Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada; Stem Cell Research Center, Tissue Engineering and Regenerative Medicine Institute, Tehran Central Branch, Islamic Azad University, Tehran, Islamic Republic of Iran.
Stem Cell Research Center, Tissue Engineering and Regenerative Medicine Institute, Tehran Central Branch, Islamic Azad University, Tehran, Islamic Republic of Iran; Department of Endodontics, Faculty of Dentistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Islamic Republic of Iran.
Dent Mater. 2023 Aug;39(8):718. doi: 10.1016/j.dental.2023.06.008. Epub 2023 Jun 29.
Injectable biomaterials that can completely fill the root canals and provide an appropriate environment will have potential application for pulp regeneration in endodontics. This study aimed to fabricate and characterize a novel injectable human amniotic membrane (HAM) hydrogel scaffold crosslinked with genipin, enabling the proliferation of Dental Pulp Stem Cells (DPSCs) and optimizing pulp regeneration.
HAM extracellular matrix (ECM) hydrogels (15, 22.5, and 30 mg/ml) crosslinked with different genipin concentrations (0, 0.1, 0.5, 1, 5, and 10 mM) were evaluated for mechanical properties, tooth discoloration, cell viability, and proliferation of DPSCs. The hydrogels were subcutaneously injected in rats to assess their immunogenicity. The hydrogels were applied in a root canal model and subcutaneously implanted in rats to determine their regenerative potential for eight weeks, and histological and immunostaining analyses were performed.
Hydrogels crosslinked with low genipin concentration demonstrated low tooth discoloration, but 0.1 mM genipin crosslinked hydrogels were excluded due to their unfavourable mechanical properties. The degradation ratio was lower in hydrogels crosslinked with 0.5 mM genipin. The 30 mg/ml-0.5 mM crosslinked hydrogel exhibited a microporous structure, and the modulus of elasticity was 1200 PA. In vitro, cell culture showed maximum viability and proliferation in 30 mg/ml-0.5 mM crosslinked hydrogel. All groups elicited minimum immunological responses, and highly vascularized pulp-like tissue was formed in human tooth roots in both groups with/without DPSCs.
Genipin crosslinking improved the biodegradability of injectable HAM hydrogels and conferred higher biocompatibility. Hydrogels encapsulated with DPSCs can support stem cell viability and proliferation. In addition, highly vascularized pulp-like tissue formation by this biomaterial displayed potential for pulp regeneration.
可完全填充根管并提供适宜环境的注射型生物材料将有望在牙髓再生的牙髓内应用。本研究旨在制备和表征一种新型的、用京尼平交联的可注射人羊膜(HAM)水凝胶支架,促进牙髓干细胞(DPSCs)的增殖,并优化牙髓再生。
评估不同浓度(0、0.1、0.5、1、5 和 10 mM)京尼平交联的 HAM 细胞外基质(ECM)水凝胶(15、22.5 和 30 mg/ml)的机械性能、牙齿变色、DPSCs 活力和增殖。将水凝胶皮下注射到大鼠体内以评估其免疫原性。将水凝胶应用于根管模型,并皮下植入大鼠体内 8 周,以确定其再生潜力,并进行组织学和免疫染色分析。
低浓度京尼平交联的水凝胶表现出低牙齿变色,但由于机械性能不佳,排除了 0.1 mM 京尼平交联的水凝胶。交联度为 0.5 mM 的水凝胶降解率较低。30 mg/ml-0.5 mM 交联水凝胶具有微孔结构,弹性模量为 1200 PA。在体外,细胞培养显示在 30 mg/ml-0.5 mM 交联水凝胶中具有最大的活力和增殖。所有组均引起最小的免疫反应,并且在载有/未载有 DPSCs 的人牙根中均形成了高度血管化的牙髓样组织。
京尼平交联提高了可注射 HAM 水凝胶的生物降解性,并赋予了更高的生物相容性。DPSCs 包封的水凝胶可支持干细胞活力和增殖。此外,该生物材料形成的高度血管化牙髓样组织显示出牙髓再生的潜力。