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IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists

Pentraxin 3 (PTX3), a member of the c-reactive protein family, is a long pentraxin protein and a pro-inflammatory marker. However, the role of PTX3 in preeclampsia (PE) remains to be elucidated. Thus, the present study aimed to investigate the biological role and mechanisms underlying PTX3 in PE. In...

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Autores principales: Wang, Xiaoxi, Zhang, Jing, Ji, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855162/
https://www.ncbi.nlm.nih.gov/pubmed/35137920
http://dx.doi.org/10.3892/mmr.2022.12631
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author Wang, Xiaoxi
Zhang, Jing
Ji, Jing
author_facet Wang, Xiaoxi
Zhang, Jing
Ji, Jing
author_sort Wang, Xiaoxi
collection PubMed
description Pentraxin 3 (PTX3), a member of the c-reactive protein family, is a long pentraxin protein and a pro-inflammatory marker. However, the role of PTX3 in preeclampsia (PE) remains to be elucidated. Thus, the present study aimed to investigate the biological role and mechanisms underlying PTX3 in PE. In the present study, PTX3 was overexpressed in trophoblasts and the subsequent changes in cell proliferation, cycle distribution and invasion were observed using Cell Counting Kit-8, flow cytometry and Transwell assays, respectively. Moreover, the expression levels of MMP2 and MMP9, proteins associated with the development of PE, were detected using reverse transcription-quantitative PCR and western blot analysis. Following treatment with interleukin (IL)-1β, the expression levels of PTX3 were measured. Furthermore, subsequent changes in cell proliferation, cycle distribution and invasion were investigated following overexpression of PTX3 and treatment with IL-1 receptor antagonist (IL-1Ra). Overexpression of PTX3 inhibited the proliferation, cycle and invasion of HTR-8/SV neo and JEG3 cells. Moreover, treatment with IL-1β increased the expression of PTX3 in HTR-8/SV neo and JEG3 cells, which was suppressed following treatment with the IL-1β antagonist. Following PTX3 overexpression and treatment with IL-1Ra, the inhibitory effects of PTX3 overexpression alone on the invasion of HTR-8/SV neo and JEG3 cells were attenuated. In conclusion, these results indicated that IL-1β could induce PTX3 upregulation, which led to the inhibition of the proliferation, invasion and cell cycle of trophoblasts, thereby promoting the progression of PE.
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spelling pubmed-88551622022-03-07 IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists Wang, Xiaoxi Zhang, Jing Ji, Jing Mol Med Rep Articles Pentraxin 3 (PTX3), a member of the c-reactive protein family, is a long pentraxin protein and a pro-inflammatory marker. However, the role of PTX3 in preeclampsia (PE) remains to be elucidated. Thus, the present study aimed to investigate the biological role and mechanisms underlying PTX3 in PE. In the present study, PTX3 was overexpressed in trophoblasts and the subsequent changes in cell proliferation, cycle distribution and invasion were observed using Cell Counting Kit-8, flow cytometry and Transwell assays, respectively. Moreover, the expression levels of MMP2 and MMP9, proteins associated with the development of PE, were detected using reverse transcription-quantitative PCR and western blot analysis. Following treatment with interleukin (IL)-1β, the expression levels of PTX3 were measured. Furthermore, subsequent changes in cell proliferation, cycle distribution and invasion were investigated following overexpression of PTX3 and treatment with IL-1 receptor antagonist (IL-1Ra). Overexpression of PTX3 inhibited the proliferation, cycle and invasion of HTR-8/SV neo and JEG3 cells. Moreover, treatment with IL-1β increased the expression of PTX3 in HTR-8/SV neo and JEG3 cells, which was suppressed following treatment with the IL-1β antagonist. Following PTX3 overexpression and treatment with IL-1Ra, the inhibitory effects of PTX3 overexpression alone on the invasion of HTR-8/SV neo and JEG3 cells were attenuated. In conclusion, these results indicated that IL-1β could induce PTX3 upregulation, which led to the inhibition of the proliferation, invasion and cell cycle of trophoblasts, thereby promoting the progression of PE. D.A. Spandidos 2022-04 2022-02-07 /pmc/articles/PMC8855162/ /pubmed/35137920 http://dx.doi.org/10.3892/mmr.2022.12631 Text en Copyright: © Wang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Xiaoxi
Zhang, Jing
Ji, Jing
IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title_full IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title_fullStr IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title_full_unstemmed IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title_short IL-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by IL-1β antagonists
title_sort il-1β-induced pentraxin 3 inhibits the proliferation, invasion and cell cycle of trophoblasts in preeclampsia and is suppressed by il-1β antagonists
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855162/
https://www.ncbi.nlm.nih.gov/pubmed/35137920
http://dx.doi.org/10.3892/mmr.2022.12631
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