Hydrogen peroxide-induced oxidative stress alters protein expression in two rat salivary acinar cell lines

IF 2.2 4区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Golnaz Golnarnik , Bernd Thiede , Tine M. Søland , Hilde K. Galtung , Trude M. Haug
{"title":"Hydrogen peroxide-induced oxidative stress alters protein expression in two rat salivary acinar cell lines","authors":"Golnaz Golnarnik ,&nbsp;Bernd Thiede ,&nbsp;Tine M. Søland ,&nbsp;Hilde K. Galtung ,&nbsp;Trude M. Haug","doi":"10.1016/j.archoralbio.2025.106254","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to investigate the impact of hydrogen peroxide-induced oxidative stress on the protein expression profiles of submandibular and parotid acinar cells using a proteomic approach. We sought to evaluate how oxidative stress might contribute to salivary gland dysfunction and whether the two glands respond differently.</div></div><div><h3>Design</h3><div>Immortalized rat parotid gland (PG) and submandibular gland (SMG) acinar epithelial cell lines were exposed to 50 µM and 150 µM hydrogen peroxide for 24 hr, followed by protein identification and quantification via liquid chromatography-mass spectrometry. Immunofluorescence microscopy and western blot analysis validated selected protein expressions, and cell viability was assessed using trypan blue exclusion assays.</div></div><div><h3>Results</h3><div>Compared to controls, histone H4 expression increased in both cell types after hydrogen peroxide exposure, whereas voltage-dependent anion-selective channel 1, keratin 7, and keratin 8 increased only in parotid gland cells. Conversely, mitochondrial aldehyde dehydrogenase and kidney isoform glutaminase were downregulated in parotid gland cells. Basal expression of mitochondrial aldehyde dehydrogenase and catalase was higher in submandibular gland cells. At higher hydrogen peroxide concentrations, antioxidant proteins expression and cell viability were greater in submandibular gland cells compared to parotid gland cells.</div></div><div><h3>Conclusions</h3><div>Our results suggest that submandibular gland acinar cells exhibit greater resistance to oxidative stress compared to parotid gland cells, potentially due to distinct antioxidant and metabolic coping strategies. Understanding these gland-specific responses may contribute to future approaches to protect salivary glands from oxidative damage under pathological conditions.</div></div>","PeriodicalId":8288,"journal":{"name":"Archives of oral biology","volume":"175 ","pages":"Article 106254"},"PeriodicalIF":2.2000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of oral biology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003996925000822","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives

This study aimed to investigate the impact of hydrogen peroxide-induced oxidative stress on the protein expression profiles of submandibular and parotid acinar cells using a proteomic approach. We sought to evaluate how oxidative stress might contribute to salivary gland dysfunction and whether the two glands respond differently.

Design

Immortalized rat parotid gland (PG) and submandibular gland (SMG) acinar epithelial cell lines were exposed to 50 µM and 150 µM hydrogen peroxide for 24 hr, followed by protein identification and quantification via liquid chromatography-mass spectrometry. Immunofluorescence microscopy and western blot analysis validated selected protein expressions, and cell viability was assessed using trypan blue exclusion assays.

Results

Compared to controls, histone H4 expression increased in both cell types after hydrogen peroxide exposure, whereas voltage-dependent anion-selective channel 1, keratin 7, and keratin 8 increased only in parotid gland cells. Conversely, mitochondrial aldehyde dehydrogenase and kidney isoform glutaminase were downregulated in parotid gland cells. Basal expression of mitochondrial aldehyde dehydrogenase and catalase was higher in submandibular gland cells. At higher hydrogen peroxide concentrations, antioxidant proteins expression and cell viability were greater in submandibular gland cells compared to parotid gland cells.

Conclusions

Our results suggest that submandibular gland acinar cells exhibit greater resistance to oxidative stress compared to parotid gland cells, potentially due to distinct antioxidant and metabolic coping strategies. Understanding these gland-specific responses may contribute to future approaches to protect salivary glands from oxidative damage under pathological conditions.
过氧化氢诱导的氧化应激改变了两种大鼠唾液腺泡细胞系的蛋白表达
目的应用蛋白质组学方法研究过氧化氢诱导的氧化应激对颌下腺和腮腺腺泡细胞蛋白表达谱的影响。我们试图评估氧化应激如何导致唾液腺功能障碍,以及这两种腺体的反应是否不同。永生化大鼠腮腺(PG)和下颌骨腺(SMG)腺泡上皮细胞系分别暴露于50 µM和150 µM过氧化氢中24 小时,通过液相色谱-质谱联用法对蛋白进行鉴定和定量。免疫荧光显微镜和western blot分析验证了选择的蛋白表达,并用台盼蓝排除法评估细胞活力。结果与对照组相比,过氧化氢暴露后两种细胞类型的组蛋白H4表达均增加,而电压依赖性阴离子选择通道1、角蛋白7和角蛋白8仅在腮腺细胞中增加。相反,线粒体醛脱氢酶和肾异构体谷氨酰胺酶在腮腺细胞中下调。颌下腺细胞中线粒体醛脱氢酶和过氧化氢酶的基础表达量较高。过氧化氢浓度较高时,与腮腺细胞相比,颌下腺细胞的抗氧化蛋白表达和细胞活力更高。结论与腮腺细胞相比,颌下腺腺泡细胞表现出更强的抗氧化应激能力,这可能是由于其具有不同的抗氧化和代谢应对策略。了解这些腺体特异性反应可能有助于未来在病理条件下保护唾液腺免受氧化损伤的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Archives of oral biology
Archives of oral biology 医学-牙科与口腔外科
CiteScore
5.10
自引率
3.30%
发文量
177
审稿时长
26 days
期刊介绍: Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including: Cell and molecular biology Molecular genetics Immunology Pathogenesis Cellular microbiology Embryology Syndromology Forensic dentistry
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信