Prrx2, the paired-related homeobox transcription factor, functions as a potential regulator of pannexin 3 expression in odontoblast differentiation

IF 2.6 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Oral Biosciences Pub Date : 2024-12-27 DOI:10.1016/j.job.2024.100601
Manami Tanaka , Asuna Sugimoto , Kokoro Iwata , Yumiko Nakashima , Muhammad Dhiaulfikri Nauval Hadiana , Yusuke Iwabuchi , Kanae Wada , Atsushi Oishi , Tsutomu Iwamoto
{"title":"Prrx2, the paired-related homeobox transcription factor, functions as a potential regulator of pannexin 3 expression in odontoblast differentiation","authors":"Manami Tanaka ,&nbsp;Asuna Sugimoto ,&nbsp;Kokoro Iwata ,&nbsp;Yumiko Nakashima ,&nbsp;Muhammad Dhiaulfikri Nauval Hadiana ,&nbsp;Yusuke Iwabuchi ,&nbsp;Kanae Wada ,&nbsp;Atsushi Oishi ,&nbsp;Tsutomu Iwamoto","doi":"10.1016/j.job.2024.100601","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to elucidate the roles of Prrx1 and Prrx2, homeobox transcription factors, in tooth development and determine whether Prrx2 regulates pannexin 3 (Panx3) expression, which is important in preodontoblasts.</div></div><div><h3>Methods</h3><div>Tooth sections were prepared from 13.5-, 15.5-, and 18.5-day-old embryonic ICR mice, and Prrx1- and Prrx2-expressing cells were identified by <em>in situ</em> hybridization. To clarify the direct relationship between Prrx2 and Panx3, dual-luciferase reporter assay and electrophoretic mobility shift assay (EMSA) were performed. The effect of endogenous Prrx2 suppression on Panx3 expression was analyzed using an siRNA assay.</div></div><div><h3>Results</h3><div><em>In situ</em> hybridization revealed that in the molars, Prrx1 and Prrx2 were similarly expressed in the bud and cap stages; however, only Prrx2 was expressed in preodontoblasts at the bell stage. In the incisors, Prrx2-expressing cells were observed from dental papilla cells to preodontoblasts. In serial sections, Prrx2-expressing cells in preodontoblasts corresponded to Panx3-expressing cells. Luciferase reporter assay using luciferase reporter plasmids containing Panx3 promoter revealed that Prrx2 overexpression in HEK293 cells significantly increased luciferase activity. EMSA of nuclear extract proteins from Prrx2-overexpressing HEK293 cells or mouse dental papilla-derived cells to the Panx3 promoter showed the protein-probe complex bands. SiRNA assay revealed that Prrx2 knockdown inhibited Panx3 expression.</div></div><div><h3>Conclusions</h3><div>Our results suggest that Prrx2 may regulate Panx3 expression during odontoblastic differentiation.</div></div>","PeriodicalId":45851,"journal":{"name":"Journal of Oral Biosciences","volume":"67 1","pages":"Article 100601"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Biosciences","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1349007924002500","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives

This study aimed to elucidate the roles of Prrx1 and Prrx2, homeobox transcription factors, in tooth development and determine whether Prrx2 regulates pannexin 3 (Panx3) expression, which is important in preodontoblasts.

Methods

Tooth sections were prepared from 13.5-, 15.5-, and 18.5-day-old embryonic ICR mice, and Prrx1- and Prrx2-expressing cells were identified by in situ hybridization. To clarify the direct relationship between Prrx2 and Panx3, dual-luciferase reporter assay and electrophoretic mobility shift assay (EMSA) were performed. The effect of endogenous Prrx2 suppression on Panx3 expression was analyzed using an siRNA assay.

Results

In situ hybridization revealed that in the molars, Prrx1 and Prrx2 were similarly expressed in the bud and cap stages; however, only Prrx2 was expressed in preodontoblasts at the bell stage. In the incisors, Prrx2-expressing cells were observed from dental papilla cells to preodontoblasts. In serial sections, Prrx2-expressing cells in preodontoblasts corresponded to Panx3-expressing cells. Luciferase reporter assay using luciferase reporter plasmids containing Panx3 promoter revealed that Prrx2 overexpression in HEK293 cells significantly increased luciferase activity. EMSA of nuclear extract proteins from Prrx2-overexpressing HEK293 cells or mouse dental papilla-derived cells to the Panx3 promoter showed the protein-probe complex bands. SiRNA assay revealed that Prrx2 knockdown inhibited Panx3 expression.

Conclusions

Our results suggest that Prrx2 may regulate Panx3 expression during odontoblastic differentiation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
配对相关的同源盒转录因子Prrx2在成牙细胞分化过程中可能调控pannexin 3的表达。
目的:本研究旨在阐明同源盒转录因子Prrx1和Prrx2在牙齿发育中的作用,并确定Prrx2是否调控pannexin 3 (Panx3)的表达,pannexin 3在成牙前细胞中起重要作用。方法:分别取13.5、15.5、18.5日龄ICR小鼠胚牙切片,原位杂交鉴定表达Prrx1和prrx2的细胞。为了明确Prrx2和Panx3之间的直接关系,我们进行了双荧光素酶报告基因实验和电泳迁移量转移实验(EMSA)。采用siRNA法分析内源性Prrx2抑制对Panx3表达的影响。结果:原位杂交结果显示,Prrx1和Prrx2在臼齿的芽和帽期表达相似;而在钟形期,只有Prrx2在成牙胚中表达。在门牙中,从牙乳头细胞到成牙前细胞均有表达prrx2的细胞。在连续切片中,原成牙细胞中表达prrx2的细胞与表达panx3的细胞相对应。利用含有Panx3启动子的荧光素酶报告质粒进行荧光素酶报告基因检测发现,在HEK293细胞中过表达Prrx2可显著提高荧光素酶活性。过表达prrx2的HEK293细胞或小鼠牙乳头源性细胞的核提取物蛋白对Panx3启动子的EMSA显示蛋白探针复合物带。SiRNA分析显示,Prrx2敲低抑制了Panx3的表达。结论:Prrx2可能在成牙细胞分化过程中调控Panx3的表达。
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 去求助
来源期刊
Journal of Oral Biosciences
Journal of Oral Biosciences DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.40
自引率
12.50%
发文量
57
审稿时长
37 days
期刊最新文献
TMPRSS2 expression in oral mucosal cells induced by transfected double-stranded RNA and IL-1β. Oral biosciences: The annual review 2024. MDP/NOD2 enhances RANKL-induced osteoclast differentiation of RAW264.7 cells The genetic basis of micro-structural fragility in murine dentin: Insights from type 2 diabetes mellitus Dietary texture-driven masticatory activity and its impact on stress tolerance
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1