The Role of PI3K/AKT/HIF-1α Pathway in the Effect of Nano-TiO2 on Lactate Production in TM4 Cells.

IF 2.7 4区 医学 Q3 TOXICOLOGY
Hongmei Chang, Siqi Zhao, Yuzhu Lei, Yunhua Hu, Yizhong Yan, Guanling Song
{"title":"The Role of PI3K/AKT/HIF-1α Pathway in the Effect of Nano-TiO<sub>2</sub> on Lactate Production in TM4 Cells.","authors":"Hongmei Chang, Siqi Zhao, Yuzhu Lei, Yunhua Hu, Yizhong Yan, Guanling Song","doi":"10.1002/jat.4725","DOIUrl":null,"url":null,"abstract":"<p><p>Titanium dioxide nanoparticles (nano-TiO<sub>2</sub>) can cause a reduction in sperm counts, and lactate production in Sertoli cells plays a key role in spermatogenesis. The aim of this study was to evaluate the effect of nano-TiO<sub>2</sub> on lactate production in mouse Sertoli cell line (TM4 cells) and to investigate whether the effect is mediated through the PI3K/AKT/HIF-1α pathway. After TM4 cells were treated with different concentrations of nano-TiO<sub>2</sub> for 48 h, cell viability, contents of glucose and lactate, and the expression levels of GLUT3 and key enzymes (HK1, HK2, PFKM, ENO1, LDH) during lactate production were detected. PI3K/AKT/HIF-1α pathway proteins were measured. In addition, PI3K agonist (IGF-1) was added to explore whether nano-TiO<sub>2</sub> regulates HIF-1α through PI3K/AKT pathway, thereby affecting the production of lactate in TM4 cells. The results showed that nano-TiO<sub>2</sub> significantly inhibited TM4 cell viability, increased glucose content, decreased lactate content, and downregulated the expression levels of GLUT3 and key enzymes during lactate production. Meanwhile, nano-TiO<sub>2</sub> decreased the expression of PI3K/AKT pathway phosphorylated proteins and HIF-1α, and IGF attenuated this effect of nano-TiO<sub>2</sub>. Collectively, nano-TiO<sub>2</sub> downregulated the expression level of proteins and enzymes related to lactate production in TM4 cells by inhibiting PI3K/AKT/HIF-1α pathway, resulting in the decrease of lactate production in TM4 cells.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jat.4725","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Titanium dioxide nanoparticles (nano-TiO2) can cause a reduction in sperm counts, and lactate production in Sertoli cells plays a key role in spermatogenesis. The aim of this study was to evaluate the effect of nano-TiO2 on lactate production in mouse Sertoli cell line (TM4 cells) and to investigate whether the effect is mediated through the PI3K/AKT/HIF-1α pathway. After TM4 cells were treated with different concentrations of nano-TiO2 for 48 h, cell viability, contents of glucose and lactate, and the expression levels of GLUT3 and key enzymes (HK1, HK2, PFKM, ENO1, LDH) during lactate production were detected. PI3K/AKT/HIF-1α pathway proteins were measured. In addition, PI3K agonist (IGF-1) was added to explore whether nano-TiO2 regulates HIF-1α through PI3K/AKT pathway, thereby affecting the production of lactate in TM4 cells. The results showed that nano-TiO2 significantly inhibited TM4 cell viability, increased glucose content, decreased lactate content, and downregulated the expression levels of GLUT3 and key enzymes during lactate production. Meanwhile, nano-TiO2 decreased the expression of PI3K/AKT pathway phosphorylated proteins and HIF-1α, and IGF attenuated this effect of nano-TiO2. Collectively, nano-TiO2 downregulated the expression level of proteins and enzymes related to lactate production in TM4 cells by inhibiting PI3K/AKT/HIF-1α pathway, resulting in the decrease of lactate production in TM4 cells.

PI3K/AKT/HIF-1α通路在纳米二氧化钛影响TM4细胞乳酸生成中的作用
纳米二氧化钛(nano-TiO2)可导致精子数量减少,而Sertoli细胞中乳酸的产生在精子发生过程中起着关键作用。本研究旨在评估纳米二氧化钛对小鼠Sertoli细胞系(TM4细胞)乳酸生成的影响,并探讨这种影响是否通过PI3K/AKT/HIF-1α途径介导。用不同浓度的纳米二氧化钛处理 TM4 细胞 48 小时后,检测细胞活力、葡萄糖和乳酸含量、GLUT3 和乳酸生成过程中关键酶(HK1、HK2、PFKM、ENO1、LDH)的表达水平。检测了 PI3K/AKT/HIF-1α 通路蛋白。此外,还加入了PI3K激动剂(IGF-1),以探讨纳米二氧化钛是否通过PI3K/AKT途径调节HIF-1α,从而影响TM4细胞乳酸的产生。结果表明,纳米二氧化钛显著抑制了TM4细胞的活力,增加了葡萄糖含量,降低了乳酸含量,并下调了GLUT3和乳酸生成过程中关键酶的表达水平。同时,纳米二氧化钛降低了 PI3K/AKT 通路磷酸化蛋白和 HIF-1α 的表达,而 IGF 则减弱了纳米二氧化钛的这种效应。总之,纳米二氧化钛通过抑制PI3K/AKT/HIF-1α通路,下调了TM4细胞中与乳酸生成相关的蛋白和酶的表达水平,导致TM4细胞乳酸生成减少。
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
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
×
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