• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

长非编码 RNA IGFBP7-AS1 通过自噬促进人脱落乳牙干细胞的牙源性分化:一项体外研究。

Long non-coding RNA IGFBP7-AS1 promotes odontogenic differentiation of stem cells from human exfoliated deciduous teeth through autophagy: An in vitro study.

机构信息

Department of Pediatric Dentistry, School and Hospital of Stomatology, Peking University, Beijing, China.

Department of Pediatric Dentistry, School and Hospital of Stomatology, Peking University, Beijing, China.

出版信息

Arch Oral Biol. 2022 Sep;141:105492. doi: 10.1016/j.archoralbio.2022.105492. Epub 2022 Jun 22.

DOI:10.1016/j.archoralbio.2022.105492
PMID:35772254
Abstract

OBJECTIVE

In the present study, we aimed to investigate whether long non-coding RNA (lncRNA) insulin-like growth factor binding protein 7-antisense 1 (IGFBP7-AS1) regulates the odonto-differentiation of stem cells from human exfoliated deciduous teeth (SHED) and its underlying mechanism.

DESIGN

Real-time polymerase chain reaction (PCR) and correlation analysis were used to determine the expression of IGFBP7-AS1 during odontogenesis. Alkaline phosphate staining, alizarin red S staining, and real-time PCR in vitro were performed to investigate the effects of IGFBP7-AS1 during odontogenesis. Western blot and immunostaining (with or without chloroquine treatment) were applied to detect the expression of the autophagy-related markers, microtubule-associated proteins 1A/1B light chain 3B (LC3B) and p62. The autophagy inhibitor 3-methyladenine was used to further clarify the effect of autophagy in odonto-differentiation as promoted by IGFBP7-AS1.

RESULTS

The expression of lncRNA IGFBP7-AS1 is significantly upregulated during odonto-differentiation of SHED and promotes odontogenesis of SHED in vitro. IGFBP7-AS1 promotes autophagy during odontogenesis.

CONCLUSIONS

IGFBP7-AS1 elicits odontogenic differentiation of SHED through autophagy. Furthermore, IGFBP7-AS1 shows promise as a gene target in the regeneration of dental hard tissue and dental-pulp complex.

摘要

目的

本研究旨在探讨长链非编码 RNA(lncRNA)胰岛素样生长因子结合蛋白 7 反义 1(IGFBP7-AS1)是否调节人乳牙脱落干细胞(SHED)的牙向分化及其潜在机制。

设计

实时聚合酶链反应(PCR)和相关分析用于确定 IGFBP7-AS1 在牙发生过程中的表达。体外碱性磷酸酶染色、茜素红 S 染色和实时 PCR 用于研究 IGFBP7-AS1 在牙发生过程中的作用。Western blot 和免疫染色(有或没有氯喹处理)用于检测自噬相关标志物微管相关蛋白 1A/1B 轻链 3B(LC3B)和 p62 的表达。自噬抑制剂 3-甲基腺嘌呤用于进一步阐明 IGFBP7-AS1 促进牙向分化过程中自噬的作用。

结果

lncRNA IGFBP7-AS1 在 SHED 的牙向分化过程中表达显著上调,并在体外促进 SHED 的牙发生。IGFBP7-AS1 促进牙发生过程中的自噬。

结论

IGFBP7-AS1 通过自噬引发 SHED 的牙向分化。此外,IGFBP7-AS1 有望成为牙硬组织和牙髓复合体再生的基因靶点。

相似文献

1
Long non-coding RNA IGFBP7-AS1 promotes odontogenic differentiation of stem cells from human exfoliated deciduous teeth through autophagy: An in vitro study.长非编码 RNA IGFBP7-AS1 通过自噬促进人脱落乳牙干细胞的牙源性分化:一项体外研究。
Arch Oral Biol. 2022 Sep;141:105492. doi: 10.1016/j.archoralbio.2022.105492. Epub 2022 Jun 22.
2
Long non-coding RNA IGFBP7-AS1 accelerates the odontogenic differentiation of stem cells from human exfoliated deciduous teeth by regulating IGFBP7 expression.长非编码 RNA IGFBP7-AS1 通过调节 IGFBP7 的表达加速人脱落乳牙干细胞的成牙分化。
Hum Cell. 2022 Nov;35(6):1697-1707. doi: 10.1007/s13577-022-00763-9. Epub 2022 Aug 29.
3
MiR-335-3p/miR-155-5p Involved in IGFBP7-AS1-Enhanced Odontogenic Differentiation.miR-335-3p/miR-155-5p 参与 IGFBP7-AS1 增强的成牙本质分化。
Int Dent J. 2023 Jun;73(3):362-369. doi: 10.1016/j.identj.2022.07.008. Epub 2022 Aug 20.
4
Long Noncoding RNA IGFBP7-AS1 Promotes Odontogenesis of Stem Cells from Human Exfoliated Deciduous Teeth via the p38 MAPK Pathway.长链非编码RNA IGFBP7-AS1通过p38丝裂原活化蛋白激酶途径促进人乳牙干细胞的牙发生
Stem Cells Int. 2022 Apr 16;2022:9227248. doi: 10.1155/2022/9227248. eCollection 2022.
5
DLX6-AS1 regulates odonto/osteogenic differentiation in dental pulp cells under the control of BMP9 via the miR-128-3p/MAPK14 axis: A laboratory investigation.DLX6-AS1 通过 miR-128-3p/MAPK14 轴调控 BMP9 诱导的牙髓细胞成牙/成骨分化:一项实验室研究。
Int Endod J. 2024 Nov;57(11):1623-1638. doi: 10.1111/iej.14120. Epub 2024 Jul 7.
6
Chondrogenic potential of stem cells from human exfoliated deciduous teeth in vitro and in vivo.人脱落乳牙干细胞在体内外的成软骨潜能
Acta Odontol Scand. 2014 Nov;72(8):664-72. doi: 10.3109/00016357.2014.888756. Epub 2014 Mar 3.
7
Extracellular IL-37 promotes osteogenic and odontogenic differentiation of human dental pulp stem cells via autophagy.细胞外白细胞介素-37 通过自噬促进人牙髓干细胞的成骨和成牙分化。
Exp Cell Res. 2021 Oct 1;407(1):112780. doi: 10.1016/j.yexcr.2021.112780. Epub 2021 Aug 16.
8
Ectopic Hard Tissue Formation by Odonto/Osteogenically In Vitro Differentiated Human Deciduous Teeth Pulp Stem Cells.体外牙本质/成骨分化的人乳牙牙髓干细胞异位硬组织形成
Calcif Tissue Int. 2015 Jul;97(1):80-9. doi: 10.1007/s00223-015-9989-1. Epub 2015 Apr 17.
9
Differences in osteogenic and odontogenic differentiation potential of DPSCs and SHED.DPSCs 和 SHED 成骨和成牙分化潜能的差异。
J Dent. 2020 Oct;101:103413. doi: 10.1016/j.jdent.2020.103413. Epub 2020 Jun 22.
10
LncRNA LEF1-AS1 promotes osteogenic differentiation of dental pulp stem cells via sponging miR-24-3p.长链非编码 RNA LEF1-AS1 通过海绵吸附 miR-24-3p 促进牙髓干细胞的成骨分化。
Mol Cell Biochem. 2020 Dec;475(1-2):161-169. doi: 10.1007/s11010-020-03868-7. Epub 2020 Aug 11.

引用本文的文献

1
The role of non-coding RNA regulates stem cell programmed death in disease therapy.非编码RNA在疾病治疗中调节干细胞程序性死亡的作用。
Noncoding RNA Res. 2025 Apr 23;13:57-70. doi: 10.1016/j.ncrna.2025.04.005. eCollection 2025 Aug.
2
Impacts of Circular RNAs on the Osteogenic Differentiation of Dental Stem Cells.环状RNA对牙干细胞成骨分化的影响
Stem Cells Int. 2025 May 8;2025:8338337. doi: 10.1155/sci/8338337. eCollection 2025.