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DNMTi@ZIF-8通过表观遗传调控增强仿生牙髓再生。

DNMTi@ZIF-8 Enhances Biomimetic Pulp Regeneration via Epigenetic Regulation.

作者信息

Li Z, Wan M, Cui D, Tian Q, Li Y, Yu S, Zheng L, Ye L

机构信息

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

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

出版信息

J Dent Res. 2025 Jul;104(7):743-752. doi: 10.1177/00220345251315468. Epub 2025 Mar 27.

Abstract

Regenerating the functional dentin-pulp complex remains a significant challenge in endodontics. Conventional regenerative endodontic therapies often result in the formation of non-pulp-like tissue due to the uncontrolled induction of stem cells and cytokines. Mimicking developmental processes to promote regeneration represents a promising yet challenging approach in regenerative medicine. This study aimed to develop a biomimetic regenerative therapy that integrates a DNMTi@ZIF-8 nanoplatform with dental pulp stem cell (DPSC) spheroids to effectively regenerate the dentin-pulp complex. First, a progressive reduction in 5-methylcytosine content was revealed to be a core signal in the odontogenic differentiation process. Based on this discovery, DNA methyltransferase inhibitors (DNMTi) were further used to simulate this regulatory process. The results showed that DNMTi not only significantly promoted odontogenic differentiation but also inhibited the angiogenesis process. To address this dual effect, in situ synthesized zeolitic imidazolate framework-8 (ZIF-8) was used for the delivery of DNMTi. This DNMTi@ZIF-8 system not only prolonged drug activity but also enhanced angiogenesis-promoting efficacy by activating the PI3K-AKT signaling pathway through the sustained release of zinc ions, assessed via angiogenic assays including scratch assays, tube formation assay, and chick chorioallantoic membrane assay. When integrated with DPSC spheroids engineered via agarose microwells, analyzed through odontogenic differentiation assays, this system demonstrated significantly enhanced odontogenic differentiation capabilities. Moreover, the introduced biomimetic regenerative therapy successfully regenerated the dentin-pulp complex in a semi-orthotopic in vivo model. This biomimetic developmental approach not only addresses critical gaps in dental tissue engineering but also highlights a new direction for treating pulp and periapical diseases, underscoring its broader implications in regenerative medicine.

摘要

在牙髓病学中,再生功能性牙本质-牙髓复合体仍然是一项重大挑战。传统的再生牙髓治疗常常由于干细胞和细胞因子的诱导不受控制而导致非牙髓样组织的形成。模仿发育过程以促进再生是再生医学中一种有前景但具有挑战性的方法。本研究旨在开发一种仿生再生疗法,将DNMTi@ZIF-8纳米平台与牙髓干细胞(DPSC)球状体整合,以有效再生牙本质-牙髓复合体。首先,5-甲基胞嘧啶含量的逐步降低被揭示为牙源性分化过程中的核心信号。基于这一发现,进一步使用DNA甲基转移酶抑制剂(DNMTi)来模拟这一调控过程。结果表明,DNMTi不仅显著促进牙源性分化,还抑制血管生成过程。为了解决这种双重作用,原位合成的沸石咪唑酯骨架-8(ZIF-8)被用于递送DNMTi。通过划痕试验、管形成试验和鸡胚绒毛尿囊膜试验等血管生成试验评估,该DNMTi@ZIF-8系统不仅延长了药物活性,还通过锌离子的持续释放激活PI3K-AKT信号通路增强了促血管生成功效。当与通过琼脂糖微孔工程化的DPSC球状体整合时,通过牙源性分化试验分析,该系统显示出显著增强的牙源性分化能力。此外,引入的仿生再生疗法在半原位体内模型中成功再生了牙本质-牙髓复合体。这种仿生发育方法不仅填补了牙科组织工程中的关键空白,还突出了治疗牙髓和根尖周疾病的新方向,强调了其在再生医学中的更广泛意义。

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