Evidence map›Paper›PMID 39256850›Full record

ArticleStem cell research & therapy2024

Fgf9 promotes incisor dental epithelial stem cell survival and enamel formation.

Lingyun Tang, Mingmei Chen, Min Wu, Hui Liang, Haoyang Ge, Yan Ma, Yan Shen, Shunyuan Lu, Chunling Shen, Hongxin Zhang and 2 more

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Challenges of Studying Amelogenesis in Gene-Targeted Mouse Models.International journal of molecular sciences · 2025
    Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Lingyun Tang *State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Mingmei Chen *State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Min WuShanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to SJTUSM, Shanghai, China.
Hui LiangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Haoyang GeState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Yan MaRuijin Hospital Lu Wan Branch, Shanghai Jiaotong University School of Medicine, Shanghai, P.R. China.
Yan ShenState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Shunyuan LuState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Chunling ShenState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Hongxin ZhangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China.
Chenping ZhangKey Laboratory of Head & Neck Cancer Translational Research of Zhejiang Province, Department of Head and Neck Surgery, Zhejiang Cancer Hospital, Hangzhou, 310022, Zhejiang, P.R. China. zhang.chenping@hotmail.com.
Zhugang WangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Rui- Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Road II, Building #17, Shanghai, 200025, P.R. China. zhugangw@shsmu.edu.cn.ORCID 0000-0002-2626-4122

Funding

National Natural Science Foundation of China 81900799National Natural Science Foundation of China 81901529National Natural Science Foundation of China 81971462National Natural Science Foundation of China 82100163Science and Technology Commission of Shanghai Municipality 19YF1429700Science and Technology Commission of Shanghai Municipality 19YF1430400Shanghai Municipal Health Commission 2020YJZX0135
6 · The paper itself

Abstract

backgroundUnderstanding the role of cytokines in tooth development is critical for advancing dental tissue engineering. Fibroblast growth factor 9 (FGF9) is the only FGF consistently expressed throughout dental epithelial tissue, from the initiation of tooth bud formation to tooth maturation. However, mice lacking Fgf9 (Fgf9

methodsTo dissect the role of Fgf9 in tooth development, we performed the micro-CT, histomorphological analysis and gene expression assay in mice and embryos with S99N mutation. In addition, we assessed the effect of FGF9 on the DESC survival and dental epithelial differentiation by DESC sphere formation assay and tooth explant culture. Cell/tissue culture methods, gene expression analysis, specific inhibitors, and antibody blockage analysis were employed to explore how Fgf9 regulates enamel differentiation and DESC survival through both direct and indirect mechanisms.

resultsThe Fgf9

conclusionsOur study demonstrates that Fgf9 is essential for DESC survival and enamel formation. Fgf9 performs as a dual-directional regulator of the dental enamel epithelium, not only inhibiting DESC differentiation into ameloblasts to preserve the stemness of DESC, but also promoting ameloblast differentiation through epithelial-mesenchymal interactions.

Indexed as

Dental EnamelEpithelial CellsFibroblast Growth Factor 9Stem CellsAnimalsCell DifferentiationCell SurvivalIncisorMiceFgf9 protein, mouseFibroblast Growth Factor 9Cell survivalDental epithelial stem cellsEnamelEpithelial-mesenchymal interactionFibroblast growth factors

Identifiers

PMID39256850
PMCPMC11389439

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.