pulp–dentin complex regeneration

  • 文章类型: Journal Article
    生物活性陶瓷,主要由生物活性玻璃组成,玻璃陶瓷,正磷酸钙陶瓷,硅酸钙陶瓷和碳酸钙陶瓷,在过去的几十年中,由于它们的生物相容性和在刺激细胞增殖方面的优异生物活性,分化和组织再生。最近的研究试图将生物活性陶瓷与生物活性离子相结合,聚合物,生物活性蛋白质和其他化学物质,以改善其机械和生物学特性,从而使它们在组织工程支架中更有效。这篇综述介绍了生物活性陶瓷基材料在牙科中的有益性能和潜在应用。特别是在牙齿硬组织的修复和再生中,牙髓牙本质复合物,牙周组织和骨组织。此外,对生物活性陶瓷的机理和陶瓷基材料的发展提供了更多的见解。
    [方框:见正文]。
    Bioactive ceramics, primarily consisting of bioactive glasses, glass-ceramics, calcium orthophosphate ceramics, calcium silicate ceramics and calcium carbonate ceramics, have received great attention in the past decades given their biocompatible nature and excellent bioactivity in stimulating cell proliferation, differentiation and tissue regeneration. Recent studies have tried to combine bioactive ceramics with bioactive ions, polymers, bioactive proteins and other chemicals to improve their mechanical and biological properties, thus rendering them more valid in tissue engineering scaffolds. This review presents the beneficial properties and potential applications of bioactive ceramic-based materials in dentistry, particularly in the repair and regeneration of dental hard tissue, pulp-dentin complex, periodontal tissue and bone tissue. Moreover, greater insights into the mechanisms of bioactive ceramics and the development of ceramic-based materials are provided.
    [Box: see text].
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  • 文章类型: Journal Article
    牙髓炎是牙科诊所的常见病。尽管重要的牙髓治疗和根管治疗可以阻止炎症的进展,它们不允许牙髓牙本质复合物的真正结构再生和功能重建。近年来,随着组织工程和再生医学的发展,基于干细胞的再生牙髓治疗(RET)的研究取得了令人满意的初步结果,显着提高其临床转化前景。作为关键的旁分泌效应之一,外泌体在牙髓-牙本质复合体再生中的作用和功能得到了广泛的关注。由于它们的成本效益优势,来源广泛,良好的生物相容性,和高安全性,外泌体被认为是促进牙髓再生的有前途的治疗工具。因此,在这篇文章中,我们首先关注外泌体的生物学特性,包括它们的生物发生,摄取,隔离,和表征。然后,从细胞增殖的角度来看,迁移,牙本质发生,血管生成,和神经发生,我们的目的是揭示外泌体在再生牙髓中的作用和机制。最后,为说明外泌体应用于牙髓再生的临床策略和影响因素,例如亲代细胞的类型,亲本细胞的培养条件,外泌体浓度,和脚手架材料,试图为探索和促进基于外泌体的再生牙髓手术的治疗策略奠定坚实的基础。
    Pulpitis is a common and frequent disease in dental clinics. Although vital pulp therapy and root canal treatment can stop the progression of inflammation, they do not allow for genuine structural regeneration and functional reconstruction of the pulp-dentin complex. In recent years, with the development of tissue engineering and regenerative medicine, research on stem cell-based regenerative endodontic therapy (RET) has achieved satisfactory preliminary results, significantly enhancing its clinical translational prospects. As one of the crucial paracrine effectors, the roles and functions of exosomes in pulp-dentin complex regeneration have gained considerable attention. Due to their advantages of cost-effectiveness, extensive sources, favorable biocompatibility, and high safety, exosomes are considered promising therapeutic tools to promote dental pulp regeneration. Accordingly, in this article, we first focus on the biological properties of exosomes, including their biogenesis, uptake, isolation, and characterization. Then, from the perspectives of cell proliferation, migration, odontogenesis, angiogenesis, and neurogenesis, we aim to reveal the roles and mechanisms of exosomes involved in regenerative endodontics. Lastly, immense efforts are made to illustrate the clinical strategies and influencing factors of exosomes applied in dental pulp regeneration, such as types of parental cells, culture conditions of parent cells, exosome concentrations, and scaffold materials, in an attempt to lay a solid foundation for exploring and facilitating the therapeutic strategy of exosome-based regenerative endodontic procedures.
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  • 文章类型: Journal Article
    牙髓干细胞(DPSC)是一种间充质干细胞,可以分化为成牙本质细胞样细胞并保护牙髓。DPSC的分化可以受到体外或体内激活不同信号通路的生物材料或生长因子的影响。在这次审查中,我们总结了参与DPSCs牙源性分化的6个主要通路,Wnt信号通路,Smad信号通路,MAPK信号通路,NF-kB信号通路,PI3K/AKT/mTOR信号通路,和Notch信号通路。多种因素可以通过一个或多个信号通路影响DPSC的牙源性分化。通过了解这些信号通路之间的相互作用,我们可以扩大对牙髓牙本质复合体再生机制的认识。
    Dental pulp stem cells (DPSCs) are a type of mesenchymal stem cells that can differentiate into odontoblast-like cells and protect the pulp. The differentiation of DPSCs can be influenced by biomaterials or growth factors that activate different signaling pathways in vitro or in vivo. In this review, we summarized six major pathways involved in the odontogenic differentiation of DPSCs, Wnt signaling pathways, Smad signaling pathways, MAPK signaling pathways, NF-kB signaling pathways, PI3K/AKT/mTOR signaling pathways, and Notch signaling pathways. Various factors can influence the odontogenic differentiation of DPSCs through one or more signaling pathways. By understanding the interactions between these signaling pathways, we can expand our knowledge of the mechanisms underlying the regeneration of the pulp-dentin complex.
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