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人输卵管类器官为精子运动提供了有利环境。

Human fallopian tube organoids provide a favourable environment for sperm motility.

作者信息

Gatimel Nicolas, Perez Guillaume, Bruno Eloïse, Sagnat David, Rolland Corinne, Tanguy-Le-Gac Yan, Di Donato Emeline, Racaud Claire, Léandri Roger, Bettiol Célia, Deraison Céline, Motta Jean-Paul, Huyghe Eric, Vergnolle Nathalie

机构信息

Department of Reproductive Medicine, Hôpital Paule de Viguier, CHU Toulouse, Toulouse, France.

IRSD, Université de Toulouse, INSERM, INRAE, ENVT, Univ Toulouse III-Paul Sabatier (UPS), Toulouse, France.

出版信息

Hum Reprod. 2025 Mar 1;40(3):503-517. doi: 10.1093/humrep/deae258.

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.

摘要

研究问题

人输卵管(HFT)类器官模型是否能为人类精子的存活和运动提供良好的顶端环境?

总结答案

分化后,一种新型HFT类器官模型的顶端腔室为精子运动提供了良好的环境,优于商业培养基。

已知信息

输卵管是实现持续妊娠的关键重大事件发生的场所,如配子的存活和功能、受精步骤以及植入前胚胎发育。为了更好地理解参与这些生殖功能的输卵管生理学和输卵管因素,并改善体外受精过程中配子制备和胚胎培养仍不理想的条件,我们试图从分离的成体干细胞开发一种HFT类器官模型,以便在顶端腔室进行精子共培养。

研究设计、规模、持续时间:在2年的时间里,从10名因确定性绝育而接受腹腔镜双侧输卵管切除术的“供体”患者身上收集输卵管组织用于类器官培养。组织消化后,将从峡部和壶腹部区域分离的细胞分别接种到3D基质胶中,并用常规生长因子进行类器官培养,用特定因子进行女性生殖道分化培养。

参与者/材料、环境、方法:通过光学显微镜、扫描和透射电子显微镜、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,将来自五名供体的精子置于对照培养基或结肠或HFT类器官(分别为峡部和壶腹部)的顶端腔室中96小时。在每个条件下对200个精子在0、48和96小时时的活力、运动能力和运动学参数进行评估,一式两份,并使用Wilcoxon检验进行比较。

主要结果及偶然性的作用

通过免疫荧光、转录组分析和电子显微镜观察证实了我们模型中特定的输卵管分化,观察到了纤毛细胞和分泌细胞。我们成功地将精子释放到HFT类器官的顶端腔室中,并将其回收用于精子分析。HFT类器官和商业精子培养基中的精子活力值相似。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,我们证明了HFT类器官顶端腔室对精子运动能力具有优越性。在孵育48小时时,HFT类器官(壶腹部31%±17,峡部29%±15)顶端腔室中的进行性精子运动能力高于商业受精培养基(15%±15)(P<0.05),并与所有其他条件相比。在96小时时,除了HFT类器官中的精子外,所有条件下进行性精子运动能力几乎为零(<1%)(P<0.05):壶腹部和峡部类器官中分别为12%±15和13%±17。计算机辅助精子分析(CASA)分析还表明,与商业体外受精培养基相比,类器官能够显著维持更高水平的运动学参数(曲线速度、平均路径速度、直线速度和头部横向运动幅度),因此具有更高的运动效率。

大规模数据

无。

局限性、谨慎原因:这是一项体外研究,其中类器官培养条件无法完全模拟输卵管细胞外基质和血管化的体内环境。

研究结果的更广泛意义

这项工作为更好地理解HFT生理学开辟了前景。首次强调了开发用于生殖目的的HFT类器官的可能性。未来,它可能有助于我们改善人类辅助生殖技术中配子的受精能力和胚胎培养条件。

研究资金/利益冲突:本研究由奥克西塔尼地区的一项赠款以及DEFE和IRSD研究团队的资金分配资助。作者没有利益冲突需要报告。

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