Co-Culture of Mouse Blastocysts on A Human Recellularized Endometrial Scaffold: An In Vitro Model for Future Implantation Studies.

IF 1.7 4区 生物学 Q4 CELL BIOLOGY Cell Journal Pub Date : 2023-08-01 DOI:10.22074/cellj.2023.1989926.1236
Elham Sadeghi, Mojtaba Rezazadeh Valojerdi, Mojdeh Salehnia
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Abstract

Objective: This study evaluates the interaction of mouse blastocysts as a surrogate embryo on a recellularized endometrial scaffold by seeding human endometrial mesenchymal cells (hEMCs).

Materials and methods: In this experimental study, prepared decellularized human endometrial tissues were characterized by morphological staining, DNA content analysis, and scanning electron microscopic (SEM) analysis. The scaffolds were subsequently recellularized by hEMCs. After seven days of cultivation, the mouse blastocysts were co-cultured on the recellularized scaffolds for 48 hours. Embryo attachment and implantation within these scaffolds were evaluated at the morphological, ultrastructural, molecular, and hormonal levels.

Results: There was no morphological evidence of cells and nuclei in the decellularized scaffold. DNA content significantly decreased by 89.92% compared to the control group (P<0.05). Both decellularized and native tissues had similar patterns of collagen bundles and elastin fibers, and glycosaminoglycan (GAGs) distribution in the stroma. After recellularization, the hEMCs attached to the scaffold surface and penetrated different parts of these scaffolds. In the co-cultured group, the embryo attached to the surface of the scaffold after 24 hours and penetrated the recellularized endometrial tissue after 48 hours. We observed multi-layered organoid-like structures formed by hEMC proliferation. The relative expressions of epithelial-related genes, ZO-1 and COL4A1, and SSP1, MMP2, and PRL, as decidualizationrelated genes, were significantly higher in the recellularized group on day 9 in the presence of the embryo compared to the other groups (P<0.05). Beta human chorionic gonadotropin (β-hCG) and prolactin were statistically increased in the recellularized group on day 9 group (P<0.05).

Conclusion: hEMCs and mouse embryo co-cultured on a decellularized endometrial scaffold provides an alternative model to study embryo implantation and the earlier stage of embryo development.

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在人再细胞化子宫内膜支架上共同培养小鼠芽细胞:用于未来植入研究的体外模型。
目的:通过接种人子宫内膜间充质细胞(hEMCs),评价小鼠胚泡作为替代胚胎在再细胞化子宫内膜支架上的相互作用,以及扫描电子显微镜(SEM)分析。支架随后通过hEMCs进行再细胞化。培养7天后,将小鼠胚泡在再细胞支架上共培养48小时。胚胎在这些支架内的附着和植入在形态学、超微结构、分子和激素水平上进行了评估。结果:脱细胞支架中没有细胞和细胞核的形态学证据。与对照组相比,DNA含量显著降低了89.92%(PZO-1和COL4A1,SSP1、MMP2和PRL,作为蜕膜化相关基因,在胚胎存在的第9天,再细胞化组的DNA含量显著高于其他组结论:hEMCs和小鼠胚胎在脱细胞子宫内膜支架上共同培养,为研究胚胎植入和胚胎发育早期提供了一种替代模型。
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来源期刊
Cell Journal
Cell Journal CELL BIOLOGY-
CiteScore
3.40
自引率
5.00%
发文量
0
审稿时长
12 months
期刊介绍: The “Cell Journal (Yakhteh)“, formerly published as “Yakhteh Medical Journal”, is a quarterly English publication of Royan Institute. This journal focuses on topics relevant to cellular and molecular scientific areas, besides other related fields. The Cell J has been certified by Ministry of Culture and Islamic Guidance in 1999 and was accredited as a scientific and research journal by HBI (Health and Biomedical Information) Journal Accreditation Commission in 2000 which is an open access journal.
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