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生物矿化启发的矿化水凝胶促进牙本质/骨硬组织的修复和再生。

Biomineralization-inspired mineralized hydrogel promotes the repair and regeneration of dentin/bone hard tissue.

作者信息

Wen Bo, Dai Yuguo, Han Xue, Huo Fangjun, Xie Li, Yu Mei, Wang Yuru, An Ning, Li Zhonghan, Guo Weihua

机构信息

State Key Laboratory of Oral Disease & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.

National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.

出版信息

NPJ Regen Med. 2023 Feb 25;8(1):11. doi: 10.1038/s41536-023-00286-3.


DOI:10.1038/s41536-023-00286-3
PMID:36841873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9968336/
Abstract

Maxillofacial hard tissue defects caused by trauma or infection often affect craniofacial function. Taking the natural hard tissue structure as a template, constructing an engineered tissue repair module is an important scheme to realize the functional regeneration and repair of maxillofacial hard tissue. Here, inspired by the biomineralization process, we constructed a composite mineral matrix hydrogel PAA-CMC-TDM containing amorphous calcium phosphates (ACPs), polyacrylic acid (PAA), carboxymethyl chitosan (CMC) and dentin matrix (TDM). The dynamic network composed of Ca·COO coordination and ACPs made the hydrogel loaded with TDM, and exhibited self-repairing ability and injectability. The mechanical properties of PAA-CMC-TDM can be regulated, but the functional activity of TDM remains unaffected. Cytological studies and animal models of hard tissue defects show that the hydrogel can promote the odontogenesis or osteogenic differentiation of mesenchymal stem cells, adapt to irregular hard tissue defects, and promote in situ regeneration of defective tooth and bone tissues. In summary, this paper shows that the injectable TDM hydrogel based on biomimetic mineralization theory can induce hard tissue formation and promote dentin/bone regeneration.

摘要

由创伤或感染引起的颌面硬组织缺损常影响颅面功能。以天然硬组织结构为模板,构建工程化组织修复模块是实现颌面硬组织功能再生与修复的重要方案。在此,受生物矿化过程启发,我们构建了一种复合矿物基质水凝胶PAA-CMC-TDM,其包含无定形磷酸钙(ACP)、聚丙烯酸(PAA)、羧甲基壳聚糖(CMC)和牙本质基质(TDM)。由Ca·COO配位和ACP组成的动态网络使水凝胶负载TDM,并表现出自我修复能力和可注射性。PAA-CMC-TDM的力学性能可被调控,但TDM的功能活性不受影响。硬组织缺损的细胞学研究和动物模型表明,该水凝胶可促进间充质干细胞的成牙或成骨分化,适应不规则硬组织缺损,并促进缺损牙齿和骨组织的原位再生。综上所述,本文表明基于仿生矿化理论的可注射TDM水凝胶可诱导硬组织形成并促进牙本质/骨再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/21266fbbb440/41536_2023_286_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/06a6687c446b/41536_2023_286_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/9ed1854b2728/41536_2023_286_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/8a427f6f9516/41536_2023_286_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/63264d5bbece/41536_2023_286_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/1c00d0ba0c94/41536_2023_286_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/60c9448e461d/41536_2023_286_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/e701cd8512c0/41536_2023_286_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/3738c9c8b1f2/41536_2023_286_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/c82870973859/41536_2023_286_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/21266fbbb440/41536_2023_286_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/06a6687c446b/41536_2023_286_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/9ed1854b2728/41536_2023_286_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/8a427f6f9516/41536_2023_286_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/63264d5bbece/41536_2023_286_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/1c00d0ba0c94/41536_2023_286_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/60c9448e461d/41536_2023_286_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/e701cd8512c0/41536_2023_286_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/3738c9c8b1f2/41536_2023_286_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/c82870973859/41536_2023_286_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8145/9968336/21266fbbb440/41536_2023_286_Fig10_HTML.jpg

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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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本文引用的文献

[1]
A review on design of scaffold for osteoinduction: Toward the unification of independent design variables.

Biomech Model Mechanobiol. 2023-2

[2]
Dentin Particulate for Bone Regeneration: An In Vitro Study.

Int J Mol Sci. 2022-8-18

[3]
Demineralized Dentin Matrix for Dental and Alveolar Bone Tissues Regeneration: An Innovative Scope Review.

Tissue Eng Regen Med. 2022-8

[4]
Cells and material-based strategies for regenerative endodontics.

Bioact Mater. 2021-11-30

[5]
Mesenchymal Stem Cell-Immune Cell Interaction and Related Modulations for Bone Tissue Engineering.

Stem Cells Int. 2022-2-1

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Bone tissue engineering: Anionic polysaccharides as promising scaffolds.

Carbohydr Polym. 2022-5-1

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Biotechnol J. 2022-4

[8]
High-Strength and Injectable Supramolecular Hydrogel Self-Assembled by Monomeric Nucleoside for Tooth-Extraction Wound Healing.

Adv Mater. 2022-4

[9]
Experimental study on the biocompatibility and osteogenesis induction ability of PLLA/DDM scaffolds.

Odontology. 2022-7

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Emerging concepts in bone repair and the premise of soft materials.

Curr Opin Biotechnol. 2022-4

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