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

IF 5.7 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Z. Li, M. Wan, D. Cui, Q. Tian, Y. Li, S. Yu, L. Zheng, L. Ye
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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.
DNMTi@ZIF-8通过表观遗传调控增强仿生牙髓再生
再生功能性牙本质-牙髓复合体仍然是牙髓学的一个重大挑战。由于干细胞和细胞因子不受控制的诱导,传统的再生牙髓治疗经常导致非髓样组织的形成。模拟发育过程来促进再生是再生医学中一个有希望但又具有挑战性的方法。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)球体结合起来,有效地再生牙本质-牙髓复合体。首先,5-甲基胞嘧啶含量的逐渐减少被发现是牙源性分化过程中的核心信号。基于这一发现,DNA甲基转移酶抑制剂(DNMTi)被进一步用于模拟这一调控过程。结果表明,DNMTi不仅能显著促进牙源性分化,还能抑制血管生成过程。为了解决这种双重效应,原位合成的沸石咪唑酸框架-8 (ZIF-8)被用于递送DNMTi。该DNMTi@ZIF-8系统不仅延长了药物活性,而且通过锌离子的持续释放激活PI3K-AKT信号通路,增强了促进血管生成的功效,通过血管生成实验(包括划痕实验、管形成实验和鸡绒毛膜尿囊膜实验)进行了评估。当与琼脂糖微孔设计的DPSC球体集成时,通过牙源分化实验进行分析,该系统显示出显着增强的牙源分化能力。此外,引入的仿生再生疗法在半原位体内模型中成功地再生了牙本质-牙髓复合体。这种仿生发育方法不仅解决了牙组织工程的关键空白,而且突出了牙髓和根尖周疾病治疗的新方向,强调了其在再生医学中的广泛意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Dental Research
Journal of Dental Research 医学-牙科与口腔外科
CiteScore
15.30
自引率
3.90%
发文量
155
审稿时长
3-8 weeks
期刊介绍: The Journal of Dental Research (JDR) is a peer-reviewed scientific journal committed to sharing new knowledge and information on all sciences related to dentistry and the oral cavity, covering health and disease. With monthly publications, JDR ensures timely communication of the latest research to the oral and dental community.
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