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胰岛素和雄激素信号在体外蜕膜化、细胞迁移和滋养细胞侵袭中的相互作用。

Interaction between insulin and androgen signalling in decidualization, cell migration and trophoblast invasion in vitro.

机构信息

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Department of Gynecology and Reproductive Medicine, Karolinska University Hospital, Stockholm, Sweden.

出版信息

J Cell Mol Med. 2021 Oct;25(20):9523-9532. doi: 10.1111/jcmm.16892. Epub 2021 Aug 31.

Abstract

Finely tuned decidualization of endometrial stromal fibroblasts into decidual cells is crucial for successful implantation and a healthy pregnancy. Both insulin and androgens are known to modulate decidualization, however, their complex effect on this process has not been fully elucidated. As hyperinsulinemia and hyperandrogenism are associated in clinical conditions, we aimed to investigate the interaction between insulin and androgens on decidualization. Primary human endometrial stromal cells were decidualized in vitro in the presence of insulin and/or androgens (dihydrotestosterone (DHT), testosterone). Gene or protein expressions of decidualization markers were measured, and cells size characteristics were determined. Migration of decidualizing endometrial stromal cells and invasion of HTR-8/SVneo trophoblast spheroids were assessed. We found that insulin and androgens in combination enhanced the upregulation of several decidualization markers including prolactin, tissue factor, tissue inhibitor of matrix metalloproteinase 3 and connexin-43, and also interacted in modulating cell size characteristics resulting in enlarged decidualizing cells. However, insulin and DHT together restricted the migration of decidualizing cells and invasion of trophoblast spheroids. Our findings suggest that insulin and androgens interact to potentiate the process of decidualization. On the other hand, inhibited cell migration and trophoblast invasion might negatively impact the function of decidualizing endometrial stromal cells.

摘要

精细调节子宫内膜基质成纤维细胞向蜕膜细胞的蜕膜化对于成功着床和健康妊娠至关重要。胰岛素和雄激素都已知可以调节蜕膜化,然而,它们对这一过程的复杂影响尚未完全阐明。由于高胰岛素血症和高雄激素血症在临床条件下是相关的,我们旨在研究胰岛素和雄激素对蜕膜化的相互作用。原代人子宫内膜基质细胞在体外培养,存在胰岛素和/或雄激素(二氢睾酮(DHT),睾酮)。测量蜕膜化标记物的基因或蛋白表达,并确定细胞大小特征。蜕膜化子宫内膜基质细胞的迁移和 HTR-8/SVneo 滋养层球体的侵袭也进行了评估。我们发现胰岛素和雄激素联合增强了几种蜕膜化标记物的上调,包括催乳素、组织因子、基质金属蛋白酶 3 的组织抑制剂和连接蛋白-43,并且还相互作用调节细胞大小特征,导致蜕膜化细胞增大。然而,胰岛素和 DHT 一起限制了蜕膜化细胞的迁移和滋养层球体的侵袭。我们的研究结果表明,胰岛素和雄激素相互作用以增强蜕膜化过程。另一方面,抑制细胞迁移和滋养层侵袭可能会对蜕膜化子宫内膜基质细胞的功能产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e634/8505820/00598628d9ac/JCMM-25-9523-g003.jpg

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