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Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts
The aim of this study was to explore the effect of zearalenone (ZEA) exposure on uterine development in weaned gilts by quantitative proteome analysis with tandem mass spectrometry tags (TMT). A total of 16 healthy weaned gilts were randomly divided into control (basal diet) and ZEA3.0 treatments gr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610722/ https://www.ncbi.nlm.nih.gov/pubmed/36287961 http://dx.doi.org/10.3390/toxins14100692 |
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author | Liu, Xinglin Wang, Zengchun Jiang, Yanping Huang, Libo Yuan, Xuejun Li, Yang Jiao, Ning Yang, Weiren Jiang, Shuzhen |
author_facet | Liu, Xinglin Wang, Zengchun Jiang, Yanping Huang, Libo Yuan, Xuejun Li, Yang Jiao, Ning Yang, Weiren Jiang, Shuzhen |
author_sort | Liu, Xinglin |
collection | PubMed |
description | The aim of this study was to explore the effect of zearalenone (ZEA) exposure on uterine development in weaned gilts by quantitative proteome analysis with tandem mass spectrometry tags (TMT). A total of 16 healthy weaned gilts were randomly divided into control (basal diet) and ZEA3.0 treatments groups (basal diet supplemented with 3.0 mg/kg ZEA). Results showed that vulva size and uterine development index were increased (p < 0.05), whereas serum follicle stimulation hormone, luteinizing hormone and gonadotropin-releasing hormone were decreased in gilts fed the ZEA diet (p < 0.05). ZEA, α-zearalenol (α-ZOL) and β-zearalenol (β-ZOL) were detected in the uteri of gilts fed a 3.0 mg/kg ZEA diet (p < 0.05). The relative protein expression levels of creatine kinase M-type (CKM), atriopeptidase (MME) and myeloperoxidase (MPO) were up-regulated (p < 0.05), whereas aldehyde dehydrogenase 1 family member (ALDH1A2), secretogranin-1 (CHGB) and SURP and G-patch domain containing 1 (SUGP1) were down-regulated (p < 0.05) in the ZEA3.0 group by western blot, which indicated that the proteomics data were dependable. In addition, the functions of differentially expressed proteins (DEPs) mainly involved the cellular process, biological regulation and metabolic process in the biological process category. Some important signaling pathways were changed in the ZEA3.0 group, such as extracellular matrix (ECM)-receptor interaction, focal adhesion and the phosphoinositide 3-kinase–protein kinase B (PI3K-AKT) signaling pathway (p < 0.01). This study sheds new light on the molecular mechanism of ZEA in the uterine development of gilts. |
format | Online Article Text |
id | pubmed-9610722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96107222022-10-28 Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts Liu, Xinglin Wang, Zengchun Jiang, Yanping Huang, Libo Yuan, Xuejun Li, Yang Jiao, Ning Yang, Weiren Jiang, Shuzhen Toxins (Basel) Article The aim of this study was to explore the effect of zearalenone (ZEA) exposure on uterine development in weaned gilts by quantitative proteome analysis with tandem mass spectrometry tags (TMT). A total of 16 healthy weaned gilts were randomly divided into control (basal diet) and ZEA3.0 treatments groups (basal diet supplemented with 3.0 mg/kg ZEA). Results showed that vulva size and uterine development index were increased (p < 0.05), whereas serum follicle stimulation hormone, luteinizing hormone and gonadotropin-releasing hormone were decreased in gilts fed the ZEA diet (p < 0.05). ZEA, α-zearalenol (α-ZOL) and β-zearalenol (β-ZOL) were detected in the uteri of gilts fed a 3.0 mg/kg ZEA diet (p < 0.05). The relative protein expression levels of creatine kinase M-type (CKM), atriopeptidase (MME) and myeloperoxidase (MPO) were up-regulated (p < 0.05), whereas aldehyde dehydrogenase 1 family member (ALDH1A2), secretogranin-1 (CHGB) and SURP and G-patch domain containing 1 (SUGP1) were down-regulated (p < 0.05) in the ZEA3.0 group by western blot, which indicated that the proteomics data were dependable. In addition, the functions of differentially expressed proteins (DEPs) mainly involved the cellular process, biological regulation and metabolic process in the biological process category. Some important signaling pathways were changed in the ZEA3.0 group, such as extracellular matrix (ECM)-receptor interaction, focal adhesion and the phosphoinositide 3-kinase–protein kinase B (PI3K-AKT) signaling pathway (p < 0.01). This study sheds new light on the molecular mechanism of ZEA in the uterine development of gilts. MDPI 2022-10-09 /pmc/articles/PMC9610722/ /pubmed/36287961 http://dx.doi.org/10.3390/toxins14100692 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Xinglin Wang, Zengchun Jiang, Yanping Huang, Libo Yuan, Xuejun Li, Yang Jiao, Ning Yang, Weiren Jiang, Shuzhen Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title | Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title_full | Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title_fullStr | Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title_full_unstemmed | Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title_short | Quantitative Proteomic Analysis of Zearalenone Exposure on Uterine Development in Weaned Gilts |
title_sort | quantitative proteomic analysis of zearalenone exposure on uterine development in weaned gilts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610722/ https://www.ncbi.nlm.nih.gov/pubmed/36287961 http://dx.doi.org/10.3390/toxins14100692 |
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