Literature DB >> 31499015

Smad7 Regulates Dental Epithelial Proliferation during Tooth Development.

Z Liu1,2,3, T Chen1,2,4, D Bai1,4, W Tian1,3, Y Chen2.   

Abstract

Tooth morphogenesis involves dynamic changes in shape and size as it proceeds through the bud, cap, and bell stages. This process requires exact regulation of cell proliferation and differentiation. Smad7, a general antagonist against transforming growth factor-β (TGF-β) signaling, is necessary for maintaining homeostasis and proper functionality in many organs. While TGF-β signaling is widely involved in tooth morphogenesis, the precise role of Smad7 in tooth development remains unknown. In this study, we showed that Smad7 is expressed in the developing mouse molars with a high level in the dental epithelium but a moderate to weak level in the dental mesenchyme. Smad7 deficiency led to a profound decrease in tooth size primarily due to a severely compromised cell proliferation capability in the dental epithelium. Consistent with the tooth shrinkage phenotype, RNA sequencing (RNA-seq) analysis revealed that Smad7 ablation downregulated genes referred to epithelial cell proliferation and cell cycle G1/S phase transition, whereas the upregulated genes were involved in responding to TGF-β signaling and cell cycle arrest. Among these genes, the expression of Cdkn1a (encoding p21), a negative cell proliferation regulator, was remarkably elevated in parallel with the diminution of Ccnd1 encoding the crucial cell cycle regulator cyclin D1 in the dental epithelium. Meanwhile, the expression level of p-Smad2/3 was ectopically elevated in the developing tooth germ of Smad7 null mice, indicating the hyperactivation of the canonical TGF-β signaling. These effects were reversed by addition of TGF-β signaling inhibitor in cell cultures of Smad7-/- molar tooth germs, with rescued expression of cyclin D1 and cell proliferation rate. In sum, our studies demonstrate that Smad7 functions primarily as a positive regulator of cell proliferation via inhibition of the canonical TGF-β signaling during dental epithelium development and highlight a crucial role for Smad7 in regulating tooth size.

Entities:  

Keywords:  TGF-β signaling; cell proliferation; dental epithelium; negative modulator; tooth morphogenesis; tooth size

Mesh:

Substances:

Year:  2019        PMID: 31499015      PMCID: PMC6806130          DOI: 10.1177/0022034519872487

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  40 in total

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Journal:  J Biol Chem       Date:  2003-06-24       Impact factor: 5.157

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4.  Inhibition of transforming growth factor-beta type II receptor signaling accelerates tooth formation in mouse first branchial arch explants.

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Journal:  Mech Dev       Date:  1999-08       Impact factor: 1.882

5.  Distinct roles of transforming growth factor-β signaling and transforming growth factor-β receptor inhibitor SB431542 in the regulation of p21 expression.

Authors:  Bon-Hun Koo; Yeaji Kim; Yang Je Cho; Doo-Sik Kim
Journal:  Eur J Pharmacol       Date:  2015-07-14       Impact factor: 4.432

6.  Wnt5a regulates growth, patterning, and odontoblast differentiation of developing mouse tooth.

Authors:  Minkui Lin; Lu Li; Chao Liu; Hongbing Liu; Fenglei He; Fuhua Yan; Yanding Zhang; Yiping Chen
Journal:  Dev Dyn       Date:  2011-02       Impact factor: 3.780

7.  Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown.

Authors:  Mihaela Pertea; Daehwan Kim; Geo M Pertea; Jeffrey T Leek; Steven L Salzberg
Journal:  Nat Protoc       Date:  2016-08-11       Impact factor: 13.491

8.  Cyclin-dependent kinases regulate the antiproliferative function of Smads.

Authors:  Isao Matsuura; Natalia G Denissova; Guannan Wang; Dongming He; Jianyin Long; Fang Liu
Journal:  Nature       Date:  2004-07-08       Impact factor: 49.962

9.  Smad7 in T cells drives T helper 1 responses in multiple sclerosis and experimental autoimmune encephalomyelitis.

Authors:  Ingo Kleiter; Jian Song; Dominika Lukas; Maruf Hasan; Bernhard Neumann; Andrew L Croxford; Xiomara Pedré; Nadine Hövelmeyer; Nir Yogev; Alexander Mildner; Marco Prinz; Elena Wiese; Kurt Reifenberg; Stefan Bittner; Heinz Wiendl; Lawrence Steinman; Christoph Becker; Ulrich Bogdahn; Markus F Neurath; Andreas Steinbrecher; Ari Waisman
Journal:  Brain       Date:  2010-03-30       Impact factor: 13.501

Review 10.  Smad-dependent and Smad-independent pathways in TGF-beta family signalling.

Authors:  Rik Derynck; Ying E Zhang
Journal:  Nature       Date:  2003-10-09       Impact factor: 49.962

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1.  USP34 regulates tooth root morphogenesis by stabilizing NFIC.

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2.  Differential lncRNA/mRNA Expression Profiling and Functional Network Analyses in Bmp2 Deletion of Mouse Dental Papilla Cells.

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Journal:  Front Genet       Date:  2021-12-22       Impact factor: 4.599

3.  Discovery and functional assessment of a novel adipocyte population driven by intracellular Wnt/β-catenin signaling in mammals.

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4.  A Rare Case of Concrescence of Mandibular Third Molar and Supernumerary Fourth Molar.

Authors:  Jiao Wang; Errui Wang; Xin Yang; Lu Yuan; Zhige Li; Jie Zhang; Baoping Zhang
Journal:  Case Rep Dent       Date:  2022-08-31

Review 5.  Tooth Formation: Are the Hardest Tissues of Human Body Hard to Regenerate?

Authors:  Juliana Baranova; Dominik Büchner; Werner Götz; Margit Schulze; Edda Tobiasch
Journal:  Int J Mol Sci       Date:  2020-06-04       Impact factor: 5.923

  5 in total

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