牙细胞片仿生牙胚模型

Dental cell sheet biomimetic tooth bud model.

作者信息

Monteiro Nelson, Smith Elizabeth E, Angstadt Shantel, Zhang Weibo, Khademhosseini Ali, Yelick Pamela C

机构信息

Department of Orthodontics, Division of Craniofacial and Molecular Genetics, Tufts University, 136 Harrison Avenue, M824, Boston, MA 02111, USA.

Division of Health Sciences and Technology, Harvard-MIT, Biomaterials Innovations Research Center, Division of Biomedical Engineering, Brigham and Women's Hospital, Harvard Medical School, 65 Landsdowne Street Cambridge, MA 02139, USA.

出版信息

Biomaterials. 2016 Nov;106:167-79. doi: 10.1016/j.biomaterials.2016.08.024. Epub 2016 Aug 17.

Abstract

Tissue engineering and regenerative medicine technologies offer promising therapies for both medicine and dentistry. Our long-term goal is to create functional biomimetic tooth buds for eventual tooth replacement in humans. Here, our objective was to create a biomimetic 3D tooth bud model consisting of dental epithelial (DE) - dental mesenchymal (DM) cell sheets (CSs) combined with biomimetic enamel organ and pulp organ layers created using GelMA hydrogels. Pig DE or DM cells seeded on temperature-responsive plates at various cell densities (0.02, 0.114 and 0.228 cells 10(6)/cm(2)) and cultured for 7, 14 and 21 days were used to generate DE and DM cell sheets, respectively. Dental CSs were combined with GelMA encapsulated DE and DM cell layers to form bioengineered 3D tooth buds. Biomimetic 3D tooth bud constructs were cultured in vitro, or implanted in vivo for 3 weeks. Analyses were performed using micro-CT, H&E staining, polarized light (Pol) microscopy, immunofluorescent (IF) and immunohistochemical (IHC) analyses. H&E, IHC and IF analyses showed that in vitro cultured multilayered DE-DM CSs expressed appropriate tooth marker expression patterns including SHH, BMP2, RUNX2, tenascin and syndecan, which normally direct DE-DM interactions, DM cell condensation, and dental cell differentiation. In vivo implanted 3D tooth bud constructs exhibited mineralized tissue formation of specified size and shape, and SHH, BMP2 and RUNX2and dental cell differentiation marker expression. We propose our biomimetic 3D tooth buds as models to study optimized DE-DM cell interactions leading to functional biomimetic replacement tooth formation.

摘要

组织工程和再生医学技术为医学和牙科提供了有前景的治疗方法。我们的长期目标是创建功能性仿生牙胚,以便最终在人类中进行牙齿替换。在此,我们的目标是创建一个仿生三维牙胚模型,该模型由牙上皮(DE)-牙间充质(DM)细胞片(CSs)与使用甲基丙烯酰化明胶(GelMA)水凝胶创建的仿生釉器和牙髓器层组成。将猪的DE或DM细胞以不同细胞密度(0.02、0.114和0.228×10⁶个细胞/cm²)接种在温度响应板上,并分别培养7、14和21天,以生成DE和DM细胞片。将牙CSs与GelMA包裹的DE和DM细胞层结合,形成生物工程三维牙胚。将仿生三维牙胚构建体进行体外培养,或体内植入3周。使用微型计算机断层扫描(micro-CT)、苏木精-伊红(H&E)染色、偏振光(Pol)显微镜、免疫荧光(IF)和免疫组织化学(IHC)分析进行检测。H&E、IHC和IF分析表明,体外培养的多层DE-DM CSs表达了适当的牙齿标记物表达模式,包括音猬因子(SHH)、骨形态发生蛋白2(BMP2)、 Runt相关转录因子2(RUNX2)、腱生蛋白和多功能蛋白聚糖,这些通常指导DE-DM相互作用、DM细胞凝聚和牙细胞分化。体内植入的三维牙胚构建体表现出特定大小和形状的矿化组织形成,以及SHH、BMP2和RUNX2以及牙细胞分化标记物的表达。我们提出将我们的仿生三维牙胚作为模型,以研究导致功能性仿生替换牙形成的优化DE-DM细胞相互作用。

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