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PRX1 阳性间充质干细胞驱动磨牙形态发生。

PRX1-positive mesenchymal stem cells drive molar morphogenesis.

机构信息

Department of Implantology, Stomatological Hospital and Dental School of Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, China.

出版信息

Int J Oral Sci. 2024 Feb 19;16(1):15. doi: 10.1038/s41368-024-00277-0.


DOI:10.1038/s41368-024-00277-0
PMID:38369512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10874978/
Abstract

Mammalian teeth, developing inseparable from epithelial-mesenchymal interaction, come in many shapes and the key factors governing tooth morphology deserve to be answered. By merging single-cell RNA sequencing analysis with lineage tracing models, we have unearthed a captivating correlation between the contrasting morphology of mouse molars and the specific presence of PRX1 cells within M1. These PRX1 cells assume a profound responsibility in shaping tooth morphology through a remarkable divergence in dental mesenchymal cell proliferation. Deeper into the mechanisms, we have discovered that Wnt5a, bestowed by mesenchymal PRX1 cells, stimulates mesenchymal cell proliferation while orchestrating molar morphogenesis through WNT signaling pathway. The loss of Wnt5a exhibits a defect phenotype similar to that of siPrx1. Exogenous addition of WNT5A can successfully reverse the inhibited cell proliferation and consequent deviant appearance exhibited in Prx1-deficient tooth germs. These findings bestow compelling evidence of PRX1-positive mesenchymal cells to be potential target in regulating tooth morphology.

摘要

哺乳动物的牙齿在发育过程中与上皮-间充质相互作用密不可分,其形态各异,值得深入研究控制牙齿形态的关键因素。通过将单细胞 RNA 测序分析与谱系追踪模型相结合,我们发现了一个引人注目的关联,即小鼠磨牙的形态对比与 M1 中 PRX1 细胞的存在之间存在关联。这些 PRX1 细胞通过在牙齿间充质细胞增殖方面的显著差异,对牙齿形态的形成具有深远的影响。深入研究其机制,我们发现由间充质 PRX1 细胞赋予的 Wnt5a 通过 WNT 信号通路刺激间充质细胞增殖,同时协调磨牙形态发生。缺失 Wnt5a 会表现出与 siPrx1 相似的缺陷表型。外源性添加 WNT5A 可以成功逆转 Prx1 缺陷牙胚中抑制的细胞增殖和随后的异常外观。这些发现为 PRX1 阳性间充质细胞作为调节牙齿形态的潜在靶点提供了有力证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/3964844fbdac/41368_2024_277_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f5b051ab3f2c/41368_2024_277_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/c8efaaf46815/41368_2024_277_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/1ebc533064db/41368_2024_277_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/71dc09e91b63/41368_2024_277_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f9d561163a80/41368_2024_277_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/df8e04f287e0/41368_2024_277_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f7101e9a49fa/41368_2024_277_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/b7cc2cf09ac8/41368_2024_277_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/3964844fbdac/41368_2024_277_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f5b051ab3f2c/41368_2024_277_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/c8efaaf46815/41368_2024_277_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/1ebc533064db/41368_2024_277_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/71dc09e91b63/41368_2024_277_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f9d561163a80/41368_2024_277_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/df8e04f287e0/41368_2024_277_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/f7101e9a49fa/41368_2024_277_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/b7cc2cf09ac8/41368_2024_277_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/811d/10874978/3964844fbdac/41368_2024_277_Fig9_HTML.jpg

相似文献

[1]
PRX1-positive mesenchymal stem cells drive molar morphogenesis.

Int J Oral Sci. 2024-2-19

[2]
Tracing PRX1 cells during molar formation and periodontal ligament reconstruction.

Int J Oral Sci. 2022-1-25

[3]
The Prx1 homeobox gene is critical for molar tooth morphogenesis.

J Dent Res. 2006-10

[4]
Activin and Bmp4 Signaling Converge on Wnt Activation during Odontogenesis.

J Dent Res. 2017-9

[5]
Hepatocyte growth factor stimulates root growth during the development of mouse molar teeth.

J Periodontal Res. 2011-8-21

[6]
Smad7 Regulates Dental Epithelial Proliferation during Tooth Development.

J Dent Res. 2019-9-9

[7]
Hepatocyte growth factor is involved in the morphogenesis of tooth germ in murine molars.

Development. 1996-4

[8]
Fgfr2b mediated epithelial-mesenchymal interactions coordinate tooth morphogenesis and dental trigeminal axon patterning.

Mech Dev. 2007

[9]
Glucose uptake mediated by glucose transporter 1 is essential for early tooth morphogenesis and size determination of murine molars.

Dev Biol. 2011-12-20

[10]
Role of PTH1R Signaling in Prx1 Mesenchymal Progenitors during Eruption.

J Dent Res. 2020-10

本文引用的文献

[1]
Cuspal Shape Alterations by Bmp4 Directing Cell Proliferation and Apoptosis.

J Dent Res. 2023-7

[2]
Loss of Stat3 in Osterix cells impairs dental hard tissues development.

Cell Biosci. 2023-4-23

[3]
Plasticity of Dental Cell Types in Development, Regeneration, and Evolution.

J Dent Res. 2023-6

[4]
Dental niche cells directly contribute to tooth reconstitution and morphogenesis.

Cell Rep. 2022-12-6

[5]
Periodic spatial patterning with a single morphogen.

Cell Syst. 2022-12-21

[6]
Spatiotemporal single-cell regulatory atlas reveals neural crest lineage diversification and cellular function during tooth morphogenesis.

Nat Commun. 2022-8-16

[7]
Stromal changes in the aged lung induce an emergence from melanoma dormancy.

Nature. 2022-6

[8]
Post natal expression of Prx1 labels appendicular restricted progenitor cell populations of multiple tissues.

J Cell Physiol. 2022-5

[9]
Tracing PRX1 cells during molar formation and periodontal ligament reconstruction.

Int J Oral Sci. 2022-1-25

[10]
Wnt5a Promotes Lysosomal Cholesterol Egress and Protects Against Atherosclerosis.

Circ Res. 2022-1-21

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