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使用基于胶原蛋白的组织工程技术对功能性体内马子宫内膜进行从头重建。

De novo reconstruction of a functional in vivo-like equine endometrium using collagen-based tissue engineering.

机构信息

Department of Obstetrics, Gynecology and Reproduction, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

CU-Animal Fertility Research Unit, Chulalongkorn University, Bangkok, Thailand.

出版信息

Sci Rep. 2024 Apr 19;14(1):9012. doi: 10.1038/s41598-024-59471-z.

Abstract

To better understand molecular aspects of equine endometrial function, there is a need for advanced in vitro culture systems that more closely imitate the intricate 3-dimensional (3D) in vivo endometrial structure than current techniques. However, development of a 3D in vitro model of this complex tissue is challenging. This study aimed to develop an in vitro 3D endometrial tissue (3D-ET) with an epithelial cell phenotype optimized by treatment with a Rho-associated protein kinase (ROCK) inhibitor. Equine endometrial epithelial (eECs) and mesenchymal stromal (eMSCs) cells were isolated separately, and eECs cultured in various concentrations of Rock inhibitor (0, 5, 10 µmol) in epithelial medium (EC-medium) containing 10% knock-out serum replacement (KSR). The optimal concentration of Rock inhibitor for enhancing eEC proliferation and viability was 10 µM. However, 10 µM Rock inhibitor in the 10% KSR EC-medium was able to maintain mucin1 (Muc1) gene expression for only a short period. In contrast, fetal bovine serum (FBS) was able to maintain Muc1 gene expression for longer culture durations. An in vitro 3D-ET was successfully constructed using a collagen-based scaffold to support the eECs and eMSCs. The 3D-ET closely mimicked in vivo endometrium by displaying gland-like eEC-derived structures positive for the endometrial gland marker, Fork headbox A2 (FOXA2), and by mimicking the 3D morphology of the stromal compartment. In addition, the 3D-ET expressed the secretory protein MUC1 on its glandular epithelial surface and responded to LPS challenge by upregulating the expression of the interleukin-6 (IL6) and prostaglandin F synthase (PGFS) genes (P < 0.01), along with an increase in their secretory products, IL-6 (P < 0.01) and prostaglandin F2alpha (PGF2α) (P < 0.001) respectively. In the future, this culture system can be used to study both normal physiology and pathological processes of the equine endometrium.

摘要

为了更好地了解马子宫内膜功能的分子方面,需要开发更能模拟当前技术复杂的 3 维(3D)体内子宫内膜结构的先进体外培养系统。然而,开发这种复杂组织的 3D 体外模型具有挑战性。本研究旨在开发一种具有上皮细胞表型的体外 3D 子宫内膜组织(3D-ET),该表型通过用 Rho 相关蛋白激酶(ROCK)抑制剂处理来优化。马子宫内膜上皮(eECs)和间质基质(eMSCs)细胞分别分离,eECs 在含有 10%无蛋白血清替代物(KSR)的上皮培养基(EC 培养基)中,用不同浓度的 ROCK 抑制剂(0、5、10 μmol)培养。促进 eEC 增殖和活力的最佳 ROCK 抑制剂浓度为 10 μM。然而,在含有 10%KSR 的 EC 培养基中,10 μM ROCK 抑制剂只能维持 Muc1 基因表达很短的时间。相比之下,胎牛血清(FBS)能够维持更长时间的 Muc1 基因表达。使用基于胶原蛋白的支架成功构建了体外 3D-ET,以支持 eECs 和 eMSCs。3D-ET 通过显示具有子宫内膜腺标记物叉头框 A2(FOXA2)阳性的腺样 eEC 衍生结构,以及模拟基质腔室的 3D 形态,紧密模拟体内子宫内膜。此外,3D-ET 在其腺上皮表面表达分泌蛋白 MUC1,并通过上调白细胞介素 6(IL6)和前列腺素 F 合酶(PGFS)基因的表达对 LPS 挑战做出反应(P<0.01),同时其分泌产物 IL-6(P<0.01)和前列腺素 F2alpha(PGF2α)(P<0.001)分别增加。将来,这种培养系统可用于研究马子宫内膜的正常生理和病理过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e973/11031578/fb906baadb49/41598_2024_59471_Fig1_HTML.jpg

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