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PAX9通过调节细胞外基质参与人诱导多能干细胞向牙周膜干细胞样分化。

PAX9 Is Involved in Periodontal Ligament Stem Cell-like Differentiation of Human-Induced Pluripotent Stem Cells by Regulating Extracellular Matrix.

作者信息

Sugiura Risa, Hamano Sayuri, Tomokiyo Atsushi, Hasegawa Daigaku, Yoshida Shinichiro, Sugii Hideki, Fujino Shoko, Adachi Orie, Kadowaki Masataka, Yamashita Daiki, Maeda Hidefumi

机构信息

Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, Japan.

OBT Research Center, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Biomedicines. 2022 Sep 22;10(10):2366. doi: 10.3390/biomedicines10102366.


DOI:10.3390/biomedicines10102366
PMID:36289626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9598762/
Abstract

Periodontal ligament stem cells (PDLSCs) play central roles in periodontal ligament (PDL) tissue homeostasis, repair, and regeneration. Previously, we established a protocol to differentiate human-induced pluripotent stem cell-derived neural crest-like cells (iNCs) into PDLSC-like cells (iPDLSCs) using human PDL cell-derived extracellular matrix (ECM). However, it remained unclear what factors principally regulate the differentiation of iNCs into iPDLSCs. In this study, we aimed to identify the transcription factor regulating production of human PDL cell-derived ECM, which is responsible for the generation of iPDLSCs. We cultured iNCs on ECMs of two human PDL cell lines (HPDLC-3S and HPDLC-3U) and of human dermal fibroblasts (HDF). iNCs cultured on HPDLC-3U demonstrated higher iPDLSC-associated gene expression and mesenchymal differentiation capacity than cells cultured on HDF or HPDLC-3S. The transcription factor was highly expressed in HPDLC-3U compared with HDF and HPDLC-3S. iNCs cultured on siPAX9-transfected HPDLC-3U displayed downregulation of iPDLSC-associated marker expression and adipocytic differentiation capacity relative to controls. Our findings suggest that PAX9 is one of the transcription factors regulating ECM production in human PDL cells, which is responsible for the differentiation of iNCs into iPDLSCs.

摘要

牙周膜干细胞(PDLSCs)在牙周膜(PDL)组织稳态、修复和再生中发挥核心作用。此前,我们建立了一种方案,利用人牙周膜细胞衍生的细胞外基质(ECM)将人诱导多能干细胞来源的神经嵴样细胞(iNCs)分化为牙周膜干细胞样细胞(iPDLSCs)。然而,尚不清楚哪些因素主要调节iNCs向iPDLSCs的分化。在本研究中,我们旨在鉴定调节人牙周膜细胞衍生的ECM产生的转录因子,该ECM负责iPDLSCs的生成。我们将iNCs培养在两种人牙周膜细胞系(HPDLC - 3S和HPDLC - 3U)以及人皮肤成纤维细胞(HDF)的ECM上。与培养在HDF或HPDLC - 3S上的细胞相比,培养在HPDLC - 3U上的iNCs表现出更高的iPDLSC相关基因表达和间充质分化能力。与HDF和HPDLC - 3S相比,转录因子PAX9在HPDLC - 3U中高表达。与对照组相比,培养在转染了siPAX9的HPDLC - 3U上的iNCs显示出iPDLSC相关标志物表达和脂肪细胞分化能力的下调。我们的研究结果表明,PAX9是调节人牙周膜细胞中ECM产生的转录因子之一,其负责iNCs向iPDLSCs的分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/1116fef45cbe/biomedicines-10-02366-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/6f3157fb3201/biomedicines-10-02366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/19c381860458/biomedicines-10-02366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/7a70ffabb590/biomedicines-10-02366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/63847617af9f/biomedicines-10-02366-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/b0ec7be21886/biomedicines-10-02366-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/dc3a82fe7c83/biomedicines-10-02366-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/1116fef45cbe/biomedicines-10-02366-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/6f3157fb3201/biomedicines-10-02366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/19c381860458/biomedicines-10-02366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/7a70ffabb590/biomedicines-10-02366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/63847617af9f/biomedicines-10-02366-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/b0ec7be21886/biomedicines-10-02366-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/dc3a82fe7c83/biomedicines-10-02366-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c200/9598762/1116fef45cbe/biomedicines-10-02366-g007.jpg

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
The Use of MSCs, iPSCs, and EVs in the Repair of Human MSK Tissues: Is Ultimate Success Dependent on Developing Excellent Implant Materials as Well as Creating an Optimal Environment for Implantation? What Is the Rationale for These Choices?

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[2]
Induction of periodontal ligament-derived mesenchymal stromal cell-like cells from human induced pluripotent stem cells.

Regen Ther. 2024-7-6

[3]
Microbial Poly(hydroxybutyrate-co-hydroxyvalerate) Scaffold for Periodontal Tissue Engineering.

Polymers (Basel). 2023-2-9

[4]
Current Application of iPS Cells in the Dental Tissue Regeneration.

Biomedicines. 2022-12-16

本文引用的文献

[1]
PAX9 in Cancer Development.

Int J Mol Sci. 2022-5-17

[2]
Single Cell RNA Sequencing Reveals Critical Functions of in Periodontal Ligament Homeostasis.

Front Cell Dev Biol. 2022-2-4

[3]
Secreted Frizzled-Related Protein 1 Promotes Odontoblastic Differentiation and Reparative Dentin Formation in Dental Pulp Cells.

Cells. 2021-9-21

[4]
The Nrf2 transcription factor: A multifaceted regulator of the extracellular matrix.

Matrix Biol Plus. 2021-2-20

[5]
The role of interleukin-6/interleukin-6 receptor signaling in the mechanical stress-induced extracellular matrix remodeling of bladder smooth muscle.

Arch Biochem Biophys. 2021-5-15

[6]
Pluripotent stem cell-based gene therapy approach: human de novo synthesized chromosomes.

Cell Mol Life Sci. 2021-2

[7]
A Modular Differentiation System Maps Multiple Human Kidney Lineages from Pluripotent Stem Cells.

Cell Rep. 2020-4-7

[8]
Extracellular matrix derived from human urine-derived stem cells enhances the expansion, adhesion, spreading, and differentiation of human periodontal ligament stem cells.

Stem Cell Res Ther. 2019-12-18

[9]
Extracellular matrix composition of connective tissues: a systematic review and meta-analysis.

Sci Rep. 2019-7-22

[10]
Generation of Human iPSC-Derived Intestinal Epithelial Cell Monolayers by CDX2 Transduction.

Cell Mol Gastroenterol Hepatol. 2019-6-19

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