fertilizing abilities and embryo culture conditions during human ARTs. STUDY FUNDING/COMPETING INTEREST(S) This study was funded by a grant from the Occitanie region, and by financial allocations from the DEFE and IRSD research teams. The authors have no conflicts of interest to report.
人类输卵管类器官为精子运动提供了有利的环境
研究问题:人类输卵管(HFT)类器官模型是否为人类精子的存活和活动提供了有利的根尖环境?新型HFT类器官模型分化后,其顶室为精子活动提供了良好的环境,优于商业培养基。HFTs是实现持续妊娠至关重要的重大事件发生的场所,如配子存活和能力、受精步骤和着床前胚胎发育。为了更好地了解输卵管生理学和输卵管因素参与这些生殖功能,并改善试管婴儿过程中配子制备和胚胎培养的体外条件,我们试图利用分离的成体干细胞建立HFT类器官模型,使精子能够在根尖室中共同培养。研究设计、大小、持续时间在2年多的时间里,我们收集了10例通过腹腔镜双侧输卵管切除术进行最终绝育的“供体”患者的输卵管组织用于类器官培养。组织消化后,从峡部和壶腹区分离细胞,分别在3D基质中播种,用常规生长因子进行类器官培养,并用特异性因子进行女性生殖道分化。参与者/材料、环境、方法采用光镜、扫描和透射电镜、免疫荧光和转录组分析对HFT类器官进行表征。在特定插入物上同时进行类器官培养后,将来自5个供体的精子分别置于对照培养基或结肠或HFT类器官的顶室(分别为地部和壶腹)中96小时。在每种情况下分别对200个精子进行0、48和96小时的活力、运动和运动学参数评估,并使用Wilcoxon测试进行比较。通过免疫荧光、转录组分析和电镜观察证实,我们的模型中出现了纤毛细胞和分泌细胞。我们成功地将精子释放到HFT类器官的顶室中,并将其恢复用于精子分析。精子活力值在HFT类器官和商业精子介质中相似。我们证明了与其他对照(结肠类器官、类器官培养基和传统商业精子受精培养基)相比,HFT类器官根尖室在精子活力方面的优势。孵育48 h时,HFT类器官顶端室(壶腹31%±17,峡部29%±15)的精子运动率高于商业受精介质(15%±15)(P <;0.05),与其他条件比较。96 h时,除了HFT类器官中的精子(P <1%)外,在所有条件下,精子的进行性运动几乎为零(<1%)。0.05):壶腹和峡部类器官分别为12%±15和13%±17。计算机辅助精子分析(CASA)分析也表明,类器官能够保持明显更高水平的运动学参数(曲线速度、平均路径速度、直线线速度和头部横向运动幅度),因此与商业试管婴儿培养基相比,更有效的流动性。大规模数据。这是一项体外研究,类器官培养的条件不能完全模拟细胞外基质和输卵管血管化的体内环境。这项工作为更好地理解高频交易生理学开辟了新的视角。它首次强调了开发用于生殖目的的高频交易类器官的可能性。在未来,它可以帮助我们改善人类抗逆转录病毒过程中配子的受精能力和胚胎培养条件。研究经费/竞争利益(S)本研究由奥西达尼地区的拨款以及国防部和IRSD研究团队的财政拨款资助。作者没有利益冲突需要报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human reproduction
Human reproduction 医学-妇产科学
CiteScore
10.90
自引率
6.60%
发文量
1369
审稿时长
1 months
期刊介绍: Human Reproduction features full-length, peer-reviewed papers reporting original research, concise clinical case reports, as well as opinions and debates on topical issues. Papers published cover the clinical science and medical aspects of reproductive physiology, pathology and endocrinology; including andrology, gonad function, gametogenesis, fertilization, embryo development, implantation, early pregnancy, genetics, genetic diagnosis, oncology, infectious disease, surgery, contraception, infertility treatment, psychology, ethics and social issues.
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