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表皮生长因子样生长因子上调人颗粒黄体细胞中五聚素 3 的表达。

EGF-like growth factors upregulate pentraxin 3 expression in human granulosa-lutein cells.

机构信息

Department of Obstetrics and Gynecology, BC Children's Hospital Research Institute, University of British Columbia, Room 317, 950 West 28th Avenue, Vancouver, BC, V5Z 4H4, Canada.

Center for Reproductive Medicine, The First Affiliated Hospital of Zhengzhou University, 40, Daxue Road, Zhengzhou, 450052, Henan, China.

出版信息

J Ovarian Res. 2024 May 8;17(1):97. doi: 10.1186/s13048-024-01404-5.

Abstract

The epidermal growth factor (EGF)-like factors, comprising amphiregulin (AREG), betacellulin (BTC), and epiregulin (EREG), play a critical role in regulating the ovulatory process. Pentraxin 3 (PTX3), an essential ovulatory protein, is necessary for maintaining extracellular matrix (ECM) stability during cumulus expansion. The aim of this study was to investigate the impact of EGF-like factors, AREG, BTC, and EREG on the expression and production of PTX3 in human granulosa-lutein (hGL) cells and the molecular mechanisms involved. Our results demonstrated that AREG, BTC, and EREG could regulate follicular function by upregulating the expression and increasing the production of PTX3 in both primary (obtained from 20 consenting patients undergoing IVF treatment) and immortalized hGL cells. The upregulation of PTX3 expression was primarily facilitated by the activation of the extracellular signal-regulated kinase 1 and 2 (ERK1/2) signaling pathway, induced by these EGF-like factors. In addition, we found that the upregulation of PTX3 expression triggered by the EGF-like factors was completely reversed by either pretreatment with the epidermal growth factor receptor (EGFR) inhibitor, AG1478, or knockdown of EGFR, suggesting that EGFR is crucial for activating the ERK1/2 signaling pathway in hGL cells. Overall, our findings indicate that AREG, BTC, and EREG may modulate human cumulus expansion during the periovulatory stage through the upregulation of PTX3.

摘要

表皮生长因子(EGF)样因子,包括双调蛋白(AREG)、β细胞素(BTC)和表皮调节素(EREG),在调节排卵过程中起着关键作用。Pentraxin 3(PTX3),一种必需的排卵蛋白,对于在卵丘扩展过程中维持细胞外基质(ECM)稳定性是必要的。本研究旨在探讨 EGF 样因子 AREG、BTC 和 EREG 对人颗粒黄体(hGL)细胞中 PTX3 的表达和产生的影响及其涉及的分子机制。我们的结果表明,AREG、BTC 和 EREG 可以通过上调原代(从 20 名同意接受 IVF 治疗的患者中获得)和永生化 hGL 细胞中 PTX3 的表达和增加其产生来调节卵泡功能。PTX3 表达的上调主要是通过这些 EGF 样因子激活细胞外信号调节激酶 1 和 2(ERK1/2)信号通路来实现的。此外,我们发现 EGF 样因子诱导的 PTX3 表达上调可被表皮生长因子受体(EGFR)抑制剂 AG1478 预处理或 EGFR 敲低完全逆转,表明 EGFR 对于激活 hGL 细胞中的 ERK1/2 信号通路至关重要。总之,我们的研究结果表明,AREG、BTC 和 EREG 可能通过上调 PTX3 来调节人卵丘在排卵前阶段的扩展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6393/11077866/5a4361040972/13048_2024_1404_Fig1_HTML.jpg

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