C5a complement receptor modulates odontogenic dental pulp stem cell differentiation under hypoxia.

IF 2.8 4区 医学 Q3 CELL BIOLOGY
Ryan Pasiewicz, Yessenia Valverde, Raghuvaran Narayanan, Ji-Hyun Kim, Muhammad Irfan, Nam-Seob Lee, Anne George, Lyndon F Cooper, Satish B Alapati, Seung Chung
{"title":"C5a complement receptor modulates odontogenic dental pulp stem cell differentiation under hypoxia.","authors":"Ryan Pasiewicz,&nbsp;Yessenia Valverde,&nbsp;Raghuvaran Narayanan,&nbsp;Ji-Hyun Kim,&nbsp;Muhammad Irfan,&nbsp;Nam-Seob Lee,&nbsp;Anne George,&nbsp;Lyndon F Cooper,&nbsp;Satish B Alapati,&nbsp;Seung Chung","doi":"10.1080/03008207.2021.1924696","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Alterations in the microenvironment change the phenotypes of dental pulp stem cells (DPSCs). The role of complement component C5a in the differentiation of DPSCs is unknown, especially under oxygen-deprived conditions. The aim of this study was to determine the effect of C5a on the odontogenic differentiation of DPSCs under normoxia and hypoxia.</p><p><strong>Material and methods: </strong>Human DPSCs were subjected to odontogenic differentiation in osteogenic media and treated with the C5a receptor antagonist-W54011 under normal and hypoxic conditions (2% oxygen). Immunochemistry, western blot, and PCR analysis for the various odontogenic differentiation genes/proteins were performed.</p><p><strong>Results: </strong>Our results demonstrated that C5a plays a positive role in the odontogenic differentiation of DPSCs. C5a receptor inhibition resulted in a significant decrease in odontogenic differentiation genes, such as DMP1, ON, RUNX2, DSPP compared with the control. This observation was further supported by the Western blot data for DSPP and DMP1 and immunohistochemical analysis. The hypoxic condition reversed this effect.</p><p><strong>Conclusions: </strong>Our results demonstrate that C5a regulates the odontogenic DPSC differentiation under normoxia. Under hypoxia, C5a exerts a reversed function for DPSC differentiation. Taken together, we identified that C5a and oxygen levels are key initial signals during pulp inflammation to control the odontogenic differentiation of DPSCs, thereby, providing a mechanism for potential therapeutic interventions for dentin repair and vital tooth preservation.</p>","PeriodicalId":10661,"journal":{"name":"Connective Tissue Research","volume":"63 4","pages":"339-348"},"PeriodicalIF":2.8000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/03008207.2021.1924696","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Connective Tissue Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/03008207.2021.1924696","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 5

Abstract

Aim: Alterations in the microenvironment change the phenotypes of dental pulp stem cells (DPSCs). The role of complement component C5a in the differentiation of DPSCs is unknown, especially under oxygen-deprived conditions. The aim of this study was to determine the effect of C5a on the odontogenic differentiation of DPSCs under normoxia and hypoxia.

Material and methods: Human DPSCs were subjected to odontogenic differentiation in osteogenic media and treated with the C5a receptor antagonist-W54011 under normal and hypoxic conditions (2% oxygen). Immunochemistry, western blot, and PCR analysis for the various odontogenic differentiation genes/proteins were performed.

Results: Our results demonstrated that C5a plays a positive role in the odontogenic differentiation of DPSCs. C5a receptor inhibition resulted in a significant decrease in odontogenic differentiation genes, such as DMP1, ON, RUNX2, DSPP compared with the control. This observation was further supported by the Western blot data for DSPP and DMP1 and immunohistochemical analysis. The hypoxic condition reversed this effect.

Conclusions: Our results demonstrate that C5a regulates the odontogenic DPSC differentiation under normoxia. Under hypoxia, C5a exerts a reversed function for DPSC differentiation. Taken together, we identified that C5a and oxygen levels are key initial signals during pulp inflammation to control the odontogenic differentiation of DPSCs, thereby, providing a mechanism for potential therapeutic interventions for dentin repair and vital tooth preservation.

C5a补体受体在缺氧条件下调控牙源性牙髓干细胞的分化。
目的:微环境的改变会改变牙髓干细胞(DPSCs)的表型。补体成分C5a在DPSCs分化中的作用尚不清楚,特别是在缺氧条件下。本研究旨在探讨C5a在常氧和缺氧条件下对DPSCs成牙分化的影响。材料和方法:将人DPSCs在成骨培养基中进行成牙分化,并在正常和低氧条件下(2%氧气)用C5a受体拮抗剂w54011处理。免疫化学、western blot和PCR分析各种牙源性分化基因/蛋白。结果:我们的研究结果表明,C5a在DPSCs的成牙分化中起着积极的作用。C5a受体抑制导致成牙分化基因DMP1、ON、RUNX2、DSPP较对照组显著降低。DSPP和DMP1的Western blot数据和免疫组织化学分析进一步支持了这一观察结果。缺氧条件逆转了这种作用。结论:我们的研究结果表明,在正常缺氧条件下,C5a调节牙源性DPSC的分化。在缺氧条件下,C5a对DPSC的分化发挥相反的作用。综上所述,我们发现C5a和氧水平是牙髓炎症过程中控制DPSCs成牙分化的关键初始信号,从而为牙本质修复和重要牙齿保存提供了潜在的治疗干预机制。
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
Connective Tissue Research
Connective Tissue Research 生物-细胞生物学
CiteScore
6.60
自引率
3.40%
发文量
37
审稿时长
2 months
期刊介绍: The aim of Connective Tissue Research is to present original and significant research in all basic areas of connective tissue and matrix biology. The journal also provides topical reviews and, on occasion, the proceedings of conferences in areas of special interest at which original work is presented. The journal supports an interdisciplinary approach; we present a variety of perspectives from different disciplines, including Biochemistry Cell and Molecular Biology Immunology Structural Biology Biophysics Biomechanics Regenerative Medicine The interests of the Editorial Board are to understand, mechanistically, the structure-function relationships in connective tissue extracellular matrix, and its associated cells, through interpretation of sophisticated experimentation using state-of-the-art technologies that include molecular genetics, imaging, immunology, biomechanics and tissue engineering.
×
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