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

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

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

2024
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Overview
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.